diff --git a/src/ontology/modules/administration.owl b/src/ontology/modules/administration.owl
index c0141b5e..0ad3c632 100644
--- a/src/ontology/modules/administration.owl
+++ b/src/ontology/modules/administration.owl
@@ -177,7 +177,7 @@
intraperitoneal injection
- is the injection of a material entity (bearing the administered substance role) into the peritoneum (bearing the target role) of an organism using a syringe
+ is the injection of a material entity (bearing the administered substance role) into the peritoneum (bearing the target role) of an organism using a syringe
BP
intraperitoneal injection
@@ -222,7 +222,7 @@
intraperitoneal administration
Rats were injected intraperitoneally with either rrIL-6 (250 ng/0.5 ml) or equal-volume sterile saline twice within an interval of 24 h
- The administration of a substance into the peritoneum of an organism
+ The administration of a substance into the peritoneum of an organism
Person:Bjoern Peters
intraperitoneal administration
@@ -270,7 +270,7 @@
oral ingestion of pill
- An adding a material entity to target with the entity is a pill and the target is the mouth
+ An adding a material entity to target with the entity is a pill and the target is the mouth
Person:Alan Ruttenberg
2009/09/28 Alan Ruttenberg. Fucoidan-use-case
oral ingestion of pill
@@ -323,7 +323,7 @@
intramuscular injection
- is the injection of a material entity (bearing the administered substance role) into the muscle (bearing the target role) of an organism using a syringe
+ is the injection of a material entity (bearing the administered substance role) into the muscle (bearing the target role) of an organism using a syringe
intramuscular injection
@@ -368,7 +368,7 @@
intradermal injection
- is the injection of a material entity (bearing the administered substance role) into the dermis (bearing the target role) of an organism using a syringe
+ is the injection of a material entity (bearing the administered substance role) into the dermis (bearing the target role) of an organism using a syringe
PERSON: Melanie Courtot
intradermal injection
@@ -400,7 +400,7 @@
oral administration
- An administering substance in vivo into the mouth of an organism
+ An administering substance in vivo into the mouth of an organism
PERSON: Melanie Courtot
oral administration
@@ -446,7 +446,7 @@
subcutaneous injection
- is the injection of a material entity (bearing the administered substance role) into the hypodermis (bearing the target role) of an organism using a syringe
+ is the injection of a material entity (bearing the administered substance role) into the hypodermis (bearing the target role) of an organism using a syringe
PERSON: Melanie Courtot
subcutaneous injection
@@ -478,7 +478,7 @@
intranasal mucosal administration
- The administration of a substance into the intranasal mucosis of an organism
+ The administration of a substance into the intranasal mucosis of an organism
PERSON: Melanie Courtot
intranasal mucosal administration
@@ -524,7 +524,7 @@
intravenous injection
- is the injection of a material entity (bearing the administered substance role) into the vein (bearing the target role) of an organism using a syringe
+ is the injection of a material entity (bearing the administered substance role) into the vein (bearing the target role) of an organism using a syringe
PERSON: Melanie Courtot
intravenous injection
@@ -553,7 +553,7 @@
passive immunization
Giving VIG (concentrated antibodies from vaccinated donors) to a patient that is infected with smallpox. Transferring epitope specific T cells from one mouse into another.
- The injection of immune effector material (antibodies, T cells or B cells) into an organism so that the organisms immune system gains its immune effector function to recognize specific antigens.
+ The injection of immune effector material (antibodies, T cells or B cells) into an organism so that the organisms immune system gains its immune effector function to recognize specific antigens.
PERSON: Bjoern Peters, Randi Vita, Jason Greenbaum
adoptive transfer
passive immunization
@@ -582,7 +582,7 @@
antibiotic administration process
- Administering substance in vivo where an antibiotic substance is administered to a living organism.
+ Administering substance in vivo where an antibiotic substance is administered to a living organism.
Chris Stoeckert
Cristian Cocos
Jie Zheng
@@ -602,7 +602,7 @@
- An administration of substance in vivo with the intention to induce disease in the organism.
+ An administration of substance in vivo with the intention to induce disease in the organism.
IEDB
IEDB
administering substance in vivo to cause disease
@@ -628,7 +628,7 @@
- An administration of substance in vivo with the intention to reduce the symptoms of or prevent development of a disease in the organism.
+ An administration of substance in vivo with the intention to reduce the symptoms of or prevent development of a disease in the organism.
IEDB
IEDB
administering substance in vivo to reduce or prevent disease
@@ -641,7 +641,7 @@
in vivo challenge
- The administration of a challenge to a live host.
+ The administration of a challenge to a live host.
Hector Guzman-Orozco
IEDB
in vivo challenge
@@ -669,7 +669,7 @@
- An administration of a substance into the stomach of an organism.
+ An administration of a substance into the stomach of an organism.
Sebastian Duesing
https://github.com/obi-ontology/obi/issues/1703
intragastric administration
@@ -697,7 +697,7 @@
- An administration of a substance into the colon of an organism.
+ An administration of a substance into the colon of an organism.
Sebastian Duesing
https://github.com/obi-ontology/obi/issues/1703
intracolonic administration
@@ -725,7 +725,7 @@
- An administration of a substance into the vagina of an organism.
+ An administration of a substance into the vagina of an organism.
Sebastian Duesing
https://github.com/obi-ontology/obi/issues/1703
vaginal administration
@@ -753,7 +753,7 @@
- An administration of a substance onto the surface of the skin of an organism.
+ An administration of a substance onto the surface of the skin of an organism.
Sebastian Duesing
percutaneous administration
transcutaneous administration
@@ -783,7 +783,7 @@
- An administration of a substance to the cervix of an organism.
+ An administration of a substance to the cervix of an organism.
Sebastian Duesing
https://github.com/obi-ontology/obi/issues/1703
cervical administration
@@ -811,7 +811,7 @@
- An administration of a substance to the conjunctiva of an organism.
+ An administration of a substance to the conjunctiva of an organism.
Sebastian Duesing
https://github.com/obi-ontology/obi/issues/1703
conjunctival administration
@@ -839,7 +839,7 @@
- An administration of a substance into the trachea of an organism.
+ An administration of a substance into the trachea of an organism.
Sebastian Duesing
https://github.com/obi-ontology/obi/issues/1703
intratracheal administration
@@ -867,7 +867,7 @@
- An administration of a substance into the amnion of an organism.
+ An administration of a substance into the amnion of an organism.
Sebastian Duesing
https://github.com/obi-ontology/obi/issues/1703
intra-amniotic administration
@@ -895,7 +895,7 @@
- An administration of a substance into the artery of an organism.
+ An administration of a substance into the artery of an organism.
Sebastian Duesing
https://github.com/obi-ontology/obi/issues/1703
intra-arterial administration
@@ -923,7 +923,7 @@
- An administration of a substance into the cerebrum of an organism.
+ An administration of a substance into the cerebrum of an organism.
Sebastian Duesing
https://github.com/obi-ontology/obi/issues/1703
intracerebral administration
@@ -951,7 +951,7 @@
- An administration of a substance into the cranium of an organism.
+ An administration of a substance into the cranium of an organism.
Sebastian Duesing
https://github.com/obi-ontology/obi/issues/1703
intracranial administration
@@ -979,7 +979,7 @@
- An administration of a substance into the epidermis of an organism.
+ An administration of a substance into the epidermis of an organism.
Sebastian Duesing
https://github.com/obi-ontology/obi/issues/1703
intraepidermal administration
@@ -1012,7 +1012,7 @@
- An administration of a substance into the lymphatic system of an organism.
+ An administration of a substance into the lymphatic system of an organism.
Sebastian Duesing
https://github.com/obi-ontology/obi/issues/1703
intralymphatic administration
@@ -1040,7 +1040,7 @@
- An intralymphatic administration in which the substance is administered into a lymph node.
+ An intralymphatic administration in which the substance is administered into a lymph node.
Sebastian Duesing
https://github.com/obi-ontology/obi/issues/1703
lymph node administration
@@ -1068,7 +1068,7 @@
- An administration of a substance into the urethra of an organism.
+ An administration of a substance into the urethra of an organism.
Sebastian Duesing
https://github.com/obi-ontology/obi/issues/1703
urethral administration
@@ -1102,7 +1102,7 @@
- An intraepidermal administration in which the skin is scratched before the substance is administered to the skin.
+ An intraepidermal administration in which the skin is scratched before the substance is administered to the skin.
Sebastian Duesing
https://github.com/obi-ontology/obi/issues/1703
skin scarification administration
@@ -1130,7 +1130,7 @@
- An adminstration of a substance into the uterus of an organism.
+ An adminstration of a substance into the uterus of an organism.
Sebastian Duesing
https://github.com/obi-ontology/obi/issues/1703
intrauteral administration
@@ -1158,7 +1158,7 @@
- An intra-arterial administration in which the substance is administered into the carotid artery.
+ An intra-arterial administration in which the substance is administered into the carotid artery.
Sebastian Duesing
i.c.
i.c. administration
@@ -1188,7 +1188,7 @@
- An administration of a substance to the eye of an organism.
+ An administration of a substance to the eye of an organism.
Sebastian Duesing
https://github.com/obi-ontology/obi/issues/1703
intraocular administration
@@ -1216,7 +1216,7 @@
- An administration of a substance into the placenta of an organism.
+ An administration of a substance into the placenta of an organism.
Sebastian Duesing
https://github.com/obi-ontology/obi/issues/1703
intraplacental administration
@@ -1244,7 +1244,7 @@
- An administration of a substance into the rectum of an organism.
+ An administration of a substance into the rectum of an organism.
Sebastian Duesing
https://github.com/obi-ontology/obi/issues/1703
intrarectal administration
@@ -1272,7 +1272,7 @@
- An administration of a substance into the spleen of an organism.
+ An administration of a substance into the spleen of an organism.
Sebastian Duesing
https://github.com/obi-ontology/obi/issues/1703
intrasplenic administration
@@ -1306,7 +1306,7 @@
- An administration of a substance into a tumor of an organism.
+ An administration of a substance into a tumor of an organism.
Sebastian Duesing
intratumoral administration
@@ -1364,7 +1364,7 @@
administration in vivo with infectious agent
- is an administration of an infectious agent to a host organism
+ is an administration of an infectious agent to a host organism
IEDB
IEDB
administration in vivo with infectious agent
diff --git a/src/ontology/modules/antibody-purification.owl b/src/ontology/modules/antibody-purification.owl
index 6f796e67..2bdaa098 100644
--- a/src/ontology/modules/antibody-purification.owl
+++ b/src/ontology/modules/antibody-purification.owl
@@ -286,7 +286,7 @@
- An antibody purification of MHC protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of MHC class I protein complex, while others contain impurities and are not of interest.
+ An antibody purification of MHC protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of MHC class I protein complex, while others contain impurities and are not of interest.
Randi Vita
Sebastian Duesing
Randi Vita
@@ -309,7 +309,7 @@
- An antibody purification of MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of human MHC class I protein complex, while others contain impurities and are not of interest.
+ An antibody purification of MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of human MHC class I protein complex, while others contain impurities and are not of interest.
Randi Vita
Sebastian Duesing
Randi Vita
@@ -332,7 +332,7 @@
- An antibody purification of human MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of HLA protein complex with A2 serotype, while others contain impurities and are not of interest.
+ An antibody purification of human MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of HLA protein complex with A2 serotype, while others contain impurities and are not of interest.
Randi Vita
Sebastian Duesing
Randi Vita
@@ -355,7 +355,7 @@
- An antibody purification of human MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of HLA protein complex with A24 serotype, while others contain impurities and are not of interest.
+ An antibody purification of human MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of HLA protein complex with A24 serotype, while others contain impurities and are not of interest.
Randi Vita
Sebastian Duesing
Randi Vita
@@ -385,7 +385,7 @@
- An antibody purification of human MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of HLA protein complex with A2 serotype and/or HLA protein complex with A28 serotype, while others contain impurities and are not of interest.
+ An antibody purification of human MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of HLA protein complex with A2 serotype and/or HLA protein complex with A28 serotype, while others contain impurities and are not of interest.
Randi Vita
Sebastian Duesing
Randi Vita
@@ -408,7 +408,7 @@
- An antibody purification of human MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of HLA protein complex with A29 serotype, while others contain impurities and are not of interest.
+ An antibody purification of human MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of HLA protein complex with A29 serotype, while others contain impurities and are not of interest.
Randi Vita
Sebastian Duesing
Randi Vita
@@ -431,7 +431,7 @@
- An antibody purification of human MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of HLA protein complex with B27 serotype, while others contain impurities and are not of interest.
+ An antibody purification of human MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of HLA protein complex with B27 serotype, while others contain impurities and are not of interest.
Randi Vita
Sebastian Duesing
Randi Vita
@@ -454,7 +454,7 @@
- An antibody purification of human MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of HLA-C protein complex, while others contain impurities and are not of interest.
+ An antibody purification of human MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of HLA-C protein complex, while others contain impurities and are not of interest.
Randi Vita
Sebastian Duesing
Randi Vita
@@ -477,7 +477,7 @@
- An antibody purification of MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of pig MHC class I protein complex, while others contain impurities and are not of interest.
+ An antibody purification of MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of pig MHC class I protein complex, while others contain impurities and are not of interest.
Randi Vita
Sebastian Duesing
Randi Vita
@@ -500,7 +500,7 @@
- An antibody purification of MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of cattle MHC class I protein complex, while others contain impurities and are not of interest.
+ An antibody purification of MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of cattle MHC class I protein complex, while others contain impurities and are not of interest.
Randi Vita
Sebastian Duesing
Randi Vita
@@ -523,7 +523,7 @@
- An antibody purification of MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of rat MHC class I protein complex, while others contain impurities and are not of interest.
+ An antibody purification of MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of rat MHC class I protein complex, while others contain impurities and are not of interest.
Randi Vita
Sebastian Duesing
Randi Vita
@@ -546,7 +546,7 @@
- An antibody purification of MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of mouse MHC class I protein complex, while others contain impurities and are not of interest.
+ An antibody purification of MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of mouse MHC class I protein complex, while others contain impurities and are not of interest.
Randi Vita
Sebastian Duesing
Randi Vita
@@ -569,7 +569,7 @@
- An antibody purification of mouse MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of H2-Dd protein complex, while others contain impurities and are not of interest.
+ An antibody purification of mouse MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of H2-Dd protein complex, while others contain impurities and are not of interest.
Randi Vita
Sebastian Duesing
Randi Vita
@@ -592,7 +592,7 @@
- An antibody purification of mouse MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of H2-Db protein complex, while others contain impurities and are not of interest.
+ An antibody purification of mouse MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of H2-Db protein complex, while others contain impurities and are not of interest.
Randi Vita
Sebastian Duesing
Randi Vita
@@ -615,7 +615,7 @@
- An antibody purification of mouse MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of H2-Kd protein complex, while others contain impurities and are not of interest.
+ An antibody purification of mouse MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of H2-Kd protein complex, while others contain impurities and are not of interest.
Randi Vita
Sebastian Duesing
Randi Vita
@@ -646,7 +646,7 @@
- An antibody purification of mouse MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of H2-Ld protein complex, H2-Db protein complex, and/or H2-Dq protein complex while others contain impurities and are not of interest.
+ An antibody purification of mouse MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of H2-Ld protein complex, H2-Db protein complex, and/or H2-Dq protein complex while others contain impurities and are not of interest.
Randi Vita
Sebastian Duesing
Randi Vita
@@ -676,7 +676,7 @@
- An antibody purification of mouse MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of H2-Dd protein complex and/or H2-Kd protein complex while others contain impurities and are not of interest.
+ An antibody purification of mouse MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of H2-Dd protein complex and/or H2-Kd protein complex while others contain impurities and are not of interest.
Randi Vita
Sebastian Duesing
Randi Vita
@@ -706,7 +706,7 @@
- An antibody purification of mouse MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of mouse MHC class I protein complex with H2-b haplotype and/or mouse MHC protein complex with H2-p haplotype while others contain impurities and are not of interest.
+ An antibody purification of mouse MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of mouse MHC class I protein complex with H2-b haplotype and/or mouse MHC protein complex with H2-p haplotype while others contain impurities and are not of interest.
Randi Vita
Sebastian Duesing
Randi Vita
@@ -737,7 +737,7 @@
- An antibody purification of mouse MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of mouse H2-Kb protein complex, H2-Ks protein complex, and/or H2-Kq protein complex while others contain impurities and are not of interest.
+ An antibody purification of mouse MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of mouse H2-Kb protein complex, H2-Ks protein complex, and/or H2-Kq protein complex while others contain impurities and are not of interest.
Randi Vita
Sebastian Duesing
Randi Vita
@@ -768,7 +768,7 @@
- An antibody purification of MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of pig MHC class I protein complex, cattle MHC class I protein complex, and/or human MHC class I protein complex, while others contain impurities and are not of interest.
+ An antibody purification of MHC class I protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of pig MHC class I protein complex, cattle MHC class I protein complex, and/or human MHC class I protein complex, while others contain impurities and are not of interest.
Randi Vita
Sebastian Duesing
Randi Vita
@@ -791,7 +791,7 @@
- An antibody purification of MHC protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of MHC class II protein complex, while others contain impurities and are not of interest.
+ An antibody purification of MHC protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of MHC class II protein complex, while others contain impurities and are not of interest.
Randi Vita
Sebastian Duesing
Randi Vita
@@ -814,7 +814,7 @@
- An antibody purification of MHC class II protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of cattle MHC class II protein complex, while others contain impurities and are not of interest.
+ An antibody purification of MHC class II protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of cattle MHC class II protein complex, while others contain impurities and are not of interest.
Randi Vita
Sebastian Duesing
Randi Vita
@@ -837,7 +837,7 @@
- An antibody purification of MHC class II protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of human MHC class II protein complex, while others contain impurities and are not of interest.
+ An antibody purification of MHC class II protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of human MHC class II protein complex, while others contain impurities and are not of interest.
Randi Vita
Sebastian Duesing
Randi Vita
@@ -860,7 +860,7 @@
- An antibody purification of human MHC class II protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of HLA-DP protein complex, while others contain impurities and are not of interest.
+ An antibody purification of human MHC class II protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of HLA-DP protein complex, while others contain impurities and are not of interest.
Randi Vita
Sebastian Duesing
Randi Vita
@@ -883,7 +883,7 @@
- An antibody purification of human MHC class II protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of HLA-DR protein complex, while others contain impurities and are not of interest.
+ An antibody purification of human MHC class II protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of HLA-DR protein complex, while others contain impurities and are not of interest.
Randi Vita
Sebastian Duesing
Randi Vita
@@ -906,7 +906,7 @@
- An antibody purification of human MHC class II protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of HLA protein complex with DQ3 serotype, while others contain impurities and are not of interest.
+ An antibody purification of human MHC class II protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of HLA protein complex with DQ3 serotype, while others contain impurities and are not of interest.
Randi Vita
Sebastian Duesing
Randi Vita
@@ -929,7 +929,7 @@
- An antibody purification of MHC class II protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of mouse MHC class II protein complex, while others contain impurities and are not of interest.
+ An antibody purification of MHC class II protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of mouse MHC class II protein complex, while others contain impurities and are not of interest.
Randi Vita
Sebastian Duesing
Randi Vita
@@ -952,7 +952,7 @@
- An antibody purification of mouse MHC class II protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of H2-IA protein complex, while others contain impurities and are not of interest.
+ An antibody purification of mouse MHC class II protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of H2-IA protein complex, while others contain impurities and are not of interest.
Randi Vita
Sebastian Duesing
Randi Vita
@@ -975,7 +975,7 @@
- An antibody purification of mouse MHC class II protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of H2-IAg7 protein complex, while others contain impurities and are not of interest.
+ An antibody purification of mouse MHC class II protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of H2-IAg7 protein complex, while others contain impurities and are not of interest.
Randi Vita
Sebastian Duesing
Randi Vita
@@ -998,7 +998,7 @@
- An antibody purification of mouse MHC class II protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of H2-IAd protein complex, while others contain impurities and are not of interest.
+ An antibody purification of mouse MHC class II protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of H2-IAd protein complex, while others contain impurities and are not of interest.
Randi Vita
Sebastian Duesing
Randi Vita
@@ -1028,7 +1028,7 @@
- An antibody purification of MHC class II protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of mouse MHC class II protein complex and/or rat MHC class II protein complex with RT1-A haplotype, while others contain impurities and are not of interest.
+ An antibody purification of MHC class II protein complex to separate a material entity into different compositions of which one fraction contains a higher concentration of mouse MHC class II protein complex and/or rat MHC class II protein complex with RT1-A haplotype, while others contain impurities and are not of interest.
Randi Vita
Sebastian Duesing
Randi Vita
diff --git a/src/ontology/modules/biobank-specimens.owl b/src/ontology/modules/biobank-specimens.owl
index a10afdaf..01aa098a 100644
--- a/src/ontology/modules/biobank-specimens.owl
+++ b/src/ontology/modules/biobank-specimens.owl
@@ -166,7 +166,7 @@
- A specimen that is derived from amniotic fluid.
+ A specimen that is derived from amniotic fluid.
Chris Stoeckert
Chris Stoeckert, Penn Medicine Biobank
amniotic fluid specimen
@@ -206,7 +206,7 @@
- A specimen that is derived from bile.
+ A specimen that is derived from bile.
Chris Stoeckert
Chris Stoeckert, Penn Medicine Biobank
bile specimen
@@ -246,7 +246,7 @@
- A specimen that is derived from cerbrospinal fluid.
+ A specimen that is derived from cerbrospinal fluid.
Chris Stoeckert
Chris Stoeckert, Penn Medicine Biobank
cerebrospinal fluid specimen
@@ -286,7 +286,7 @@
- A specimen that is derived from feces.
+ A specimen that is derived from feces.
Chris Stoeckert
stool specimen
Chris Stoeckert, Penn Medicine Biobank
@@ -327,7 +327,7 @@
- A specimen that is derived from digestive system fluid or secretion.
+ A specimen that is derived from digestive system fluid or secretion.
Chris Stoeckert
gastric fluid specimen
Chris Stoeckert, Penn Medicine Biobank
@@ -368,7 +368,7 @@
- A specimen that is derived from milk.
+ A specimen that is derived from milk.
Chris Stoeckert
Chris Stoeckert, Penn Medicine Biobank
milk specimen
@@ -408,7 +408,7 @@
- A specimen that is derived from pericardial fluid.
+ A specimen that is derived from pericardial fluid.
Chris Stoeckert
Chris Stoeckert, Penn Medicine Biobank
pericardial fluid specimen
@@ -448,7 +448,7 @@
- A specimen that is derived from saliva.
+ A specimen that is derived from saliva.
Chris Stoeckert
Chris Stoeckert, Penn Medicine Biobank
saliva specimen
@@ -488,7 +488,7 @@
- A specimen that is derived from sputum.
+ A specimen that is derived from sputum.
Chris Stoeckert
Chris Stoeckert, Penn Medicine Biobank
sputum specimen
@@ -528,7 +528,7 @@
- A specimen that is derived from sweat.
+ A specimen that is derived from sweat.
Chris Stoeckert
Chris Stoeckert, Penn Medicine Biobank
sweat specimen
@@ -568,7 +568,7 @@
- A specimen that is derived from synovial fluid.
+ A specimen that is derived from synovial fluid.
Chris Stoeckert
Chris Stoeckert, Penn Medicine Biobank
synovial fluid specimen
@@ -618,7 +618,7 @@
- A specimen that is derived from vireous humor.
+ A specimen that is derived from vireous humor.
Chris Stoeckert
vitreous fluid specimen
Chris Stoeckert, Penn Medicine Biobank
@@ -659,7 +659,7 @@
- A specimen that is derived from bone marrow.
+ A specimen that is derived from bone marrow.
Chris Stoeckert
Chris Stoeckert, Penn Medicine Biobank
bone marrow specimen
@@ -709,7 +709,7 @@
- A specimen that is derived from placenta.
+ A specimen that is derived from placenta.
Chris Stoeckert
Chris Stoeckert, Penn Medicine Biobank
placenta specimen
@@ -749,7 +749,7 @@
- A specimen that is derived from peritoneal fluid.
+ A specimen that is derived from peritoneal fluid.
Chris Stoeckert
Chris Stoeckert, Penn Medicine Biobank
peritoneal fluid specimen
@@ -789,7 +789,7 @@
- A specimen that is derived from pleural fluid.
+ A specimen that is derived from pleural fluid.
Chris Stoeckert
Chris Stoeckert, Penn Medicine Biobank
pleural fluid specimen
@@ -839,7 +839,7 @@
- A specimen that is derived from brain.
+ A specimen that is derived from brain.
Chris Stoeckert
Chris Stoeckert, NCI BBRB
brain specimen
@@ -879,7 +879,7 @@
- A specimen that is derived from hair.
+ A specimen that is derived from hair.
Chris Stoeckert
Chris Stoeckert, NCI BBRB
hair specimen
@@ -929,7 +929,7 @@
- A specimen that is derived from prostate gland.
+ A specimen that is derived from prostate gland.
Chris Stoeckert
Chris Stoeckert, NCI BBRB
prostate gland specimen
@@ -969,7 +969,7 @@
- A specimen that is derived from skeletal muscle.
+ A specimen that is derived from skeletal muscle.
Chris Stoeckert
Chris Stoeckert, NCI BBRB
skeletal muscle tissue specimen
@@ -1019,7 +1019,7 @@
- A specimen that is derived from heart.
+ A specimen that is derived from heart.
Chris Stoeckert
Chris Stoeckert, NCI BBRB
heart specimen
@@ -1069,7 +1069,7 @@
- A specimen that is derived from renal medulla.
+ A specimen that is derived from renal medulla.
Chris Stoeckert
kidney medulla specimen
Chris Stoeckert, NCI BBRB
@@ -1120,7 +1120,7 @@
- A specimen that is derived from adrenal gland.
+ A specimen that is derived from adrenal gland.
Chris Stoeckert
Chris Stoeckert, NCI BBRB
adrenal gland specimen
@@ -1170,7 +1170,7 @@
- A specimen that is derived from breast.
+ A specimen that is derived from breast.
Chris Stoeckert
mammary tissue specimen
Chris Stoeckert, NCI BBRB
@@ -1221,7 +1221,7 @@
- A specimen that is derived from urinary bladder.
+ A specimen that is derived from urinary bladder.
Chris Stoeckert
Chris Stoeckert, NCI BBRB
urinary bladder specimen
@@ -1271,7 +1271,7 @@
- A specimen that is derived from tibial artery.
+ A specimen that is derived from tibial artery.
Chris Stoeckert
Chris Stoeckert, NCI BBRB
tibial artery specimen
@@ -1321,7 +1321,7 @@
- A specimen that is derived from skin.
+ A specimen that is derived from skin.
Chris Stoeckert
skin specimen
Chris Stoeckert, NCI BBRB
@@ -1372,7 +1372,7 @@
- A specimen that is derived from pancreas.
+ A specimen that is derived from pancreas.
Chris Stoeckert
Chris Stoeckert, NCI BBRB
pancreas specimen
@@ -1422,7 +1422,7 @@
- A specimen that is derived from stomach.
+ A specimen that is derived from stomach.
Chris Stoeckert
Chris Stoeckert, NCI BBRB
stomach specimen
@@ -1472,7 +1472,7 @@
- A specimen that is derived from pituitary gland.
+ A specimen that is derived from pituitary gland.
Chris Stoeckert
Chris Stoeckert, NCI BBRB
pituitary gland specimen
@@ -1512,7 +1512,7 @@
- A specimen that is derived from adipose tissue.
+ A specimen that is derived from adipose tissue.
Chris Stoeckert
Chris Stoeckert, NCI BBRB
adipose tissue specimen
@@ -1562,7 +1562,7 @@
- A specimen that is derived from cortex of kidney.
+ A specimen that is derived from cortex of kidney.
Chris Stoeckert
kidney cortex specimen
Chris Stoeckert, NCI BBRB
@@ -1613,7 +1613,7 @@
- A specimen that is derived from esophagus mucosa.
+ A specimen that is derived from esophagus mucosa.
Chris Stoeckert
Chris Stoeckert, NCI BBRB
esophagus mucosa specimen
@@ -1663,7 +1663,7 @@
- A specimen that is derived from colon.
+ A specimen that is derived from colon.
Chris Stoeckert
Chris Stoeckert, NCI BBRB
colon specimen
@@ -1713,7 +1713,7 @@
- A specimen that is derived from lung.
+ A specimen that is derived from lung.
Chris Stoeckert
Chris Stoeckert, NCI BBRB
lung specimen
@@ -1763,7 +1763,7 @@
- A specimen that is derived from esophagus muscularis mucosa.
+ A specimen that is derived from esophagus muscularis mucosa.
Chris Stoeckert
esophagus muscularis specimen
Chris Stoeckert, NCI BBRB
@@ -1814,7 +1814,7 @@
- A specimen that is derived from cerebral cortex.
+ A specimen that is derived from cerebral cortex.
Chris Stoeckert
brain cortex specimen
Chris Stoeckert, NCI BBRB
@@ -1865,7 +1865,7 @@
- A specimen that is derived from thyroid gland.
+ A specimen that is derived from thyroid gland.
Chris Stoeckert
Chris Stoeckert, NCI BBRB
thyroid gland specimen
@@ -1915,7 +1915,7 @@
- A specimen that is derived from cerebellum.
+ A specimen that is derived from cerebellum.
Chris Stoeckert
brain cerebellum specimen
Chris Stoeckert, NCI BBRB
@@ -1966,7 +1966,7 @@
- A specimen that is derived from tibial nerve.
+ A specimen that is derived from tibial nerve.
Chris Stoeckert
Chris Stoeckert, NCI BBRB
tibial nerve specimen
@@ -2016,7 +2016,7 @@
- A specimen that is derived from coronary artery.
+ A specimen that is derived from coronary artery.
Chris Stoeckert
Chris Stoeckert, NCI BBRB
coronary artery specimen
@@ -2066,7 +2066,7 @@
- A specimen that is derived from spleen.
+ A specimen that is derived from spleen.
Chris Stoeckert
Chris Stoeckert, NCI BBRB
spleen specimen
@@ -2116,7 +2116,7 @@
- A specimen that is derived from aorta.
+ A specimen that is derived from aorta.
Chris Stoeckert
Chris Stoeckert, NCI BBRB
aorta specimen
@@ -2166,7 +2166,7 @@
- A specimen that is derived from the atrium auricular region.
+ A specimen that is derived from the atrium auricular region.
Chris Stoeckert
Chris Stoeckert, NCI BBRB
atrial appendage specimen
@@ -2216,7 +2216,7 @@
- A specimen that is derived from the esophagogastric junction.
+ A specimen that is derived from the esophagogastric junction.
Chris Stoeckert
Chris Stoeckert, NCI BBRB
esophagogastric junction specimen
@@ -2266,7 +2266,7 @@
- A specimen that is derived from ileum.
+ A specimen that is derived from ileum.
Chris Stoeckert
Chris Stoeckert, NCI BBRB
ileum specimen
@@ -2316,7 +2316,7 @@
- A specimen that is derived from liver.
+ A specimen that is derived from liver.
Chris Stoeckert
Chris Stoeckert, NCI BBRB
liver specimen
@@ -2366,7 +2366,7 @@
- A specimen that is derived from minor salivary gland.
+ A specimen that is derived from minor salivary gland.
Chris Stoeckert
Chris Stoeckert, NCI BBRB
minor salivary gland specimen
@@ -2416,7 +2416,7 @@
- A specimen that is derived from omentum.
+ A specimen that is derived from omentum.
Chris Stoeckert
Chris Stoeckert, NCI BBRB
omentum specimen
@@ -2466,7 +2466,7 @@
- A specimen that is derived from female gonad.
+ A specimen that is derived from female gonad.
Chris Stoeckert
Chris Stoeckert, NCI BBRB
ovary specimen
@@ -2516,7 +2516,7 @@
- A specimen that is derived from sigmoid colon.
+ A specimen that is derived from sigmoid colon.
Chris Stoeckert
Chris Stoeckert, NCI BBRB
sigmoid colon specimen
@@ -2566,7 +2566,7 @@
- A specimen that is derived from suprapubic skin.
+ A specimen that is derived from suprapubic skin.
Chris Stoeckert
Chris Stoeckert, NCI BBRB
suprapubic skin specimen
@@ -2616,7 +2616,7 @@
- A specimen that is derived from testis.
+ A specimen that is derived from testis.
Chris Stoeckert
Chris Stoeckert, NCI BBRB
testis specimen
@@ -2666,7 +2666,7 @@
- A specimen that is derived from uterus.
+ A specimen that is derived from uterus.
Chris Stoeckert
Chris Stoeckert, NCI BBRB
uterus specimen
@@ -2716,7 +2716,7 @@
- A specimen that is derived from vagina.
+ A specimen that is derived from vagina.
Chris Stoeckert
Chris Stoeckert, NCI BBRB
vagina specimen
@@ -2768,7 +2768,7 @@
- A specimen that is collected with a swab from the surface of an areola of a breast.
+ A specimen that is collected with a swab from the surface of an areola of a breast.
Chris Stoeckert
Chris Stoeckert, OBIB
areolar swab specimen
@@ -2814,7 +2814,7 @@
- A specimen that is collected with a swab from the surface of a breast.
+ A specimen that is collected with a swab from the surface of a breast.
Chris Stoeckert
Chris Stoeckert, OBIB
breast swab specimen
@@ -2860,7 +2860,7 @@
- A specimen that is collected with a swab from the cheek portion of the inside surface of a mouth.
+ A specimen that is collected with a swab from the cheek portion of the inside surface of a mouth.
Chris Stoeckert
Chris Stoeckert, OBIB
cheek swab specimen
@@ -2906,7 +2906,7 @@
- A specimen that is collected with a swab from the surface of a nasopharynx.
+ A specimen that is collected with a swab from the surface of a nasopharynx.
Chris Stoeckert
Chris Stoeckert, OBIB
nasopharyngeal swab specimen
@@ -2952,7 +2952,7 @@
- A specimen that is collected with a swab from the inside surface of a mouth.
+ A specimen that is collected with a swab from the inside surface of a mouth.
Chris Stoeckert
Chris Stoeckert, OBIB
oral swab specimen
@@ -2998,7 +2998,7 @@
- A specimen that is collected with a swab from the surface of a oropharynx.
+ A specimen that is collected with a swab from the surface of a oropharynx.
Chris Stoeckert
Chris Stoeckert, OBIB
oropharyngeal swab specimen
@@ -3044,7 +3044,7 @@
- A specimen that is collected with a swab from the surface of a rectum.
+ A specimen that is collected with a swab from the surface of a rectum.
Chris Stoeckert
Chris Stoeckert, OBIB
rectal swab specimen
@@ -3090,7 +3090,7 @@
- A specimen that is collected with a swab from the surface of a tongue.
+ A specimen that is collected with a swab from the surface of a tongue.
Chris Stoeckert
Chris Stoeckert, OBIB
tongue swab specimen
@@ -3136,7 +3136,7 @@
- A specimen that is collected with a swab from the surface of a vagina.
+ A specimen that is collected with a swab from the surface of a vagina.
Chris Stoeckert
Chris Stoeckert, OBIB
vagina swab specimen
@@ -3182,7 +3182,7 @@
- A specimen that is collected with a swab from the surface of a feces.
+ A specimen that is collected with a swab from the surface of a feces.
Chris Stoeckert
stool swab specimen
Chris Stoeckert, OBIB
@@ -3229,7 +3229,7 @@
- A specimen that is collected with a swab from the surface of an environmenal material.
+ A specimen that is collected with a swab from the surface of an environmenal material.
Chris Stoeckert
Chris Stoeckert, OBIB
environmental swab specimen
@@ -3272,7 +3272,7 @@
- A sputum specimen that is collected from an organism following its inhalation of a nebulized salt solution.
+ A sputum specimen that is collected from an organism following its inhalation of a nebulized salt solution.
John Judkins
PMC3297553
induced sputum specimen
@@ -3315,7 +3315,7 @@
- A specimen that is collected with a suctioning tube from the trachea.
+ A specimen that is collected with a suctioning tube from the trachea.
Asiyah Yu Lin ORCID:0000-0003-2620-0345
tracheal wash specimen
PMID:25338241
@@ -3361,7 +3361,7 @@
- A specimen that is collected with a mid-turbinate nasal swab from the turbinate area of the nasal cavity.
+ A specimen that is collected with a mid-turbinate nasal swab from the turbinate area of the nasal cavity.
Asiyah Yu Lin ORCID:0000-0003-2620-0345
https://seattlechildrenslab.testcatalog.org/catalogs/185/files/11633
mid-turbinate nasal swab specimen
@@ -3406,7 +3406,7 @@
- A specimen that is collected with a suctioning tube from the nasal cavity.
+ A specimen that is collected with a suctioning tube from the nasal cavity.
Asiyah Yu Lin ORCID:0000-0003-2620-0345
nasal wash specimen
nasopharyngeal aspirate
@@ -3453,7 +3453,7 @@
- A specimen that is collected with a suctioning tube from the lower respiratory tract.
+ A specimen that is collected with a suctioning tube from the lower respiratory tract.
Asiyah Yu Lin ORCID:0000-0003-2620-0345
lower respiratory tract wash specimen
Asiyah Yu Lin ORCID:0000-0003-2620-0345
@@ -3499,7 +3499,7 @@
- A specimen that is derived from the upper respiratory tract
+ A specimen that is derived from the upper respiratory tract
Asiyah Yu Lin ORCID:0000-0003-2620-0345
Asiyah Yu Lin ORCID:0000-0003-2620-0345
upper respiratory specimen
@@ -3531,7 +3531,7 @@
- A specimen that is derived from the lower respiratory tract.
+ A specimen that is derived from the lower respiratory tract.
Asiyah Yu Lin ORCID:0000-0003-2620-0345
Asiyah Yu Lin ORCID:0000-0003-2620-0345
lower respiratory tract specimen
@@ -3576,7 +3576,7 @@
- A specimen that is derived from the anterior nasal wall
+ A specimen that is derived from the anterior nasal wall
Asiyah Yu Lin ORCID:0000-0003-2620-0345
Asiyah Yu Lin ORCID:0000-0003-2620-0345
anterior nasal swab specimen
@@ -3619,7 +3619,7 @@
- A specimen that derives from a biofilm that forms on the inner surface of an endotracheal tube while the tube is in the trachea. The specimen is collected upon removal of the tube from the trachea.
+ A specimen that derives from a biofilm that forms on the inner surface of an endotracheal tube while the tube is in the trachea. The specimen is collected upon removal of the tube from the trachea.
John Judkins ORCID:0000-0001-6595-0902
https://bmcpulmmed.biomedcentral.com/articles/10.1186/s12890-019-0926-3
endotracheal tube specimen
@@ -3656,7 +3656,7 @@
- A specimen that derives from a biofilm that forms on the inner surface of an endotracheal tube while the tube is in the trachea. The specimen is collected by suction without removing the tube.
+ A specimen that derives from a biofilm that forms on the inner surface of an endotracheal tube while the tube is in the trachea. The specimen is collected by suction without removing the tube.
John Judkins ORCID:0000-0001-6595-0902
https://bmcpulmmed.biomedcentral.com/articles/10.1186/s12890-019-0926-3
endotracheal aspirate specimen
@@ -3693,7 +3693,7 @@
- A blood specimen that is located in a vacutainer.
+ A blood specimen that is located in a vacutainer.
John Judkins
Vacutainer sample
VEuPathDB
@@ -3731,7 +3731,7 @@
- A blood specimen that is located on a filter paper.
+ A blood specimen that is located on a filter paper.
Chris Stoeckert
Jie Zheng
Filter paper sample
@@ -3772,7 +3772,7 @@
- A specimen that is derived from placental blood.
+ A specimen that is derived from placental blood.
John Judkins
VEuPathDB
placental blood specimen
@@ -3809,7 +3809,7 @@
- A processed specimen that is extracted from whole blood using gradient centrifugation that separates the blood into a layer of peripheral blood mononuclear cells under the top layer of plasma. It contains lymphocytes, monocytes or macrophages that are critical components in the immune system.
+ A processed specimen that is extracted from whole blood using gradient centrifugation that separates the blood into a layer of peripheral blood mononuclear cells under the top layer of plasma. It contains lymphocytes, monocytes or macrophages that are critical components in the immune system.
Chris Stoeckert
Jie Zheng
PBMC specimen
@@ -3858,7 +3858,7 @@
- A specimen that is derived from a portion of lymph collected from an organism.
+ A specimen that is derived from a portion of lymph collected from an organism.
John Judkins ORCID:0000-0001-6595-0902
VEuPathDB
lymph specimen
@@ -3905,7 +3905,7 @@
- A specimen that is derived from part of a digestive tract.
+ A specimen that is derived from part of a digestive tract.
John Judkins ORCID:0000-0001-6595-0902
VEuPathDB
digestive tract specimen
@@ -3948,7 +3948,7 @@
- A specimen collected through nasal cavity lavage that contains the reagents used to for the lavage process, organisms, cells, cellular secretions, and other biomaterials present in the nasal cavity space.
+ A specimen collected through nasal cavity lavage that contains the reagents used to for the lavage process, organisms, cells, cellular secretions, and other biomaterials present in the nasal cavity space.
Randi Vita
Sebastian Duesing
nasal lavage fluid
@@ -4009,7 +4009,7 @@
- A specimen that is derived from some uterine cervix
+ A specimen that is derived from some uterine cervix
Christian Stoeckert ORCID:0000-0002-5714-991X
Mark A. Miller ORCID:0000-0001-9076-6066
Christian Stoeckert ORCID:0000-0002-5714-991X
@@ -4060,7 +4060,7 @@
- A specimen that is derived from some urethra
+ A specimen that is derived from some urethra
Christian Stoeckert ORCID:0000-0002-5714-991X
Mark A. Miller ORCID:0000-0001-9076-6066
Christian Stoeckert ORCID:0000-0002-5714-991X
@@ -4101,7 +4101,7 @@
- A specimen that is derived from some cervical mucus
+ A specimen that is derived from some cervical mucus
Christian Stoeckert ORCID:0000-0002-5714-991X
Mark A. Miller ORCID:0000-0001-9076-6066
Christian Stoeckert ORCID:0000-0002-5714-991X
@@ -4152,7 +4152,7 @@
- A specimen that is derived from some throat
+ A specimen that is derived from some throat
Christian Stoeckert ORCID:0000-0002-5714-991X
Mark A. Miller ORCID:0000-0001-9076-6066
Christian Stoeckert ORCID:0000-0002-5714-991X
@@ -4203,7 +4203,7 @@
- A specimen that is derived from some eye
+ A specimen that is derived from some eye
Christian Stoeckert ORCID:0000-0002-5714-991X
Mark A. Miller ORCID:0000-0001-9076-6066
Christian Stoeckert ORCID:0000-0002-5714-991X
@@ -4254,7 +4254,7 @@
- A specimen that is derived from some respiratory system
+ A specimen that is derived from some respiratory system
Christian Stoeckert ORCID:0000-0002-5714-991X
Mark A. Miller ORCID:0000-0001-9076-6066
Christian Stoeckert ORCID:0000-0002-5714-991X
@@ -4305,7 +4305,7 @@
- A specimen that is derived from some upper respiratory tract
+ A specimen that is derived from some upper respiratory tract
Christian Stoeckert ORCID:0000-0002-5714-991X
Mark A. Miller ORCID:0000-0001-9076-6066
Christian Stoeckert ORCID:0000-0002-5714-991X
@@ -4356,7 +4356,7 @@
- A specimen that is derived from some nasopharynx
+ A specimen that is derived from some nasopharynx
Christian Stoeckert ORCID:0000-0002-5714-991X
Mark A. Miller ORCID:0000-0001-9076-6066
Christian Stoeckert ORCID:0000-0002-5714-991X
@@ -4397,7 +4397,7 @@
- A specimen that is derived from some semen
+ A specimen that is derived from some semen
Christian Stoeckert ORCID:0000-0002-5714-991X
Mark A. Miller ORCID:0000-0001-9076-6066
Christian Stoeckert ORCID:0000-0002-5714-991X
@@ -4438,7 +4438,7 @@
- A specimen that is derived from some bodily fluid
+ A specimen that is derived from some bodily fluid
Christian Stoeckert ORCID:0000-0002-5714-991X
Mark A. Miller ORCID:0000-0001-9076-6066
Christian Stoeckert ORCID:0000-0002-5714-991X
@@ -4489,7 +4489,7 @@
- A specimen that is derived from some chorionic villus
+ A specimen that is derived from some chorionic villus
Christian Stoeckert ORCID:0000-0002-5714-991X
Mark A. Miller ORCID:0000-0001-9076-6066
Christian Stoeckert ORCID:0000-0002-5714-991X
@@ -4530,7 +4530,7 @@
- A specimen that is derived from some meconium
+ A specimen that is derived from some meconium
Christian Stoeckert ORCID:0000-0002-5714-991X
Mark A. Miller ORCID:0000-0001-9076-6066
Christian Stoeckert ORCID:0000-0002-5714-991X
@@ -4571,7 +4571,7 @@
- A specimen that is derived from some umbilical cord blood
+ A specimen that is derived from some umbilical cord blood
Christian Stoeckert ORCID:0000-0002-5714-991X
Mark A. Miller ORCID:0000-0001-9076-6066
Christian Stoeckert ORCID:0000-0002-5714-991X
@@ -4612,7 +4612,7 @@
- A specimen that is derived from some arterial blood
+ A specimen that is derived from some arterial blood
Christian Stoeckert ORCID:0000-0002-5714-991X
Mark A. Miller ORCID:0000-0001-9076-6066
Christian Stoeckert ORCID:0000-0002-5714-991X
@@ -4653,7 +4653,7 @@
- A specimen that is derived from some venous blood
+ A specimen that is derived from some venous blood
Christian Stoeckert ORCID:0000-0002-5714-991X
Mark A. Miller ORCID:0000-0001-9076-6066
Christian Stoeckert ORCID:0000-0002-5714-991X
@@ -4694,7 +4694,7 @@
- A specimen that is derived from some capillary blood
+ A specimen that is derived from some capillary blood
Christian Stoeckert ORCID:0000-0002-5714-991X
Mark A. Miller ORCID:0000-0001-9076-6066
Christian Stoeckert ORCID:0000-0002-5714-991X
@@ -4739,7 +4739,7 @@
- A specimen that is derived from some erythrocytes
+ A specimen that is derived from some erythrocytes
Christian Stoeckert ORCID:0000-0002-5714-991X
Mark A. Miller ORCID:0000-0001-9076-6066
Christian Stoeckert ORCID:0000-0002-5714-991X
@@ -4784,7 +4784,7 @@
- A specimen that is derived from some reticulocytes
+ A specimen that is derived from some reticulocytes
Christian Stoeckert ORCID:0000-0002-5714-991X
Mark A. Miller ORCID:0000-0001-9076-6066
Christian Stoeckert ORCID:0000-0002-5714-991X
@@ -4829,7 +4829,7 @@
- A specimen that is derived from some leukocytes
+ A specimen that is derived from some leukocytes
Christian Stoeckert ORCID:0000-0002-5714-991X
Mark A. Miller ORCID:0000-0001-9076-6066
Christian Stoeckert ORCID:0000-0002-5714-991X
diff --git a/src/ontology/modules/biopsy.owl b/src/ontology/modules/biopsy.owl
index 43cf512c..48c01296 100644
--- a/src/ontology/modules/biopsy.owl
+++ b/src/ontology/modules/biopsy.owl
@@ -146,7 +146,7 @@
Biopsy of a potentially cancerous mole.
- A specimen collection that obtains a sample of tissue or cell from a living multicellular organism body for diagnostic purposes by means intended to be minimally invasive.
+ A specimen collection that obtains a sample of tissue or cell from a living multicellular organism body for diagnostic purposes by means intended to be minimally invasive.
Damion Dooley
Nicole Vasilevsky
https://en.wikipedia.org/wiki/Biopsy
@@ -161,7 +161,7 @@
Image-guided needle biopsy allows a doctor to biopsy suspicious areas that aren't readily seen or felt through skin, such as in a prostate gland.
- A biopsy which uses an imaging procedure to guide a needle biopsy.
+ A biopsy which uses an imaging procedure to guide a needle biopsy.
Damion Dooley
image guided needle biopsy
image-guided biopsy
@@ -184,7 +184,7 @@
A CT Guided Biopsy is a procedure performed by a radiologist to obtain a small tissue sample through a needle.
- A needle biopsy guided by real-time computed tomography (CT) scan images.
+ A needle biopsy guided by real-time computed tomography (CT) scan images.
Damion Dooley
CT Assisted Biopsy
CT Guided Biopsy
@@ -202,7 +202,7 @@
An ultrasound-guided needle biopsy uses sound waves to help locate a nodule or abnormality within the thyroid.
- A needle biopsy guided by ultrasound visualization.
+ A needle biopsy guided by ultrasound visualization.
Damion Dooley
https://www.oncolink.org/cancer-treatment/procedures-diagnostic-tests/biopsy-procedures/ultrasound-guided-needle-biopsy
ultrasound-guided needle biopsy
@@ -222,7 +222,7 @@
A needle biopsy is often used on suspicious breast lumps and enlarged lymph nodes that a doctor can feel through a patient's skin.
- A biopsy that uses a hollow needle to extract cells.
+ A biopsy that uses a hollow needle to extract cells.
Damion Dooley
https://www.mayoclinic.org/tests-procedures/needle-biopsy/about/pac-20394749
needle biopsy
@@ -236,7 +236,7 @@
A fine needle aspiration biopsy is commonly performed in order to test for cancer.
- A biopsy that uses a thin needle to extract cells.
+ A biopsy that uses a thin needle to extract cells.
Chris Stoeckert, Helena Ellis, Jie Zheng
FNA
FNAB
@@ -253,7 +253,7 @@
A core needle biopsy can remove more tissue than a fine needle biopsy, and therefore can provide more information about the cells and tissue removed.
- A biopsy that uses a hollow tube to collect a core of tissue.
+ A biopsy that uses a hollow tube to collect a core of tissue.
Chris Stoeckert, Helena Ellis, Jie Zheng
CNB
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5769667/
@@ -269,7 +269,7 @@
Surgical biopsy may be required to collect hard-to-reach tissue.
- A biopsy involving a surgical incision into an organism to access the biopsy material.
+ A biopsy involving a surgical incision into an organism to access the biopsy material.
Damion Dooley
excisional biopsy
open biopsy
@@ -291,7 +291,7 @@
The makeup of fat in the abdominal wall can be investigated by fat biopsy.
- A biopsy involving the collection of a small part of the abdominal wall fat pad.
+ A biopsy involving the collection of a small part of the abdominal wall fat pad.
Nicole Vasilevsky, Damion Dooley
abdominal wall biopsy
fat biopsy
@@ -313,7 +313,7 @@
A mouse tail biopsy was performed to collect material for DNA extraction.
- A biopsy involving the collection of the tip of a mamallian tail.
+ A biopsy involving the collection of the tip of a mamallian tail.
Nicole Vasilevsky, Damion Dooley
snip
http://web.jhu.edu/animalcare/policies/Tail%20Biopsy%20of%20Mice.pdf
@@ -334,7 +334,7 @@
A bone marrow biopsy removes bone with the marrow inside to look at under a microscope
- A biopsy where a small amount of bone and a small amount of fluid and bone marrow are collected.
+ A biopsy where a small amount of bone and a small amount of fluid and bone marrow are collected.
Nicole Vasilevsky
http://www.webmd.com/cancer/bone-marrow-aspiration-and-biopsy
bone marrow biopsy
@@ -354,7 +354,7 @@
A three or four millimeter punch is used in s skinpunch biopsy proceedure.
- A biopsy that involves the collection of a cylinder of skin (including epidermis, dermis and superficial fat) using a punch tool.
+ A biopsy that involves the collection of a cylinder of skin (including epidermis, dermis and superficial fat) using a punch tool.
Nicole Vasilevsky
punch biopsy; skin biopsy
http://healthlibrary.epnet.com/GetContent.aspx?token=b93d114e-5009-4f6a-9917-6c594254fcc7&chunkiid=14861
@@ -381,7 +381,7 @@
A vacuum assisted biopsy can remove an area of abnormal cells from breast tissue.
- A biopsy performed with a needle augmented with a vacuum device.
+ A biopsy performed with a needle augmented with a vacuum device.
Damion Dooley
VAB
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5769667/
diff --git a/src/ontology/modules/data-sets.owl b/src/ontology/modules/data-sets.owl
index f553bb20..cab821ed 100644
--- a/src/ontology/modules/data-sets.owl
+++ b/src/ontology/modules/data-sets.owl
@@ -121,13 +121,13 @@
The output produced by a digital imaging technique, such as microscopy, MRI, or CT.
- A data set that is comprised of multidimensional structured measurements and metadata required for a morphological representation of an entity. An image data set can be the source from which an image (such as a 2D image using pixels or a 3D image using voxels) is produced.
- https://orcid.org/0000-0001-9625-1899 "William D. Duncan"
- https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
- https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
- https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
- https://orcid.org/0000-0002-7245-3450 "Lauren M. Wishnie"
- https://orcid.org/0000-0002-9821-4132 "Mackenzie T. Smith"
+ A data set that is comprised of multidimensional structured measurements and metadata required for a morphological representation of an entity. An image data set can be the source from which an image (such as a 2D image using pixels or a 3D image using voxels) is produced.
+ https://orcid.org/0000-0001-9625-1899 "William D. Duncan"
+ https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
+ https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
+ https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
+ https://orcid.org/0000-0002-7245-3450 "Lauren M. Wishnie"
+ https://orcid.org/0000-0002-9821-4132 "Mackenzie T. Smith"
https://github.com/obi-ontology/obi/issues/1481
image data set
@@ -149,13 +149,13 @@
The DICOM file produced by an MRI machine when a multiple sclerosis patient undergoes a brain scan.
- An image data set whose information content originates from some MR imaging assay and is about some MRI participant.
- https://orcid.org/0000-0001-9625-1899 "William D. Duncan"
- https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
- https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
- https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
- https://orcid.org/0000-0002-7245-3450 "Lauren M. Wishnie"
- https://orcid.org/0000-0002-9821-4132 "Mackenzie T. Smith"
+ An image data set whose information content originates from some MR imaging assay and is about some MRI participant.
+ https://orcid.org/0000-0001-9625-1899 "William D. Duncan"
+ https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
+ https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
+ https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
+ https://orcid.org/0000-0002-7245-3450 "Lauren M. Wishnie"
+ https://orcid.org/0000-0002-9821-4132 "Mackenzie T. Smith"
MRI at a Glance, ISBN 10: 1119053552
https://github.com/obi-ontology/obi/issues/1481
magnetic resonance image data set
@@ -173,15 +173,15 @@
- The untransformed ("k-space") data produced by an MRI machine, prior to mathematical transformation into a form that corresponds to the anatomical structure of the brain.
- An image data set that encodes measurement values produced by some instrument before undergoing a data transformation.
- https://orcid.org/0000-0001-9625-1899 "William D. Duncan"
- https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
- https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
- https://orcid.org/0000-0002-1604-3078 "Alan Ruttenberg"
- https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
- https://orcid.org/0000-0002-7245-3450 "Lauren M. Wishnie"
- https://orcid.org/0000-0002-9821-4132 "Mackenzie T. Smith"
+ The untransformed ("k-space") data produced by an MRI machine, prior to mathematical transformation into a form that corresponds to the anatomical structure of the brain.
+ An image data set that encodes measurement values produced by some instrument before undergoing a data transformation.
+ https://orcid.org/0000-0001-9625-1899 "William D. Duncan"
+ https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
+ https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
+ https://orcid.org/0000-0002-1604-3078 "Alan Ruttenberg"
+ https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
+ https://orcid.org/0000-0002-7245-3450 "Lauren M. Wishnie"
+ https://orcid.org/0000-0002-9821-4132 "Mackenzie T. Smith"
https://github.com/obi-ontology/obi/issues/1481
raw image data set
@@ -203,13 +203,13 @@
The production of JPEG file by a digital camera.
- An image data set that is the output of an image data set analysis.
- https://orcid.org/0000-0001-9625-1899 "William D. Duncan"
- https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
- https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
- https://orcid.org/0000-0002-1604-3078 "Alan Ruttenberg"
- https://orcid.org/0000-0002-7245-3450 "Lauren M. Wishnie"
- https://orcid.org/0000-0002-9821-4132 "Mackenzie T. Smith"
+ An image data set that is the output of an image data set analysis.
+ https://orcid.org/0000-0001-9625-1899 "William D. Duncan"
+ https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
+ https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
+ https://orcid.org/0000-0002-1604-3078 "Alan Ruttenberg"
+ https://orcid.org/0000-0002-7245-3450 "Lauren M. Wishnie"
+ https://orcid.org/0000-0002-9821-4132 "Mackenzie T. Smith"
https://github.com/obi-ontology/obi/issues/1481
computed image data set
@@ -230,14 +230,14 @@
- The product of a mathematical transformation of raw "k-space" data produced by an MRI machine into a form that represents the anatomical structure of the brain.
- An image data set that is the direct output of a raw magnetic resonance image data set reconstruction or a transformation of another MR image data set.
- https://orcid.org/0000-0001-9625-1899 "William D. Duncan"
- https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
- https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
- https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
- https://orcid.org/0000-0002-7245-3450 "Lauren M. Wishnie"
- https://orcid.org/0000-0002-9821-4132 "Mackenzie T. Smith"
+ The product of a mathematical transformation of raw "k-space" data produced by an MRI machine into a form that represents the anatomical structure of the brain.
+ An image data set that is the direct output of a raw magnetic resonance image data set reconstruction or a transformation of another MR image data set.
+ https://orcid.org/0000-0001-9625-1899 "William D. Duncan"
+ https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
+ https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
+ https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
+ https://orcid.org/0000-0002-7245-3450 "Lauren M. Wishnie"
+ https://orcid.org/0000-0002-9821-4132 "Mackenzie T. Smith"
https://github.com/obi-ontology/obi/issues/1481
reconstructed magnetic resonance image data set
@@ -249,9 +249,9 @@
MRI used for assessing structural integrity of brain axons and visualizing ischemia.
- A type of magnetic resonance image data set collected using at least three diffusion gradients of some factor "b," which is a function of the amplitude, duration, and interval of the gradiants.
- https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
- https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
+ A type of magnetic resonance image data set collected using at least three diffusion gradients of some factor "b," which is a function of the amplitude, duration, and interval of the gradiants.
+ https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
+ https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
https://github.com/obi-ontology/obi/issues/1481
diffusion weighted magnetic resonance image data set
@@ -263,11 +263,11 @@
MRI used for assessing brain activity via blood oxygen level dependent signal.
- An magnetic resonance image data set collected as a 4D time series representing changes in brain metabolism (i.e. BOLD), typically used as a proxy for brain activity.
- https://orcid.org/0000-0001-9625-1899 "William D. Duncan"
- https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
- https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
- https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
+ An magnetic resonance image data set collected as a 4D time series representing changes in brain metabolism (i.e. BOLD), typically used as a proxy for brain activity.
+ https://orcid.org/0000-0001-9625-1899 "William D. Duncan"
+ https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
+ https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
+ https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
https://github.com/obi-ontology/obi/issues/1481
functional magnetic resonance image data set
@@ -279,10 +279,10 @@
An fMRI used for assessing functional connectivity of brain regions at rest.
- A type of functional MRI in which the participant is not given a task, but just rests during acquisision
- https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
- https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
- https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
+ A type of functional MRI in which the participant is not given a task, but just rests during acquisision
+ https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
+ https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
+ https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
https://github.com/obi-ontology/obi/issues/1481
resting state functional magnetic resonance image data set
@@ -294,10 +294,10 @@
fMRI type used for assessing brain activity while performing an action or in response to stimuli.
- A type of functional MRI in which the participant is given a task or tasks, which are timed with the acquisition
- https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
- https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
- https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
+ A type of functional MRI in which the participant is given a task or tasks, which are timed with the acquisition
+ https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
+ https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
+ https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
https://github.com/obi-ontology/obi/issues/1481
task-based functional magnetic resonance image data set
@@ -309,9 +309,9 @@
MRI used for evaluating ischemia.
- An magnetic resonance image data set that captures volume and flow of blood in the brain.
- https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
- https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
+ An magnetic resonance image data set that captures volume and flow of blood in the brain.
+ https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
+ https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
https://github.com/obi-ontology/obi/issues/1481
perfusion weighted magnetic resonance image data set
@@ -323,10 +323,10 @@
MRI used for visualizing structure of tissue.
- An magnetic resonance image data set in which the contrast emphasizes density of protons, supressing T1 and T2 effects
- https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
- https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
- https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
+ An magnetic resonance image data set in which the contrast emphasizes density of protons, supressing T1 and T2 effects
+ https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
+ https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
+ https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
https://github.com/obi-ontology/obi/issues/1481
proton density magnetic resonance image data set
@@ -338,10 +338,10 @@
MRI used for visualizing structure of tissue where fluid is hypointense.
- An magnetic resonance image acquired using a T1 weighted magnetic resonance image acquisition sequence.
- https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
- https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
- https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
+ An magnetic resonance image acquired using a T1 weighted magnetic resonance image acquisition sequence.
+ https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
+ https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
+ https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
https://github.com/obi-ontology/obi/issues/1481
T1 weighted magnetic resonance image data set
@@ -353,10 +353,10 @@
MRI used for assessing breakdown of blood brain barrier.
- A T1 weighted image data set where gadolidium contrast agent has been administered to the participant before image acquistion.
- https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
- https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
- https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
+ A T1 weighted image data set where gadolidium contrast agent has been administered to the participant before image acquistion.
+ https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
+ https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
+ https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
https://github.com/obi-ontology/obi/issues/1481
post-Gd T1 weighted magnetic resonance image data set
@@ -368,10 +368,10 @@
MRI used for computational research on the structure of tissue.
- T1 weighted image data set collected using a gradient recall echo sequence.
- https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
- https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
- https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
+ T1 weighted image data set collected using a gradient recall echo sequence.
+ https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
+ https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
+ https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
https://github.com/obi-ontology/obi/issues/1481
T1 weighted GRE magnetic resonance image data set
@@ -383,10 +383,10 @@
MRI used for computational segmentation of tissue due to high quality.
- A T1-weighted image data set acquired from an NMR/MRI machine with at least a 3 Tesla magnet and in which the voxel size is isotropic.
- https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
- https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
- https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
+ A T1-weighted image data set acquired from an NMR/MRI machine with at least a 3 Tesla magnet and in which the voxel size is isotropic.
+ https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
+ https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
+ https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
https://github.com/obi-ontology/obi/issues/1481
high resolution T1 weighted magnetic resonance image data set
@@ -398,10 +398,10 @@
First MRI acquired as part of longitudinal study.
- A T1w image data set collected at an evaluant's first visit in a study.
- https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
- https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
- https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
+ A T1w image data set collected at an evaluant's first visit in a study.
+ https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
+ https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
+ https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
https://github.com/obi-ontology/obi/issues/1481
baseline high resolution T1 weighted magnetic resonance image data set
@@ -413,10 +413,10 @@
MRI acquired after the first scan as part of longitudinal study.
- A T1w image data set collected at a later time than the evaluant's first scan.
- https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
- https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
- https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
+ A T1w image data set collected at a later time than the evaluant's first scan.
+ https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
+ https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
+ https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
https://github.com/obi-ontology/obi/issues/1481
follow-up high resolution T1 weighted magnetic resonance image data set
@@ -428,10 +428,10 @@
MRI used for visualizing structure of tissue, often of lower quality than a GRE sequence.
- A T1 weighted image data set acquired using a spin echo sequence.
- https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
- https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
- https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
+ A T1 weighted image data set acquired using a spin echo sequence.
+ https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
+ https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
+ https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
https://github.com/obi-ontology/obi/issues/1481
T1 weighted SE magnetic resonance image data set
@@ -443,10 +443,10 @@
MRI used for visualizing structure of tissue where fluid is hyperintense.
- A magnetic resonance image produced by a T2 weighted magnetic resonance image acquisition sequence.
- https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
- https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
- https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
+ A magnetic resonance image produced by a T2 weighted magnetic resonance image acquisition sequence.
+ https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
+ https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
+ https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
https://github.com/obi-ontology/obi/issues/1481
T2 weighted magnetic resonance image data set
@@ -458,10 +458,10 @@
MRI used for visualizing lesions in multiple sclerosis.
- A T2 weighted image data set collected using a FLAIR sequence.
- https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
- https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
- https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
+ A T2 weighted image data set collected using a FLAIR sequence.
+ https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
+ https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
+ https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
https://github.com/obi-ontology/obi/issues/1481
T2 weighted FLAIR magnetic resonance image data set
@@ -473,10 +473,10 @@
MRI used for visualizing structure of tissue with fast acquisition times.
- T2 weighted image collected using a fast/turbo spin echo sequence.
- https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
- https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
- https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
+ T2 weighted image collected using a fast/turbo spin echo sequence.
+ https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
+ https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
+ https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
T2 weighted TSE magnetic resonance image data set
https://github.com/obi-ontology/obi/issues/1481
T2 weighted FSE magnetic resonance image data set
@@ -489,10 +489,10 @@
MRI used for visualizing structure of tissue, often longer acquisition than FSE sequence.
- A type of T2-weighted image in which the acquisition is performed using a 2D spin-echo technique
- https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
- https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
- https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
+ A type of T2-weighted image in which the acquisition is performed using a 2D spin-echo technique
+ https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
+ https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
+ https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
https://github.com/obi-ontology/obi/issues/1481
T2 weighted SE magnetic resonance image data set
@@ -504,9 +504,9 @@
MRI used for visualizing structure of tissue where signal from fat is suppressed.
- A T2 weighted magnetic resonance image data set collected using a STIR sequence to suppress the signal coming from fat.
- https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
- https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
+ A T2 weighted magnetic resonance image data set collected using a STIR sequence to suppress the signal coming from fat.
+ https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
+ https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
https://github.com/obi-ontology/obi/issues/1481
T2 weighted STIR magnetic resonance image data set
@@ -518,10 +518,10 @@
MRI better suited for identifying focal pathology than T2w SE sequences.
- T2* weighted image data set collected using a gradient echo sequence.
- https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
- https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
- https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
+ T2* weighted image data set collected using a gradient echo sequence.
+ https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
+ https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
+ https://orcid.org/0000-0002-2104-0568 "Lucas M. Serra"
https://github.com/obi-ontology/obi/issues/1481
T2* weighted GRE magnetic resonance image data set
@@ -546,10 +546,10 @@
- The untransformed ("k-space") data produced by an MRI machine, prior to mathematical transformation into a form that corresponds to the anatomical structure of the brain.
- An image data set that is the direct output of an magnetic resonance imaging assay and whose values encode spatial frequencies produced by the NMR or MRI instrument.
- https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
- https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
+ The untransformed ("k-space") data produced by an MRI machine, prior to mathematical transformation into a form that corresponds to the anatomical structure of the brain.
+ An image data set that is the direct output of an magnetic resonance imaging assay and whose values encode spatial frequencies produced by the NMR or MRI instrument.
+ https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
+ https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
https://github.com/obi-ontology/obi/issues/1481
raw magnetic resonance image data set
@@ -573,12 +573,12 @@
The Desikan-Killiany brain region atlas used by the FreeSurfer software suite.
- An image data set consisting of values computed from multiple image data sets encoded to represent the spatial location of individual functional or structural regions of a canonical brain.
- https://orcid.org/0000-0001-9625-1899 "William D. Duncan"
- https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
- https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
- https://orcid.org/0000-0002-7245-3450 "Lauren M. Wishnie"
- https://orcid.org/0000-0002-9821-4132 "Mackenzie T. Smith"
+ An image data set consisting of values computed from multiple image data sets encoded to represent the spatial location of individual functional or structural regions of a canonical brain.
+ https://orcid.org/0000-0001-9625-1899 "William D. Duncan"
+ https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
+ https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
+ https://orcid.org/0000-0002-7245-3450 "Lauren M. Wishnie"
+ https://orcid.org/0000-0002-9821-4132 "Mackenzie T. Smith"
https://github.com/obi-ontology/obi/issues/1481
brain region atlas image data set
@@ -590,10 +590,10 @@
A brain atlas of resting-state functional networks derived from the probability that disparate brains regions are active at the same time.
- A brain atlas consisting of weighted values that respresent the probability that a voxel X is part of some brain component Y, typically derived from multiple image data sets.
- https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
- https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
- https://orcid.org/0000-0002-9821-4132 "Mackenzie T. Smith"
+ A brain atlas consisting of weighted values that respresent the probability that a voxel X is part of some brain component Y, typically derived from multiple image data sets.
+ https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
+ https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
+ https://orcid.org/0000-0002-9821-4132 "Mackenzie T. Smith"
https://github.com/obi-ontology/obi/issues/1481
probabilistic brain region atlas image dataset
@@ -605,10 +605,10 @@
The JHU white-matter tractography atlas used for mapping brain connectomes.
- A brain atlas consisting of discrete integer values where a value X denotes a voxel is part of some brain component Y.
- https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
- https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
- https://orcid.org/0000-0002-9821-4132 "Mackenzie T. Smith"
+ A brain atlas consisting of discrete integer values where a value X denotes a voxel is part of some brain component Y.
+ https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
+ https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
+ https://orcid.org/0000-0002-9821-4132 "Mackenzie T. Smith"
https://github.com/obi-ontology/obi/issues/1481
deterministic brain region atlas image data set
@@ -620,12 +620,12 @@
The output of an algorithm that identifies pedestrians walking in a street from an image data set, where the output contains values only in the segment where the pedestrian is present.
- An image data set of integer values in which each value corresponds to some shared characteristic or computed property. The values often belong to a group of pixels or voxels that share the same characteristic, such as a tissue type or anatomical region.
- https://orcid.org/0000-0001-9625-1899 "William D. Duncan"
- https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
- https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
- https://orcid.org/0000-0002-7245-3450 "Lauren M. Wishnie"
- https://orcid.org/0000-0002-9821-4132 "Mackenzie T. Smith"
+ An image data set of integer values in which each value corresponds to some shared characteristic or computed property. The values often belong to a group of pixels or voxels that share the same characteristic, such as a tissue type or anatomical region.
+ https://orcid.org/0000-0001-9625-1899 "William D. Duncan"
+ https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
+ https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
+ https://orcid.org/0000-0002-7245-3450 "Lauren M. Wishnie"
+ https://orcid.org/0000-0002-9821-4132 "Mackenzie T. Smith"
https://github.com/obi-ontology/obi/issues/1481
image segmentation map
@@ -637,9 +637,9 @@
The output produced by a manual or automated segmentation of lesions from a brain MRI.
- An image data set where voxel intensity values greater than zero encode the location of some brain lesion and voxels outside the lesion have an intensity value of zero.
- https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
- https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
+ An image data set where voxel intensity values greater than zero encode the location of some brain lesion and voxels outside the lesion have an intensity value of zero.
+ https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
+ https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
https://github.com/obi-ontology/obi/issues/1481
lesion mask
@@ -651,9 +651,9 @@
The output produced by a manual or automated segmentation of lesions from a T1w MRI.
- A lesion mask where the lesions are derived from a T1 weighted image data set.
- https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
- https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
+ A lesion mask where the lesions are derived from a T1 weighted image data set.
+ https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
+ https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
https://github.com/obi-ontology/obi/issues/1481
T1 lesion mask
@@ -665,9 +665,9 @@
The output produced by a manual or automated segmentation of lesions from a T2w FLAIR MRI.
- A lesion mask where the lesions are derived from a T2 FLAIR image data set.
- https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
- https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
+ A lesion mask where the lesions are derived from a T2 FLAIR image data set.
+ https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
+ https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
https://github.com/obi-ontology/obi/issues/1481
T2 FLAIR lesion mask
diff --git a/src/ontology/modules/data-transformations.owl b/src/ontology/modules/data-transformations.owl
index 682dd8da..919f15f2 100644
--- a/src/ontology/modules/data-transformations.owl
+++ b/src/ontology/modules/data-transformations.owl
@@ -144,7 +144,7 @@
- The process of deriving a data item from an image data set using computer algorithms. The produced data item can be an image data set, data measurement, or any other data item.
+ The process of deriving a data item from an image data set using computer algorithms. The produced data item can be an image data set, data measurement, or any other data item.
https://orcid.org/0000-0001-9625-1899 "William D. Duncan"
https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
@@ -176,7 +176,7 @@
A Fourier transform of raw "k-space" data produced into an image data set that represents the anatomical structure of the tissue examined.
- A process that transforms raw magnetic resonance image data from an NMR/MRI machine into a reconstructed magnetic resonance image data set.
+ A process that transforms raw magnetic resonance image data from an NMR/MRI machine into a reconstructed magnetic resonance image data set.
https://orcid.org/0000-0001-9625-1899 "William D. Duncan"
https://orcid.org/0000-0001-9676-7377 "Alexander D. Bartnik"
https://orcid.org/0000-0001-9990-8331 "Alexander D. Diehl"
diff --git a/src/ontology/modules/devices.owl b/src/ontology/modules/devices.owl
index 4e31ff82..745ec45a 100644
--- a/src/ontology/modules/devices.owl
+++ b/src/ontology/modules/devices.owl
@@ -228,7 +228,7 @@
chromatography column
- Chromatography column in chemistry is a tube and contents (typically glass) used to purify individual chemical compounds from mixtures of compounds. It is often used for preparative applications on scales from micrograms up to kilograms.
+ Chromatography column in chemistry is a tube and contents (typically glass) used to purify individual chemical compounds from mixtures of compounds. It is often used for preparative applications on scales from micrograms up to kilograms.
Frank Gibson
http://en.wikipedia.org/wiki/Column_chromatography
open tracker https://sourceforge.net/tracker/index.php?func=detail&aid=2881353&group_id=177891&atid=886178
@@ -249,7 +249,7 @@
pump valve switch
- A pump valve switch is a cardinal part of a liquid chromatography instrument that controls the flow.
+ A pump valve switch is a cardinal part of a liquid chromatography instrument that controls the flow.
FG:I would assume this should be a pump valve control switch and it would not be specific to a liquid chromatography instrument
OBI Instrument branch
OBI
@@ -288,7 +288,7 @@
chromatography device
- A device that facilitates the separation of mixtures. The function of a chromatography device involves passing a mixture dissolved in a "mobile phase" through a stationary phase, which separates the analyte to be measured from other molecules in the mixture and allows it to be isolated.
+ A device that facilitates the separation of mixtures. The function of a chromatography device involves passing a mixture dissolved in a "mobile phase" through a stationary phase, which separates the analyte to be measured from other molecules in the mixture and allows it to be isolated.
Frank Gibson
chromatography instrument
http://en.wikipedia.org/wiki/Chromatography
@@ -329,7 +329,7 @@
mass spectrometer
LCQ Fleet Ion Trap MSn manufactured by thermo fisher scientific
- A mass spectrometer is an instrument which is used to measure the mass to charge ratio of ions. All mass spectrometers consist of three basic parts: an ion source, a mass analyzer, and a detector system. The stages within the mass spectrometer are: 1. Production of ions from the sample 2. Separation of ions with different masses 3. Detection of the number of ions of each mass produced 4.Collection of data to generate the mass spectrum
+ A mass spectrometer is an instrument which is used to measure the mass to charge ratio of ions. All mass spectrometers consist of three basic parts: an ion source, a mass analyzer, and a detector system. The stages within the mass spectrometer are: 1. Production of ions from the sample 2. Separation of ions with different masses 3. Detection of the number of ions of each mass produced 4.Collection of data to generate the mass spectrum
Frank Gibson
http://en.wikipedia.org/wiki/Mass_spectrometry
mass spectrometer
@@ -367,7 +367,7 @@
liquid chromatography mass spectrometry platform
- A liquid chromatography mass spectrometry platform is a platform that is the collection of instrument, software and reagents needed to perform a liquid chromatography mass spectrometry protocol. definition_source: OBI.
+ A liquid chromatography mass spectrometry platform is a platform that is the collection of instrument, software and reagents needed to perform a liquid chromatography mass spectrometry protocol. definition_source: OBI.
OBI instrument branch
OBI Instrument branch
liquid chromatography mass spectrometry platform
@@ -393,7 +393,7 @@
microarray platform
- A microarray platform is a platform that contains the instruments, software and reagents needed to perform a microarray protocol. definition_source: OBI.
+ A microarray platform is a platform that contains the instruments, software and reagents needed to perform a microarray protocol. definition_source: OBI.
OBI Instrument branch
OBI Instrument branch
microarray platform
@@ -414,7 +414,7 @@
gamma counter
A Geiger counter
- A processed material which measures gamma radiation
+ A processed material which measures gamma radiation
Frank Gibson
http://en.wikipedia.org/wiki/Gamma_counter
gamma counter
@@ -435,7 +435,7 @@
polystyrene tube
Polystyrene tubes can be used to contain tissue culture cells during centrifgation
- A polystyrene tube is a test tube made of polystyrene
+ A polystyrene tube is a test tube made of polystyrene
PERSON: Chris Stoeckert
PERSON: Chris Stoeckert
polystyrene tube
@@ -456,7 +456,7 @@
incubator
Incubators are used in microbiology for culturing (growing) bacteria and other microorganisms. Incubators in tissue culture rooms are used for culturing stem cells, lymphocytes, skin fibroblasts and other types of cells
- A device in which environmental conditions (light, photoperiod, temperature, humidity, etc.) can be controlled
+ A device in which environmental conditions (light, photoperiod, temperature, humidity, etc.) can be controlled
Frank Gibson
http://www.medterms.com/script/main/art.asp?articlekey=18426
incubator
@@ -476,7 +476,7 @@
supernatant collection system harvesting frame
- A device that is designed for collecting 90% of the supernatant in a microplate well and separating the living cell with no stress, eliminating centrifugation and other similar techniques. It can be used in a variety of release assays with different radioactive isotopes, such as Cr51 or I125.
+ A device that is designed for collecting 90% of the supernatant in a microplate well and separating the living cell with no stress, eliminating centrifugation and other similar techniques. It can be used in a variety of release assays with different radioactive isotopes, such as Cr51 or I125.
Daniel Schober
google
supernatant collection system harvesting frame
@@ -496,7 +496,7 @@
filter paper
- A device manufacture with the intent to provide a porous unsized paper used for filtering.
+ A device manufacture with the intent to provide a porous unsized paper used for filtering.
Frank Gibson
sep:00107
filter paper
@@ -517,7 +517,7 @@
microtiter plate
A microtiter plate with 6, 24, 96, 384 or 1536 sample wells used in the enzyme-linked immunosorbent assay (ELISA)
- A microtiter_plate is a flat plate with multiple wells used as small test tubes.
+ A microtiter_plate is a flat plate with multiple wells used as small test tubes.
Melanie Courtot
microplate
http://en.wikipedia.org/wiki/Microtiter_plate
@@ -545,7 +545,7 @@
mass analyzer
The mass analyzer of the Voyager-DE(tm) STR Biospectrometry Workstation
- A Mass analyzer is a device that separates ions according to their mass-to-charge ratio. All mass spectrometers are based on dynamics of charged particles in electric and magnetic fields in vacuum where the two laws of Lorentz force law and Newton's second law of motion apply.
+ A Mass analyzer is a device that separates ions according to their mass-to-charge ratio. All mass spectrometers are based on dynamics of charged particles in electric and magnetic fields in vacuum where the two laws of Lorentz force law and Newton's second law of motion apply.
Frank Gibson
PERSON: Daniel Schober
http://en.wikipedia.org/wiki/Mass_spectrometry#Mass_analyzer
@@ -567,7 +567,7 @@
ion source
The ion source of a Voyager-DE??? STR Biospectrometry Workstation
- An ion source is a device that is part of a mass spectrometer that ionizes the material under analysis. The ions are then transported by magnetic or electric fields to the mass analyzer. Techniques for ionization have been key to determining what types of samples can be analyzed by mass spectrometry. Electron ionization and chemical ionization are used for gases and vapors. In chemical ionization sources, the material is ionized by chemical ion-molecule reactions during collisions in the source. Two techniques often used with liquid and solid biological samples include electrospray ionization (due to John Fenn PMID 2675315.) and matrix-assisted laser desorption/ionization (MALDI, due to M. Karas and F. Hillenkamp (Measuring Mass: From Positive Rays to Proteins by Michael A. Grayson (Editor) (ISBN 0-941901-31-9))).
+ An ion source is a device that is part of a mass spectrometer that ionizes the material under analysis. The ions are then transported by magnetic or electric fields to the mass analyzer. Techniques for ionization have been key to determining what types of samples can be analyzed by mass spectrometry. Electron ionization and chemical ionization are used for gases and vapors. In chemical ionization sources, the material is ionized by chemical ion-molecule reactions during collisions in the source. Two techniques often used with liquid and solid biological samples include electrospray ionization (due to John Fenn PMID 2675315.) and matrix-assisted laser desorption/ionization (MALDI, due to M. Karas and F. Hillenkamp (Measuring Mass: From Positive Rays to Proteins by Michael A. Grayson (Editor) (ISBN 0-941901-31-9))).
Frank Gibson
http://en.wikipedia.org/wiki/Mass_spectrometry#Ion_source
ion source
@@ -588,7 +588,7 @@
ion detector
The ion detector of the Voyager-DE(tm) STR Biospectrometry Workstation
- An ion detector is a device that measures and records the charge induced or current produced when an ion passes by or hits a surface. Example: In a scanning instrument the signal produced in the detector during the course of the scan versus where the instrument is in the scan (at what m/Q) will produce a mass spectrum, a record of ions as a function of m/Q.
+ An ion detector is a device that measures and records the charge induced or current produced when an ion passes by or hits a surface. Example: In a scanning instrument the signal produced in the detector during the course of the scan versus where the instrument is in the scan (at what m/Q) will produce a mass spectrum, a record of ions as a function of m/Q.
Frank Gibson
http://en.wikipedia.org/wiki/Mass_spectrometry#Detector
ion detector
@@ -716,7 +716,7 @@
isoelectric focusing device
- An isoelectric focusing device is a device in which isoelectric focusing can be performed. An isoelectric focussing device had the function to contain and control the contained environment and transfer electrical energy from a power supply to a separation medium and the charged material to be separated.
+ An isoelectric focusing device is a device in which isoelectric focusing can be performed. An isoelectric focussing device had the function to contain and control the contained environment and transfer electrical energy from a power supply to a separation medium and the charged material to be separated.
Frank Gibson
isoelectric focusing unit
sep:00097
@@ -743,7 +743,7 @@
thermostatic circulator
- A thermostatic circulator is a device which cools or heats a circulating liquid. It has the function to contain control the contained environment and transfer energy from or to the circulating liquid
+ A thermostatic circulator is a device which cools or heats a circulating liquid. It has the function to contain control the contained environment and transfer energy from or to the circulating liquid
Frank Gibson
sep:00098
thermostatic circulator
@@ -775,7 +775,7 @@
blot module
- A blot module is a device which has the function to conatin and facilitate the material transfer process blotting to be realised
+ A blot module is a device which has the function to conatin and facilitate the material transfer process blotting to be realised
Frank Gibson
sep:00092
blot module
@@ -811,7 +811,7 @@
image acquisition device
- An image creation device is a device which captures a digitized image of an object
+ An image creation device is a device which captures a digitized image of an object
Frank Gibson
image acquisition device
sep:00096
@@ -856,7 +856,7 @@
gel dryer
- A gel dryer is a device which has the function to contain and to control the contained environment to facilitate the drying of gels
+ A gel dryer is a device which has the function to contain and to control the contained environment to facilitate the drying of gels
Frank Gibson
sep:00094
gel dryer
@@ -883,7 +883,7 @@
syringe
Accuracy of oral liquid measuring devices: comparison of dosing cup and oral dosing syringe.Ann Pharmacother. 2008 Jan;42(1):46-52. Epub 2007 Dec 4. PMID: 18056832
- A processed material which is used to introduce or draw fluids from a material entity. A syringe is made of a piston and body. the movement of the piston in the body determines the amount/volume of fluid to inject or draw
+ A processed material which is used to introduce or draw fluids from a material entity. A syringe is made of a piston and body. the movement of the piston in the body determines the amount/volume of fluid to inject or draw
Philippe Rocca-Serra
OBI Instrument adapted from Wikipedia
syringe
@@ -904,7 +904,7 @@
needle
Ovarian carcinoma presenting with axillary lymph node metastasis: A case diagnosed by fine-needle aspiration and brief review of the literature. Diagn Cytopathol. 2008 Oct 16. PMID: 18925569
- A needle is a sharp, hollow device used to penetrate tissue or soft material. When attached to a syringe. it allows delivery of a specific volume of liquid or gaseous mixture.
+ A needle is a sharp, hollow device used to penetrate tissue or soft material. When attached to a syringe. it allows delivery of a specific volume of liquid or gaseous mixture.
Philippe Rocca-Serra
OBI Instrument
needle
@@ -918,7 +918,7 @@
packed column
- A packed column is a chromatography column where the particles of the solid stationary phase or the support coated with a liquid stationary phase may fill the whole inside volume of the tube.
+ A packed column is a chromatography column where the particles of the solid stationary phase or the support coated with a liquid stationary phase may fill the whole inside volume of the tube.
PERSON:Daniel Schober
WEB:<http:www.iupac.org/publications/pac/1993/pdf/6504x0819.pdf>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01218
@@ -945,7 +945,7 @@
column chromatography detector
- There is a wide range of detectors available for both GC and LC each having their own particular areas of application. In general the more catholic the response, the less sensitive the detector and the most sensitive detectors are those that have a specific response. The performance of all detectors should be properly specified so that the user can determine which is most suitable for a specific application. Such specifications are also essential to compare the performance of different detectors supplied by alternative instrument manufactures. Detector specifications should be presented in a standard form and in standard units, so that detectors can be compared that function on widely different principles.
+ There is a wide range of detectors available for both GC and LC each having their own particular areas of application. In general the more catholic the response, the less sensitive the detector and the most sensitive detectors are those that have a specific response. The performance of all detectors should be properly specified so that the user can determine which is most suitable for a specific application. Such specifications are also essential to compare the performance of different detectors supplied by alternative instrument manufactures. Detector specifications should be presented in a standard form and in standard units, so that detectors can be compared that function on widely different principles.
PERSON:Daniel Schober
WEB:<http://www.chromatography-online.org/Principles/Basic-Chromatograph/Detector/rs56.html>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01077
@@ -961,7 +961,7 @@
Bruker autosampler
- A Bruker autosampler is an autosampler made by Bruker.
+ A Bruker autosampler is an autosampler made by Bruker.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400209
@@ -976,7 +976,7 @@
organic acid column
- An organic acid column is a chromatography column which enables (reversed-phase) separation of hydrophilic aliphatic and aromatic organic acids with UV detection. Organic acid columns allow retention of polar and apolar organic acids and are hydrolysis resistant.
+ An organic acid column is a chromatography column which enables (reversed-phase) separation of hydrophilic aliphatic and aromatic organic acids with UV detection. Organic acid columns allow retention of polar and apolar organic acids and are hydrolysis resistant.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01099
@@ -991,7 +991,7 @@
thermal conductivity detector
- The most commonly used detector in preparative GC is the thermal conductivity detector (hot wire detector). Even this detector, however, is often too sensitive and has too high a flow impedance. Under such circumstances, the procedure mentioned above must be employed. The eluent from the preparative column is split and a small portion diverted through the detector (sometimes with further dilution with carrier gas to reduce sensitivity).
+ The most commonly used detector in preparative GC is the thermal conductivity detector (hot wire detector). Even this detector, however, is often too sensitive and has too high a flow impedance. Under such circumstances, the procedure mentioned above must be employed. The eluent from the preparative column is split and a small portion diverted through the detector (sometimes with further dilution with carrier gas to reduce sensitivity).
PERSON:Daniel Schober
TCD, hot wire detector
WEB:<http://www.chromatography-online.org/Preparative/Apparatus/Detectors/rs27.html>
@@ -1007,7 +1007,7 @@
Bruker US 2 NMR magnet
- An actively-shielded superconducting magnet from Bruker that combines Bruker BioSpin's advanced, proprietary UltraShield active shielding and UltraStabilized sub-cooling technologies. This shielded and stabilized (US2) magnet system delivers high sensitivity and spectral dispersion.
+ An actively-shielded superconducting magnet from Bruker that combines Bruker BioSpin's advanced, proprietary UltraShield active shielding and UltraStabilized sub-cooling technologies. This shielded and stabilized (US2) magnet system delivers high sensitivity and spectral dispersion.
PERSON:Daniel Schober
WEB:<http://www.bruker-biospin.com/nmr_magnets_950us2.html>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400189
@@ -1023,7 +1023,7 @@
protein column
- A protein column is a chromatography column used for the separation of complex protein mixtures. Protein columns enable sample desalting, followed by chromatographic separation or fractionation of complex protein samples, e.g. immunodepleted serum or plasma proteins.
+ A protein column is a chromatography column used for the separation of complex protein mixtures. Protein columns enable sample desalting, followed by chromatographic separation or fractionation of complex protein samples, e.g. immunodepleted serum or plasma proteins.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01238
@@ -1039,7 +1039,7 @@
solvent mixer
- A liquid chromatography device that mixes different solvents, e.g. under high pressure and in differrent volumes ranging from 5 ml to 5 L capacity. Powerful magnetic mixers provide vigorous agitation required for high pressure reaction chemistry.
+ A liquid chromatography device that mixes different solvents, e.g. under high pressure and in differrent volumes ranging from 5 ml to 5 L capacity. Powerful magnetic mixers provide vigorous agitation required for high pressure reaction chemistry.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01072
@@ -1054,7 +1054,7 @@
Bruker NMR Case sample changer
- The NMR Case is an economical NMR sample changer for laboratories with modest automation needs. It expands the maximum number of samples your spectrometer can process during unattended operation to 24. The NMR Case consists of multiple components. The NMR Case exchange module installed atop your cryostat. The two front legs are adjustable, making the NMR Case compatible with many different cryostats.
+ The NMR Case is an economical NMR sample changer for laboratories with modest automation needs. It expands the maximum number of samples your spectrometer can process during unattended operation to 24. The NMR Case consists of multiple components. The NMR Case exchange module installed atop your cryostat. The two front legs are adjustable, making the NMR Case compatible with many different cryostats.
PERSON:Daniel Schober
WEB:<http://www.bruker-biospin.com/automation.html>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400203
@@ -1070,7 +1070,7 @@
nano pump system
- A pump system optimized for nano flow chromatography.
+ A pump system optimized for nano flow chromatography.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01052
@@ -1085,7 +1085,7 @@
Bruker AutoClean system
- NMR tubes are often used once and discarded, creating needless waste. With the Bruker BioSpin Autoclean system you can now recycle 5mm, 3mm, or 5mm/3mm step-down (Wilmad 520-1B) NMR tubes. AutoClean NMR Tube Washing System is a simple way to recoup the substantial investment your organization makes in quality NMR tubes, and cut back on needless waste material.
+ NMR tubes are often used once and discarded, creating needless waste. With the Bruker BioSpin Autoclean system you can now recycle 5mm, 3mm, or 5mm/3mm step-down (Wilmad 520-1B) NMR tubes. AutoClean NMR Tube Washing System is a simple way to recoup the substantial investment your organization makes in quality NMR tubes, and cut back on needless waste material.
washing system/NMR tube washing system, XPS: device has function washing
PERSON:Daniel Schober
WEB:<http://www.used-line.com/c5983250s10028-Bruker_Biospin_NMR_Autoclean_Nuclear_Magnetic_Resonance_Organic_Solvents.htm>
@@ -1101,7 +1101,7 @@
manual injection system
- The traditional hardware system that allows a human to inject a sample into an inlet by hand, using a syringe.
+ The traditional hardware system that allows a human to inject a sample into an inlet by hand, using a syringe.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01064
@@ -1116,7 +1116,7 @@
Varian GEMINI spectrometer
- An older Varian Broadband NMR spectrometer.
+ An older Varian Broadband NMR spectrometer.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400239
@@ -1132,7 +1132,7 @@
column connector
- A device that connects two or more columns together in a functional way with leak-tight connection, low dead volume, low thermal mass and high inertness.
+ A device that connects two or more columns together in a functional way with leak-tight connection, low dead volume, low thermal mass and high inertness.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01236
@@ -1148,7 +1148,7 @@
solid NMR probe
- An NMR probe that is designed to hold a solid sample.
+ An NMR probe that is designed to hold a solid sample.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400243
@@ -1164,7 +1164,7 @@
Bruker high resolution probe
- BRUKER BIOSPIN's experienced Research & Development group not only delivers top-performance probes for the more common experiments, but also a wealth of special probes for almost any application. For high resolution (HR) NMR we offer probes with a variety of important characteristics and features.
+ BRUKER BIOSPIN's experienced Research & Development group not only delivers top-performance probes for the more common experiments, but also a wealth of special probes for almost any application. For high resolution (HR) NMR we offer probes with a variety of important characteristics and features.
PERSON:Daniel Schober
HR Probe
GROUP:<http://msi-ontology.sourceforge.net>
@@ -1181,7 +1181,7 @@
chromatography detector
- A chromatography detector is a device that locates in the dimensions of space and time, the positions of the components of a mixture that has been subjected to a chromatographic process and thus permits the senses to appreciate the nature of the separation. Defining characteristics are Dynamic Range, Response Index or Linearity, Linear Dynamic range, Detector Response, Detector Noise Level, Detector Sensitivity or Minimum Detectable Concentration, Total System Dispersion, Sensor Dimensions, Detector Time Constant, Pressure Sensitivity, Flow Sensitivity, Operating Temperature Range.
+ A chromatography detector is a device that locates in the dimensions of space and time, the positions of the components of a mixture that has been subjected to a chromatographic process and thus permits the senses to appreciate the nature of the separation. Defining characteristics are Dynamic Range, Response Index or Linearity, Linear Dynamic range, Detector Response, Detector Noise Level, Detector Sensitivity or Minimum Detectable Concentration, Total System Dispersion, Sensor Dimensions, Detector Time Constant, Pressure Sensitivity, Flow Sensitivity, Operating Temperature Range.
PERSON:Daniel Schober
WEB:<http://www.chromatography-online.org/GC-Detectors/Classification/rs1.html>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01012
@@ -1196,7 +1196,7 @@
normal phase column
- A normal phase column is a chromatography column in which the stationary phase is more polar than the mobile phase. Its counterpart is the reversed phase column.
+ A normal phase column is a chromatography column in which the stationary phase is more polar than the mobile phase. Its counterpart is the reversed phase column.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01097
@@ -1211,7 +1211,7 @@
APOLLO console
- The APOLLO is a compact, modular, multiple-DSP, Windows XP Professional-based console that can be equipped with up to 8 DDS-based RF transmitter channels configurable from 2 kHz to 3.5 GHz. Each transmitter channel produces a nominal 1V output and has the most agile frequency, phase and amplitude control of any system on the market. An array of additional options are available including multiple RF transmitters, linear high-power RF amplifiers, digital receiver arrays, low noise figure preamplifiers, a gradient control system, shim unit, MAS spin-speed controller, variable temperature unit, digital lock system and probe/coil interface. With its numerous options, the Apollo can be configured for any NMR, NQR or MRI application.
+ The APOLLO is a compact, modular, multiple-DSP, Windows XP Professional-based console that can be equipped with up to 8 DDS-based RF transmitter channels configurable from 2 kHz to 3.5 GHz. Each transmitter channel produces a nominal 1V output and has the most agile frequency, phase and amplitude control of any system on the market. An array of additional options are available including multiple RF transmitters, linear high-power RF amplifiers, digital receiver arrays, low noise figure preamplifiers, a gradient control system, shim unit, MAS spin-speed controller, variable temperature unit, digital lock system and probe/coil interface. With its numerous options, the Apollo can be configured for any NMR, NQR or MRI application.
PERSON:Daniel Schober
WEB:<http://www.tecmag.com/apollo.htm>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400249
@@ -1227,7 +1227,7 @@
NMR sample holder
- An NMR sample holder is the part of an NMR instrument, which carries the NMR probe,sample tube and the nmr sample.
+ An NMR sample holder is the part of an NMR instrument, which carries the NMR probe,sample tube and the nmr sample.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400212
@@ -1249,7 +1249,7 @@
chromatography instrument
- Any instrument that is used to carry out a chromatography experiment.
+ Any instrument that is used to carry out a chromatography experiment.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01262
@@ -1265,7 +1265,7 @@
continuous wave NMR instrument
- Continuous wave NMR spectrometers are similar to optical spectrometers, but the sample is held in a strong magnetic field, where the frequency of the source is slowly scanned (in some instruments, the source frequency is held constant, and the field is scanned).
+ Continuous wave NMR spectrometers are similar to optical spectrometers, but the sample is held in a strong magnetic field, where the frequency of the source is slowly scanned (in some instruments, the source frequency is held constant, and the field is scanned).
PERSON:Daniel Schober
WEB:<http://teaching.shu.ac.uk/hwb/chemistry/tutorials/molspec/nmr3.htm>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400283
@@ -1281,7 +1281,7 @@
fourier transformation NMR instrument
- In fourier transformation NMR, all frequencies in a spectrum are irradiated simultaneously with a radio frequency pulse. Following the pulse, the nuclei return to thermal equilibrium. A time domain emission signal is recorded by the instrument as the nuclei relax. A frequency domain spectrum is obtained by Fourier transformation.
+ In fourier transformation NMR, all frequencies in a spectrum are irradiated simultaneously with a radio frequency pulse. Following the pulse, the nuclei return to thermal equilibrium. A time domain emission signal is recorded by the instrument as the nuclei relax. A frequency domain spectrum is obtained by Fourier transformation.
PERSON:Daniel Schober
GROUP:<http://teaching.shu.ac.uk/hwb/chemistry/tutorials/molspec/nmr3.htm>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400284
@@ -1297,7 +1297,7 @@
nitrogen phosphorous detector
- The nitrogen phosphorus detector (NPD) (sometimes called the thermionic detector) is a very sensitive, specific detector the design of which, is based on the FID. Physically the sensor appears to be very similar to the FID but, in fact, operates on an entirely different principle. The nitrogen phosphorous detector (sometimes called the thermionic detector) is a very sensitive but specific detector that responds almost exclusively to nitrogen and phosphorous compounds. It is based on the flame ionization detector but differs in that it contains a rubidium or cesium silicate (glass) bead situated in a heater coil, a little distance from the hydrogen flame. If the detector is to respond to both nitrogen and phosphorous then the hydrogen flow should be minimal so that the gas does not ignite at the jet. If the detector is to respond to phosphorous only, a large flow of hydrogen is used which is burnt at the jet. The heated bead emits electrons by thermionic emission. These electrons are collected under a potential of a few volts by an appropriately placed anode, and provides a background current. When a solute containing nitrogen or phosphorous is eluted from the column, the partially combusted nitrogen and phosphorous materials are adsorbed on the surface of the bead. The adsorbed material reduces the work function of the surface and, as consequence, the emission of electrons is increased which raises the current collected at the electrode. The sensitivity of the detector to phosphorous is about 10-12 gram per ml and for nitrogen about 10-11 gram per ml at a signal to nose ratio of 2. The alkali bead as a finite life and needs regular replacement.
+ The nitrogen phosphorus detector (NPD) (sometimes called the thermionic detector) is a very sensitive, specific detector the design of which, is based on the FID. Physically the sensor appears to be very similar to the FID but, in fact, operates on an entirely different principle. The nitrogen phosphorous detector (sometimes called the thermionic detector) is a very sensitive but specific detector that responds almost exclusively to nitrogen and phosphorous compounds. It is based on the flame ionization detector but differs in that it contains a rubidium or cesium silicate (glass) bead situated in a heater coil, a little distance from the hydrogen flame. If the detector is to respond to both nitrogen and phosphorous then the hydrogen flow should be minimal so that the gas does not ignite at the jet. If the detector is to respond to phosphorous only, a large flow of hydrogen is used which is burnt at the jet. The heated bead emits electrons by thermionic emission. These electrons are collected under a potential of a few volts by an appropriately placed anode, and provides a background current. When a solute containing nitrogen or phosphorous is eluted from the column, the partially combusted nitrogen and phosphorous materials are adsorbed on the surface of the bead. The adsorbed material reduces the work function of the surface and, as consequence, the emission of electrons is increased which raises the current collected at the electrode. The sensitivity of the detector to phosphorous is about 10-12 gram per ml and for nitrogen about 10-11 gram per ml at a signal to nose ratio of 2. The alkali bead as a finite life and needs regular replacement.
PERSON:Daniel Schober
WEB:<http://www.chromatography-online.org/topics/nitrogen/phosphorus/detector.html>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01089
@@ -1312,7 +1312,7 @@
cation exchange column
- A cation exchange column is a chromatography column that is used in cation exchange chromatography.
+ A cation exchange column is a chromatography column that is used in cation exchange chromatography.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01096
@@ -1327,7 +1327,7 @@
direct detection NMR probe
- An NMR probe designed to allow the direct detection of acquisition nuclei.
+ An NMR probe designed to allow the direct detection of acquisition nuclei.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400280
@@ -1343,7 +1343,7 @@
Bruker B-ACS system
- The Bruker Automatic Sample Changer (B-ACS 60/120), used in conjunction with Bruker DISNMR, UXNMR or XWIN-NMR software, provides dialog-guided facilities which allow the user to easily and effectively perform automatic (continuous) experiments. Features include a 60 or 120 sample capacity, random accessing of samples, positive sample identification with the optional bar code reader, and temperature control of individual samples with the optional sample heater unit.
+ The Bruker Automatic Sample Changer (B-ACS 60/120), used in conjunction with Bruker DISNMR, UXNMR or XWIN-NMR software, provides dialog-guided facilities which allow the user to easily and effectively perform automatic (continuous) experiments. Features include a 60 or 120 sample capacity, random accessing of samples, positive sample identification with the optional bar code reader, and temperature control of individual samples with the optional sample heater unit.
PERSON:Daniel Schober
WEB:<http://www.bruker-biospin.com/automation.html>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400210
@@ -1365,7 +1365,7 @@
rapid resolution column
- A rapid resolution column is a chromatography column as marketed by Agilent, which is used with a rapid resolution cartridge to ensure a fast chromatography process with good separation resolution.
+ A rapid resolution column is a chromatography column as marketed by Agilent, which is used with a rapid resolution cartridge to ensure a fast chromatography process with good separation resolution.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01102
@@ -1380,7 +1380,7 @@
liquid chromatography autosampler
- Designed to perform capillary LC with injection of sample volumes ranging from nL to L.
+ Designed to perform capillary LC with injection of sample volumes ranging from nL to L.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01061
@@ -1395,7 +1395,7 @@
vacuum degasser
- A degassing system used for degassing solvents in liquid chromatography. Dissolved gasses, usually nitrogen and oxygen from the air, tend to be evolved in the mobile phase as the pressure is reduced when the mobile phase leaves the liquid chromatography column and enters the detector. Gasses in the mobile phase in the detector can produce completely unacceptable noise and, thus, must be removed. The dissolved gasses were originally removed under vacuum but, unfortunately, are soon replaced if the solvent is left in contact with air at atmospheric pressure. For this reason degassing is now usually carried out by bubbling helium through the mobile phase reservoirs. Secondly, vacuum is used in the thermionic detector. This consists of a device, very similar in design to the thermionic valve which is attached to a vacuum and a small quantity of the eluent from a gas chromatography column allowed to bleed through it. Helium is used as the carrier gas. The presence of solute vapor causes the thermionic current to fall. This type of detector tends to become contaminated rather readily.
+ A degassing system used for degassing solvents in liquid chromatography. Dissolved gasses, usually nitrogen and oxygen from the air, tend to be evolved in the mobile phase as the pressure is reduced when the mobile phase leaves the liquid chromatography column and enters the detector. Gasses in the mobile phase in the detector can produce completely unacceptable noise and, thus, must be removed. The dissolved gasses were originally removed under vacuum but, unfortunately, are soon replaced if the solvent is left in contact with air at atmospheric pressure. For this reason degassing is now usually carried out by bubbling helium through the mobile phase reservoirs. Secondly, vacuum is used in the thermionic detector. This consists of a device, very similar in design to the thermionic valve which is attached to a vacuum and a small quantity of the eluent from a gas chromatography column allowed to bleed through it. Helium is used as the carrier gas. The presence of solute vapor causes the thermionic current to fall. This type of detector tends to become contaminated rather readily.
PERSON:Daniel Schober
WEB:<http://www.chromatography-online.org/topics/vacuum.html>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01053
@@ -1410,7 +1410,7 @@
capillary column
- A capillary column is a thin tube with a small inner diameter, usually around 0.5 mm.
+ A capillary column is a thin tube with a small inner diameter, usually around 0.5 mm.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01066
@@ -1425,7 +1425,7 @@
sample inlet
- The column inlet (or injector) provides the means to introduce a sample into a continuous flow of carrier gas. The inlet is a piece of hardware attached to the column head.
+ The column inlet (or injector) provides the means to introduce a sample into a continuous flow of carrier gas. The inlet is a piece of hardware attached to the column head.
PERSON:Daniel Schober
WEB:<http://en.wikipedia.org/wiki/Gas_chromatography#Inlets>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01044
@@ -1441,7 +1441,7 @@
NMR tube washing system
- An automatic cleaning system for NMR tubes that removes previous probe and sample residues in order to allow for tube recycling.
+ An automatic cleaning system for NMR tubes that removes previous probe and sample residues in order to allow for tube recycling.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400204
@@ -1457,7 +1457,7 @@
NMR console
- A component of an NMR instrument that controls the activities of the other components.
+ A component of an NMR instrument that controls the activities of the other components.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400015
@@ -1473,7 +1473,7 @@
dual loop autosampler
- A dual loop autosampler is an autosampler that is designed for handling both analytical (10 mL/min flow rate) to preparative scale sample purification (100 mL/min flow rate).
+ A dual loop autosampler is an autosampler that is designed for handling both analytical (10 mL/min flow rate) to preparative scale sample purification (100 mL/min flow rate).
PERSON:Daniel Schober
WEB:<http://www.chem.agilent.com/scripts/pds.asp?lpage=17149>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01063
@@ -1494,7 +1494,7 @@
variable wavelength detector
- A chromatography detector, that can detect signals within a certain range at user-defined wavelengths.
+ A chromatography detector, that can detect signals within a certain range at user-defined wavelengths.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01079
@@ -1509,7 +1509,7 @@
Bruker LC-NMR platform
- The LC-NMR/MS setup was first introduced by Bruker BioSpin in 1999. An LC-NMR system including a Bruker Peak Sampling Unit (BPSU-36) was coupled with a Bruker Daltonics esquire series ion trap mass spectrometer via a Bruker NMR-MS interface (BNMI). Since October 2004 the Bruker Daltonics microTOF-LC time-of-flight mass spectrometer can also be integrated in an LC-NMR setup.
+ The LC-NMR/MS setup was first introduced by Bruker BioSpin in 1999. An LC-NMR system including a Bruker Peak Sampling Unit (BPSU-36) was coupled with a Bruker Daltonics esquire series ion trap mass spectrometer via a Bruker NMR-MS interface (BNMI). Since October 2004 the Bruker Daltonics microTOF-LC time-of-flight mass spectrometer can also be integrated in an LC-NMR setup.
PERSON:Daniel Schober
WEB:<http://www.bruker-biospin.com/hyphenation_lcnmr_ms.html>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400276
@@ -1526,7 +1526,7 @@
sample injection system
- An automated chromatography system that injects the sample into the chromatography columns in order to increase speed and minimize human involvement in the purification process for better reproducibility.
+ An automated chromatography system that injects the sample into the chromatography columns in order to increase speed and minimize human involvement in the purification process for better reproducibility.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01057
@@ -1548,7 +1548,7 @@
multiple wavelength detector
- A chromatography detector, that can detect many discrete wavelengths in parallel and produces a multiple wavelength chromatographic profile.
+ A chromatography detector, that can detect many discrete wavelengths in parallel and produces a multiple wavelength chromatographic profile.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01078
@@ -1563,7 +1563,7 @@
photoionization detector
- The selective determination of aromatic hydrocarbons or organo-heteroatom species is the job of the photoionization detector (PID). This device uses ultraviolet light as a means of ionizing an analyte exiting from a GC column. The ions produced by this process are collected by electrodes. The current generated is therefore a measure of the analyte concentration. f the amount of ionization is reproducible for a given compound, pressure, and light source then the current collected at the PID's reaction cell electrodes is reproducibly proportional to the amount of that compound entering the cell. The reason why the compounds that are routinely analyzed are either aromatic hydrocarbons or heteroatom containing compounds (like organosulfur or organophosphorus species) is because these species have ionization potentials (IP) that are within reach of commercially available UV lamps. The available lamp energies range from 8.3 to 11.7 ev, that is, lambda max ranging from 150 nm to 106 nm. Although most PIDs have only one lamp, lamps in the PID are exchanged depending on the compound selectivity required in the analysis.
+ The selective determination of aromatic hydrocarbons or organo-heteroatom species is the job of the photoionization detector (PID). This device uses ultraviolet light as a means of ionizing an analyte exiting from a GC column. The ions produced by this process are collected by electrodes. The current generated is therefore a measure of the analyte concentration. f the amount of ionization is reproducible for a given compound, pressure, and light source then the current collected at the PID's reaction cell electrodes is reproducibly proportional to the amount of that compound entering the cell. The reason why the compounds that are routinely analyzed are either aromatic hydrocarbons or heteroatom containing compounds (like organosulfur or organophosphorus species) is because these species have ionization potentials (IP) that are within reach of commercially available UV lamps. The available lamp energies range from 8.3 to 11.7 ev, that is, lambda max ranging from 150 nm to 106 nm. Although most PIDs have only one lamp, lamps in the PID are exchanged depending on the compound selectivity required in the analysis.
PERSON:Daniel Schober
PID
WEB:<http://www.chemistry.adelaide.edu.au/external/soc-rel/content/pid.htm>
@@ -1579,7 +1579,7 @@
gas generator
- An instrument that generates gases for use with the gas chromatograph. Previously gas was obtained from gas tanks or gas cylinders. However, over the past decade the use of gas generators have become more popular as it avoids having gases at high pressure in the laboratory which is perceived by some as potentially dangerous. In addition, the use of a hydrogen generator avoids the use of a cylinder of hydrogen at high pressure which is also perceived by some as a serious fire hazard despite the fact that they have been used in laboratories, quite safely for nearly a century.
+ An instrument that generates gases for use with the gas chromatograph. Previously gas was obtained from gas tanks or gas cylinders. However, over the past decade the use of gas generators have become more popular as it avoids having gases at high pressure in the laboratory which is perceived by some as potentially dangerous. In addition, the use of a hydrogen generator avoids the use of a cylinder of hydrogen at high pressure which is also perceived by some as a serious fire hazard despite the fact that they have been used in laboratories, quite safely for nearly a century.
PERSON:Daniel Schober
WEB:<http://www.chromatography-online.org/GC/Gas-Supplies/Pure-Air-Generators./rs5.html>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01033
@@ -1595,7 +1595,7 @@
column jacket
- A column jacket is a piece of column chromatography equipment that covers a column in order to ensure thermoisolation and create a controllable thermostatic microenvironment.
+ A column jacket is a piece of column chromatography equipment that covers a column in order to ensure thermoisolation and create a controllable thermostatic microenvironment.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01276
@@ -1611,7 +1611,7 @@
electron capture detector
- The electron capture detector is a GC detector that uses a radioactive Beta emitter (electrons) to ionize some of the carrier gas and produce a current between a biased pair of electrodes. When organic molecules that contain electronegative functional groups, such as halogens, phosphorous, and nitro groups pass by the detector, they capture some of the electrons and reduce the current measured between the electrodes.
+ The electron capture detector is a GC detector that uses a radioactive Beta emitter (electrons) to ionize some of the carrier gas and produce a current between a biased pair of electrodes. When organic molecules that contain electronegative functional groups, such as halogens, phosphorous, and nitro groups pass by the detector, they capture some of the electrons and reduce the current measured between the electrodes.
PERSON:Daniel Schober
ECD
WEB:<http://homepages.onsnet.nu/%7Ealkema/html/whatisgc.html>
@@ -1627,7 +1627,7 @@
reversed phase column
- A reversed phase column is a chromatography column in which the mobile phase is more polar than the stationary phase. Its counterpart is the normal phase column.
+ A reversed phase column is a chromatography column in which the mobile phase is more polar than the stationary phase. Its counterpart is the normal phase column.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01106
@@ -1642,7 +1642,7 @@
injector lubricant
- A lubricant used in liquid chromatography that eases sample injector penetration.
+ A lubricant used in liquid chromatography that eases sample injector penetration.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01118
@@ -1657,7 +1657,7 @@
DISCOVERY console
- The Discovery console is a Windows XP Professional-based, integrated console designed especially for Solid-State NMR. The console includes everything needed to interface to any magnet and solids probe - from computer to cables to duplexing network.
+ The Discovery console is a Windows XP Professional-based, integrated console designed especially for Solid-State NMR. The console includes everything needed to interface to any magnet and solids probe - from computer to cables to duplexing network.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400247
@@ -1673,7 +1673,7 @@
Bruker AMX series NMR instrument
- A series of older Bruker NMR magnets, now out of production. The Bruker AMX500 has proven an extremely reliable workhorse, with excellent lineshape yielding superior water suppression even without gradients. The Oxford 11.7 Tesla 5.2 cm bore magnet rests on a TMC vibration damping table. Homogeneity is controlled by a BSN-18 and BSN-2 with 19 shim controls. In addition to the 5 mm triple resonance probe, the AMX is equipped with a 10mm broadband observe probe.
+ A series of older Bruker NMR magnets, now out of production. The Bruker AMX500 has proven an extremely reliable workhorse, with excellent lineshape yielding superior water suppression even without gradients. The Oxford 11.7 Tesla 5.2 cm bore magnet rests on a TMC vibration damping table. Homogeneity is controlled by a BSN-18 and BSN-2 with 19 shim controls. In addition to the 5 mm triple resonance probe, the AMX is equipped with a 10mm broadband observe probe.
PERSON:Daniel Schober
WEB:<http://www.tufts.edu/med/biochemistry/NMR/amx500.html>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400240
@@ -1689,7 +1689,7 @@
chromatofocusing column
- A chromatofocusing column is a chromatography column in which a resin is equilibrated at one pH and eluted at a second pH. The use of a weak ion-exchange resin causes a pH gradient to be formed at the solvent front owing to the buffering action of the resin. This pH gradient in turn leads to an ordering of proteins by isoelectric point. Molecules of charge sign opposite the resin bind; those of charge sign like the resin do not bind.
+ A chromatofocusing column is a chromatography column in which a resin is equilibrated at one pH and eluted at a second pH. The use of a weak ion-exchange resin causes a pH gradient to be formed at the solvent front owing to the buffering action of the resin. This pH gradient in turn leads to an ordering of proteins by isoelectric point. Molecules of charge sign opposite the resin bind; those of charge sign like the resin do not bind.
PERSON:Daniel Schober
WEB:<http://www.bioprocessintl.com/default.asp?page=glossary&TopicID=1>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01209
@@ -1716,7 +1716,7 @@
NMR probe
- Part of an NMR instrument that detects the signals emitted from a sample. No single probe can perform the full range of experiments, and probes that are designed to perform more than one type of measurement usually suffer from performance compromises. The probe represents a rather fragile single point of failure that can render an NMR system completely unusable if the probe is dropped or otherwise damaged. Probes are usually characterised by Sample diameter and Frequency.n alt The instrument that transmits and receives radiofrequency to and from the NMR sample.
+ Part of an NMR instrument that detects the signals emitted from a sample. No single probe can perform the full range of experiments, and probes that are designed to perform more than one type of measurement usually suffer from performance compromises. The probe represents a rather fragile single point of failure that can render an NMR system completely unusable if the probe is dropped or otherwise damaged. Probes are usually characterised by Sample diameter and Frequency.n alt The instrument that transmits and receives radiofrequency to and from the NMR sample.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400014
@@ -1732,7 +1732,7 @@
NMR magnet
- A magnet which induces a certain frequency (MHz) and which has a certain bore diameter.n alt The NMR signal is a natural physical property of the certain atomic nuclei but it can only be detected with an external magnetic field. A magnet is a fundamental part of an NMR instrument which induces an electromagnetic force field (RF pulse) and by this excites and aligns the spins of the electrons of the NMR acquisition nucleus. It is usually a big (superconducting) electromagnet which is cooled by liquid helium and can be adjusted to a frequency between 200 and 950 MHz. The magnetic field strength is measured in Tesla or Gauss.
+ A magnet which induces a certain frequency (MHz) and which has a certain bore diameter.n alt The NMR signal is a natural physical property of the certain atomic nuclei but it can only be detected with an external magnetic field. A magnet is a fundamental part of an NMR instrument which induces an electromagnetic force field (RF pulse) and by this excites and aligns the spins of the electrons of the NMR acquisition nucleus. It is usually a big (superconducting) electromagnet which is cooled by liquid helium and can be adjusted to a frequency between 200 and 950 MHz. The magnetic field strength is measured in Tesla or Gauss.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400185
@@ -1748,7 +1748,7 @@
trap column
- A trap column is a chromatography column which is used prior to a, e.g. mass spectrometry, separation to clean up or concentrate controlled amounts of samples prior to elution to a detector.
+ A trap column is a chromatography column which is used prior to a, e.g. mass spectrometry, separation to clean up or concentrate controlled amounts of samples prior to elution to a detector.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01261
@@ -1763,7 +1763,7 @@
flow probe
- An NMR probe that allows the automatized flow-through of a sample. The sample is aspirated via a syringe pump into the Flow probe, the NMR spectrum is acquired and when the experiment is complete, the sample is returned to back to an external source (well plate) or flushed to waste. Sometimes pulsed field gradients (PFG) can be established in flow probes.
+ An NMR probe that allows the automatized flow-through of a sample. The sample is aspirated via a syringe pump into the Flow probe, the NMR spectrum is acquired and when the experiment is complete, the sample is returned to back to an external source (well plate) or flushed to waste. Sometimes pulsed field gradients (PFG) can be established in flow probes.
PERSON:Daniel Schober
WEB:<http://www.varianinc.com/cgi-bin/nav?products/NMR/accessory/auto_samplers/vast/index&cid=HFIH>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400131
@@ -1779,7 +1779,7 @@
flame ionization detector
- A flame ionization detector is a GC detector that consist of a hydrogen/air flame and a collector plate which are normally heated independently of the chromatographic oven. Heating is necessary in order to prevent condensation of water generated by the flame and also to prevent any hold-up of solutes as they pass from the column to the flame. There is an electrode above the flame to collect the ions formed at a hydrogen/air flame. The number of ions hitting the collector is measured and a signal is generated. Flame ionization detectors are most widely used and generally applicable for gas chromatography and hence is used for routine and general purpose analysis. It is easy to use but destructive of the sample.
+ A flame ionization detector is a GC detector that consist of a hydrogen/air flame and a collector plate which are normally heated independently of the chromatographic oven. Heating is necessary in order to prevent condensation of water generated by the flame and also to prevent any hold-up of solutes as they pass from the column to the flame. There is an electrode above the flame to collect the ions formed at a hydrogen/air flame. The number of ions hitting the collector is measured and a signal is generated. Flame ionization detectors are most widely used and generally applicable for gas chromatography and hence is used for routine and general purpose analysis. It is easy to use but destructive of the sample.
PERSON:Daniel Schober
FID
WEB:<http://homepages.onsnet.nu/%7Ealkema/html/whatisgc.html>
@@ -1795,7 +1795,7 @@
vial
- A container made from solid material and primarily used for holding liquid.
+ A container made from solid material and primarily used for holding liquid.
https://orcid.org/0000-0002-8844-9165
https://en.wikipedia.org/wiki/Vial
vial
@@ -1815,7 +1815,7 @@
magic angle spinning rotor
- A rotor device that holds the NMR sample and enables the adjustment of the orientation of the rotation axis for a sample in a NMR instrument in the magic angle.
+ A rotor device that holds the NMR sample and enables the adjustment of the orientation of the rotation axis for a sample in a NMR instrument in the magic angle.
PERSON:Daniel Schober
MAS rotor
WEB:<http://www.freepatentsonline.com/4352066.html>
@@ -1832,7 +1832,7 @@
Varian VXR spectrometer
- A Varian NMR spectrometer.
+ A Varian NMR spectrometer.
PERSON:Daniel Schober
WEB:<http://www.scs.uiuc.edu/NMR/instruments/vxr500.php>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400238
@@ -1848,7 +1848,7 @@
splitless GC injector
- Injected sample enters column immediately (while split valve to split vent is closed). Here a sample is introduced into a heated small chamber via a syringe through a septum - the heat facilitates volatilization of the sample and sample matrix. The carrier gas then either sweeps the entirety (splitless mode) or a portion (split mode) of the sample into the column. In split mode, a part of the sample/carrier gas mixture in the injection chamber is exhausted through the split vent.
+ Injected sample enters column immediately (while split valve to split vent is closed). Here a sample is introduced into a heated small chamber via a syringe through a septum - the heat facilitates volatilization of the sample and sample matrix. The carrier gas then either sweeps the entirety (splitless mode) or a portion (split mode) of the sample into the column. In split mode, a part of the sample/carrier gas mixture in the injection chamber is exhausted through the split vent.
PERSON:Daniel Schober
WEB:<http://en.wikipedia.org/wiki/Gas_chromatography>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01060
@@ -1863,7 +1863,7 @@
preparative autosampler
- For preparative LC with injection of sample volumes ranging from L to mL ranges.
+ For preparative LC with injection of sample volumes ranging from L to mL ranges.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01062
@@ -1878,7 +1878,7 @@
flow high resolution probe
- Hyphenated analytical techniques combining mass spectrometry and chromatography are well-established laboratory tools. The combination of chromatography and NMR has also made its way into the analytical laboratory. Further developments even combine all three techniques into an LC-NMR/NMR-MS system. The use of solid phase extraction provides an efficient interface between chromatography and NMR with demands for special type of flow probes.
+ Hyphenated analytical techniques combining mass spectrometry and chromatography are well-established laboratory tools. The combination of chromatography and NMR has also made its way into the analytical laboratory. Further developments even combine all three techniques into an LC-NMR/NMR-MS system. The use of solid phase extraction provides an efficient interface between chromatography and NMR with demands for special type of flow probes.
PERSON:Daniel Schober
flow HR-probe
GROUP:<http://msi-ontology.sourceforge.net>
@@ -1895,7 +1895,7 @@
liquid chromatography valve
- A sample valve that must be able to sustain pressures up to 10,000 p.s.i., although it is most likely to operate on a continuous basis, at pressures of 3,000 p.s.i. or less. The higher the operating pressure the tighter the valve seating surfaces must be forced together to eliminate any leak. It follows that any abrasive material, however fine, that passes into the valve can cause the valve seating to become scored each time it is rotated which will ultimately lead to leaks. This will cause the sample size to vary between samples and eventually affect the accuracy of the analysis. It follows that any solid material must be carefully removed from any sample before filling the valve. The sample volume of an internal loop valve is situated in the connecting slot of the valve rotor and can be used only for relatively small sample volumes. Internal sample loop valves provide samples with volumes ranging from 0.1 ml to about 0.5 ml. Valve operation is shown in figure 6. The left-hand side diagram shows the load position. The sample occupies the rotor slot and has been filled by passing the sample from an appropriate syringe through the rotor slot to waste. While loading the sample, the mobile phase supply is passed through the valve directly to the column. To place the sample onto the column, the valve is then rotated and the valve slot containing the sample is now placed between the solvent supply and the column. As a result, the sample is passed into the column by the flow of solvent.
+ A sample valve that must be able to sustain pressures up to 10,000 p.s.i., although it is most likely to operate on a continuous basis, at pressures of 3,000 p.s.i. or less. The higher the operating pressure the tighter the valve seating surfaces must be forced together to eliminate any leak. It follows that any abrasive material, however fine, that passes into the valve can cause the valve seating to become scored each time it is rotated which will ultimately lead to leaks. This will cause the sample size to vary between samples and eventually affect the accuracy of the analysis. It follows that any solid material must be carefully removed from any sample before filling the valve. The sample volume of an internal loop valve is situated in the connecting slot of the valve rotor and can be used only for relatively small sample volumes. Internal sample loop valves provide samples with volumes ranging from 0.1 ml to about 0.5 ml. Valve operation is shown in figure 6. The left-hand side diagram shows the load position. The sample occupies the rotor slot and has been filled by passing the sample from an appropriate syringe through the rotor slot to waste. While loading the sample, the mobile phase supply is passed through the valve directly to the column. To place the sample onto the column, the valve is then rotated and the valve slot containing the sample is now placed between the solvent supply and the column. As a result, the sample is passed into the column by the flow of solvent.
PERSON:Daniel Schober
WEB:<http://www.chromatography-online.org/EC-Dispersion/HPLC-Sample-Valves/rs16.html>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01110
@@ -1911,7 +1911,7 @@
JEOL NMR probe
- An NMR probe that is manufactured by JEOL.
+ An NMR probe that is manufactured by JEOL.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400232
@@ -1927,7 +1927,7 @@
Bruker UltraShield Plus NMR magnet
- An NMR magnet of which Brukers claims it is the latest and most advanced self-shielding NMR magnet technology ever developed. These magnets are the ultimate advancement in high performance, actively-shielded NMR solutions. They offer unprecedented shielding performance whilst ensuring no compromise in system homogeneity, stability or cryogenic specifications.
+ An NMR magnet of which Brukers claims it is the latest and most advanced self-shielding NMR magnet technology ever developed. These magnets are the ultimate advancement in high performance, actively-shielded NMR solutions. They offer unprecedented shielding performance whilst ensuring no compromise in system homogeneity, stability or cryogenic specifications.
PERSON:Daniel Schober
WEB:<http://www.bruker-biospin.com/nmr_magnets_usplus.html>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400190
@@ -1943,7 +1943,7 @@
Bruker CryoProbe
- The Bruker BioSpin CryoProbe is a high-performance cryogenically cooled probe developed for high-resolution applications. It has improved signal/noise (S/N) ratios obtained by reducing the operating temperature of the coil and the pre-amplifier. As a result, the efficiency of the coil is improved and the noise of the coil and the pre-amplifier are reduced.The dramatic increase in the S/N ratio by a factor of 3-4, as compared to conventional probes, leads to a possible reduction in experiment time of up to 16 or a reduction in required sample concentration by a factor of up to 4. The CryoProbes possess key characteristics for NMR analysis:n Significant S/N gains (with moderately salty samples also)n Short pulse widthsn Short ring down timesn Linear behavior in power responsen Gradient capabilityn CryoProbes are available as Triple Resonance, Dual, Selective X Detection, MicroImaging, and Quad Nucleus Probes configurations at 400 MHz and highern All high resolution probes have a lock circuitn All high resolution probes have Z-gradient.
+ The Bruker BioSpin CryoProbe is a high-performance cryogenically cooled probe developed for high-resolution applications. It has improved signal/noise (S/N) ratios obtained by reducing the operating temperature of the coil and the pre-amplifier. As a result, the efficiency of the coil is improved and the noise of the coil and the pre-amplifier are reduced.The dramatic increase in the S/N ratio by a factor of 3-4, as compared to conventional probes, leads to a possible reduction in experiment time of up to 16 or a reduction in required sample concentration by a factor of up to 4. The CryoProbes possess key characteristics for NMR analysis:n Significant S/N gains (with moderately salty samples also)n Short pulse widthsn Short ring down timesn Linear behavior in power responsen Gradient capabilityn CryoProbes are available as Triple Resonance, Dual, Selective X Detection, MicroImaging, and Quad Nucleus Probes configurations at 400 MHz and highern All high resolution probes have a lock circuitn All high resolution probes have Z-gradient.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400191
@@ -1959,7 +1959,7 @@
column cartridge
- A device that binds the chromatography column and additional connector elements and / or valves or syringes into one physical unity for further processing.
+ A device that binds the chromatography column and additional connector elements and / or valves or syringes into one physical unity for further processing.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01055
@@ -1974,7 +1974,7 @@
affinity column
- An affinity column is a chromatography column that is used in affinity chromatography. Differences in the affinity of molecules to be separated to a stationary phase are used for discriminate retention.
+ An affinity column is a chromatography column that is used in affinity chromatography. Differences in the affinity of molecules to be separated to a stationary phase are used for discriminate retention.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01094
@@ -1989,7 +1989,7 @@
tecmag NMR instrument
- An NMR instrument that is manufactured by tecmag.
+ An NMR instrument that is manufactured by tecmag.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400250
@@ -2005,7 +2005,7 @@
gel filtration column
- A Gel filtration column is a chromatography column for size-exclusion chromatography, in which the stationary phase is a gel. The main application of gel filtration chromatography is the fractionation of proteins and other water-soluble polymers.
+ A Gel filtration column is a chromatography column for size-exclusion chromatography, in which the stationary phase is a gel. The main application of gel filtration chromatography is the fractionation of proteins and other water-soluble polymers.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01104
@@ -2020,7 +2020,7 @@
fraction collector
- A fraction detector is a device that allows regular or specified samples to be taken from a column eluate and stored in a retrievable form. The storage vessels are usually small sample tubes or vials that are oriented in a rotating disk or in a moving belt, there movement usually being controlled by a microprocessor. On receiving a signal from the microprocessor, the next vial is placed under the column outlet and the eluate collected until receiving another signal from the computer. Once the properties of the chromatogram that describes the separation has been ascertained, then the collection program can be defined. The fractions can be collected on a basis of time either at regular intervals or a specific times to collect specific peaks. Alternatively the fractions can be collected by monitoring the detector output and when a peak starts to elute the fraction collector is activated and the peak collected in a specific vial. When the peak returns to base line the column eluate is then directed to waste until the next peak starts eluting. Fraction collectors are in common use with most liquid chromatographs. They are used to collect samples for further purification, subsequent examination by spectroscopic techniques or for biological or organoleptic testing.
+ A fraction detector is a device that allows regular or specified samples to be taken from a column eluate and stored in a retrievable form. The storage vessels are usually small sample tubes or vials that are oriented in a rotating disk or in a moving belt, there movement usually being controlled by a microprocessor. On receiving a signal from the microprocessor, the next vial is placed under the column outlet and the eluate collected until receiving another signal from the computer. Once the properties of the chromatogram that describes the separation has been ascertained, then the collection program can be defined. The fractions can be collected on a basis of time either at regular intervals or a specific times to collect specific peaks. Alternatively the fractions can be collected by monitoring the detector output and when a peak starts to elute the fraction collector is activated and the peak collected in a specific vial. When the peak returns to base line the column eluate is then directed to waste until the next peak starts eluting. Fraction collectors are in common use with most liquid chromatographs. They are used to collect samples for further purification, subsequent examination by spectroscopic techniques or for biological or organoleptic testing.
PERSON:Daniel Schober
WEB:<http://www.chromatography-online.org/topics/fraction/collector.html>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01073
@@ -2035,7 +2035,7 @@
in-line filter
- A solvent filter that sits between the pump and the injection valve that prevents dust particles, general debris and, to some extent, bacteria from entering the chromatography system. Contaminants can interfere with the low-pressure gradient former or the pump and particles entering valves may interfere with the proper function. The result could cause an increased baseline noise, non-repeatable gradient forming, unreliable flow rate or other interferences. Solvent in-line filters are low-pressure filters and will allow a high flow rate due to a large surface area and large porosity.
+ A solvent filter that sits between the pump and the injection valve that prevents dust particles, general debris and, to some extent, bacteria from entering the chromatography system. Contaminants can interfere with the low-pressure gradient former or the pump and particles entering valves may interfere with the proper function. The result could cause an increased baseline noise, non-repeatable gradient forming, unreliable flow rate or other interferences. Solvent in-line filters are low-pressure filters and will allow a high flow rate due to a large surface area and large porosity.
PERSON:Daniel Schober
WEB:<http://www.appliedporous.com/frits-chromatography.htm>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01123
@@ -2050,7 +2050,7 @@
imaging NMR probe
- An NMR probe that is designed for generating pictures from sample states via NMR imaging.
+ An NMR probe that is designed for generating pictures from sample states via NMR imaging.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400244
@@ -2066,7 +2066,7 @@
Bruker AC series NMR instrument
- A series of older Bruker NMR magnets, now out of production.
+ A series of older Bruker NMR magnets, now out of production.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400241
@@ -2082,7 +2082,7 @@
gas chromatography equipment
- Any device used in a gas chromatography experiment.
+ Any device used in a gas chromatography experiment.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01030
@@ -2098,7 +2098,7 @@
syringe filter
- A small membrane filter of defined pore size, that filters samples from a syringe.
+ A small membrane filter of defined pore size, that filters samples from a syringe.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01122
@@ -2119,7 +2119,7 @@
Bruker SampleRail system
- This Instrument system automatically prepares an NMR sample, inserts it into an NMR magnet, performs NMR experiments on the sample, and transports it back to the preparation system. The SampleRail fulfills the transporting tasks from the preparation system into the NMR magnet and back.
+ This Instrument system automatically prepares an NMR sample, inserts it into an NMR magnet, performs NMR experiments on the sample, and transports it back to the preparation system. The SampleRail fulfills the transporting tasks from the preparation system into the NMR magnet and back.
PERSON:Daniel Schober
WEB:<http://www.bruker-biospin.com/automation.html>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400207
@@ -2135,7 +2135,7 @@
column compartment
- For chromatography analyses, the ability to maintain a stable column environment regardless of ambient temperature fluctuations is critical for maintaining retention time precision. In order to ensure such stable conditions at different chromatography steps a column compartment can be installed that ensures e.g. stable temperature of the column in a given step.
+ For chromatography analyses, the ability to maintain a stable column environment regardless of ambient temperature fluctuations is critical for maintaining retention time precision. In order to ensure such stable conditions at different chromatography steps a column compartment can be installed that ensures e.g. stable temperature of the column in a given step.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01068
@@ -2150,7 +2150,7 @@
capillary pump system
- A pump system optimized for capillary chromatography.
+ A pump system optimized for capillary chromatography.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01051
@@ -2171,7 +2171,7 @@
evaporative light scattering detector
- The evaporative light scattering detector, as its name implies, utilizes a spray that continuously atomizes the column eluent into small droplets. These droplets are allowed to evaporate, leaving the solutes as fine particulate matter suspended in the atomizing gas.
+ The evaporative light scattering detector, as its name implies, utilizes a spray that continuously atomizes the column eluent into small droplets. These droplets are allowed to evaporate, leaving the solutes as fine particulate matter suspended in the atomizing gas.
PERSON:Daniel Schober
WEB:<http://www.chromatography-online.org/HPLC-Detectors/Evaporative-Light-Scattering/rs73.html>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01082
@@ -2186,7 +2186,7 @@
column cartridger
- A chromatography device where the column cartridge is inserted into and stabilised.
+ A chromatography device where the column cartridge is inserted into and stabilised.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01054
@@ -2201,7 +2201,7 @@
nitrogen generator
- A gas generator that generates nitrogen gas.
+ A gas generator that generates nitrogen gas.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01034
@@ -2216,7 +2216,7 @@
needle assembly
- The needle assembly attached to the autosampler, comprises the injector needle that feeds a sample or carrier gas into the inlet
+ The needle assembly attached to the autosampler, comprises the injector needle that feeds a sample or carrier gas into the inlet
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01065
@@ -2231,7 +2231,7 @@
Bruker Capillary LC-NMR platform
- Capillary LC-NMR is a hyphenated technique coupling capillary liquid chromatography and NMR, which increases sensitivity dramatically through the use of miniaturization of the chromatographic techniques and NMR detection volume. LC-NMR hyphenated systems separate a mixture into its pure components and couple the output to NMR for automatic sample analysis. The ever increasing need to measure lower sample amounts and lower level impurities demands the highest NMR sensitivity. Traditional LC-NMR systems with relatively large peak volumes are not optimized for such low levels of detection. Bruker BioSpin, together with Waters and Protasis has developed a Capillary LC-NMR system. The latest capillary LC attributes and highest capillary flow probe sensitivity combine with state of the art NMR systems technology. Greater mass sensitivity and faster spectral analysis with smaller sample volumes is possible. This system is ideal for analysis of metabolites and impurities associated with the drug development process.
+ Capillary LC-NMR is a hyphenated technique coupling capillary liquid chromatography and NMR, which increases sensitivity dramatically through the use of miniaturization of the chromatographic techniques and NMR detection volume. LC-NMR hyphenated systems separate a mixture into its pure components and couple the output to NMR for automatic sample analysis. The ever increasing need to measure lower sample amounts and lower level impurities demands the highest NMR sensitivity. Traditional LC-NMR systems with relatively large peak volumes are not optimized for such low levels of detection. Bruker BioSpin, together with Waters and Protasis has developed a Capillary LC-NMR system. The latest capillary LC attributes and highest capillary flow probe sensitivity combine with state of the art NMR systems technology. Greater mass sensitivity and faster spectral analysis with smaller sample volumes is possible. This system is ideal for analysis of metabolites and impurities associated with the drug development process.
PERSON:Daniel Schober
WEB:<http://www.bruker-biospin.com/hyphenation_caplcnmr.html>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400279
@@ -2248,7 +2248,7 @@
gas chromatography oven
- A gas chromatography oven is an oven with a heated connection between the GC and the MS instrument in a GCMS-analysis, that keeps compounds in the gas phase as they leave the GC oven.
+ A gas chromatography oven is an oven with a heated connection between the GC and the MS instrument in a GCMS-analysis, that keeps compounds in the gas phase as they leave the GC oven.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01039
@@ -2264,7 +2264,7 @@
autosampler
- An optional part of an NMR instrument used to hold samples prior to NMR analysis and that sequentially loads these samples into the analytical part of the NMR instrument. n alt The autosampler is an automatic sample changer device.
+ An optional part of an NMR instrument used to hold samples prior to NMR analysis and that sequentially loads these samples into the analytical part of the NMR instrument. n alt The autosampler is an automatic sample changer device.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400002
@@ -2280,7 +2280,7 @@
isocratic pump system
- A pump system optimized for isocratic chromatography.
+ A pump system optimized for isocratic chromatography.
PERSON:Daniel Schober
WEB:<http://www.buchi.com/Isocratic-Pump-System.253.0.html>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01049
@@ -2295,7 +2295,7 @@
flash pump system
- Any pump system used in flash column chromatography to push the solvent through the column. Better flow rates can be achieved by using a pump or by using compressed gas (e.g. air, nitrogen, or argon) to push the solvent through the column (flash column chromatography).
+ Any pump system used in flash column chromatography to push the solvent through the column. Better flow rates can be achieved by using a pump or by using compressed gas (e.g. air, nitrogen, or argon) to push the solvent through the column (flash column chromatography).
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01048
@@ -2310,7 +2310,7 @@
Varian UNITY INOVA spectrometer
- The UNITY INOVA is also the easiest spectrometer to use and is also the choice of those interested in using advanced NMR techniques in their own research, but without becoming, or hiring, an NMR expert. A complete set of turnkey operating environments is available for the UNITY INOVA covering the structure and dynamics of biological macromolecules, small molecules, solids, and imaging. These packages put the combined NMR expertise of the entire Varian NMR community at your fingertips.
+ The UNITY INOVA is also the easiest spectrometer to use and is also the choice of those interested in using advanced NMR techniques in their own research, but without becoming, or hiring, an NMR expert. A complete set of turnkey operating environments is available for the UNITY INOVA covering the structure and dynamics of biological macromolecules, small molecules, solids, and imaging. These packages put the combined NMR expertise of the entire Varian NMR community at your fingertips.
PERSON:Daniel Schober
WEB:<http://www.varianinc.com/cgi-bin/nav?products/NMR/spectromet/inova/index&cid=HFIH>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400236
@@ -2326,7 +2326,7 @@
liquid NMR probe
- An NMR probe that is designed to hold a liquid sample.
+ An NMR probe that is designed to hold a liquid sample.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400242
@@ -2342,7 +2342,7 @@
ion exchange column
- An ion exchange column is a chromatography column that is used in ion exchange chromatography and anion or cation exchange resins to enable separation.
+ An ion exchange column is a chromatography column that is used in ion exchange chromatography and anion or cation exchange resins to enable separation.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01105
@@ -2357,7 +2357,7 @@
Bruker NMR probe
- An NMR probe that is manufactured by Bruker.
+ An NMR probe that is manufactured by Bruker.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400231
@@ -2373,7 +2373,7 @@
anion trap column
- An anion trap column is a trap column and ion-exchange column which contains cationic anion-exchange resins.
+ An anion trap column is a trap column and ion-exchange column which contains cationic anion-exchange resins.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01277
@@ -2394,7 +2394,7 @@
fluorescene detector
- A single wavelength detector, where the excitation light wavelength is normally a mercury lamp generated high intensity UV light at 253.7 nm. Many substances that fluoresce will be excited by light of this wavelength and hence be detected.
+ A single wavelength detector, where the excitation light wavelength is normally a mercury lamp generated high intensity UV light at 253.7 nm. Many substances that fluoresce will be excited by light of this wavelength and hence be detected.
PERSON:Daniel Schober
WEB:<http://www.chromatography-online.org/HPLC-Detectors/Fluorescence/Single-Wavelength-Excitation/rs57.html>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01080
@@ -2409,7 +2409,7 @@
tecmag EAGLE probe
- The Eagle is a 4 mm 1H/X solid-state MAS probe with a top spinning speed of 18 kHz. Its simple design is robust, reliable and easy to spin. Configurations are available for 200 to 600 MHz wide bore magnets on Tecmag, Bruker, Chemagnetics, JEOL and Varian spectrometers.
+ The Eagle is a 4 mm 1H/X solid-state MAS probe with a top spinning speed of 18 kHz. Its simple design is robust, reliable and easy to spin. Configurations are available for 200 to 600 MHz wide bore magnets on Tecmag, Bruker, Chemagnetics, JEOL and Varian spectrometers.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400248
@@ -2431,7 +2431,7 @@
electrical conductivity detector
- The electrical conductivity detector measures the conductivity of the mobile phase. There is usually background conductivity which must be backed-off by suitable electronic adjustments. If the mobile phase contains buffers, the detector gives a base signal that completely overwhelms that from any solute usually making detection impossible. Thus, the electrical conductivity detector a bulk property detector. and senses all ions whether they are from a solute or from the mobile phase. In order to prevent polarization of the sensing electrodes, AC voltages must be used and so it is the impedance not the resistance of the electrode system that is actually measured. From a physical chemistry stand point the conductivity of a solution is more important than its resistance. However, it is the resistance (impedance) of the electrode system that determines the current across it. The resistance of any conductor varies directly as its length and inversely as its cross sectional area.
+ The electrical conductivity detector measures the conductivity of the mobile phase. There is usually background conductivity which must be backed-off by suitable electronic adjustments. If the mobile phase contains buffers, the detector gives a base signal that completely overwhelms that from any solute usually making detection impossible. Thus, the electrical conductivity detector a bulk property detector. and senses all ions whether they are from a solute or from the mobile phase. In order to prevent polarization of the sensing electrodes, AC voltages must be used and so it is the impedance not the resistance of the electrode system that is actually measured. From a physical chemistry stand point the conductivity of a solution is more important than its resistance. However, it is the resistance (impedance) of the electrode system that determines the current across it. The resistance of any conductor varies directly as its length and inversely as its cross sectional area.
PERSON:Daniel Schober
WEB:<http://www.chromatography-online.org/HPLC-Detectors/Electrical-Conductivity/rs83.html>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01239
@@ -2452,7 +2452,7 @@
NMR instrument
- An Instrument which is used to carry out a NMR analysis of some sample.
+ An Instrument which is used to carry out a NMR analysis of some sample.
PERSON:Daniel Schober
MRI scanner
NMR instrument
@@ -2471,7 +2471,7 @@
Bruker UltraShield NMR magnet
- An NMR magnet manufactured by Bruker that ensures field homogeneity without amplified effects from vibrations or thermal changes. This magnet technology uses active shielding and optimizes coil design.
+ An NMR magnet manufactured by Bruker that ensures field homogeneity without amplified effects from vibrations or thermal changes. This magnet technology uses active shielding and optimizes coil design.
PERSON:Daniel Schober
WEB:<http://www.bruker-biospin.com/nmr_magnets_us.html?&print=http%3A%2Fitsupportunit.com%2Fawstats%2Ficon%2Fnisum%2Fivuj%2F>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400187
@@ -2487,7 +2487,7 @@
piston-seal
- The seal made by a piston in a diaphragm pump. The unique property of the reciprocating diaphragm pump is that the actuating piston does not come into direct contact with the mobile phase and thus, the demands on the piston-cylinder seal are not so great. The diaphragm has a relatively high surface area and thus, the movement of the diaphragm is relatively small and consequently the pump can be operated at a fairly high frequency. High frequency pumping results in a very significant reduction in pulse amplitude and, in addition, high frequency pulses are more readily damped by the column system. Nevertheless, it must be emphasized that diaphragm pumps are not pulseless.
+ The seal made by a piston in a diaphragm pump. The unique property of the reciprocating diaphragm pump is that the actuating piston does not come into direct contact with the mobile phase and thus, the demands on the piston-cylinder seal are not so great. The diaphragm has a relatively high surface area and thus, the movement of the diaphragm is relatively small and consequently the pump can be operated at a fairly high frequency. High frequency pumping results in a very significant reduction in pulse amplitude and, in addition, high frequency pulses are more readily damped by the column system. Nevertheless, it must be emphasized that diaphragm pumps are not pulseless.
PERSON:Daniel Schober
WEB:<http://www.chromatography-online.org/HPLC/Basic-HPLC/Pump/Diaphragm/rs15.html>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01116
@@ -2502,7 +2502,7 @@
mass selective detector
- A mass selective detector is a GC detector that uses mass spectrometry. It is based upon the ionization of solute molecules in the ion source and the separation of the ions generated on the basis of their mass/charge ratio by an analyzer unit. This may be a magnetic sector analyzer, a quadruple mass filter, or an ion trap. Ions are detected by a dynode electron multiplier.
+ A mass selective detector is a GC detector that uses mass spectrometry. It is based upon the ionization of solute molecules in the ion source and the separation of the ions generated on the basis of their mass/charge ratio by an analyzer unit. This may be a magnetic sector analyzer, a quadruple mass filter, or an ion trap. Ions are detected by a dynode electron multiplier.
PERSON:Daniel Schober
mass spectrometry detector
WEB:<http://homepages.onsnet.nu/%7Ealkema/html/whatisgc.html>
@@ -2518,7 +2518,7 @@
spin column
- A spin column is a chromatography column which is suitable for putting it into a centrifuge. A spin column enforces separation through increased G-forces while spinning the column in a centrifuge. It is often used in DNA gel extraction kits.
+ A spin column is a chromatography column which is suitable for putting it into a centrifuge. A spin column enforces separation through increased G-forces while spinning the column in a centrifuge. It is often used in DNA gel extraction kits.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01232
@@ -2533,7 +2533,7 @@
transfer line
- A combination of devices that are used in connection with a sampling head for transferring components of an applied sample to the analyzing part of a chromatography system.
+ A combination of devices that are used in connection with a sampling head for transferring components of an applied sample to the analyzing part of a chromatography system.
PERSON:Daniel Schober
WEB:<http://www.freepatentsonline.com/5702671.html>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01235
@@ -2549,7 +2549,7 @@
gradient pump system
- A pump system optimized for gradient chromatography.
+ A pump system optimized for gradient chromatography.
PERSON:Daniel Schober
WEB:<http://www.buchi.com/Gradient-Pump-System.531.0.html>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01050
@@ -2564,7 +2564,7 @@
high temperature column
- A high temperature column is a chromatography column which is suitable for and withstands very high temperatures in chromatography ovens.
+ A high temperature column is a chromatography column which is suitable for and withstands very high temperatures in chromatography ovens.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01233
@@ -2579,7 +2579,7 @@
Bruker Ultrastabilized NMR magnet
- An NMR magnet manufactured by Bruker for Ultra-High Field NMR, available from 750 MHz to 900 MHz, which provides reliable operation at reduced temperature and ambient pressure via being rigidly mounted and stabilized.
+ An NMR magnet manufactured by Bruker for Ultra-High Field NMR, available from 750 MHz to 900 MHz, which provides reliable operation at reduced temperature and ambient pressure via being rigidly mounted and stabilized.
PERSON:Daniel Schober
WEB:<http://www.bruker-biospin.com/nmr_magnets_ultrastabilized.html?&print=http%3A%2Fitsupportunit.com%2Fawstats%2Ficon%2Fnisum%2Fivuj%2F>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400188
@@ -2601,7 +2601,7 @@
NMR sample tube
- The sample-tube holds the NMR sample and sits in the nmr probe. It is usually a glass tube of 5-20mm diameter.
+ The sample-tube holds the NMR sample and sits in the nmr probe. It is usually a glass tube of 5-20mm diameter.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400132
@@ -2617,7 +2617,7 @@
Varian UNITY spectrometer
- The predecessor series of the Varian UNITY INOVA spectrometer.
+ The predecessor series of the Varian UNITY INOVA spectrometer.
PERSON:Daniel Schober
WEB:<http://www.scs.uiuc.edu/NMR/instruments/u400.php>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400237
@@ -2633,7 +2633,7 @@
AVANCE II spectrometer
- A spectrometer suitable for metabolomics and in vivo NMR studies but structural analysis of small molecules and low molecular weight proteins can also be performed. To accomplish these studies there are six probe-heads available. A successor, the AVANCE III came out recently.
+ A spectrometer suitable for metabolomics and in vivo NMR studies but structural analysis of small molecules and low molecular weight proteins can also be performed. To accomplish these studies there are six probe-heads available. A successor, the AVANCE III came out recently.
PERSON:Daniel Schober
WEB:<http://cermax.itqb.unl.pt/mambo/en/index.php?option=com_content&task=view&id=36&Itemid=93>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400197
@@ -2649,7 +2649,7 @@
y-column connector
- A column connector that connects one column on one side with two columns at the other side, hence building a Y shaped structure.
+ A column connector that connects one column on one side with two columns at the other side, hence building a Y shaped structure.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01237
@@ -2664,7 +2664,7 @@
Bruker LC-NMR/MS platform
- Includes the connection to a high-resolution TOF-LC-MS system.
+ Includes the connection to a high-resolution TOF-LC-MS system.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400277
@@ -2687,7 +2687,7 @@
refractive index detector
- For analyzing non-UV absorbing substances, such as carbohydrates, lipids and polymers. This is also the detector of choice for gel permeation chromatography. The refractive index detector is one of the least sensitive LC detectors. It is very sensitive to changes in ambient temperature, pressure changes, flow-rate changes and can not be used for gradient elution. Despite these many disadvantages, this detector is extremely useful for detecting those compounds that are nonionic, do not adsorb in the UV, and do not fluoresce. There are many optical systems used in refractive index detectors but one of the most common is the differential refractive index detector.
+ For analyzing non-UV absorbing substances, such as carbohydrates, lipids and polymers. This is also the detector of choice for gel permeation chromatography. The refractive index detector is one of the least sensitive LC detectors. It is very sensitive to changes in ambient temperature, pressure changes, flow-rate changes and can not be used for gradient elution. Despite these many disadvantages, this detector is extremely useful for detecting those compounds that are nonionic, do not adsorb in the UV, and do not fluoresce. There are many optical systems used in refractive index detectors but one of the most common is the differential refractive index detector.
PERSON:Daniel Schober
WEB:<http://www.chromatography-online.org/HPLC/Refractive-Index/rs33.html>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01081
@@ -2702,7 +2702,7 @@
anion exchange column
- An anion exchange column is a chromatography column that is used in anion exchange chromatography and which enables the separation of anion mixtures.
+ An anion exchange column is a chromatography column that is used in anion exchange chromatography and which enables the separation of anion mixtures.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01095
@@ -2717,7 +2717,7 @@
plunger column
- A plunger column is a chromatography column with adjustable heigth control. By means of an adjustable endpiece (plunger) the user can adjust the column length without disturbing the packed bed. Plunger columns can equalize volume changes and thus avoids dead volumes within the column.
+ A plunger column is a chromatography column with adjustable heigth control. By means of an adjustable endpiece (plunger) the user can adjust the column length without disturbing the packed bed. Plunger columns can equalize volume changes and thus avoids dead volumes within the column.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01108
@@ -2732,7 +2732,7 @@
flame photometric detector
- The determination of sulfur or phosphorus containing compounds is the job of the flame photometric detector (FPD). This device uses the chemiluminescent reactions of these compounds in a hydrogen/air flame as a source of analytical information that is relatively specific for substances containing these two kinds of atoms. The emitting species for sulfur compounds is excited S2. The lambda max for emission of excited S2 is approximately 394 nm. The emitter for phosphorus compounds in the flame is excited HPO (lambda max = doublet 510-526 nm). In order to selectively detect one or the other family of compounds as it elutes from the GC column, an interference filter is used between the flame and the photomultiplier tube (PMT) to isolate the appropriate emission band. The drawback here being that the filter must be exchanged between chromatographic runs if the other family of compounds is to be detected.
+ The determination of sulfur or phosphorus containing compounds is the job of the flame photometric detector (FPD). This device uses the chemiluminescent reactions of these compounds in a hydrogen/air flame as a source of analytical information that is relatively specific for substances containing these two kinds of atoms. The emitting species for sulfur compounds is excited S2. The lambda max for emission of excited S2 is approximately 394 nm. The emitter for phosphorus compounds in the flame is excited HPO (lambda max = doublet 510-526 nm). In order to selectively detect one or the other family of compounds as it elutes from the GC column, an interference filter is used between the flame and the photomultiplier tube (PMT) to isolate the appropriate emission band. The drawback here being that the filter must be exchanged between chromatographic runs if the other family of compounds is to be detected.
PERSON:Daniel Schober
FPD
WEB:<http://www.shsu.edu/~chemistry/FPD/FPD.html>
@@ -2748,7 +2748,7 @@
chromatography pump system
- Better flow rates can be achieved by using a pump or by using compressed gas (e.g. air, nitrogen, or argon) to push the solvent through the column (flash column chromatography).
+ Better flow rates can be achieved by using a pump or by using compressed gas (e.g. air, nitrogen, or argon) to push the solvent through the column (flash column chromatography).
PERSON:Daniel Schober
WEB:<http://en.wikipedia.org/wiki/Column_chromatography>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01046
@@ -2763,7 +2763,7 @@
Bruker 1mm MicroProbe
- Over the past few years there has been a significantly growing demand for miniaturization in all areas ofmodern research and development. Evoked by many exciting applications, there is a need for analytical methods which require less amounts of sample. Bruker BioSpin meets this challenge with a revolutionary NMR probe design: The 1mm MicroProbe. It operates with disposable 1mm capillary sample tubes and the sample volume of 5 microliters enables the use of lowest amounts of sample to run all high resolution NMR experiments with outstanding sensitivity and up to 16 times faster measurements. Due to the TXI-type probe design, the z-gradient coil and the automatic matching and tuning accessory, the 1mm MicroProbe can be used for a wide variety of NMR experiments. The key advantages of this probe include:n up to 4 times higher mass sensitivity than 5mm conventional probes (with respect to the same sample amount)n excellent solvent suppression propertiesn virtually no salt effectn discrete samples in tubes that can be sealed and storedn automation accessory for sample preparation and handling available.
+ Over the past few years there has been a significantly growing demand for miniaturization in all areas ofmodern research and development. Evoked by many exciting applications, there is a need for analytical methods which require less amounts of sample. Bruker BioSpin meets this challenge with a revolutionary NMR probe design: The 1mm MicroProbe. It operates with disposable 1mm capillary sample tubes and the sample volume of 5 microliters enables the use of lowest amounts of sample to run all high resolution NMR experiments with outstanding sensitivity and up to 16 times faster measurements. Due to the TXI-type probe design, the z-gradient coil and the automatic matching and tuning accessory, the 1mm MicroProbe can be used for a wide variety of NMR experiments. The key advantages of this probe include:n up to 4 times higher mass sensitivity than 5mm conventional probes (with respect to the same sample amount)n excellent solvent suppression propertiesn virtually no salt effectn discrete samples in tubes that can be sealed and storedn automation accessory for sample preparation and handling available.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400194
@@ -2779,7 +2779,7 @@
Bruker BEST NMR system
- The introduction of biological screening and combinatorial chemistry for chemical synthesis has also introduced new requirements for NMR automation, e.g., the use of well plates for sample input, increased demands on throughput, and the need for quick and simple interpretation of the acquired NMR data.
+ The introduction of biological screening and combinatorial chemistry for chemical synthesis has also introduced new requirements for NMR automation, e.g., the use of well plates for sample input, increased demands on throughput, and the need for quick and simple interpretation of the acquired NMR data.
PERSON:Daniel Schober
Bruker Efficient Sample Transfer NMR
WEB:<http://www.bruker-biospin.com/automation.html>
@@ -2796,7 +2796,7 @@
chromatography detector filter
- An optical filter that is used to obtain monochromatic light of a defined wavelength from detector lamps.
+ An optical filter that is used to obtain monochromatic light of a defined wavelength from detector lamps.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01121
@@ -2811,7 +2811,7 @@
cation trap column
- A cation trap column is a trap column and ion-exchange column which contains anionic cation-exchange resins.
+ A cation trap column is a trap column and ion-exchange column which contains anionic cation-exchange resins.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01278
@@ -2826,7 +2826,7 @@
column adapter
- An Adapter that enabled the connection of a column to additional devices.
+ An Adapter that enabled the connection of a column to additional devices.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01113
@@ -2848,7 +2848,7 @@
pulsed amperometric detector
- A chromatography detector as used by high-performance anion exchange chromatography that provides sensitive and specific detection of carbohydrates. Pulsed Electrochemical Detection (PED) allows simple, sensitive, and direct detection of numerous polar aliphatic compounds, especially carbohydrates. This technique exploits the electrocatalytic activity of noble metal electrode surfaces to oxidize various polar functional groups. In PED, multi-step potential-time waveforms at Au and Pt electrodes realize amperometric/coulometric detection while maintaining uniform and reproducible electrode activity. The response mechanisms in PED are dominated by the surface properties of the electrode, and, as a consequence, members of each chemical class of compounds produce virtually identical voltammetric responses. Thus, the full potential is realized when combined with high performance liquid chromatography (HPLC).
+ A chromatography detector as used by high-performance anion exchange chromatography that provides sensitive and specific detection of carbohydrates. Pulsed Electrochemical Detection (PED) allows simple, sensitive, and direct detection of numerous polar aliphatic compounds, especially carbohydrates. This technique exploits the electrocatalytic activity of noble metal electrode surfaces to oxidize various polar functional groups. In PED, multi-step potential-time waveforms at Au and Pt electrodes realize amperometric/coulometric detection while maintaining uniform and reproducible electrode activity. The response mechanisms in PED are dominated by the surface properties of the electrode, and, as a consequence, members of each chemical class of compounds produce virtually identical voltammetric responses. Thus, the full potential is realized when combined with high performance liquid chromatography (HPLC).
PERSON:Daniel Schober
PAD
WEB:<http://adsabs.harvard.edu/abs/2004SPIE.5261..103L>
@@ -2864,7 +2864,7 @@
Bruker NMR instrument
- An NMR instrument that is manufactured by Bruker.
+ An NMR instrument that is manufactured by Bruker.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400198
@@ -2880,7 +2880,7 @@
Bruker NMR magnet
- An NMR magnet that is manufactured by Bruker.
+ An NMR magnet that is manufactured by Bruker.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400186
@@ -2896,7 +2896,7 @@
ozone-induced chemiluminescence detector
- Although there are many direct ozone chemiluminescent reactions with various gaseous molecules, the incorporation of a conversion step to convert various non-chemiluminescent analytes to a species capable of reacting with ozone to produce chemiluminescence broadens the horizon of this technique tremendously. The conversion of nearly all nitrogen- and sulfur-containing compounds to their respective chemiluminescent species for universal nitrogen and sulfur detection has made nitrogen/sulfur chemiluminescence detection the most widely used analytical methods based upon ozone-induced chemiluminescence. In addition to non-chromatographic applications, nitrogen/sulfur chemiluminescence detection has been adapted to various chromatographic techniques from gas chromatography to liquid and supercritical fluid chromatography as specialized element-specific detectors. The characteristics of these detectors are evaluated and compared to other element-selective detection techniques. The unique features of the chemiluminescence detectors have made them powerful tools in many diverse fields of analytical chemistry.
+ Although there are many direct ozone chemiluminescent reactions with various gaseous molecules, the incorporation of a conversion step to convert various non-chemiluminescent analytes to a species capable of reacting with ozone to produce chemiluminescence broadens the horizon of this technique tremendously. The conversion of nearly all nitrogen- and sulfur-containing compounds to their respective chemiluminescent species for universal nitrogen and sulfur detection has made nitrogen/sulfur chemiluminescence detection the most widely used analytical methods based upon ozone-induced chemiluminescence. In addition to non-chromatographic applications, nitrogen/sulfur chemiluminescence detection has been adapted to various chromatographic techniques from gas chromatography to liquid and supercritical fluid chromatography as specialized element-specific detectors. The characteristics of these detectors are evaluated and compared to other element-selective detection techniques. The unique features of the chemiluminescence detectors have made them powerful tools in many diverse fields of analytical chemistry.
PERSON:Daniel Schober
WEB:<http://sangerhinxtongbr.library.ingentaconnect.com/content/els/00219673/1999/00000842/00000001/art00177>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01088
@@ -2911,7 +2911,7 @@
tecmag NMR console
- An NMR console manufactured by tecmac.
+ An NMR console manufactured by tecmac.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400246
@@ -2927,7 +2927,7 @@
JEOL NMR instrument
- An NMR instrument that is manufactured by JEOL.
+ An NMR instrument that is manufactured by JEOL.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400226
@@ -2943,7 +2943,7 @@
chromatography consumable
- A chromatography consumable is a consumable that is used in a chromatography experiment.
+ A chromatography consumable is a consumable that is used in a chromatography experiment.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01115
@@ -2959,7 +2959,7 @@
column frit
- A part of the column content that separates column packing compartments. In radial columns the packing is supported between two cylindrical frits and the gap between represents the bed height or column length. The outer frit is the column inlet and consequently the sample initially has a large area of stationary phase with which to interact. Frits are porous metal products to prevent unwanted particles from entering the chromatography system. These particles may come from the sample, the solvent or debris generated by the chromatography system itself. Such particles entering the system may lead to clogging of capillaries, interference with the chromatography by changing chromatographic parameters or disturbance of the detector function. Characteristics of a frit, besides the diameter and the thickness, is the porosity (pore distribution, density).
+ A part of the column content that separates column packing compartments. In radial columns the packing is supported between two cylindrical frits and the gap between represents the bed height or column length. The outer frit is the column inlet and consequently the sample initially has a large area of stationary phase with which to interact. Frits are porous metal products to prevent unwanted particles from entering the chromatography system. These particles may come from the sample, the solvent or debris generated by the chromatography system itself. Such particles entering the system may lead to clogging of capillaries, interference with the chromatography by changing chromatographic parameters or disturbance of the detector function. Characteristics of a frit, besides the diameter and the thickness, is the porosity (pore distribution, density).
PERSON:Daniel Schober
WEB:<http://www.chromatography-online.org/topics/radial/columns.html>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01070
@@ -2975,7 +2975,7 @@
liquid chromatography column
- A liquid chromatography column is a chromatography column that is used in liquid chromatography, i.e. a column that is provided with a liquid sample mix.
+ A liquid chromatography column is a chromatography column that is used in liquid chromatography, i.e. a column that is provided with a liquid sample mix.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01227
@@ -2990,7 +2990,7 @@
detector lamp
- A lamp used in a chromatography detector that excites sample molecules at certain frequencies / emission wavelengths, e.g. Mercury Vapor Lamp (253.7 nm), Zinc Vapor Lamp (2123.9 nm and 307.6 nm), Cadmium Vapor Lamp (228.8, 326.1,340.3, and 346.6 nm). To obtain monochromatic light an appropriate light filter would be needed.
+ A lamp used in a chromatography detector that excites sample molecules at certain frequencies / emission wavelengths, e.g. Mercury Vapor Lamp (253.7 nm), Zinc Vapor Lamp (2123.9 nm and 307.6 nm), Cadmium Vapor Lamp (228.8, 326.1,340.3, and 346.6 nm). To obtain monochromatic light an appropriate light filter would be needed.
PERSON:Daniel Schober
WEB:<http://www.chromatography-online.org/HPLC/UV-Detectors/Fixed-Wavelength/rs23.html>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01119
@@ -3005,7 +3005,7 @@
chart recorder
- The chart recorder is a device that transduces signal-intensities into a graphical peak output: As the separated components of the gas sample emerge into the detector, the change in voltage in the detecting bridge circuit causes a representative peak to be drawn on a chart recorder. The position of the peak along the time axis of the chart measures the component's retention time, which identifies the component. This is directly related to carrier gas flow rate, temperature and column packing and dimensions. The area under each peak is proportional to the concentration of the component of the sample. The area of the peaks inscribed on the chart recorder can be determined by multiplying the height of the peak in mm, by the width of the peak in mm at 1/2 the peak height. The calibration curves for use with the chart recorder are therefore peak area plotted against concentration.
+ The chart recorder is a device that transduces signal-intensities into a graphical peak output: As the separated components of the gas sample emerge into the detector, the change in voltage in the detecting bridge circuit causes a representative peak to be drawn on a chart recorder. The position of the peak along the time axis of the chart measures the component's retention time, which identifies the component. This is directly related to carrier gas flow rate, temperature and column packing and dimensions. The area under each peak is proportional to the concentration of the component of the sample. The area of the peaks inscribed on the chart recorder can be determined by multiplying the height of the peak in mm, by the width of the peak in mm at 1/2 the peak height. The calibration curves for use with the chart recorder are therefore peak area plotted against concentration.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01069
@@ -3021,7 +3021,7 @@
open tubular column
- An open tubular column is a chromatography column in which the particles of the solid stationary phase or the support coated with a liquid stationary phase are concentrated on or along the inside tube wall leaving an open, unrestricted path for the mobile phase in the middle part of the tube.
+ An open tubular column is a chromatography column in which the particles of the solid stationary phase or the support coated with a liquid stationary phase are concentrated on or along the inside tube wall leaving an open, unrestricted path for the mobile phase in the middle part of the tube.
PERSON:Daniel Schober
WEB:<http:www.iupac.org/publications/pac/1993/pdf/6504x0819.pdf>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01219
@@ -3036,7 +3036,7 @@
high resolution magic angle spin probe
- Samples that are neither solid nor liquid, being of biological, chemical, or pharmaceutical interest, reveal highly resolved spectra when magic angle spinning is applied. The correct solution is a gradient, such that the field varies along the spinner axis. This so-called Magic Angle Gradient is employed in Brukers high resolution Magic Angle Spinning (hr-MAS) probes, and is implemented in such a way that it is compatible with the stator and does not interfere with the sample eject or insert. Bruker BioSpin has developed a series of dedicated probes for standard bore magnets to accommodate the rapidly expanding field of hr-MAS. These probes are available in double (e.g. 1H and 13C) and triple resonance (e.g. 1H, 13C, 15N) modes and come equipped with a deuterium lock channel. The probes have automatic sample ejection and insertion capability, with the availability of an optional sample changer, enabling fully automated sample runs. Probes can be equipped with an optional B0 gradient, directed along the magic angle, so that gradient spectroscopy can be done used.
+ Samples that are neither solid nor liquid, being of biological, chemical, or pharmaceutical interest, reveal highly resolved spectra when magic angle spinning is applied. The correct solution is a gradient, such that the field varies along the spinner axis. This so-called Magic Angle Gradient is employed in Brukers high resolution Magic Angle Spinning (hr-MAS) probes, and is implemented in such a way that it is compatible with the stator and does not interfere with the sample eject or insert. Bruker BioSpin has developed a series of dedicated probes for standard bore magnets to accommodate the rapidly expanding field of hr-MAS. These probes are available in double (e.g. 1H and 13C) and triple resonance (e.g. 1H, 13C, 15N) modes and come equipped with a deuterium lock channel. The probes have automatic sample ejection and insertion capability, with the availability of an optional sample changer, enabling fully automated sample runs. Probes can be equipped with an optional B0 gradient, directed along the magic angle, so that gradient spectroscopy can be done used.
PERSON:Daniel Schober
high resolution MAS, hr-MAS
GROUP:<http://msi-ontology.sourceforge.net>
@@ -3053,7 +3053,7 @@
hydrogen generator
- A gas generator that generates hydrogen gas.
+ A gas generator that generates hydrogen gas.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01035
@@ -3068,7 +3068,7 @@
glass column
- A glass column is a chromatography column made out of glass that is usually used for larger scale and preparative liquid chromatography separations.
+ A glass column is a chromatography column made out of glass that is usually used for larger scale and preparative liquid chromatography separations.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01101
@@ -3083,7 +3083,7 @@
auto injector
- A gas chromatography device that can auto-inject a small number of samples an inlet.
+ A gas chromatography device that can auto-inject a small number of samples an inlet.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01058
@@ -3098,7 +3098,7 @@
Varian NMR instrument
- An NMR instrument that is manufactured by Varian.
+ An NMR instrument that is manufactured by Varian.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400234
@@ -3114,7 +3114,7 @@
Bruker MATCH tube holder system
- The Bruker Multiple Adjustable Tube Clamp Holder MATCH system is a holder for 100 mm long NMR sample tubes with diameters ranging from micro tubes up to 5 mm NMR tubes. The MATCH insert fits into a standard 10 mm Bruker spinner and is suitable for all non-spinning applications.n The MATCH system provides an easy and cost efficient means of optimizing the signal-to-noise ratio of each sample. By matching the NMR tube diameter to the size of the sample, most of the sample can be placed in the active column of the NMR coil. This leads to an enhanced signal detection compared to diluting the same sample quantity in a larger tube.
+ The Bruker Multiple Adjustable Tube Clamp Holder MATCH system is a holder for 100 mm long NMR sample tubes with diameters ranging from micro tubes up to 5 mm NMR tubes. The MATCH insert fits into a standard 10 mm Bruker spinner and is suitable for all non-spinning applications.n The MATCH system provides an easy and cost efficient means of optimizing the signal-to-noise ratio of each sample. By matching the NMR tube diameter to the size of the sample, most of the sample can be placed in the active column of the NMR coil. This leads to an enhanced signal detection compared to diluting the same sample quantity in a larger tube.
PERSON:Daniel Schober
Bruker Multiple Adjustable Tube Clamp Holder
GROUP:<http://msi-ontology.sourceforge.net>
@@ -3131,7 +3131,7 @@
Bruker SPE-NMR platform
- A Solid Phase Extraction (SPE) system provides an interface between liquid chromatography (LC) and NMR. For the process of LC-SPE NMR a chromatographic separation is done and the peaks of interest are trapped on an individual SPE cartridge after the column. The peak selection is done either by UV detection or by evaluation of the on-line registered MS or MSn spectra.
+ A Solid Phase Extraction (SPE) system provides an interface between liquid chromatography (LC) and NMR. For the process of LC-SPE NMR a chromatographic separation is done and the peaks of interest are trapped on an individual SPE cartridge after the column. The peak selection is done either by UV detection or by evaluation of the on-line registered MS or MSn spectra.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400278
@@ -3148,7 +3148,7 @@
guard column
- Guard columns are installed between the injection valve and the analytical or preparative column and here will remove contaminants and prolong the lifetime of the columns.
+ Guard columns are installed between the injection valve and the analytical or preparative column and here will remove contaminants and prolong the lifetime of the columns.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01111
@@ -3164,7 +3164,7 @@
high resolution probe with automatic tuning and matching
- The Automatic Tuning and Matching (ATM) option for AVANCE spectrometers is available for double resonance probes in fixed-frequency and broadband tunable configurations with either direct or indirect detection. Thus, for multinuclear operation, as often required for applications in inorganic chemistry, ATM facilitates the accurate setting of 90 degree pulse widths on both observe and decoupling channels for each chosen nucleus and each individual sample - even with full automation. Triple resonance probes in fixed-frequency configurations, as typically used for inverse detection with high-field systems.
+ The Automatic Tuning and Matching (ATM) option for AVANCE spectrometers is available for double resonance probes in fixed-frequency and broadband tunable configurations with either direct or indirect detection. Thus, for multinuclear operation, as often required for applications in inorganic chemistry, ATM facilitates the accurate setting of 90 degree pulse widths on both observe and decoupling channels for each chosen nucleus and each individual sample - even with full automation. Triple resonance probes in fixed-frequency configurations, as typically used for inverse detection with high-field systems.
PERSON:Daniel Schober
High Resolution Probes with Automatic Tuning and Matching, HR_probe_with_ATM
GROUP:<http://msi-ontology.sourceforge.net>
@@ -3181,7 +3181,7 @@
fluorine-induced chemiluminescence detector
- A gas chromatographic detection system based on the low pressure, gas phase chemiluminescence of the reaction mixture of molecular fluorine with organo-sulfur, -selenium, and -tellurium compounds separated from (gas phase) headspace samples. This detector was originally developed in the research group of John Birks at the University of Colorado, USA and was manufactured and sold by Sievers Instruments (Boulder Colorado, USA). This system can be divided up into three parts: the chromatograph, transfer line, and reaction cell; PMT and photon counting electronics; and the molecular fluorine generator.
+ A gas chromatographic detection system based on the low pressure, gas phase chemiluminescence of the reaction mixture of molecular fluorine with organo-sulfur, -selenium, and -tellurium compounds separated from (gas phase) headspace samples. This detector was originally developed in the research group of John Birks at the University of Colorado, USA and was manufactured and sold by Sievers Instruments (Boulder Colorado, USA). This system can be divided up into three parts: the chromatograph, transfer line, and reaction cell; PMT and photon counting electronics; and the molecular fluorine generator.
PERSON:Daniel Schober
WEB:<http://www.shsu.edu/~chm_tgc/publications/JPP/chasteen.htm>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01087
@@ -3196,7 +3196,7 @@
size exclusion column
- A size exclusion column is a chromatography column as used in size exclusion chromatography and which enables the separation of mixtures according to differrences in molecular size.
+ A size exclusion column is a chromatography column as used in size exclusion chromatography and which enables the separation of mixtures according to differrences in molecular size.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01100
@@ -3211,7 +3211,7 @@
chromatography splitter
- An adjustable restriction that is placed in the waste outlet to allow the necessary pressure to develop at the column inlet to force a flow (q ml/min) through the column. If the flow of mobile phase is Q ml/min then the waste flow will be (Q-q) ml/min. by adjusting the waste flow, the proportion of the sample entering the capillary column can be varied over a wide range of values and the necessary minimum permissible volume for the particular column in use can be selected for analysis. Unfortunately, the fraction taken in this way may not be representative of the original sample. This is due to the individual solutes in the mixture having different diffusivities and, thus, they distribute themselves across the sampling tube in an irregular manner. In general, the components with higher diffusivities (e.g., those solutes of lower molecular weight) will diffuse away from the bulk sample more quickly than those having lower diffusivities.
+ An adjustable restriction that is placed in the waste outlet to allow the necessary pressure to develop at the column inlet to force a flow (q ml/min) through the column. If the flow of mobile phase is Q ml/min then the waste flow will be (Q-q) ml/min. by adjusting the waste flow, the proportion of the sample entering the capillary column can be varied over a wide range of values and the necessary minimum permissible volume for the particular column in use can be selected for analysis. Unfortunately, the fraction taken in this way may not be representative of the original sample. This is due to the individual solutes in the mixture having different diffusivities and, thus, they distribute themselves across the sampling tube in an irregular manner. In general, the components with higher diffusivities (e.g., those solutes of lower molecular weight) will diffuse away from the bulk sample more quickly than those having lower diffusivities.
PERSON:Daniel Schober
WEB:<http://www.chromatography-online.org/EC-Dispersion/GC-Capillary-Columns/rs13.html>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01041
@@ -3227,7 +3227,7 @@
Bruker micro imaging probe
- For medical, biological and material sciences research, avance imaging systems provide optimal object handling and performance with a variety of samples types. Two classes of imaging probes are available: in vivo probes for handling and sustaining live objects such as animals and plants, and conventional imaging probes for materials samples.
+ For medical, biological and material sciences research, avance imaging systems provide optimal object handling and performance with a variety of samples types. Two classes of imaging probes are available: in vivo probes for handling and sustaining live objects such as animals and plants, and conventional imaging probes for materials samples.
PERSON:Daniel Schober
WEB:<http://www.bruker-biospin.com/probes_microimaging.html>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400225
@@ -3243,7 +3243,7 @@
custom made column
- A custom made column ia a chromatography column which is specifically tailored according to the needs of the separation as requested by a scientist or working group.
+ A custom made column ia a chromatography column which is specifically tailored according to the needs of the separation as requested by a scientist or working group.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01234
@@ -3258,7 +3258,7 @@
gel permeation column
- A gel permeation column is a chromatography column which is used in gel permeation chromatography and which employs as the stationary phase a swollen gel made by polymerizing and cross-linking styrene in the presence of a diluent which is a nonsolvent for the styrene polymer. The polymer to be analyzed is introduced at the top of the column and then is elutriated with a solvent. The polymer molecules diffuse through the gel at rates depending on their molecular size.
+ A gel permeation column is a chromatography column which is used in gel permeation chromatography and which employs as the stationary phase a swollen gel made by polymerizing and cross-linking styrene in the presence of a diluent which is a nonsolvent for the styrene polymer. The polymer to be analyzed is introduced at the top of the column and then is elutriated with a solvent. The polymer molecules diffuse through the gel at rates depending on their molecular size.
PERSON:Daniel Schober
WEB:<http://composite.about.com/od/glossaries/l/bldef_g2419.htm>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01103
@@ -3273,7 +3273,7 @@
Bruker SampleJet system
- Bruker BioSpin introduces the SampleJet, a robot for NMR tube automation. The SampleJet has been consciously designed to meet the growing customer demand for simplicity, versatility and higher throughput in NMR sample tube automation.n The SampleJet utilizes the modern-day industry standard for sample arrangements-the 96 well plate array. Therefore, the samples may be handled by standard lab automation devices before or after the NMR measurement.
+ Bruker BioSpin introduces the SampleJet, a robot for NMR tube automation. The SampleJet has been consciously designed to meet the growing customer demand for simplicity, versatility and higher throughput in NMR sample tube automation.n The SampleJet utilizes the modern-day industry standard for sample arrangements-the 96 well plate array. Therefore, the samples may be handled by standard lab automation devices before or after the NMR measurement.
PERSON:Daniel Schober
WEB:<http://www.bruker-biospin.com/automation.html>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400208
@@ -3289,7 +3289,7 @@
JEOL ECX NMR spectrometer
- The ECX series of NMR spectrometers is designed for any laboratory needing an easy-to-use, reliable, routine NMR system. The ECX NMR series is available from 300 to 500 MHz. The console is designed around a modular, digital NMR electronics chassis controlled by an intelligent acquisition computer. For unprecedented flexibility, the JEOL NMR system offers a Windows XP, Mac OSX or LINUX. Both the workstation and spectrometer may be connected to a standard network, allowing seamless remote operation anywhere in the world.
+ The ECX series of NMR spectrometers is designed for any laboratory needing an easy-to-use, reliable, routine NMR system. The ECX NMR series is available from 300 to 500 MHz. The console is designed around a modular, digital NMR electronics chassis controlled by an intelligent acquisition computer. For unprecedented flexibility, the JEOL NMR system offers a Windows XP, Mac OSX or LINUX. Both the workstation and spectrometer may be connected to a standard network, allowing seamless remote operation anywhere in the world.
PERSON:Daniel Schober
WEB:<http://www.jeol.com/PRODUCTS/AnalyticalInstruments/NuclearMagneticResonance/ECX/tabid/145/Default.aspx>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400227
@@ -3305,7 +3305,7 @@
quaternary pump system
- A pump system that pump and mix up to four different solvents in parallel.
+ A pump system that pump and mix up to four different solvents in parallel.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01047
@@ -3320,7 +3320,7 @@
carbon nanotube column
- Carbon nanotubes (CNTs) are known to have high thermal and mechanical stability and have the potential to be high-performance separation media that utilize the nanoscale interactions. CNT can be applied in long capillary tubes for the development of gas chromatography columns. A film of CNTs can be deposited by chemical vapor deposition (CVD) to form the stationary phase in the open tubular format. Altering the CVD conditions can vary the thickness and the morphology of the CNT film, which opens the possibility of selectivity tuning. The ability to fabricate long tubes coated with CNTs can be readily employed in other gas- and liquid-phase separations as well.
+ Carbon nanotubes (CNTs) are known to have high thermal and mechanical stability and have the potential to be high-performance separation media that utilize the nanoscale interactions. CNT can be applied in long capillary tubes for the development of gas chromatography columns. A film of CNTs can be deposited by chemical vapor deposition (CVD) to form the stationary phase in the open tubular format. Altering the CVD conditions can vary the thickness and the morphology of the CNT film, which opens the possibility of selectivity tuning. The ability to fabricate long tubes coated with CNTs can be readily employed in other gas- and liquid-phase separations as well.
PERSON:Daniel Schober
WEB:<http://pubs.acs.org/cgi-bin/abstract.cgi/ancham/2005/77/i21/abs/ac050812j.html>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01107
@@ -3335,7 +3335,7 @@
Bruker solid magic angle spinning probe
- Magic angle spinning, nowadays a routine technique for solids NMR, still offers the capability of innovation. The high mechanical performance of MAS probes in conjunction with efficient rf pulse techniques open new exciting fields in solids NMR of biological samples and in the field of quadrupolar nuclei.
+ Magic angle spinning, nowadays a routine technique for solids NMR, still offers the capability of innovation. The high mechanical performance of MAS probes in conjunction with efficient rf pulse techniques open new exciting fields in solids NMR of biological samples and in the field of quadrupolar nuclei.
PERSON:Daniel Schober
solid MAS probe
GROUP:<http://msi-ontology.sourceforge.net>
@@ -3352,7 +3352,7 @@
Varian MERCURY spectrometer
- MERCURYplus spectrometers provide superior control, stability, and performance for high-productivity environments. Surface-mount electronics enable a small footprint without compromising data quality. Modular design allows flexible configuration. Direct digital synthesis, linear amplifiers, and other innovative RF and digital technologies enable push-button operation.
+ MERCURYplus spectrometers provide superior control, stability, and performance for high-productivity environments. Surface-mount electronics enable a small footprint without compromising data quality. Modular design allows flexible configuration. Direct digital synthesis, linear amplifiers, and other innovative RF and digital technologies enable push-button operation.
PERSON:Daniel Schober
WEB:<http://www.varianinc.com/cgi-bin/nav?varinc/docs/products/NMR/spectromet/mercury/index&cid=975JINLIKLRMPGLMNOILJ>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400235
@@ -3368,7 +3368,7 @@
Bruker Metabolic Profiler
- An NMR platform for conducting metabonomics studies, traditional metabolism studies, and analysis of complex mixtures, featuring an Avance NMR spectrometer and a microTOF from Bruker Daltonics. By combining the structural resolving power of NMR with mass accuracy of the microTOF Bruker offers a complete system for metabolic research. The Metabolic Profiler provides a simple, easy to use and inexpensive base-system to acquire the spectroscopic data, needed to do basic metabolic profiling including metabonomic statistical analysis.
+ An NMR platform for conducting metabonomics studies, traditional metabolism studies, and analysis of complex mixtures, featuring an Avance NMR spectrometer and a microTOF from Bruker Daltonics. By combining the structural resolving power of NMR with mass accuracy of the microTOF Bruker offers a complete system for metabolic research. The Metabolic Profiler provides a simple, easy to use and inexpensive base-system to acquire the spectroscopic data, needed to do basic metabolic profiling including metabonomic statistical analysis.
PERSON:Daniel Schober
WEB:<http://www.bruker-biospin.com/metabolicprofiler.html>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400199
@@ -3385,7 +3385,7 @@
column heater
- The glass liner can be fitted with a separate heater and the volatilization temperature can, thus, be controlled. This flash heater system is available in most chromatographs. By using a syringe with a long needle, the tip can be made to penetrate past the liner and discharge its contents directly into the column packing. This procedure is called 'on-column injection' and, as it reduces peak dispersion on injection and thus, provides higher column efficiencies, is often the preferred procedure.
+ The glass liner can be fitted with a separate heater and the volatilization temperature can, thus, be controlled. This flash heater system is available in most chromatographs. By using a syringe with a long needle, the tip can be made to penetrate past the liner and discharge its contents directly into the column packing. This procedure is called 'on-column injection' and, as it reduces peak dispersion on injection and thus, provides higher column efficiencies, is often the preferred procedure.
PERSON:Daniel Schober
WEB:<http://www.chromatography-online.org/GC/Injection-Devices/Open-Tubular-Column/rs15.html>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01040
@@ -3400,7 +3400,7 @@
JEOL CapNMR probe
- The JEOL ECA and ECX NMR spectrometers now support the MRM/Protasis CapNMR Probe for well plate-based and microvial-based NMR analysis. The CapNMR probe is available at proton frequencies ranging from 300 MHz to 800 MHz in both indirect configurations (e.g. 1H{13C} and 1H {31P}) and also in triple resonance configurations (e.g. 1H{13C, 15N}, 1H{31P, 15N}). Both employ a high-strength z-directed field gradient. The flowprobes come with the choice of two flowcell volumes: a 5 μl flowcell with an NMR active volume of 2.5 μl, and a 10 μl flowcell with an NMR active volume of 5 μl. The fluidic connections are 75 μm i.d. and 1/32 o.d. FEP Teflon with hastelloy unions for exceptional solvent compatibility.
+ The JEOL ECA and ECX NMR spectrometers now support the MRM/Protasis CapNMR Probe for well plate-based and microvial-based NMR analysis. The CapNMR probe is available at proton frequencies ranging from 300 MHz to 800 MHz in both indirect configurations (e.g. 1H{13C} and 1H {31P}) and also in triple resonance configurations (e.g. 1H{13C, 15N}, 1H{31P, 15N}). Both employ a high-strength z-directed field gradient. The flowprobes come with the choice of two flowcell volumes: a 5 μl flowcell with an NMR active volume of 2.5 μl, and a 10 μl flowcell with an NMR active volume of 5 μl. The fluidic connections are 75 μm i.d. and 1/32 o.d. FEP Teflon with hastelloy unions for exceptional solvent compatibility.
PERSON:Daniel Schober
WEB:<http://www.jeol.com/PRODUCTS/AnalyticalInstruments/NuclearMagneticResonance/CapNMRProbe/tabid/396/Default.aspx>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400233
@@ -3422,7 +3422,7 @@
acquisition computer
- A Computer used for NMR, can be divided into central processing unit (CPU), consisting of instruction, interpretation and arithmetic unit plus fast access memory, and peripheral devices such as bulk data storage and input and output devices (including, via the interface, the spectrometer). Under software control, the computer controls the RF pulses and gradients necessary to acquire data, and process the data to produce spectra or images. Note that devices such as the spectrometer may themselves incorporate small computers.
+ A Computer used for NMR, can be divided into central processing unit (CPU), consisting of instruction, interpretation and arithmetic unit plus fast access memory, and peripheral devices such as bulk data storage and input and output devices (including, via the interface, the spectrometer). Under software control, the computer controls the RF pulses and gradients necessary to acquire data, and process the data to produce spectra or images. Note that devices such as the spectrometer may themselves incorporate small computers.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400013
@@ -3438,7 +3438,7 @@
gas chromatography detector
- A gas chromatography detector is a chromatography detector that locates in the dimensions of space and time, the positions of the components of a mixture that has been subjected to a gas chromatographic process and thus permits the senses to appreciate the nature of the separation. There is no LC detector that has an equivalent performance to the flame ionization detector (FID) used in GC. In general, LC detectors have sensitivities of two to three orders of magnitude less than their GC counterparts and linear dynamic ranges one to two orders of magnitude lower. Only highly specific LC detectors have sensitivities that can approach those of GC detectors.
+ A gas chromatography detector is a chromatography detector that locates in the dimensions of space and time, the positions of the components of a mixture that has been subjected to a gas chromatographic process and thus permits the senses to appreciate the nature of the separation. There is no LC detector that has an equivalent performance to the flame ionization detector (FID) used in GC. In general, LC detectors have sensitivities of two to three orders of magnitude less than their GC counterparts and linear dynamic ranges one to two orders of magnitude lower. Only highly specific LC detectors have sensitivities that can approach those of GC detectors.
PERSON:Daniel Schober
FID
WEB:<http://www.chromatography-online.org/GC-Detectors/Classification/rs1.html>
@@ -3455,7 +3455,7 @@
gas purifier
- Gas purifiers are instruments used for the removal of gas impurities like hydrocarbons, oxygen, and moisture from carrier gas and fuel gases for GC or GC-MS systems.
+ Gas purifiers are instruments used for the removal of gas impurities like hydrocarbons, oxygen, and moisture from carrier gas and fuel gases for GC or GC-MS systems.
PERSON:Daniel Schober
WEB:<http://www.sigmaaldrich.com/Area_of_Interest/Analytical__Chromatography/Gas_Chromatography/Accessories/SGT_Gas_Purifier.html>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01036
@@ -3471,7 +3471,7 @@
indirect detection probe
- An NMR probe designed to allow the indirect detection of acquisition nuclei.
+ An NMR probe designed to allow the indirect detection of acquisition nuclei.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400281
@@ -3487,7 +3487,7 @@
JEOL ECA NMR spectrometer
- The ECA series of NMR spectrometers is a high performance, research grade NMR system configurable to a wide range off applications. The ECA NMR is available from 300 to 930 MHz field strengths and is 1GHz ready. The system is designed around a modular, digital NMR electronics chassis controlled from a UNIX or Windows workstation and acquisition system. Both the workstation and spectrometer may be connected to a standard network, allowing seamless remote operation anywhere in the world.
+ The ECA series of NMR spectrometers is a high performance, research grade NMR system configurable to a wide range off applications. The ECA NMR is available from 300 to 930 MHz field strengths and is 1GHz ready. The system is designed around a modular, digital NMR electronics chassis controlled from a UNIX or Windows workstation and acquisition system. Both the workstation and spectrometer may be connected to a standard network, allowing seamless remote operation anywhere in the world.
PERSON:Daniel Schober
WEB:<http://www.jeol.com/PRODUCTS/AnalyticalInstruments/NuclearMagneticResonance/ECA/tabid/146/Default.aspx>
http://msi-ontology.sourceforge.net/ontology/NMR.owl#msi_400228
@@ -3503,7 +3503,7 @@
atomic emission detector
- Instead of measuring simple gas phase (carbon containing) ions created in a flame as with the flame ionization detector, or the change in background current because of electronegative element capture of thermal electrons as with the electron capture detector, the AED has a much wider applicability because it is based on the detection of atomic emissions. The strength of the AED lies in the detector's ability to simultaneously determine the atomic emissions of many of the elements in analytes that elute from a GC capillary column (called eluants or solutes in some books). As eluants come off the capillary column they are fed into a microwave powered plasma (or discharge) cavity where the compounds are destroyed and their atoms are excited by the energy of the plasma. The light that is emitted by the excited particles is separated into individual lines via a photodiode array. The associated computer then sorts out the individual emission lines and can produce chromatograms made up of peaks from eluants that contain only a specific element.
+ Instead of measuring simple gas phase (carbon containing) ions created in a flame as with the flame ionization detector, or the change in background current because of electronegative element capture of thermal electrons as with the electron capture detector, the AED has a much wider applicability because it is based on the detection of atomic emissions. The strength of the AED lies in the detector's ability to simultaneously determine the atomic emissions of many of the elements in analytes that elute from a GC capillary column (called eluants or solutes in some books). As eluants come off the capillary column they are fed into a microwave powered plasma (or discharge) cavity where the compounds are destroyed and their atoms are excited by the energy of the plasma. The light that is emitted by the excited particles is separated into individual lines via a photodiode array. The associated computer then sorts out the individual emission lines and can produce chromatograms made up of peaks from eluants that contain only a specific element.
PERSON:Daniel Schober
AED
WEB:<http://elchem.kaist.ac.kr/vt/chem-ed/sep/gc/detector/aed.htmt>
@@ -3526,7 +3526,7 @@
454 Genome Sequence 20
PMID: 18946007.Pyrosequencing analysis of the oral microflora of healthy adults. Keijser BJ, Zaura E, Huse SM, van der Vossen JM, Schuren FH, Montijn RC, ten Cate JM, Crielaard W. J Dent Res. 2008 Nov;87(11):1016-20.
- is a DNA sequencer first manufactured by 454 Life Science Corporation in 2005, and enables pyrosequencing to be performed. It comprises both optics and fluidics subsystems, which are controlled by a computer subsystem. The fluidics subsystem ensures accurate reagent dispensing. It consists of a reagents cassette (which holds the reagent containers), a sipper manifold, pumps, valves, and debubblers. The fluidics subsystem flows the sequencing reagents across the wells of the PicoTiterPlate device, and moves the spent reagents from the PicoTiterPlate device to the waste receptacle. The optics subsystem consists of a CCD camera and a camera controller. The camera captures the light emitted in the wells of the PicoTiterPlate device during each step of the sequencing cycle, and sends the digital images to the computer subsystem for processing. The computer controls the other Sequencer subsystems, and processes the digital images sent by the camera to extract the DNA sequence information.
+ is a DNA sequencer first manufactured by 454 Life Science Corporation in 2005, and enables pyrosequencing to be performed. It comprises both optics and fluidics subsystems, which are controlled by a computer subsystem. The fluidics subsystem ensures accurate reagent dispensing. It consists of a reagents cassette (which holds the reagent containers), a sipper manifold, pumps, valves, and debubblers. The fluidics subsystem flows the sequencing reagents across the wells of the PicoTiterPlate device, and moves the spent reagents from the PicoTiterPlate device to the waste receptacle. The optics subsystem consists of a CCD camera and a camera controller. The camera captures the light emitted in the wells of the PicoTiterPlate device during each step of the sequencing cycle, and sends the digital images to the computer subsystem for processing. The computer controls the other Sequencer subsystems, and processes the digital images sent by the camera to extract the DNA sequence information.
Philippe Rocca-Serra
GS 20
454 Genome Sequence 20
@@ -3546,7 +3546,7 @@
ABI 377 automated sequencer
- is a DNA sequencer which is manufactured by Applied Biosystems corporation (formerly Perkin-Elmer). It allows automated chain termination DNA sequencing. It has part polyacrylamide gel electrophoresis system and a laser -based detection system to detect fluorescence intensity emitted by the dyes attached to the dideoxyterminator nucleotides or to the primers.
+ is a DNA sequencer which is manufactured by Applied Biosystems corporation (formerly Perkin-Elmer). It allows automated chain termination DNA sequencing. It has part polyacrylamide gel electrophoresis system and a laser -based detection system to detect fluorescence intensity emitted by the dyes attached to the dideoxyterminator nucleotides or to the primers.
Philippe Rocca-Serra
Applied Biosystems
ABI 377 automated sequencer
@@ -3567,7 +3567,7 @@
AB SOLiD System
PMID: 19336255. RNA-Seq-quantitative measurement of expression through massively parallel RNA-sequencing. Wilhelm BT, Landry JR. Methods. 2009 Jul;48(3):249-57.
- is a DNA sequencer which is manufactured by Applied Biosystems and which enable DNA sequencing by ligation
+ is a DNA sequencer which is manufactured by Applied Biosystems and which enable DNA sequencing by ligation
Philippe Rocca-Serra
Applied Biosystems
AB SOLiD System
@@ -3588,7 +3588,7 @@
454 Genome Sequencer FLX
PMID: 18616967. The Genome Sequencer FLX System--longer reads, more applications, straight forward bioinformatics and more complete data sets. Droege M, Hill B. J Biotechnol. 2008 Aug 31;136(1-2):3-10.
- is a DNA sequencer which was first manufactured by 454 Life Science Corporation in 2008 and enables pyrosequencing to be performed. It comprises both optics and fluidics subsystems, which are controlled by a computer subsystem. The fluidics subsystem ensures accurate reagent dispensing. It consists of a reagents cassette (which holds the reagent containers), a sipper manifold, pumps, valves, and debubblers. The fluidics subsystem flows the sequencing reagents across the wells of the PicoTiterPlate device, and moves the spent reagents from the PicoTiterPlate device to the waste receptacle. The optics subsystem consists of a CCD camera and a camera controller. The camera captures the light emitted in the wells of the PicoTiterPlate device during each step of the sequencing cycle, and sends the digital images to the computer subsystem for processing. The computer controls the other Sequencer subsystems, and processes the digital images sent by the camera to extract the DNA sequence information. It has the ability to sequence 400-600 million base pairs per run with 400-500 base pair read lengths.
+ is a DNA sequencer which was first manufactured by 454 Life Science Corporation in 2008 and enables pyrosequencing to be performed. It comprises both optics and fluidics subsystems, which are controlled by a computer subsystem. The fluidics subsystem ensures accurate reagent dispensing. It consists of a reagents cassette (which holds the reagent containers), a sipper manifold, pumps, valves, and debubblers. The fluidics subsystem flows the sequencing reagents across the wells of the PicoTiterPlate device, and moves the spent reagents from the PicoTiterPlate device to the waste receptacle. The optics subsystem consists of a CCD camera and a camera controller. The camera captures the light emitted in the wells of the PicoTiterPlate device during each step of the sequencing cycle, and sends the digital images to the computer subsystem for processing. The computer controls the other Sequencer subsystems, and processes the digital images sent by the camera to extract the DNA sequence information. It has the ability to sequence 400-600 million base pairs per run with 400-500 base pair read lengths.
Philippe Rocca-Serra
454 GS FLX
GS-FLX
@@ -3611,7 +3611,7 @@
Illumina Genome Analyzer II
PMID: 19336255. RNA-Seq-quantitative measurement of expression through massively parallel RNA-sequencing. Wilhelm BT, Landry JR.Methods. 2009 Jul;48(3):249-57.
- is a DNA sequence which is manufactured by Illumina (Solexa) corporation. it support sequencing of single or paired end clone libraries relying on sequencing by synthesis technology
+ is a DNA sequence which is manufactured by Illumina (Solexa) corporation. it support sequencing of single or paired end clone libraries relying on sequencing by synthesis technology
Philippe Rocca-Serra
Illumina Corporation
Illumina Genome Analyzer II
@@ -3631,7 +3631,7 @@
Li-Cor 4300 DNA Analysis System
- is a DNA sequencer which is manufactured by Li-Cor corporation and enable automated chain termination based DNA sequencing
+ is a DNA sequencer which is manufactured by Li-Cor corporation and enable automated chain termination based DNA sequencing
Philippe Rocca-Serra
OBI and Li-Cor
Li-Cor 4300 DNA Analysis System
@@ -3651,7 +3651,7 @@
HeliScope Single Molecule Sequencer
- is a DNA sequencer manufacturer by Helicos Corporation to carry out Single Molecule sequencing using reversible termination chemistry
+ is a DNA sequencer manufacturer by Helicos Corporation to carry out Single Molecule sequencing using reversible termination chemistry
Philippe Rocca-Serra
HeliScope Single Molecule Sequencer
@@ -3680,7 +3680,7 @@
anticoagulant-containing test tube
- A 'blue top' test tube that contains anticoagulant for storing blood specimens'
+ A 'blue top' test tube that contains anticoagulant for storing blood specimens'
Person:Alan Ruttenberg
2009/09/28 Alan Ruttenberg. Fucoidan-use-case
anticoagulant-containing test tube
@@ -3701,7 +3701,7 @@
glucometer
Diabetic patients use glucometers to determine their glucose levels
- A measurement device with the function to measure and record the level/amount of glucose in a blood sample
+ A measurement device with the function to measure and record the level/amount of glucose in a blood sample
PERSON:Frank Gibson
PERSON:Helen Parkinson
glucose meter
@@ -3724,7 +3724,7 @@
micro electrode
A micro-electrode recording device used to record extracellular action potentialsin monkey caudate nucleus
- An electrode of very fine caliber consisting usually of a fine wire or a glass tube of capillary diameter drawn to a fine point and filled with saline or a metal used in physiological experiments to stimulate or record action currents of extracellular or intracellular origin in the nervous system.
+ An electrode of very fine caliber consisting usually of a fine wire or a glass tube of capillary diameter drawn to a fine point and filled with saline or a metal used in physiological experiments to stimulate or record action currents of extracellular or intracellular origin in the nervous system.
Helen Parkinson, Jessica Turner, Dirk Derom
micro electrode measuring device
Jessica Turner, Dirk Derom
@@ -3750,7 +3750,7 @@
measurement device
A ruler, a microarray scanner, a Geiger counter.
- A device in which a measure function inheres.
+ A device in which a measure function inheres.
GROUP:OBI Philly workshop
OBI
measurement device
@@ -3770,7 +3770,7 @@
test tube
- A test tube is a device consisting of a glass or plastic tubing, open at the top, usually with a rounded U-shaped bottom which has the function to contain material
+ A test tube is a device consisting of a glass or plastic tubing, open at the top, usually with a rounded U-shaped bottom which has the function to contain material
Bjoern Peters
collection tube
sample tube
@@ -3798,7 +3798,7 @@
Sysmex CA-6000 Coagulation Analyzer
- The Sysmex CA-6000 automated coagulation analyzer is a random access instrument that is capable of performing 20 clot-based and chromogenic assays
+ The Sysmex CA-6000 automated coagulation analyzer is a random access instrument that is capable of performing 20 clot-based and chromogenic assays
Person:Alan Ruttenberg
web:http://www.clinchem.org/cgi/content/full/43/9/1783@2009/08/06
2009/09/28 Alan Ruttenberg. Fucoidan-use-case
@@ -3819,7 +3819,7 @@
calorimeter
- A measurement device that is used to calculate the heat flow of a chemical reaction or physical change.
+ A measurement device that is used to calculate the heat flow of a chemical reaction or physical change.
PERSON:Bjoern Peters
calorimetry instrument?
http://chemistry.about.com/od/chemistryglossary/a/calorimeterdef.htm
@@ -3845,7 +3845,7 @@
material separation device
flow cytometer
- A device with a separation function realized in a planed process
+ A device with a separation function realized in a planed process
material separation device
@@ -3863,7 +3863,7 @@
positron emission tomography scanner
- A device that produces a three-dimensional image or picture of functional processes in the body. It detects pairs of gamma rays emitted indirectly by a positron-emitting radionuclide (tracer), which is introduced into the body on a biologically active molecule.
+ A device that produces a three-dimensional image or picture of functional processes in the body. It detects pairs of gamma rays emitted indirectly by a positron-emitting radionuclide (tracer), which is introduced into the body on a biologically active molecule.
PERSON:Bjoern Peters
PET scanner?
http://en.wikipedia.org/wiki/Positron_emission_tomography
@@ -3884,7 +3884,7 @@
micromanipulator
- A device that is used to physically interact with a sample under a microscope, where a level of precision of movement is necessary that cannot be achieved by the unaided human hand.
+ A device that is used to physically interact with a sample under a microscope, where a level of precision of movement is necessary that cannot be achieved by the unaided human hand.
PERSON:Bjoern Peters
http://en.wikipedia.org/wiki/Micromanipulator
micromanipulator
@@ -3898,7 +3898,7 @@
optical microscope
- A microscope that produces an image of an object by targeting it with an electro-magnetic beam in the visible frequency range
+ A microscope that produces an image of an object by targeting it with an electro-magnetic beam in the visible frequency range
PERSON:Bjoern Peters
optical microscope
@@ -3917,7 +3917,7 @@
vibration isolation table
- A device that supports another device such as a precision instrument by isolating it from vibration that is transmitted from the floor.
+ A device that supports another device such as a precision instrument by isolating it from vibration that is transmitted from the floor.
PERSON:Bjoern Peters
United States Patent 6877711
vibration isolation table
@@ -3943,7 +3943,7 @@
oscilloscope
- A device that measures and displayes signal voltages, usually as a two-dimensional graph of one or more electrical potential differences (vertical axis) plotted as a function of time or of some other voltage (horizontal axis).
+ A device that measures and displayes signal voltages, usually as a two-dimensional graph of one or more electrical potential differences (vertical axis) plotted as a function of time or of some other voltage (horizontal axis).
PERSON:Bjoern Peters
http://en.wikipedia.org/wiki/Oscilloscope
oscilloscope
@@ -3963,7 +3963,7 @@
electrode puller
- A device used in the first step in making electrodes, that applies constant tension on a glass capillary tube and eventually breaks it while heating it; this produces a very fine point on the capillary tube.
+ A device used in the first step in making electrodes, that applies constant tension on a glass capillary tube and eventually breaks it while heating it; this produces a very fine point on the capillary tube.
PERSON:Bjoern Peters
http://faculty.plattsburgh.edu/donald.slish/Puller1.html
electrode puller
@@ -3994,7 +3994,7 @@
vibrotome
- A preparation device that uses a vibrating razor blade to cut through tissue.
+ A preparation device that uses a vibrating razor blade to cut through tissue.
vibrotome
@@ -4028,7 +4028,7 @@
container
- A device that can be used to restrict the location of material entities over time
+ A device that can be used to restrict the location of material entities over time
03/21/2010: Added to allow classification of children (similar to what we want to do for 'measurement device'. Lookint at what classifies here, we may want to reconsider a contain function assigned to a part of an entity is necessarily also a function of the whole (e.g. is a centrifuge a container because it has test tubes as parts?)
PERSON: Bjoern Peters
container
@@ -4054,7 +4054,7 @@
computed tomography scanner
- An image acquisition device that generates a three-dimensional image of the inside of an object from a large series of two-dimensional X-ray images taken around a single axis of rotation.
+ An image acquisition device that generates a three-dimensional image of the inside of an object from a large series of two-dimensional X-ray images taken around a single axis of rotation.
PERSON:Bjoern Peters
CT scanner
X-ray computed tomography scanner
@@ -4081,7 +4081,7 @@
PCR instrument
- A device that is used to amplify a single or few copies of a piece of DNA across several orders of magnitude, generating thousands to millions of copies of a particular DNA sequence.
+ A device that is used to amplify a single or few copies of a piece of DNA across several orders of magnitude, generating thousands to millions of copies of a particular DNA sequence.
03/21/2010: Added because it is unclear if the thermal cycler definition is intentionally broader than PCR instrument. Contacted Melanie and Trish about this. Definitions and use of alternative terms need to be made consistent.
PCR instrument
@@ -4094,7 +4094,7 @@
electron microscope
- A microscope that produces an image of an object by targeting it with an electron beam
+ A microscope that produces an image of an object by targeting it with an electron beam
electron microscope
@@ -4112,7 +4112,7 @@
Faraday cage
- A device formed by conducting material or by a mesh of such material, that blocks out external static electric fields.
+ A device formed by conducting material or by a mesh of such material, that blocks out external static electric fields.
PERSON:Bjoern Peters
Faraday shield
Wikipedia http://en.wikipedia.org/wiki/Faraday_cage
@@ -4139,7 +4139,7 @@
light emission device
A light source is an optical subsystem that provides light for use in a distant area using a delivery system (e.g., fiber optics)
- A device which has a function to emit light.
+ A device which has a function to emit light.
Person:Helen Parkinson
OBI
light emission device
@@ -4165,7 +4165,7 @@
A homogenizer is a perturbation device.
- A perturbation device is a device which is designed to perform a perturb function
+ A perturbation device is a device which is designed to perform a perturb function
Helen Parkinson
OBI Vancouver workshop 2010
PERSON: Helen Parkinson
@@ -4199,7 +4199,7 @@
environmental control device
A growth chamber is an environmental control device.
- An environmental control device is a device which has the function to control some aspect of the environment such as temperature, or humidity.
+ An environmental control device is a device which has the function to control some aspect of the environment such as temperature, or humidity.
Helen Parkinson
OBI
environmental control device
@@ -4237,7 +4237,7 @@
angiograph
- A device that records the patterns of pulse waves inside blood vessels.
+ A device that records the patterns of pulse waves inside blood vessels.
PERSON: Erik Segerdell
http://medical-dictionary.thefreedictionary.com/angiograph
angiograph
@@ -4257,7 +4257,7 @@
capillary blotter
- A device that is used to transfer nucleic acids from agarose gels onto a membrane, based on the movement of buffer from a reservoir through the gel and the blotting membrane to a stack of dry blotting paper by capillary force. The molecules are carried to the blotting membrane on which they are adsorbed.
+ A device that is used to transfer nucleic acids from agarose gels onto a membrane, based on the movement of buffer from a reservoir through the gel and the blotting membrane to a stack of dry blotting paper by capillary force. The molecules are carried to the blotting membrane on which they are adsorbed.
PERSON: Erik Segerdell
http://www.biometra.de/
capillary blotter
@@ -4283,7 +4283,7 @@
bioreactor
- A device or system that supports a biologically active environment.
+ A device or system that supports a biologically active environment.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Bioreactor
bioreactor
@@ -4303,7 +4303,7 @@
pH meter
- A device that is used to measure the pH (acidity or alkalinity) of a liquid.
+ A device that is used to measure the pH (acidity or alkalinity) of a liquid.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/PH_meter
pH meter
@@ -4323,7 +4323,7 @@
digital camera
- An image acquisition device that takes video or still photographs, or both, digitally by recording images via an electronic image sensor.
+ An image acquisition device that takes video or still photographs, or both, digitally by recording images via an electronic image sensor.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Digital_camera
digital camera
@@ -4343,7 +4343,7 @@
chip spotting device
- A device for dropping and immobilizing a solution of biomolecules, for example, nucleic acids such as probe DNA, mRNA, and peptide nucleic acid (PNA), and proteins on a DNA microarray surface to manufacture a DNA microarray.
+ A device for dropping and immobilizing a solution of biomolecules, for example, nucleic acids such as probe DNA, mRNA, and peptide nucleic acid (PNA), and proteins on a DNA microarray surface to manufacture a DNA microarray.
PERSON: Erik Segerdell
United States Patent 7416705
chip spotting device
@@ -4357,7 +4357,7 @@
RNA extraction/purification instrument
- A device that is used to isolate and collect RNA for subsequent molecular analysis.
+ A device that is used to isolate and collect RNA for subsequent molecular analysis.
PERSON: Erik Segerdell
PERSON: Erik Segerdell
RNA extraction/purification instrument
@@ -4371,7 +4371,7 @@
two-photon laser/detector
- A light source used in fluorescence imaging that allows the imaging of living tissue up to a depth of 1 mm, based on the concept that two photons of low energy can excite a fluorophore in a quantum event, resulting in the emission of a fluorescence photon, typically at a higher energy than either of the two excitatory photons.
+ A light source used in fluorescence imaging that allows the imaging of living tissue up to a depth of 1 mm, based on the concept that two photons of low energy can excite a fluorophore in a quantum event, resulting in the emission of a fluorescence photon, typically at a higher energy than either of the two excitatory photons.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Two-photon_excitation_microscopy
two-photon laser/detector
@@ -4391,7 +4391,7 @@
electrophoresis system
- A device that moves charged particles through a medium by using an electric field induced by electrodes.
+ A device that moves charged particles through a medium by using an electric field induced by electrodes.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Category:Electrophoresis
electrophoresis system
@@ -4411,7 +4411,7 @@
PET synthesizer
- A device that is used to produce targeted molecular pharmaceuticals for use in positron emission tomography.
+ A device that is used to produce targeted molecular pharmaceuticals for use in positron emission tomography.
PERSON: Erik Segerdell
PERSON: Erik Segerdell
PET synthesizer
@@ -4431,7 +4431,7 @@
spinning-disk confocal microscope
- A confocal microscope that uses a Nipkow disk, a mechanical, geometrically operating image scanning device.
+ A confocal microscope that uses a Nipkow disk, a mechanical, geometrically operating image scanning device.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Nipkow_disk
spinning-disk confocal microscope
@@ -4445,7 +4445,7 @@
DNA synthesizer
- An oligonucleotide synthesizer that is used to custom-build DNA molecules to contain a particular sequence of nucleotides.
+ An oligonucleotide synthesizer that is used to custom-build DNA molecules to contain a particular sequence of nucleotides.
PERSON: Erik Segerdell
http://www.globalspec.com/LearnMore/Labware_Scientific_Instruments/Clinical_Research_Labware/DNA_Synthesizers
DNA synthesizer
@@ -4459,7 +4459,7 @@
high performance liquid chromatography instrument
- A liquid chromatography instrument that consists of a reservoir of mobile phase, a pump, an injector, a separation column, and a detector. The pump (rather than gravity) provides the higher pressure required to propel the mobile phase and analyte through the densely packed column.
+ A liquid chromatography instrument that consists of a reservoir of mobile phase, a pump, an injector, a separation column, and a detector. The pump (rather than gravity) provides the higher pressure required to propel the mobile phase and analyte through the densely packed column.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/High_performance_liquid_chromatography
high performance liquid chromatography instrument
@@ -4479,7 +4479,7 @@
microplate reader
- A measurement device that detects biological, chemical or physical events of samples in microtiter plates.
+ A measurement device that detects biological, chemical or physical events of samples in microtiter plates.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Plate_reader
microplate reader
@@ -4493,7 +4493,7 @@
ELISA microplate reader
- A microplate reader that is used for enzyme-linked immunosorbent assays (ELISA).
+ A microplate reader that is used for enzyme-linked immunosorbent assays (ELISA).
PERSON: Erik Segerdell
PERSON: Erik Segerdell
ELISA microplate reader
@@ -4513,7 +4513,7 @@
spot cutter
- A robotic device that is used to excise spots from gels.
+ A robotic device that is used to excise spots from gels.
PERSON: Erik Segerdell
PERSON: Erik Segerdell
spot cutter
@@ -4539,7 +4539,7 @@
microwave synthesis system
- A device that is used to apply microwave irradiation to chemical reactions.
+ A device that is used to apply microwave irradiation to chemical reactions.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Microwave_chemistry
microwave synthesis system
@@ -4559,7 +4559,7 @@
densitometer
- A device that measures the degree of darkness (the optical density) of a photographic or semitransparent material or of a reflecting surface.
+ A device that measures the degree of darkness (the optical density) of a photographic or semitransparent material or of a reflecting surface.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Densitometer
densitometer
@@ -4585,7 +4585,7 @@
automatic staining machine
- A device that is used to automatically stain tissue sections on slides or tissue specimens.
+ A device that is used to automatically stain tissue sections on slides or tissue specimens.
PERSON: Erik Segerdell
PERSON: Erik Segerdell
automatic staining machine
@@ -4611,7 +4611,7 @@
automatic tissue processor
- A device for processing histological tissue having a tissue carrier basket suspended from a turntable overlying a plurality of beakers suspended from a carrier plate. The turntable is raised, indexed, and lowered by a suitable driving mechanism to move the tissue basket sequentially through the beakers. Timers can each be programmed to control the movement of the turntable to provide various different cycles for processing the tissue. Some of the beakers are received in individual thermal baths to heat and control the temperature of the substances received in the beakers for treating the tissue.
+ A device for processing histological tissue having a tissue carrier basket suspended from a turntable overlying a plurality of beakers suspended from a carrier plate. The turntable is raised, indexed, and lowered by a suitable driving mechanism to move the tissue basket sequentially through the beakers. Timers can each be programmed to control the movement of the turntable to provide various different cycles for processing the tissue. Some of the beakers are received in individual thermal baths to heat and control the temperature of the substances received in the beakers for treating the tissue.
PERSON: Erik Segerdell
United States Patent 3762362
automatic tissue processor
@@ -4631,7 +4631,7 @@
stereo microscope
- An optical microscope that uses two separate optical paths with two objectives and two eyepieces to provide slightly different viewing angles to the left and right eyes.
+ An optical microscope that uses two separate optical paths with two objectives and two eyepieces to provide slightly different viewing angles to the left and right eyes.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Optical_microscope#Stereo_microscope
stereo microscope
@@ -4645,7 +4645,7 @@
top loading balance
- A balance that consists of a metal plate on which to place an object and a digital readout of the measurement of its mass.
+ A balance that consists of a metal plate on which to place an object and a digital readout of the measurement of its mass.
PERSON: Erik Segerdell
PERSON: Erik Segerdell
top loading balance
@@ -4665,7 +4665,7 @@
perfusion station
- A device or system in which perfusion units are integrated.
+ A device or system in which perfusion units are integrated.
PERSON: Erik Segerdell
PERSON: Erik Segerdell
perfusion station
@@ -4691,7 +4691,7 @@
SPECT scanner
- A nuclear medicine tomographic imaging device that uses gamma rays to provide 3D information, typically presented as cross-sectional slices through the specimen but with the ability to be freely reformatted or manipulated as required.
+ A nuclear medicine tomographic imaging device that uses gamma rays to provide 3D information, typically presented as cross-sectional slices through the specimen but with the ability to be freely reformatted or manipulated as required.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Single_photon_emission_computed_tomography
SPECT scanner
@@ -4711,7 +4711,7 @@
scintillation counter
- A device that is used to measure ionizing radiation.
+ A device that is used to measure ionizing radiation.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Scintillation_counter
scintillation counter
@@ -4731,7 +4731,7 @@
programmable array microscope
- A confocal microscope that uses a programmable spatial light modulator for generating an arbitrary pattern of conjugate illumination and detection apertures.
+ A confocal microscope that uses a programmable spatial light modulator for generating an arbitrary pattern of conjugate illumination and detection apertures.
PERSON: Erik Segerdell
Verveer et al, Journal of Microscopy, vol. 189, pt. 3, pp. 192-8
programmable array microscope
@@ -4763,7 +4763,7 @@
cryostat
- A device consisting of a vessel, similar in construction to a vacuum flask, that is used to maintain cold cryogenic temperatures. FIX THIS DEFINITION
+ A device consisting of a vessel, similar in construction to a vacuum flask, that is used to maintain cold cryogenic temperatures. FIX THIS DEFINITION
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Cryostat
cryostat
@@ -4783,7 +4783,7 @@
microtome knife maker
- A glass cutting and breaking device that is used to produce glass knives used in ultramicrotomy.
+ A glass cutting and breaking device that is used to produce glass knives used in ultramicrotomy.
PERSON: Erik Segerdell
PERSON: Erik Segerdell
microtome knife maker
@@ -4803,7 +4803,7 @@
cryofixation device
- A device that is used for the fixation or stabilization of biological materials as the first step in specimen preparation for electron microscopy.
+ A device that is used for the fixation or stabilization of biological materials as the first step in specimen preparation for electron microscopy.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Cryofixation
cryofixation device
@@ -4829,7 +4829,7 @@
hybridization oven
- A device that creates an appropriate environment for nucleic acid hybridization.
+ A device that creates an appropriate environment for nucleic acid hybridization.
PERSON: Erik Segerdell
PERSON: Erik Segerdell
hybridization oven
@@ -4861,7 +4861,7 @@
incubator shaker
- An incubating device that provides shaking motion for biomedical applications (e.g., cell cultures).
+ An incubating device that provides shaking motion for biomedical applications (e.g., cell cultures).
PERSON: Erik Segerdell
PERSON: Erik Segerdell
incubator shaker
@@ -4887,7 +4887,7 @@
small-animal image acquisition device
- A device that is used to image small laboratory animals (e.g., rats and mice) in vivo.
+ A device that is used to image small laboratory animals (e.g., rats and mice) in vivo.
PERSON: Erik Segerdell
PERSON: Erik Segerdell
small-animal image acquisition device
@@ -4913,7 +4913,7 @@
infrared image acquisition device
- An image acquisition device that is responsive to an infrared emissive target within a given field of view.
+ An image acquisition device that is responsive to an infrared emissive target within a given field of view.
PERSON: Erik Segerdell
United States Patent 4107530
infrared image acquisition device
@@ -4933,7 +4933,7 @@
confocal microscope
- A microscope that is used to increase micrograph contrast and/or reconstruct three-dimensional images by using a spatial pinhole to eliminate out-of-focus light in specimens that are thicker than the focal plane.
+ A microscope that is used to increase micrograph contrast and/or reconstruct three-dimensional images by using a spatial pinhole to eliminate out-of-focus light in specimens that are thicker than the focal plane.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Confocal_microscopy
confocal microscope
@@ -4953,7 +4953,7 @@
patch clamp device
- A device used in electrophysiology that allows the study of single or multiple ion channels in cells.
+ A device used in electrophysiology that allows the study of single or multiple ion channels in cells.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Patch_clamp
patch clamp device
@@ -4979,7 +4979,7 @@
gel imaging system
- A device that is used to acquire images of laboratory gels.
+ A device that is used to acquire images of laboratory gels.
PERSON: Erik Segerdell
PERSON: Erik Segerdell
gel imaging system
@@ -4999,7 +4999,7 @@
protein separation apparatus
- A device that is used for the separation of proteins.
+ A device that is used for the separation of proteins.
PERSON: Erik Segerdell
PERSON: Erik Segerdell
protein separation apparatus
@@ -5013,7 +5013,7 @@
multichannel electronic pipette
- A multichannel pipette that can be programmed by the user to aspirate a volume of liquid reagent or sample and dispense the aspirated volume or a series of aliquots in successive dispensing operations.
+ A multichannel pipette that can be programmed by the user to aspirate a volume of liquid reagent or sample and dispense the aspirated volume or a series of aliquots in successive dispensing operations.
PERSON: Erik Segerdell
http://www.faqs.org/patents/app/20090196797
multichannel electronic pipette
@@ -5033,7 +5033,7 @@
vitrification apparatus
- A device that is used to effect the transition of a substance into a glass.
+ A device that is used to effect the transition of a substance into a glass.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Glass_transition
vitrification apparatus
@@ -5059,7 +5059,7 @@
radiography instrument
- An image acquisition device that uses ionizing electromagnetic radiation such as X-rays to view objects.
+ An image acquisition device that uses ionizing electromagnetic radiation such as X-rays to view objects.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Medical_radiography
radiography instrument
@@ -5085,7 +5085,7 @@
radiation measurement device
- A device that consists of a radiosensitive detector and a means of recording the effects of radiation on the detector.
+ A device that consists of a radiosensitive detector and a means of recording the effects of radiation on the detector.
PERSON: Erik Segerdell
PERSON: Erik Segerdell
radiation measurement device
@@ -5111,7 +5111,7 @@
lyophilizer
- A device that is used to freeze dry material.
+ A device that is used to freeze dry material.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Freeze_drying
lyophilizer
@@ -5125,7 +5125,7 @@
tandem mass spectrometer
- A mass spectrometer in which ions are subjected to two or more sequential stages of analysis (which may be separated spatially or temporally) according to the quotient mass/charge.
+ A mass spectrometer in which ions are subjected to two or more sequential stages of analysis (which may be separated spatially or temporally) according to the quotient mass/charge.
PERSON: Erik Segerdell
http://goldbook.iupac.org/T06250.html
tandem mass spectrometer
@@ -5145,7 +5145,7 @@
microhardness tester
- A hardness testing device that is used in light-optical microscopes.
+ A hardness testing device that is used in light-optical microscopes.
PERSON: Erik Segerdell
United States Patent 4611487
microhardness tester
@@ -5159,7 +5159,7 @@
multimode microplate reader
- A microplate reader that can detect multiple types of absorbance, luminescence or fluorescence.
+ A microplate reader that can detect multiple types of absorbance, luminescence or fluorescence.
PERSON: Erik Segerdell
PERSON: Erik Segerdell
multimode microplate reader
@@ -5173,7 +5173,7 @@
mechanical balance
- A balance that is used to compare the weights of two bodies, to determine the difference in mass (or weight).
+ A balance that is used to compare the weights of two bodies, to determine the difference in mass (or weight).
PERSON: Erik Segerdell
http://www.britannica.com/EBchecked/topic/49765/balance
mechanical balance
@@ -5187,7 +5187,7 @@
computer cluster
- A group of linked computers, working together closely so that in many respects they form a single computer.
+ A group of linked computers, working together closely so that in many respects they form a single computer.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Cluster_(computing)
computer cluster
@@ -5207,7 +5207,7 @@
microtome knife sharpener
- A device that is used to sharpen knives used in microtomy.
+ A device that is used to sharpen knives used in microtomy.
PERSON: Erik Segerdell
PERSON: Erik Segerdell
microtome knife sharpener
@@ -5227,7 +5227,7 @@
plate shaker
- A device that provides shaking motion for microplates.
+ A device that provides shaking motion for microplates.
PERSON: Erik Segerdell
PERSON: Erik Segerdell
plate shaker
@@ -5247,7 +5247,7 @@
coagulation analyzer
- A device for automatically analyzing blood coagulation in a clinical laboratory.
+ A device for automatically analyzing blood coagulation in a clinical laboratory.
PERSON: Erik Segerdell
United States Patent 5439646
coagulation analyzer
@@ -5267,7 +5267,7 @@
laser capture microdissection microscope
- A microscope that uses low-energy laser beams and special transfer film to lift single cells from a tissue.
+ A microscope that uses low-energy laser beams and special transfer film to lift single cells from a tissue.
PERSON: Erik Segerdell
http://www.answers.com/topic/laser-capture-microdissection-microscope-in-medicine
laser capture microdissection microscope
@@ -5287,7 +5287,7 @@
liquid extraction robot
- A liquid handling device that provides automatic liquid extraction.
+ A liquid handling device that provides automatic liquid extraction.
PERSON: Erik Segerdell
PERSON: Erik Segerdell
liquid extraction robot
@@ -5313,7 +5313,7 @@
ultrasound machine
- A device that is used to visualize subcutaneous body structures including tendons, muscles, joints, vessels and internal organs.
+ A device that is used to visualize subcutaneous body structures including tendons, muscles, joints, vessels and internal organs.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Sonography
ultrasound machine
@@ -5339,7 +5339,7 @@
immunoblot scanner
- A device that is used for the imaging of immunoblots.
+ A device that is used for the imaging of immunoblots.
PERSON: Erik Segerdell
PERSON: Erik Segerdell
immunoblot scanner
@@ -5353,7 +5353,7 @@
microcentrifuge
- A type of centrifuge that is designed for small tubes (0.2 ml to 2.0 ml), has a compact design, and has a small footprint.
+ A type of centrifuge that is designed for small tubes (0.2 ml to 2.0 ml), has a compact design, and has a small footprint.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Laboratory_centrifuge
microcentrifuge
@@ -5367,7 +5367,7 @@
electronic repeater pipette
- A micropipette that can be programmed by the user to aspirate a volume of liquid reagent or sample and dispense a series of aliquots in successive dispensing operations.
+ A micropipette that can be programmed by the user to aspirate a volume of liquid reagent or sample and dispense a series of aliquots in successive dispensing operations.
PERSON: Erik Segerdell
http://www.faqs.org/patents/app/20090196797
electronic repeater pipette
@@ -5381,7 +5381,7 @@
electron paramagnetic resonance spectrometer
- An spectrophotometer that is used to investigate chemical species that have one or more unpaired electrons, such as organic and inorganic free radicals or inorganic complexes possessing a transition metal ion.
+ An spectrophotometer that is used to investigate chemical species that have one or more unpaired electrons, such as organic and inorganic free radicals or inorganic complexes possessing a transition metal ion.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Electron_paramagnetic_resonance
electron paramagnetic resonance spectrometer
@@ -5401,7 +5401,7 @@
rocker
- A device that provides three-dimensional motion for biomedical applications (e.g., gel trays).
+ A device that provides three-dimensional motion for biomedical applications (e.g., gel trays).
PERSON: Erik Segerdell
PERSON: Erik Segerdell
rocker
@@ -5415,7 +5415,7 @@
analytical balance
- A balance with weighing pan(s) inside a transparent enclosure that is used to measure mass to a very high degree of precision and accuracy.
+ A balance with weighing pan(s) inside a transparent enclosure that is used to measure mass to a very high degree of precision and accuracy.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Weighing_scale
analytical balance
@@ -5435,7 +5435,7 @@
scanning force microscope
- A microscope that forms images of surfaces using a physical probe that scans the specimen.
+ A microscope that forms images of surfaces using a physical probe that scans the specimen.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Scanning_probe_microscopy
scanning force microscope
@@ -5449,7 +5449,7 @@
pulsed-field gel electrophoresis system
- A gel electrophoresis system in which the gel matrix is subjected to an electric field that periodically changes direction.
+ A gel electrophoresis system in which the gel matrix is subjected to an electric field that periodically changes direction.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Pulsed_field_gel_electrophoresis
pulsed-field gel electrophoresis system
@@ -5469,7 +5469,7 @@
tissue embedding station
- A device that is used to perform paraffin embedding of tissue specimens.
+ A device that is used to perform paraffin embedding of tissue specimens.
PERSON: Erik Segerdell
PERSON: Erik Segerdell
tissue embedding station
@@ -5489,7 +5489,7 @@
nucleic acid sequencer
- An device that is used to determine the order of nucleotides in nucleic acid sequences.
+ An device that is used to determine the order of nucleotides in nucleic acid sequences.
PERSON: Erik Segerdell
PERSON: Erik Segerdell
nucleic acid sequencer
@@ -5515,7 +5515,7 @@
bead array reader
- A device that is used to acquire and image bead array data.
+ A device that is used to acquire and image bead array data.
PERSON: Erik Segerdell
PERSON: Erik Segerdell
bead array reader
@@ -5529,7 +5529,7 @@
real-time PCR machine
- An PCR instrument that enables both detection and quantification of one or more specific sequences in a DNA sample.
+ An PCR instrument that enables both detection and quantification of one or more specific sequences in a DNA sample.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Real-time_polymerase_chain_reaction
real-time PCR machine
@@ -5561,7 +5561,7 @@
paraffin oven
- A device that is used for the warming of paraffin embedding medium.
+ A device that is used for the warming of paraffin embedding medium.
PERSON: Erik Segerdell
PERSON: Erik Segerdell
paraffin oven
@@ -5593,7 +5593,7 @@
autoclave
- A device that is used to sterilize equipment and supplies by subjecting them to high pressure steam at 121 C or more, typically for 15 to 20 minutes depending on the size of the load and the contents.
+ A device that is used to sterilize equipment and supplies by subjecting them to high pressure steam at 121 C or more, typically for 15 to 20 minutes depending on the size of the load and the contents.
PERSON: Erik Segerdell
J. Black, Microbiology, Prentice Hall (1993) pg. 334; http://en.wikipedia.org/wiki/Autoclave
autoclave
@@ -5613,7 +5613,7 @@
microplate washer
- A device that is used to wash immunoassays in microwell strips and plates with professional accuracy. WHAT IS PROFESSIONAL ACCURACY??
+ A device that is used to wash immunoassays in microwell strips and plates with professional accuracy. WHAT IS PROFESSIONAL ACCURACY??
PERSON: Erik Segerdell
http://www.articlesnatch.com/Article/Microplate-Readers-And-Washers-For-Laboratories/948037
microplate washer
@@ -5633,7 +5633,7 @@
nucleic acid extraction/purification instrument
- A device that is used to isolate and collect nucleic acids (DNA or RNA) for subsequent molecular analysis.
+ A device that is used to isolate and collect nucleic acids (DNA or RNA) for subsequent molecular analysis.
PERSON: Erik Segerdell
PERSON: Erik Segerdell
nucleic acid extraction/purification instrument
@@ -5647,7 +5647,7 @@
ELISA microplate washer
- A microplate washer that is used for enzyme-linked immunosorbent assays (ELISA).
+ A microplate washer that is used for enzyme-linked immunosorbent assays (ELISA).
PERSON: Erik Segerdell
PERSON: Erik Segerdell
ELISA microplate washer
@@ -5667,7 +5667,7 @@
vacuum manifold
- A device that is used for the vacuum-driven processing of multiwell strips or plates, or spin columns. IS THIS AN INSTRUMENT? IS THE DEFINTION CORRECT - TO DISTRIBUTE PRESSURE EVENLY.
+ A device that is used for the vacuum-driven processing of multiwell strips or plates, or spin columns. IS THIS AN INSTRUMENT? IS THE DEFINTION CORRECT - TO DISTRIBUTE PRESSURE EVENLY.
PERSON: Erik Segerdell
PERSON: Erik Segerdell
vacuum manifold
@@ -5681,7 +5681,7 @@
DNA extraction/purification instrument
- A device that is used to isolate and collect DNA for subsequent molecular analysis.
+ A device that is used to isolate and collect DNA for subsequent molecular analysis.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/DNA_extraction
DNA extraction/purification instrument
@@ -5707,7 +5707,7 @@
multichannel pipette
- A pipetting system that has a plurality of tip fittings and is used for multi-well plate applications.
+ A pipetting system that has a plurality of tip fittings and is used for multi-well plate applications.
PERSON: Erik Segerdell
PERSON: Erik Segerdell
multichannel pipette
@@ -5727,7 +5727,7 @@
cell harvester
- A device that is used to harvest cells from microplates and deposit samples on a filter mat. NOT AN INSTRUMENT?
+ A device that is used to harvest cells from microplates and deposit samples on a filter mat. NOT AN INSTRUMENT?
PERSON: Erik Segerdell
PERSON: Erik Segerdell
cell harvester
@@ -5741,7 +5741,7 @@
portable fluorometer
- A compact fluorometer that can be carried or moved with ease.
+ A compact fluorometer that can be carried or moved with ease.
PERSON: Erik Segerdell
PERSON: Erik Segerdell
portable fluorometer
@@ -5755,7 +5755,7 @@
gel electrophoresis system
- An electrophoresis system in which an electric field is applied to a gel matrix
+ An electrophoresis system in which an electric field is applied to a gel matrix
PERSON: Erik Segerdell
https://en.wikipedia.org/wiki/Gel_electrophoresis
gel electrophoresis system
@@ -5775,7 +5775,7 @@
diffractometer
- A measurement device for analyzing the structure of a material from the scattering pattern produced when a beam of radiation or particles (e.g. X rays or neutrons) interacts with it.
+ A measurement device for analyzing the structure of a material from the scattering pattern produced when a beam of radiation or particles (e.g. X rays or neutrons) interacts with it.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Diffractometer
diffractometer
@@ -5795,7 +5795,7 @@
microdissection instrument
- A device that is used for the dissection of tissues under magnification.
+ A device that is used for the dissection of tissues under magnification.
PERSON: Erik Segerdell
http://medical-dictionary.thefreedictionary.com/microdissection
microdissection instrument
@@ -5815,7 +5815,7 @@
micropipette puller
- A device that is used to fabricate glass micropipettes.
+ A device that is used to fabricate glass micropipettes.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Micropipette
micropipette puller
@@ -5835,7 +5835,7 @@
laser scanning confocal microscope
- A confocal microscope that obtains high-resolution optical images with depth selectivity, in which a laser beam passes through a light source aperture and then is focused by an objective lens into a small (ideally diffraction limited) focal volume within or on the surface of a specimen.
+ A confocal microscope that obtains high-resolution optical images with depth selectivity, in which a laser beam passes through a light source aperture and then is focused by an objective lens into a small (ideally diffraction limited) focal volume within or on the surface of a specimen.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Confocal_laser_scanning_microscopy
laser scanning confocal microscope
@@ -5855,7 +5855,7 @@
digital microscope
- A microscope that uses optics and a charge-coupled device (CCD) camera to output a digital image to a monitor.
+ A microscope that uses optics and a charge-coupled device (CCD) camera to output a digital image to a monitor.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Digital_microscope
digital microscope
@@ -5881,7 +5881,7 @@
freeze substitution system
- A device or system for dehydrating and then chemically fixing electron microscopy samples at low temperatures in preparation for various treatments including embedding in resins.
+ A device or system for dehydrating and then chemically fixing electron microscopy samples at low temperatures in preparation for various treatments including embedding in resins.
PERSON: Erik Segerdell
doi:10.1017/S143192760707866X
freeze substitution system
@@ -5907,7 +5907,7 @@
micropipette
- A microinjection device that is used to measure very small volumes of liquids.
+ A microinjection device that is used to measure very small volumes of liquids.
PERSON: Erik Segerdell
http://www.answers.com/topic/micropipette
micropipette
@@ -5927,7 +5927,7 @@
voltage clamp device
- A device that is used to measure the ion currents across the membrane of excitable cells, such as neurons, while holding the membrane voltage at a set level.
+ A device that is used to measure the ion currents across the membrane of excitable cells, such as neurons, while holding the membrane voltage at a set level.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Voltage_clamp
voltage clamp device
@@ -5959,7 +5959,7 @@
vacuum oven
- A device that heats materials in a vacuum.
+ A device that heats materials in a vacuum.
PERSON: Erik Segerdell
PERSON: Erik Segerdell
vacuum oven
@@ -5979,7 +5979,7 @@
slide warmer
- A device that is used to heat microscope slides.
+ A device that is used to heat microscope slides.
PERSON: Erik Segerdell
PERSON: Erik Segerdell
slide warmer
@@ -5993,7 +5993,7 @@
capillary electrophoresis instrument
- An electrophoresis system that is used to separate ionic species by their charge and frictional forces and mass.
+ An electrophoresis system that is used to separate ionic species by their charge and frictional forces and mass.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Capillary_electrophoresis
capillary electrophoresis instrument
@@ -6013,7 +6013,7 @@
denaturing high-performance liquid chromatography instrument
- A high performance liquid chromatography instrument that employs temperature-dependent separation of DNA containing mismatched base pairs from PCR-amplified DNA fragments for chromatographic mutation analysis.
+ A high performance liquid chromatography instrument that employs temperature-dependent separation of DNA containing mismatched base pairs from PCR-amplified DNA fragments for chromatographic mutation analysis.
PERSON: Erik Segerdell
doi:10.1385/1-59259-850-1:173
denaturing high-performance liquid chromatography instrument
@@ -6027,7 +6027,7 @@
agarose gel electrophoresis system
- A gel electrophoresis system that is used to separate DNA or RNA molecules by size, achieved by moving negatively charged nucleic acid molecules through an agarose matrix with an electric field.
+ A gel electrophoresis system that is used to separate DNA or RNA molecules by size, achieved by moving negatively charged nucleic acid molecules through an agarose matrix with an electric field.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Agarose_gel_electrophoresis
agarose gel electrophoresis system
@@ -6053,7 +6053,7 @@
balance
- A measuring instrument that is used to determine the weight or mass of an object.
+ A measuring instrument that is used to determine the weight or mass of an object.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Weighing_scale
balance
@@ -6073,7 +6073,7 @@
surface plasmon resonance instrument
- A tool for measuring adsorption of material onto planar metal (typically gold and silver) surfaces or onto the surface of metal nanoparticles.
+ A tool for measuring adsorption of material onto planar metal (typically gold and silver) surfaces or onto the surface of metal nanoparticles.
PERSON: Erik Segerdell
http://en.wikipedia.org/wiki/Surface_plasmon_resonance
surface plasmon resonance instrument
@@ -6093,7 +6093,7 @@
protein sequencer
- An device that is used to determine the order of amino acids in protein sequences.
+ An device that is used to determine the order of amino acids in protein sequences.
PERSON: Erik Segerdell
PERSON: Erik Segerdell
protein sequencer
@@ -6113,7 +6113,7 @@
X-ray source
- A device that is used to generate X-rays.
+ A device that is used to generate X-rays.
PERSON: Erik Segerdell
x-ray generator
http://en.wikipedia.org/wiki/X-ray_generator
@@ -6128,7 +6128,7 @@
liquid chromatography instrument
- A chromatography device that dissolves a mixture in liquid mobile phase to separate the analyte to be measured from other molecules in the mixture and allows it to be isolated
+ A chromatography device that dissolves a mixture in liquid mobile phase to separate the analyte to be measured from other molecules in the mixture and allows it to be isolated
PERSON: Matthew Brush
PERSON: Matthew Brush
liquid chromatography instrument
@@ -6142,7 +6142,7 @@
SNP microarray
- A DNA microarray used to detect polymorphisms in DNA samples
+ A DNA microarray used to detect polymorphisms in DNA samples
Person: Helen Parkinson
EFO_0002703 SNP array
SNP microarray
@@ -6156,7 +6156,7 @@
tiling microarray
- A DNA microarray which has short fragments of nucleic acid immobilized on a substrate. These are designed to cover the whole genome of the target species. Tiling arrays are used to determine genome binding in ChIP assays or to identify transcribed regions.
+ A DNA microarray which has short fragments of nucleic acid immobilized on a substrate. These are designed to cover the whole genome of the target species. Tiling arrays are used to determine genome binding in ChIP assays or to identify transcribed regions.
Person: Helen Parkinson
genome tiling array
EFO_0002704: tiling array
@@ -6176,7 +6176,7 @@
- A device made to be used in an analyte assay for immobilization of substances that bind the analyte at regular spatial positions on a surface.
+ A device made to be used in an analyte assay for immobilization of substances that bind the analyte at regular spatial positions on a surface.
PERSON: Chris Stoeckert, Jie Zheng, Alan Ruttenberg
Penn Group
assay array
@@ -6195,7 +6195,7 @@
- An array that consists of 3-micron silica beads that self assemble in microwells on either of two materials: fiber optic bundles or planar silica slides.
+ An array that consists of 3-micron silica beads that self assemble in microwells on either of two materials: fiber optic bundles or planar silica slides.
PERSON: Chris Stoeckert, Jie Zheng, Alan Ruttenberg, Venkat Malladi
http://www.illumina.com/technology/beadarray_technology.ilmn
Illumina BeadChip
@@ -6248,7 +6248,7 @@
- A BeadChip made for an analyte assay that generates information about DNA methylation.
+ A BeadChip made for an analyte assay that generates information about DNA methylation.
PERSON: Chris Stoeckert, Jie Zheng, Alan Ruttenberg
Penn Group
Illumina methylation BeadChip
@@ -6267,7 +6267,7 @@
- A flow cytometer analyzer manifactured by Becton ans Dickinson. Can be configured with up to 5 lasers, 488nm, 532 or 561 nm, 640 nm, 405 nm, 355 nm for measuring up to 20 parameters simultaneously.
+ A flow cytometer analyzer manifactured by Becton ans Dickinson. Can be configured with up to 5 lasers, 488nm, 532 or 561 nm, 640 nm, 405 nm, 355 nm for measuring up to 20 parameters simultaneously.
Anna Maria Masci
http://www.bdbiosciences.com/instruments/lsrx20/index.jsp?WT.srch=1&gclid=CJjJ8JTR5LoCFXBo7AodZycAbg
LSRFortessa X-20
@@ -6280,7 +6280,7 @@
Ion 316 Chip v2
- An ion semiconductor chip manufactured by Life Technologies which detects polymerase-driven base incorporation to translate into digital form. The 316 chip is compatible with the Ion Torrent PGM and has a run time of: 3.0 hours for 200 bp reads with an output of 30-50 Mb, 4.9 hours for 400 bp reads with an output of 60 Mb-1 Gb.
+ An ion semiconductor chip manufactured by Life Technologies which detects polymerase-driven base incorporation to translate into digital form. The 316 chip is compatible with the Ion Torrent PGM and has a run time of: 3.0 hours for 200 bp reads with an output of 30-50 Mb, 4.9 hours for 400 bp reads with an output of 60 Mb-1 Gb.
Issue Tracker #774 https://sourceforge.net/p/obi/obi-terms/774/
PERSON: Sagar Jain
Ion 316 Chip
@@ -6297,7 +6297,7 @@
Ion 318 Chip v2
- An ion semiconductor chip manufactured by Life Technologies which detects polymerase-driven base incorporation to translate into digital form. The 318 chip is compatible with the Ion Torrent PGM and has a run time of: 4.4 hours for 200 bp reads with an output of 60 Mb-1 Gb, 7.3 hours for 400 bp reads with an output of 1.2 Gb-2 Gb.
+ An ion semiconductor chip manufactured by Life Technologies which detects polymerase-driven base incorporation to translate into digital form. The 318 chip is compatible with the Ion Torrent PGM and has a run time of: 4.4 hours for 200 bp reads with an output of 60 Mb-1 Gb, 7.3 hours for 400 bp reads with an output of 1.2 Gb-2 Gb.
Issue Tracker #775 https://sourceforge.net/p/obi/obi-terms/775/
PERSON: Sagar Jain
Ion 318 Chip
@@ -6314,7 +6314,7 @@
ion semiconductor chip
- An ion detector that is organized as an electronic circuit whose components, such as transistors and resistors, are etched or deposited on a single slice of semiconductor material to produce a chip. The specific chip detects ion charge induced when an ion passes by or hits a surface.
+ An ion detector that is organized as an electronic circuit whose components, such as transistors and resistors, are etched or deposited on a single slice of semiconductor material to produce a chip. The specific chip detects ion charge induced when an ion passes by or hits a surface.
Issue Tracker: #776 https://sourceforge.net/p/obi/obi-terms/776/
PERSON: Sagar Jain
ion chip
@@ -6331,7 +6331,7 @@
Ion 314 Chip v2
- An ion semiconductor chip manufactured by Life Technologies which detects polymerase-driven base incorporation to translate into digital form. The 314 chip is compatible with the Ion Torrent PGM and has a run time of: 2.3 hours for 200 bp reads with an output of 30-50 Mb, 3.7 hours for 400 bp reads with an output of 60-100 Mb.
+ An ion semiconductor chip manufactured by Life Technologies which detects polymerase-driven base incorporation to translate into digital form. The 314 chip is compatible with the Ion Torrent PGM and has a run time of: 2.3 hours for 200 bp reads with an output of 30-50 Mb, 3.7 hours for 400 bp reads with an output of 60-100 Mb.
Issue Tracker #766 https://sourceforge.net/p/obi/obi-terms/766/
PERSON: Sagar Jain
Ion 314 Chip
@@ -6349,7 +6349,7 @@
Gravina, Michael T., Jenny H. Lin, and Stuart S. Levine. "Lane-by-lane sequencing using Illumina's Genome Analyzer II." BioTechniques 54.5 (2013): 265-269. PMID: 23662897
- An Illumina Genome Analyzer II which is manufactured by the Illumina corporation. It supports sequencing of single, long or short insert paired end clone libraries relying on sequencing by synthesis technology. The Genome Analyzer IIx is the most widely adopted next-generation sequencing platform and proven and published across the broadest range of research applications.
+ An Illumina Genome Analyzer II which is manufactured by the Illumina corporation. It supports sequencing of single, long or short insert paired end clone libraries relying on sequencing by synthesis technology. The Genome Analyzer IIx is the most widely adopted next-generation sequencing platform and proven and published across the broadest range of research applications.
PERSON: Venkat Malladi, Chris Stoeckert, Jie Zheng, Alan Ruttenberg
Illumina GA IIx
Illumina Genome Analyzer IIx
@@ -6371,7 +6371,7 @@
Wang J, Qi J, Zhao H, He S, Zhang Y, Wei S, Zhao F. Metagenomic sequencing reveals microbiota and its functional potential associated with periodontal disease. Sci Rep. 2013 May;3:1843. PMID:23673380
- A DNA sequencer which is manufactured by the Illumina corporation, with two flow cells and a throughput of up to 55 Gb per day. Built upon sequencing by synthesis technology, the machine is optimized for generation of data for multiple samples in a single run.
+ A DNA sequencer which is manufactured by the Illumina corporation, with two flow cells and a throughput of up to 55 Gb per day. Built upon sequencing by synthesis technology, the machine is optimized for generation of data for multiple samples in a single run.
PERSON: Venkat Malladi, Chris Stoeckert, Jie Zheng
HiSeq 2000
http://res.illumina.com/documents/products/datasheets/datasheet_hiseq_systems.pdf
@@ -6392,7 +6392,7 @@
Spaethling, Jennifer M., and James H. Eberwine. "Single-cell transcriptomics for drug target discovery." Current opinion in pharmacology (2013). pmid:23725882
- A DNA sequencer which is manufactured by the Illumina corporation, with two flow cells and a throughput of up to 160 Gb per day. Built upon sequencing by synthesis technology, the machine is optimized for generation of data for batching multiple samples or rapid results on a few samples.
+ A DNA sequencer which is manufactured by the Illumina corporation, with two flow cells and a throughput of up to 160 Gb per day. Built upon sequencing by synthesis technology, the machine is optimized for generation of data for batching multiple samples or rapid results on a few samples.
PERSON: Venkat Malladi, Chris Stoeckert, Jie Zheng, Alan Ruttenberg
HiSeq 2500
http://res.illumina.com/documents/products/datasheets/datasheet_hiseq2500.pdf
@@ -6413,7 +6413,7 @@
Rutvisuttinunt W, Chinnawirotpisan P, Simasathien S, Shrestha SK, Yoon IK, Klungthong C, Fernandez S. Simultaneous and complete genome sequencing of influenza A and B with high coverage by Illumina MiSeq Platform. J Virol Methods. 2013 Nov;193(2):394-404. [PMID:23856301]
- A DNA sequencer which is manufactured by the Illumina corporation. Built upon sequencing by synthesis technology, the machine provides an end-to-end solution (cluster generation, amplification, sequencing, and data analysis) in a single machine.
+ A DNA sequencer which is manufactured by the Illumina corporation. Built upon sequencing by synthesis technology, the machine provides an end-to-end solution (cluster generation, amplification, sequencing, and data analysis) in a single machine.
PERSON: Venkat Malladi, Chris Stoeckert, Jie Zheng
Illumina MiSeq
http://res.illumina.com/documents/products/datasheets/datasheet_miseq.pdf
@@ -6428,7 +6428,7 @@
Naumov, Vladimir A., et al. "Genome-scale analysis of DNA methylation in colorectal cancer using Infinium HumanMethylation450 BeadChips." Epigenetics 8.9 (2013): 0-1. PMID: 23867710
- A methylation BeadChip which is manufactured by the Illumina corporation. Built upon BeadChip tehcnology, the array interrogates ~ 485,000 methylation sites per sample at single-nucleotide resolution.
+ A methylation BeadChip which is manufactured by the Illumina corporation. Built upon BeadChip tehcnology, the array interrogates ~ 485,000 methylation sites per sample at single-nucleotide resolution.
PERSON: Venkat Malladi, Chris Stoeckert, Jie Zheng, Alan Ruttenberg
Illumina Infinium Human Methylation 450K BeadChip
http://www.illumina.com/products/methylation_450_beadchip_kits.ilmn
@@ -6443,7 +6443,7 @@
Polidoro, Silvia, et al. "Effects of bisphosphonate treatment on DNA methylation in osteonecrosis of the jaw." Mutation Research/Genetic Toxicology and Environmental Mutagenesis 757.2 (2013): 104-113. PMID: 23892139
- A methylation BeadChip which is manufactured by the Illumina corporation. Built upon BeadChip tehcnology, the array interrogates ~ 27,000 CpG sites per sample at single-nucleotide resolution.
+ A methylation BeadChip which is manufactured by the Illumina corporation. Built upon BeadChip tehcnology, the array interrogates ~ 27,000 CpG sites per sample at single-nucleotide resolution.
PERSON: Venkat Malladi, Chris Stoeckert, Jie Zheng, Alan Ruttenberg
Illumina Infinium Human Methylation 27K BeadChip
http://res.illumina.com/documents/products/datasheets/datasheet_dna_methylation_analysis.pdf
@@ -6458,7 +6458,7 @@
Edwards, Todd L., et al. "Genome-Wide Association Study Confirms SNPs in SNCA and the MAPT Region as Common Risk Factors for Parkinson Disease." Annals of human genetics 74.2 (2010): 97-109. PMID: 20070850
- A BeadChip which is manufactured by the Illumina corporation. Built upon BeadChip tehcnology, the array integrates ~ 1 million markers per sample for genotyping, and copy number variation (CNV) and Cytogenetic analysis.
+ A BeadChip which is manufactured by the Illumina corporation. Built upon BeadChip tehcnology, the array integrates ~ 1 million markers per sample for genotyping, and copy number variation (CNV) and Cytogenetic analysis.
PERSON: Venkat Malladi, Chris Stoeckert, Jie Zheng, Alan Ruttenberg
Illumina Human 1M-Duo Infinium HD BeadChip
http://www.illumina.com/technology/infinium_hd_assay.ilmn
@@ -6479,7 +6479,7 @@
Vissers, Lisenka ELM, et al. "A de novo paradigm for mental retardation." Nature genetics 42.12 (2010): 1109-1112. PMID:21076407
- A DNA sequencer which is manufacted by the Applied Biosystems corporation. Built upon SOLiD sequencing technology, the machine generates greater than 1 billion mappable reads per run.
+ A DNA sequencer which is manufacted by the Applied Biosystems corporation. Built upon SOLiD sequencing technology, the machine generates greater than 1 billion mappable reads per run.
PERSON: Venkat Malladi, Chris Stoeckert, Jie Zheng, Alan Ruttenberg
Applied Biosystems SOLiD 3 Plus System
http://www3.appliedbiosystems.com/cms/groups/mcb_marketing/documents/generaldocuments/cms_072050.pdf
@@ -6500,7 +6500,7 @@
Miller, Becky Akiko. Detection and biological assessment of genome structural variation in Plasmodium falciparum. Diss. University of Notre Dame, 2012. http://etd.nd.edu/ETD-db/theses/available/etd-04182012-114744/
- A tiling array which is manufactured by the Nimblegen corporation. Built to analyze DNA sequence copy number by comparative genomic hybridization for mouse DNA against 385,000 features.
+ A tiling array which is manufactured by the Nimblegen corporation. Built to analyze DNA sequence copy number by comparative genomic hybridization for mouse DNA against 385,000 features.
PERSON: Venkat Malladi, Chris Stoeckert, Jie Zheng, Alan Ruttenberg
Nimblegen Mouse 385K Whole Genome CGH Tiling Array
http://www.nimblegen.com/downloads/support/05434483001_NG_CGHLOH_UGuide_v9p1.pdf
@@ -6521,7 +6521,7 @@
Wartman, Lukas D., et al. "Sequencing a mouse acute promyelocytic leukemia genome reveals genetic events relevant for disease progression." The Journal of clinical investigation 121.4 (2011): 1445. PMID:21436584
- A tiling array which is manufactured by the Nimblegen corporation. Built to analyze DNA sequence copy number by comparative genomic hybridization for mouse DNA against 3x720,000 features.
+ A tiling array which is manufactured by the Nimblegen corporation. Built to analyze DNA sequence copy number by comparative genomic hybridization for mouse DNA against 3x720,000 features.
PERSON: Venkat Malladi, Chris Stoeckert, Jie Zheng, Alan Ruttenberg
Nimblegen Mouse 3x720K Whole Genome CGH Tiling Array
http://www.nimblegen.com/downloads/support/05434483001_NG_CGHLOH_UGuide_v9p1.pdf
@@ -6542,7 +6542,7 @@
Deletion in Xp22.11: PTCHD1 is a candidate gene for X-linked intellectual disability with or without autism PMID:21091464
- A tiling array which is manufactured by the Nimblegen corporation. Built to analyze DNA sequence copy number by comparative genomic hybridization for human DNA against 3x720,000 features.
+ A tiling array which is manufactured by the Nimblegen corporation. Built to analyze DNA sequence copy number by comparative genomic hybridization for human DNA against 3x720,000 features.
PERSON: Venkat Malladi, Chris Stoeckert, Jie Zheng, Alan Ruttenberg
Nimblegen Human 3x720K Whole Genome CGH Tiling Array
http://www.nimblegen.com/downloads/support/05434483001_NG_CGHLOH_UGuide_v9p1.pdf
@@ -6563,7 +6563,7 @@
Filges, Isabel, et al. "Reduced expression by SETBP1 haploinsufficiency causes developmental and expressive language delay indicating a phenotype distinct from Schinzel–Giedion syndrome." Journal of medical genetics 48.2 (2011): 117-122. PMID:21037274
- A tiling array which is manufactured by the Nimblegen corporation. Built to analyze DNA sequence copy number by comparative genomic hybridization for human DNA against 2.1 million features.
+ A tiling array which is manufactured by the Nimblegen corporation. Built to analyze DNA sequence copy number by comparative genomic hybridization for human DNA against 2.1 million features.
PERSON: Venkat Malladi, Chris Stoeckert, Jie Zheng, Alan Ruttenberg
Nimblegen Human 2.1M Whole-Genome CGH Tiling Array v2.0
http://www.nimblegen.com/downloads/support/05434483001_NG_CGHLOH_UGuide_v9p1.pdf
@@ -6584,7 +6584,7 @@
Spaethling, Jennifer M., and James H. Eberwine. "Single-cell transcriptomics for drug target discovery." Current opinion in pharmacology (2013). pmid:23725882
- A DNA sequencer which is manufactured by the Pacific Biosciences corporation. Built upon single molecule real-time sequencing technology, the machine is optimized for generation with long reads and high consensus accuracy.
+ A DNA sequencer which is manufactured by the Pacific Biosciences corporation. Built upon single molecule real-time sequencing technology, the machine is optimized for generation with long reads and high consensus accuracy.
PERSON: Venkat Malladi, Chris Stoeckert, Jie Zheng, Alan Ruttenberg
Pacific Biosciences RS II
http://www.pacificbiosciences.com/products/
@@ -6605,7 +6605,7 @@
Kolbert, Christopher P., et al. "Multi-platform analysis of microRNA expression measurements in RNA from fresh frozen and FFPE tissues." PloS one 8.1 (2013): e52517. PMID:23382819
- A human array which is manufacutred by NanoString Technologies. Built upon color-coded molecular barcodes technology, the array profiles miRNA with increased specificity and sensitivty than microarrays.
+ A human array which is manufacutred by NanoString Technologies. Built upon color-coded molecular barcodes technology, the array profiles miRNA with increased specificity and sensitivty than microarrays.
PERSON: Venkat Malladi, Chris Stoeckert, Jie Zheng, Alan Ruttenberg. Mark A. Miller removed "V2" per https://github.com/obi-ontology/obi/issues/831 on 20180511.
https://www.nanostring.com/products/mirna-assays/mirna-panels
nCounter Human miRNA Expression array
@@ -6623,7 +6623,7 @@
- A DNA sequencer which is a desktop sequencer ideal for smaller-scale studies manufactured by the Illumina corporation. It supports sequencing of single, long or short insert paired end clone libraries relying on sequencing by synthesis technology.
+ A DNA sequencer which is a desktop sequencer ideal for smaller-scale studies manufactured by the Illumina corporation. It supports sequencing of single, long or short insert paired end clone libraries relying on sequencing by synthesis technology.
Person: Venkat Malladi, Chris Stoeckert, Jie Zheng
Illumina NextSeq 500
http://systems.illumina.com/systems/nextseq-sequencer.html
@@ -6642,7 +6642,7 @@
- A DNA sequencer which is manufactured by the Illumina corporation, with a single flow cell and a throughput of up to 35 Gb per day. It supports sequencing of single, long or short insert paired end clone libraries relying on sequencing by synthesis technology.
+ A DNA sequencer which is manufactured by the Illumina corporation, with a single flow cell and a throughput of up to 35 Gb per day. It supports sequencing of single, long or short insert paired end clone libraries relying on sequencing by synthesis technology.
Person: Venkat Malladi, Chris Stoeckert, Jie Zheng
HiSeq 1000
http://res.illumina.com/documents/products/datasheets/datasheet_hiseq_systems.pdf
@@ -6661,7 +6661,7 @@
- A tiling array which is a comprehensive whole human genome expression array manufactured by the Affymetrix corporation. Built to analyze DNA sequence copy number by comparative genomic hybridization for human DNA against 47,000 transcripts and variants.
+ A tiling array which is a comprehensive whole human genome expression array manufactured by the Affymetrix corporation. Built to analyze DNA sequence copy number by comparative genomic hybridization for human DNA against 47,000 transcripts and variants.
Person: Venkat Malladi, Chris Stoeckert, Jie Zheng
Affymetrix HT Human Genome U133 Plus 2 Array Plate Set
HG-U133 Plus 2
@@ -6682,7 +6682,7 @@
- An AB SOLid System which is manufacted by the Applied Biosystems corporation. Built upon SOLiD sequencing technology, the machine generates greater than 1 billion mappable reads per run.
+ An AB SOLid System which is manufacted by the Applied Biosystems corporation. Built upon SOLiD sequencing technology, the machine generates greater than 1 billion mappable reads per run.
Person: Venkat Malladi, Chris Stoeckert, Jie Zheng
Applied Biosystems SOLiD 4 System
SOLiD 4
@@ -6702,7 +6702,7 @@
- A tiling microarray which is manufactured by the Affymetrix corporation. Built to analyze 3' DNA sequence copy number by comparative genomic hybridization for human DNA against 28,000 genes. It can be used for gene expression and alternative splicing assay
+ A tiling microarray which is manufactured by the Affymetrix corporation. Built to analyze 3' DNA sequence copy number by comparative genomic hybridization for human DNA against 28,000 genes. It can be used for gene expression and alternative splicing assay
Person: Venkat Malladi, Chris Stoeckert, Jie Zheng
Affymetrix Human Exon 1.0 St Array
Human Exon 1.0
@@ -6723,7 +6723,7 @@
- A tiling array which is manufactured by the Affymetrix corporation. Built to analyze DNA sequence copy number by comparative genomic hybridization for human DNA against 39,000 transcripts and variants.
+ A tiling array which is manufactured by the Affymetrix corporation. Built to analyze DNA sequence copy number by comparative genomic hybridization for human DNA against 39,000 transcripts and variants.
Person: Venkat Malladi, Chris Stoeckert, Jie Zheng
Affymetrix HT Human Genome U133 Array Plate Set
HG-U133
@@ -6738,7 +6738,7 @@
- An Illumina Genome Analyzer II which is manufactured by the Illumina corporation. It supports sequencing of single, long or short insert paired end clone libraries relying on sequencing by synthesis technology. The Genome Analyzer IIe makes industry-leading next-generation sequencing technology accessible to more laboratories.
+ An Illumina Genome Analyzer II which is manufactured by the Illumina corporation. It supports sequencing of single, long or short insert paired end clone libraries relying on sequencing by synthesis technology. The Genome Analyzer IIe makes industry-leading next-generation sequencing technology accessible to more laboratories.
Person: Venkat Malladi, Chris Stoeckert, Jie Zheng
Illumina GA IIe
Illumina Genome Analyzer IIe
@@ -6767,7 +6767,7 @@
surface plasmon resonance sensor chip
ProteOn GLC Sensor Chip #176-5011
- A device that is used as a binding surface for ligand during a surface plasmon resonance assay, consisting of a glass plate to which a metal film is attached
+ A device that is used as a binding surface for ligand during a surface plasmon resonance assay, consisting of a glass plate to which a metal film is attached
Anna Maria Masci
SPR sensor chip
biosensor chip
@@ -6789,7 +6789,7 @@
- A DNA sequencer manufactured by Illumina corporation, with a single flow cell and a throughput of more than 200 Gb per day.
+ A DNA sequencer manufactured by Illumina corporation, with a single flow cell and a throughput of more than 200 Gb per day.
PERSON: Sagar Jain, Richard Scheuermann
HiSeq 3000
http://www.illumina.com/systems/hiseq-3000-4000.html
@@ -6809,7 +6809,7 @@
- A DNA sequencer manufactured by Illumina corporation, with two flow cell and a throughput of more than 400 Gb per day.
+ A DNA sequencer manufactured by Illumina corporation, with two flow cell and a throughput of more than 400 Gb per day.
PERSON: Sagar Jain, Richard Scheuermann
HiSeq 4000
http://www.illumina.com/systems/hiseq-3000-4000.html
@@ -6841,7 +6841,7 @@
specimen container
COPAN eSwab, CPT vacutainer, PAXgene Blood DNA tube
- A container with the function of containing a specimen.
+ A container with the function of containing a specimen.
For details see tracker item: http://sourceforge.net/p/obi/obi-terms/792/
Chris Stoeckert
Duke Biobank, OBIB
@@ -6867,7 +6867,7 @@
physical store
a freezer. a humidity controlled box.
- A container with an environmental control function.
+ A container with an environmental control function.
For details see tracker item: http://sourceforge.net/p/obi/obi-terms/793/
Chris Stoeckert
Duke Biobank, OBIB
@@ -6887,7 +6887,7 @@
- A tiling array which is manufactured by the Nimblegen corporation to analyze DNA sequence copy number by comparative genomic hybridization for human DNA against 6x630,000 features.
+ A tiling array which is manufactured by the Nimblegen corporation to analyze DNA sequence copy number by comparative genomic hybridization for human DNA against 6x630,000 features.
Term request: https://sourceforge.net/p/obi/obi-terms/791/
Jason Hilton, Chris Stoeckert, Bjoern Peters, OBI-group
NimbleGen Human 6x630K CGH Whole Genome Tiling Array
@@ -6903,7 +6903,7 @@
Illumina Genome Analyzer
- A DNA sequencer manufactured by Solexa as one of its first sequencer lines, launched in 2006, and capable of sequencing 1 gigabase (Gb) of data in a single run.
+ A DNA sequencer manufactured by Solexa as one of its first sequencer lines, launched in 2006, and capable of sequencing 1 gigabase (Gb) of data in a single run.
Person: Chris Stoeckert, Jason Hilton
Illumina Genome Analyzer I
http://www.illumina.com/technology/next-generation-sequencing/solexa-technology.html
@@ -6918,7 +6918,7 @@
Illumina HiSeq X Ten
- A DNA sequencer that consists of a set of 10 HiSeq X Sequencing Systems.
+ A DNA sequencer that consists of a set of 10 HiSeq X Sequencing Systems.
Person: Chris Stoeckert, Jason Hilton, Sagar Jain, Richard Scheuermann
HiSeq X Ten
http://www.illumina.com/systems/hiseq-x-sequencing-system/system.html
@@ -6933,7 +6933,7 @@
Illumina Infinium Omni5Exome-4 Kit
- An Illumina BeadChip which is an array that interrogates over 4.3 million whole-genome variants for genotyping and copy number variation.
+ An Illumina BeadChip which is an array that interrogates over 4.3 million whole-genome variants for genotyping and copy number variation.
Person: Chris Stoeckert, Jason Hilton
http://www.illumina.com/products/by-type/microarray-kits/infinium-omni5-exome.html
Illumina Infinium Omni5Exome-4 Kit
@@ -6947,7 +6947,7 @@
Illumina Infinium MethylationEPIC v1.0 BeadChip
- An Illumina methylation BeadChip which is an array that interrogates ~ 850,000 methylation sites per sample at single-nucleotide resolution.
+ An Illumina methylation BeadChip which is an array that interrogates ~ 850,000 methylation sites per sample at single-nucleotide resolution.
Person: Chris Stoeckert, Jason Hilton
http://www.illumina.com/content/dam/illumina-marketing/documents/products/datasheets/humanmethylationepic-data-sheet-1070-2015-008.pdf
Illumina Infinium MethylationEPIC v1.0 BeadChip
@@ -6961,7 +6961,7 @@
Leica Peloris rapid tissue processor
- An automatic tissue processor that is a dual retort tissue processor manufactured by the Leica company to provide fast, high quality tissue processing for histology laboratories.
+ An automatic tissue processor that is a dual retort tissue processor manufactured by the Leica company to provide fast, high quality tissue processing for histology laboratories.
Chris Stoeckert, Helena Ellis
http://drp8p5tqcb2p5.cloudfront.net/fileadmin/downloads_lbs/Leica%20PELORIS/User%20Manuals/Leica_Peloris_manual_EN.pdf
NCI BBRB
@@ -6976,7 +6976,7 @@
Microm Ergostar HM200
- A microtome that is manufactured by Microm and uses a vertical cutting stroke common to all rotary microtomes engaged by a horizontal sliding movement. An operating arm replaces the handwheel and is attached to both sides of the instrument for greater convenience to permit control of sectioning from the left or right.
+ A microtome that is manufactured by Microm and uses a vertical cutting stroke common to all rotary microtomes engaged by a horizontal sliding movement. An operating arm replaces the handwheel and is attached to both sides of the instrument for greater convenience to permit control of sectioning from the left or right.
Chris Stoeckert, Helena Ellis
http://www.ultra-medical.com/Microm-Ergostar-HM200-Microtome/en
NCI BBRB
@@ -6991,7 +6991,7 @@
microtome blade
- A device that is the part of a microtome used to slice specimens to a desired thickness.
+ A device that is the part of a microtome used to slice specimens to a desired thickness.
Chris Stoeckert, Helena Ellis
https://en.wikipedia.org/wiki/Microtome
NCI BBRB
@@ -7006,7 +7006,7 @@
Sakura Low profile Accu-Edge microtome blade
- A microtome blade that is manufactured by Feather and is disposable. The ultra-sharp blades section specimens without striations, distortion or chattering.
+ A microtome blade that is manufactured by Feather and is disposable. The ultra-sharp blades section specimens without striations, distortion or chattering.
Chris Stoeckert, Helena Ellis
http://www.sakura.eu/Our-products/item/8/Microtomy/29/Accu-Edge-Disposable-Microtome-Blades
NCI BBRB
@@ -7020,7 +7020,7 @@
microraft
- A material separation device also commerically known as Isoraft, that is used to isolate single cells.
+ A material separation device also commerically known as Isoraft, that is used to isolate single cells.
Stephen A. Fisher, Junhyong Kim, Dan Berrios
https://en.wikipedia.org/wiki/Microrafts
microraft
@@ -7033,7 +7033,7 @@
pipette
- A device that is a laboratory tool commonly used in chemistry, biology and medicine to transport a measured volume of liquid, often as a media dispenser.
+ A device that is a laboratory tool commonly used in chemistry, biology and medicine to transport a measured volume of liquid, often as a media dispenser.
Stephen A. Fisher, Junhyong Kim, Dan Berrios
https://en.wikipedia.org/wiki/Pipette
pipette
@@ -7053,7 +7053,7 @@
Kolbert, Christopher P., et al. "Multi-platform analysis of microRNA expression measurements in RNA from fresh frozen and FFPE tissues." PloS one 8.1 (2013): e52517. PMID:23382819
- A mouse array which is manufacutred by NanoString Technologies. Built upon color-coded molecular barcodes technology, the array profiles miRNA with increased specificity and sensitivty than microarrays.
+ A mouse array which is manufacutred by NanoString Technologies. Built upon color-coded molecular barcodes technology, the array profiles miRNA with increased specificity and sensitivty than microarrays.
PERSON: Venkat Malladi, Chris Stoeckert, Jie Zheng, Alan Ruttenberg. Mark A. Miller added based on http://purl.obolibrary.org/obo/OBI_0002013
https://www.nanostring.com/products/mirna-assays/mirna-panels
nCounter Mouse miRNA Expression array
@@ -7072,7 +7072,7 @@
digital acquisition card
- The digital acquisition card acts as the interface between the computer and a measurement device via the computer bus. It converts the signal generated by a measurement device (output from device) to a digital signal via an analog-to-digital converter, ADC. It also converts a digital signal to an analog signal via a digital-to-analog converter, DAC. This analog signal (e.g., stimulus) is fed to a measurement device (input to device).
+ The digital acquisition card acts as the interface between the computer and a measurement device via the computer bus. It converts the signal generated by a measurement device (output from device) to a digital signal via an analog-to-digital converter, ADC. It also converts a digital signal to an analog signal via a digital-to-analog converter, DAC. This analog signal (e.g., stimulus) is fed to a measurement device (input to device).
Mark A. Miller
DAQ device
digital acquisition and digital generation card
@@ -7094,7 +7094,7 @@
Illumina NovaSeq 6000
Genomic DNA of Xenophilus sp. E41 was extracted and sequenced using an Illumina NovaSeq 6000 system.
- A DNA sequencer which is manufactured by the Illumina corporation, with two flow cells and an output of up to 6000 Gb (32-40 B reads per run). The sequencer utilizes synthesis technology and patterned flow cells to optimize throughput and even spacing of sequencing clusters.
+ A DNA sequencer which is manufactured by the Illumina corporation, with two flow cells and an output of up to 6000 Gb (32-40 B reads per run). The sequencer utilizes synthesis technology and patterned flow cells to optimize throughput and even spacing of sequencing clusters.
Dan Berrios
NovaSeq 6000
http://www.illumina.com/systems/sequencing-platforms/novaseq.html
@@ -7109,7 +7109,7 @@
PacBio Sequel
The cDNAs were sequenced on the PacBio Sequel platform.
- A DNA sequencer built upon single molecule real-time sequencing technology, optimized for generation with long reads and high consensus accuracy, and manufactured by the Pacific Biosciences corporation
+ A DNA sequencer built upon single molecule real-time sequencing technology, optimized for generation with long reads and high consensus accuracy, and manufactured by the Pacific Biosciences corporation
Bonita Lam
Dan Berrios
Pacific BioSciences Sequel
@@ -7125,7 +7125,7 @@
PacBio Sequel II
The cDNAs were sequenced on the PacBio Sequel II platform.
- A DNA sequencer built upon single molecule real-time sequencing technology, optimized for generation of highly accurate ("HiFi") long reads, and which is manufactured by the Pacific Biosciences corporation.
+ A DNA sequencer built upon single molecule real-time sequencing technology, optimized for generation of highly accurate ("HiFi") long reads, and which is manufactured by the Pacific Biosciences corporation.
Bonita Lam
Dan Berrios
Pacific BioSciences Sequel II
@@ -7148,7 +7148,7 @@
vacuum-assisted biopsy needle
Vacuum-assisted biopsy needles come in two varieties: a non-tethered design and a needle design requiring tethering cable to a vacuum source.
- A core biopsy needle integrated with a vacuum system which facilitates the collection of specimen material.
+ A core biopsy needle integrated with a vacuum system which facilitates the collection of specimen material.
Damion Dooley
https://www.researchgate.net/publication/330227873
https://github.com/obi-ontology/obi/issues/1163
@@ -7169,7 +7169,7 @@
glass bottle
- A container with a narrow neck that is made of glass.
+ A container with a narrow neck that is made of glass.
VEuPathDB
VEuPathDB
https://github.com/obi-ontology/obi/issues/1117
@@ -7191,7 +7191,7 @@
glass bottle coated with insecticides
- A glass bottle that coated with material designed to control insects.
+ A glass bottle that coated with material designed to control insects.
VEuPathDB
VEuPathDB
https://github.com/obi-ontology/obi/issues/1117
@@ -7214,7 +7214,7 @@
Oxford Nanopore MinION
Approaches to Whole Mitochondrial Genome Sequencing on the Oxford Nanopore MinION
- A portable DNA sequencer which is manufactured by the Oxford Nanopore Technologies corporation, that uses consumable flow cells producing up to 30 Gb of DNA sequence data per flow cell. The sequencer produces real-time results and utilizes nanopore technology with up to 512 nanopore channels in the sensor array.
+ A portable DNA sequencer which is manufactured by the Oxford Nanopore Technologies corporation, that uses consumable flow cells producing up to 30 Gb of DNA sequence data per flow cell. The sequencer produces real-time results and utilizes nanopore technology with up to 512 nanopore channels in the sensor array.
PERSON: Bonita Lam
ONT MinION, MinION
https://nanoporetech.com/products/minion
@@ -7236,7 +7236,7 @@
Oxford Nanopore GridION Mk1
Nineteen libraries were constructed and sequenced on nineteen different R9.4 FlowCells using the GridION X5 sequencer
- A DNA sequencer that is manufactured by the Oxford Nanopore Technologies corporation, that can run and analyze up to five individual flow cells producing up to 150 Gb of data per run. The sequencer produces real-time results and utilizes nanopore technology with the option of running the flow cells concurrently or individually.
+ A DNA sequencer that is manufactured by the Oxford Nanopore Technologies corporation, that can run and analyze up to five individual flow cells producing up to 150 Gb of data per run. The sequencer produces real-time results and utilizes nanopore technology with the option of running the flow cells concurrently or individually.
PERSON: Bonita Lam
Oxford Nanopore GridION X5, GridION Mk1
https://nanoporetech.com/products/gridion
@@ -7258,7 +7258,7 @@
Oxford Nanopore PromethION
Structural variants identified by Oxford Nanopore PromethION sequencing of the human genome.
- A DNA sequencer that is manufactured by the Oxford Nanopore Technologies corporation, capable of running up to 48 flow cells and producing up to 7.6 Tb of data per run. The sequencer produces real-time results and utilizes Nanopore technology, with each flow cell allowing up to 3,000 nanopores to be sequencing simultaneously.
+ A DNA sequencer that is manufactured by the Oxford Nanopore Technologies corporation, capable of running up to 48 flow cells and producing up to 7.6 Tb of data per run. The sequencer produces real-time results and utilizes Nanopore technology, with each flow cell allowing up to 3,000 nanopores to be sequencing simultaneously.
PERSON: Bonita Lam
PromethION
https://nanoporetech.com/products/promethion
@@ -7275,7 +7275,7 @@
Examples of PPE include respirators, gloves, aprons, fall protection, and full body suits, as well as head, eye and foot protection.
PPE is equipment worn by a worker to minimize exposure to specific hazards.
- A device which is a wearable garment designed to protect the wearer's body from injury or infection.
+ A device which is a wearable garment designed to protect the wearer's body from injury or infection.
https://orcid.org/0000-0002-8844-9165
PPE
personal protective equipment
@@ -7293,7 +7293,7 @@
face mask
A systematic review on the efficacy of face coverings against respiratory viruses analyzed 19 randomized trials and concluded that use of face masks and respirators appeared to be protective in both health care and community settings
- A personal protective device worn over the nose and mouth as a respiratory filter to inhibit the flow of particles.
+ A personal protective device worn over the nose and mouth as a respiratory filter to inhibit the flow of particles.
https://orcid.org/0000-0002-8844-9165
face covering
respirator
@@ -7311,7 +7311,7 @@
non-medical mask
A non-medical mask may contain fabrics that are not regulated for use in surgical masks or respirators, or may not be designed to form a seal around the nose and mouth.
- A face mask not manufactured according to medical equipment standards.
+ A face mask not manufactured according to medical equipment standards.
https://orcid.org/0000-0002-8844-9165
cloth mask
https://www.canada.ca/en/public-health/services/diseases/2019-novel-coronavirus-infection/prevention-risks/about-non-medical-masks-face-coverings.html
@@ -7328,7 +7328,7 @@
medical mask
The finding of a much higher rate of infection in the cloth mask arm could be interpreted as harm caused by cloth masks, efficacy of medical masks, or most likely a combination of both.
- A face mask manufactured according to a recognized medical equipment standard.
+ A face mask manufactured according to a recognized medical equipment standard.
https://orcid.org/0000-0002-9578-0788
surgical mask
https://www.canada.ca/en/public-health/services/diseases/2019-novel-coronavirus-infection/prevention-risks/about-non-medical-masks-face-coverings.html
@@ -7344,7 +7344,7 @@
N95 respirator
- A face mask that meets the U.S. National Institute for Occupational Safety and Health (NIOSH) N95 classification of air filtration, meaning that it filters at least 95% of incoming airborne particles.
+ A face mask that meets the U.S. National Institute for Occupational Safety and Health (NIOSH) N95 classification of air filtration, meaning that it filters at least 95% of incoming airborne particles.
https://orcid.org/0000-0002-8844-9165
N95
N95 face mask
@@ -7363,7 +7363,7 @@
face shield
- A personal protective device used to protect the wearer's entire face (or part of it) from hazards such as flying objects and road debris, chemical splashes, or alternately potentially infectious materials.
+ A personal protective device used to protect the wearer's entire face (or part of it) from hazards such as flying objects and road debris, chemical splashes, or alternately potentially infectious materials.
https://orcid.org/0000-0002-8844-9165
faceshield
splash shield
@@ -7380,7 +7380,7 @@
patient gown
- A personal protective clothing item which is a gown designed for use by a patient to facilitate caregiving by medical staff.
+ A personal protective clothing item which is a gown designed for use by a patient to facilitate caregiving by medical staff.
https://orcid.org/0000-0002-8844-9165
hospital gown
https://en.wikipedia.org/wiki/Patient_gown
@@ -7397,7 +7397,7 @@
scrubs
Examples consist of a short-sleeve V-necked shirt and drawstring pants or a short-sleeve calf-length dress, a tie-back or bouffant-style cap, a mask, a surgical gown, latex gloves, and supportive closed-toe shoes.
- A personal protective clothing item which is sterilized and which is worn by a health care professional. It can reference a shirt and pants or dress, and depending on medical protocol, may include a medical cap.
+ A personal protective clothing item which is sterilized and which is worn by a health care professional. It can reference a shirt and pants or dress, and depending on medical protocol, may include a medical cap.
https://orcid.org/0000-0002-8844-9165
scrub clothing item
https://en.wikipedia.org/wiki/Scrubs_(clothing)
@@ -7413,7 +7413,7 @@
reusable patient gown
- A patient gown intended to be reused after being laundered.
+ A patient gown intended to be reused after being laundered.
https://orcid.org/0000-0002-8844-9165
https://en.wikipedia.org/wiki/Patient_gown
https://github.com/obi-ontology/obi/issues/1193
@@ -7428,7 +7428,7 @@
disposable patient gown
- A patient gown intended for a single period of continuous use and then disposed of.
+ A patient gown intended for a single period of continuous use and then disposed of.
https://orcid.org/0000-0002-8844-9165
https://en.wikipedia.org/wiki/Patient_gown
https://github.com/obi-ontology/obi/issues/1193
@@ -7443,7 +7443,7 @@
medical gown
- A personal protective clothing item which is a gown worn by a medical professional in order to provide a barrier between patient and professional.
+ A personal protective clothing item which is a gown worn by a medical professional in order to provide a barrier between patient and professional.
https://orcid.org/0000-0002-8844-9165
hospital gown
https://en.wikipedia.org/wiki/Medical_gown
@@ -7459,7 +7459,7 @@
apron
- A garment which is worn over other clothing and covers mainly the front of the body.
+ A garment which is worn over other clothing and covers mainly the front of the body.
https://orcid.org/0000-0002-8844-9165
https://en.wikipedia.org/wiki/Apron
https://github.com/obi-ontology/obi/issues/1193
@@ -7474,7 +7474,7 @@
surgical gown
- A medical gown which is subjected to a sterilization process and which is intended to be worn by a medical professional during surgical procedures.
+ A medical gown which is subjected to a sterilization process and which is intended to be worn by a medical professional during surgical procedures.
https://orcid.org/0000-0002-8844-9165
OBI
https://github.com/obi-ontology/obi/issues/1193
@@ -7489,7 +7489,7 @@
personal protective glove
- A personal protective device which is a glove.
+ A personal protective device which is a glove.
https://orcid.org/0000-0002-8844-9165
OBI
https://github.com/obi-ontology/obi/issues/1193
@@ -7504,7 +7504,7 @@
personal protective clothing item
- A personal protective device which consists of a garment that serves in place of or in addition to regular body clothing.
+ A personal protective device which consists of a garment that serves in place of or in addition to regular body clothing.
https://orcid.org/0000-0002-8844-9165
OBI
https://github.com/obi-ontology/obi/issues/1193
@@ -7519,7 +7519,7 @@
laboratory coat
- A personal protective clothing item which is an overcoat worn by medical or laboratory professionals.
+ A personal protective clothing item which is an overcoat worn by medical or laboratory professionals.
https://orcid.org/0000-0002-8844-9165
white coat
https://en.wikipedia.org/wiki/White_coat
@@ -7535,7 +7535,7 @@
medical glove
- A personal protective glove which is disposable and is used during medical examinations and procedures to help prevent cross-contamination between caregivers and patients.
+ A personal protective glove which is disposable and is used during medical examinations and procedures to help prevent cross-contamination between caregivers and patients.
https://orcid.org/0000-0002-8844-9165
https://en.wikipedia.org/wiki/Medical_glove
https://github.com/obi-ontology/obi/issues/1193
@@ -7550,7 +7550,7 @@
nitrile glove
- A personal protective glove which is made out of nitrile rubber.
+ A personal protective glove which is made out of nitrile rubber.
https://orcid.org/0000-0002-8844-9165
https://en.wikipedia.org/wiki/Medical_glove
https://github.com/obi-ontology/obi/issues/1193
@@ -7565,7 +7565,7 @@
transparent partition
- A device which is a transparent constructed barrier, usually made out of acrylic (Plexiglass) or polycarbonate plastic, installed in facilities to intercept respiratory droplets, encourage physical distancing requirements.
+ A device which is a transparent constructed barrier, usually made out of acrylic (Plexiglass) or polycarbonate plastic, installed in facilities to intercept respiratory droplets, encourage physical distancing requirements.
https://orcid.org/0000-0002-8844-9165
transparent partition
https://ncceh.ca/content/blog/physical-barriers-covid-19-infection-prevention-and-control-commercial-settings
@@ -7581,7 +7581,7 @@
footwear cover
- A personal protective device which is an impermiable material which covers a shoe or boot in order to prevent spread of specific environmental contaminants.
+ A personal protective device which is an impermiable material which covers a shoe or boot in order to prevent spread of specific environmental contaminants.
https://orcid.org/0000-0002-8844-9165
boot cover
shoe cover
@@ -7598,7 +7598,7 @@
disposable footwear cover
- A footwear cover which is designed for a single period of continuous use and then disposed of.
+ A footwear cover which is designed for a single period of continuous use and then disposed of.
https://orcid.org/0000-0002-8844-9165
OBI
https://github.com/obi-ontology/obi/issues/1193
@@ -7613,7 +7613,7 @@
reusable footwear cover
- A footwear cover which is designed for repeated use.
+ A footwear cover which is designed for repeated use.
https://orcid.org/0000-0002-8844-9165
OBI
https://github.com/obi-ontology/obi/issues/1193
@@ -7628,7 +7628,7 @@
surgical N95 respirator
- A N95 respirator which has been approved by the FDA as a surgical mask.
+ A N95 respirator which has been approved by the FDA as a surgical mask.
https://orcid.org/0000-0002-8844-9165
healthcare respirator
medical respirator
@@ -7647,7 +7647,7 @@
protective coverall
- A personal protective clothing item which is a loose fitting coverall for ease of movement, with sleeves, full leggings and often a hood to cover the head. These can also include overshoe pieces to cover footwear and protect against contamination.
+ A personal protective clothing item which is a loose fitting coverall for ease of movement, with sleeves, full leggings and often a hood to cover the head. These can also include overshoe pieces to cover footwear and protect against contamination.
https://orcid.org/0000-0002-8844-9165
https://www.safeopedia.com/definition/863/disposable-coveralls
https://github.com/obi-ontology/obi/issues/1193
@@ -7663,7 +7663,7 @@
protective sleeve
A protective sleeve can be designed to provide protection from heat, welding spatter or hot metal, chemicals, sharp objects, paint or other liquids.
- A personal protective clothing item which is a protective cover worn over the arm.
+ A personal protective clothing item which is a protective cover worn over the arm.
https://orcid.org/0000-0002-8844-9165
https://www.safeopedia.com/definition/974/protective-sleeves
https://github.com/obi-ontology/obi/issues/1193
@@ -7678,7 +7678,7 @@
protective apron
- A personal protective clothing item which is an apron.
+ A personal protective clothing item which is an apron.
https://orcid.org/0000-0002-8844-9165
https://en.wikipedia.org/wiki/Apron
https://github.com/obi-ontology/obi/issues/1193
@@ -7693,7 +7693,7 @@
medical cap
- A personal protective device which is worn on the head that helps prevent transmission of contaminants contained in hair and scalp.
+ A personal protective device which is worn on the head that helps prevent transmission of contaminants contained in hair and scalp.
https://orcid.org/0000-0002-8844-9165
bouffant cap
bouffant hat
@@ -7713,7 +7713,7 @@
specimen collection device
- A device used to collect a specimen.
+ A device used to collect a specimen.
https://orcid.org/0000-0002-8844-9165
specimen collection device
@@ -7726,7 +7726,7 @@
chromatography vial
- A vial with cap and container material suited to optical, sanitary and handling requirements of chromatography.
+ A vial with cap and container material suited to optical, sanitary and handling requirements of chromatography.
PERSON:Daniel Schober
GROUP:<http://msi-ontology.sourceforge.net>
http://msi-ontology.sourceforge.net/ontology/CHROM.owl#msi_01117
@@ -7742,7 +7742,7 @@
specimen pad
An absorbent pad and its accompanying container are designed to provide safe storage and transport to various degrees for diagnostic and clinical samples, infectious and hazardous materials, chemicals, pharmaceuticals and environmental samples.
- A sample collection device consisting of a soft flexible, absorbent pad usually made from natural material such as gauze or cotton, used to absorb specimen fluid or particulate matter.
+ A sample collection device consisting of a soft flexible, absorbent pad usually made from natural material such as gauze or cotton, used to absorb specimen fluid or particulate matter.
https://orcid.org/0000-0002-8844-9165
absorbant pad
polysponge
@@ -7764,7 +7764,7 @@
specimen collection swab stick
A swab stick allows a worker to collect samples without touching the inside of the bag
- A specimen collection device which is a specimen pad attached to a long handle used to collect specimen material.
+ A specimen collection device which is a specimen pad attached to a long handle used to collect specimen material.
https://orcid.org/0000-0002-8844-9165
polyprobe
sponge probe
@@ -7782,7 +7782,7 @@
cotton swab
- A device which is a cotton pad mounted on one or both ends of a stick.
+ A device which is a cotton pad mounted on one or both ends of a stick.
https://orcid.org/0000-0002-8844-9165
Q-tip
swab-sampler
@@ -7804,7 +7804,7 @@
drag swab
- A specimen collection device consisting of a specimen pad made of sterile gauze which is aseptically attached to a pole by clips or to a string
+ A specimen collection device consisting of a specimen pad made of sterile gauze which is aseptically attached to a pole by clips or to a string
https://orcid.org/0000-0002-8844-9165
https://www.fda.gov/food/laboratory-methods-food/environmental-sampling-and-detection-salmonella-poultry-houses
drag swab
@@ -7818,7 +7818,7 @@
pre-moistened swab stick
- A specimen collection swab stick that is pre-moistened with liquid prior to sampling.
+ A specimen collection swab stick that is pre-moistened with liquid prior to sampling.
https://orcid.org/0000-0002-8844-9165
pre-moistened swab stick
@@ -7832,7 +7832,7 @@
surface wipe
Surface sampling procedures involved the use of polyester wipes, swabs, contact slides (two types), and adhesive tapes; a gelatin filter was used to sample the air.
- A sample collection device consisting of a thin, less absorbent sheet, used to collect material from surfaces.
+ A sample collection device consisting of a thin, less absorbent sheet, used to collect material from surfaces.
https://orcid.org/0000-0002-8844-9165
https://www.science.gov/topicpages/s/surface+wipe+sampling.html
surface wipe
@@ -7847,7 +7847,7 @@
catheter
A catheter left inside the body, either temporarily or permanently, may be referred to as an indwelling catheter.
- A device which is a flexible tube inserted into a body and which enables transfer of fluids into or out of a body.
+ A device which is a flexible tube inserted into a body and which enables transfer of fluids into or out of a body.
https://orcid.org/0000-0002-8844-9165
http://purl.bioontology.org/ontology/MESH/D057785
catheter
@@ -7861,7 +7861,7 @@
ultraviolet light source
- A light source that provides ultraviolet (UV) light for use in a distant area using a delivery system.
+ A light source that provides ultraviolet (UV) light for use in a distant area using a delivery system.
Person: Jie Zheng
UV light source
Person: Jie Zheng
@@ -7878,7 +7878,7 @@
visible light source
- A light source that provides visible light for use in a distant area using a delivery system.
+ A light source that provides visible light for use in a distant area using a delivery system.
Person: Jie Zheng
Person: Jie Zheng
https://github.com/obi-ontology/obi/issues/1200
@@ -7894,7 +7894,7 @@
solar light source
- A light source that light is produced from solar energy.
+ A light source that light is produced from solar energy.
Person: Chris Stoeckert
Person: Jie Zheng
Person: Chris Stoeckert
@@ -7916,7 +7916,7 @@
- A device designed to catch arthropods.
+ A device designed to catch arthropods.
John Judkins
MIRO:30000011
https://github.com/obi-ontology/obi/issues/1217
@@ -7929,7 +7929,7 @@
- An arthropod trap, consisting of a pit dug in the ground to provide a space for arthropods to rest and be collected.
+ An arthropod trap, consisting of a pit dug in the ground to provide a space for arthropods to rest and be collected.
John Judkins
IRO:0000005
https://github.com/obi-ontology/obi/issues/1217
@@ -7942,7 +7942,7 @@
- An arthropod trap designed to work with an animal (which could be human) inside a netted structure. This structure is designed so that an arthropod, attracted by the animal, can fly into the netted structure but can neither escape nor reach the animal.
+ An arthropod trap designed to work with an animal (which could be human) inside a netted structure. This structure is designed so that an arthropod, attracted by the animal, can fly into the netted structure but can neither escape nor reach the animal.
John Judkins
https://github.com/obi-ontology/obi/issues/1217
baited net trap
@@ -7954,7 +7954,7 @@
- An arthropod trap consisting of a static physical barrier designed to funnel arthropods in flight into a container.
+ An arthropod trap consisting of a static physical barrier designed to funnel arthropods in flight into a container.
John Judkins
IRO:0000017
https://github.com/obi-ontology/obi/issues/1217
@@ -7973,7 +7973,7 @@
- A device manufactured by BioGents that is designed to count mosquitoes passing through the device, differentiating the mosquitoes from other arthropods.
+ A device manufactured by BioGents that is designed to count mosquitoes passing through the device, differentiating the mosquitoes from other arthropods.
John Judkins
IRO:0000143
https://github.com/obi-ontology/obi/issues/1217
@@ -7992,7 +7992,7 @@
- An arthropod trap that is manufactured by Biogents and is designed to attract arthropods through the use of a motorized fan to mimic convection currents produced by a human. The current also pulls arthropods into the trap, where a layer of gauze prevents the arthropods from escaping along with the air current.
+ An arthropod trap that is manufactured by Biogents and is designed to attract arthropods through the use of a motorized fan to mimic convection currents produced by a human. The current also pulls arthropods into the trap, where a layer of gauze prevents the arthropods from escaping along with the air current.
John Judkins
IRO:0000028
VSMO:0001906
@@ -8006,7 +8006,7 @@
- A light trap that is designed similarly to the New Jersey trap—in that it uses motorized suction and light attractant—and is powered by a six-volt battery.
+ A light trap that is designed similarly to the New Jersey trap—in that it uses motorized suction and light attractant—and is powered by a six-volt battery.
This trap is also designed to be lightweight and operate in environments in which electricity may be scarce.
John Judkins
CDC light trap
@@ -8021,7 +8021,7 @@
- A device that is designed for the collection of arthropod larvae or pupae from water and has the shape of a ladle or a pan.
+ A device that is designed for the collection of arthropod larvae or pupae from water and has the shape of a ladle or a pan.
John Judkins
dipper for immatures
VSMO:0001479
@@ -8035,7 +8035,7 @@
- A light trap that uses carbon dioxide as attractant. The trap consists of a container of dry ice with holes in the bottom to allow the carbon dioxide to flow downward into a separate container, in which a motorized fan creates suction to collect arthropods.
+ A light trap that uses carbon dioxide as attractant. The trap consists of a container of dry ice with holes in the bottom to allow the carbon dioxide to flow downward into a separate container, in which a motorized fan creates suction to collect arthropods.
John Judkins
EVS trap
IRO:0000029
@@ -8050,7 +8050,7 @@
- An arthropod trap that is designed to collect gravid female arthropods or their eggs.
+ An arthropod trap that is designed to collect gravid female arthropods or their eggs.
John Judkins
IRO:0000030
https://github.com/obi-ontology/obi/issues/1217
@@ -8063,7 +8063,7 @@
- An arthropod trap that uses light as an attractant.
+ An arthropod trap that uses light as an attractant.
John Judkins
MIRO:30000065
https://github.com/obi-ontology/obi/issues/1217
@@ -8076,7 +8076,7 @@
- A light trap designed to be placed inside a building.
+ A light trap designed to be placed inside a building.
John Judkins
indoor light trap
MIRO:30000009
@@ -8090,7 +8090,7 @@
- A light trap designed to be placed outside a building.
+ A light trap designed to be placed outside a building.
John Judkins
outdoor light trap
MIRO:30000010
@@ -8104,7 +8104,7 @@
- An arthropod trap that is powered by propane and is designed to emit a combination of carbon dioxide, heat, water, and oct-1-en-3-ol attractants while simultaneously using suction to trap arthropods.
+ An arthropod trap that is powered by propane and is designed to emit a combination of carbon dioxide, heat, water, and oct-1-en-3-ol attractants while simultaneously using suction to trap arthropods.
John Judkins
IRO:0000022
https://github.com/obi-ontology/obi/issues/1217
@@ -8117,7 +8117,7 @@
- A gravid trap consisting of an arthropod attractant and adhesive surface.
+ A gravid trap consisting of an arthropod attractant and adhesive surface.
John Judkins
IRO:0000140
https://github.com/obi-ontology/obi/issues/1217
@@ -8130,7 +8130,7 @@
- A light trap that is designed to use motorized suction to trap arthropods in a collection bag once they approach the light attractant.
+ A light trap that is designed to use motorized suction to trap arthropods in a collection bag once they approach the light attractant.
John Judkins
New Jersey trap
IRO:0000031
@@ -8144,7 +8144,7 @@
- A light trap that is designed to use motorized suction to trap arthropods in a collection bag once they approach the attractant. The light is supplied by an 8 watt tube, and the fan providing the suction has an 11-centimeter diameter.
+ A light trap that is designed to use motorized suction to trap arthropods in a collection bag once they approach the attractant. The light is supplied by an 8 watt tube, and the fan providing the suction has an 11-centimeter diameter.
John Judkins
OVI light-suction trap
IRO:0000154
@@ -8159,7 +8159,7 @@
- An arthropod trap that is positioned adjacent to a window of a building and is designed to collect arthropods flying out of the building.
+ An arthropod trap that is positioned adjacent to a window of a building and is designed to collect arthropods flying out of the building.
John Judkins
outlet window trap
MIRO:30000020
@@ -8173,7 +8173,7 @@
- An arthropod trap that consists of a container holding a mesh layer above water and is designed to trap arthropods hatched from eggs dropped over the water by gravid females.
+ An arthropod trap that consists of a container holding a mesh layer above water and is designed to trap arthropods hatched from eggs dropped over the water by gravid females.
John Judkins
oviposition trap
MIRO:30000016
@@ -8188,7 +8188,7 @@
- An arthropod trap that is designed to be attractive to an arthropod as a place to rest during a period of inactivity.
+ An arthropod trap that is designed to be attractive to an arthropod as a place to rest during a period of inactivity.
John Judkins
https://github.com/obi-ontology/obi/issues/1217
resting arthropod trap
@@ -8200,7 +8200,7 @@
- An arthropod trap that consists of a box that is open on one end. The placement of the box and modifications to it are done in such a way that it becomes attractive to an arthropod as a place to rest during a period of inactivity.
+ An arthropod trap that consists of a box that is open on one end. The placement of the box and modifications to it are done in such a way that it becomes attractive to an arthropod as a place to rest during a period of inactivity.
John Judkins
resting box catch
IRO:0000021
@@ -8214,7 +8214,7 @@
- An arthropod trap that consists of a bucket, which is lined with fabric and placed on its side, and a wet cloth inside the bucket. The placement of the box and modifications to it are done in such a way that it becomes attractive to an arthropod as a place to rest during a period of inactivity (not actively seeking a host).
+ An arthropod trap that consists of a bucket, which is lined with fabric and placed on its side, and a wet cloth inside the bucket. The placement of the box and modifications to it are done in such a way that it becomes attractive to an arthropod as a place to rest during a period of inactivity (not actively seeking a host).
John Judkins
resting bucket catch
IRO:0000141
@@ -8228,7 +8228,7 @@
- An arthropod trap that is made of cloth and netting and is designed to be suspended from above (e.g. from a tree). It is also designed so that the arthropod enters the trap from beneath, being attracted to some bait, and is prevented from escaping upward by the suspended cloth, which allows them to be collected from the upper interior of the trap.
+ An arthropod trap that is made of cloth and netting and is designed to be suspended from above (e.g. from a tree). It is also designed so that the arthropod enters the trap from beneath, being attracted to some bait, and is prevented from escaping upward by the suspended cloth, which allows them to be collected from the upper interior of the trap.
John Judkins
shannon trap catch
IRO:0000191
@@ -8242,7 +8242,7 @@
- An arthropod trap that consists of a bucket, which is lined with adhesive and placed on its side, and a wet cloth inside the bucket. The placement of the box and modifications to it are done in such a way that it becomes attractive to an arthropod as a place to rest during a period of inactivity. The trap is designed for arthropods to become caught in the adhesive so that they can be collected.
+ An arthropod trap that consists of a bucket, which is lined with adhesive and placed on its side, and a wet cloth inside the bucket. The placement of the box and modifications to it are done in such a way that it becomes attractive to an arthropod as a place to rest during a period of inactivity. The trap is designed for arthropods to become caught in the adhesive so that they can be collected.
John Judkins
sticky resting bucket catch
IRO:0000142
@@ -8256,7 +8256,7 @@
- An arthropod trap that is designed to capture arthropods resting on a surface by coating the surface with adhesive.
+ An arthropod trap that is designed to capture arthropods resting on a surface by coating the surface with adhesive.
John Judkins
sticky trap catch
IRO:0000128
@@ -8270,7 +8270,7 @@
- A device that is designed to provide a solid surface that is attractive to an arthropod as a place to rest during a period of inactivity.
+ A device that is designed to provide a solid surface that is attractive to an arthropod as a place to rest during a period of inactivity.
John Judkins
VSMO:0001355
https://github.com/obi-ontology/obi/issues/1302
@@ -8284,7 +8284,7 @@
- A device that is designed for the collection of arthropod larvae or pupae from water and consists of a conical net.
+ A device that is designed for the collection of arthropod larvae or pupae from water and consists of a conical net.
John Judkins
https://github.com/obi-ontology/obi/issues/1302
VEuPathDB
@@ -8297,7 +8297,7 @@
- An arthropod trap that uses as attractant an animal that is not human and is the size of a chicken or smaller.
+ An arthropod trap that uses as attractant an animal that is not human and is the size of a chicken or smaller.
John Judkins
trap containing small non-human animal bait
VSMO:0001595
@@ -8312,7 +8312,7 @@
- An arthropod trap that is designed to trap an arthropod as it emerges from water at the beginning of its adult stage.
+ An arthropod trap that is designed to trap an arthropod as it emerges from water at the beginning of its adult stage.
John Judkins
American Midland Naturalist, Vol. 97, No. 2 (Apr., 1977), pp. 381-389
VSMO:0001352
@@ -8328,7 +8328,7 @@
Jonsson developed a free-standing window trap consisting of a 16 x 20-cm perspex box, 16 cm high and divided in the middle by a 20 x 36-cm sheet of perspex (window). The two compartments of the box are filled to a depth of about 12 cm with 4-6% formalin containing a few drops of detergent; in winter ethylene glycol can be added to prevent freezing. One or two holes drilled in one side of the box at 12 cm and covered with fine netting prevent the trap overflowing after heavy rain. Traps are mounted on aluminium poles. Flying insects on hitting the transparent vertical plastic window fall into the formalin. The window trap may catch vectors that are seeking a host or moving for other purposes. [ISBN:9781402066658]
- An arthropod trap that consists of a transparent window placed in a box that holds a liquid solution deadly to arthropods. This trap is designed to stop an arthropod in flight, causing it to fall into the liquid and die.
+ An arthropod trap that consists of a transparent window placed in a box that holds a liquid solution deadly to arthropods. This trap is designed to stop an arthropod in flight, causing it to fall into the liquid and die.
VEuPathDB
VSMO:0001649
free-standing window trap
@@ -8346,7 +8346,7 @@
- A device manufactured by BioGents that is designed for operation with the BG-Sentinel trap and releases an attractant that mimics the scent of human skin.
+ A device manufactured by BioGents that is designed for operation with the BG-Sentinel trap and releases an attractant that mimics the scent of human skin.
VEuPathDB
BG-lure
IRO:0001060
@@ -8359,7 +8359,7 @@
- A device that consists of a network of mesh and is designed to capture adult arthropods.
+ A device that consists of a network of mesh and is designed to capture adult arthropods.
VEuPathDB
VSMO:0001522
hand-held sweep net
@@ -8372,7 +8372,7 @@
The original trap CDC gravid trap (or gravid trap of Reiter) consists of a 3 inch diameter PVC inlet tube housing a 6 V motor, as used in CDC traps, on which is mounted a four-bladed 3 inch counter-clockwise fan. The inlet tube is clamped between two vertical wooden boards that fit over a black plastic box (18.5 x 14.0 x 6.5 inches). A plastic 12 inch long PVC chimney slots into the upper end of the inlet tube. The top half consists of three struts that fit into and support a netting collecting bag. For this the middle of the collecting bag is reinforced with a circular patch of denim cloth. The oviposition attractant is made by adding 1 lb of hay and 1 oz each of dried brewer's yeast and lactalbumen powder to 30 gallons of tap water. This infusion is allowed to mature for 5 days. This original gravid mosquito trap of Reiter suffers from certain limitations, namely up to 10% of the catch of adults is damaged by passing through the fan blades, and adults tend to die of desiccation. [ISBN:9781402066658]
- A gravid trap that consists of a pan holding a hay infusion, motorized fan, and collection bag. This trap is designed to attract gravid female arthropods to the infused material, which would serve as an oviposition medium, and then draw them into the bag with the current generated by the fan.
+ A gravid trap that consists of a pan holding a hay infusion, motorized fan, and collection bag. This trap is designed to attract gravid female arthropods to the infused material, which would serve as an oviposition medium, and then draw them into the bag with the current generated by the fan.
VEuPathDB
CDC gravid trap
VSMO:0001510
@@ -8393,7 +8393,7 @@
Illumina MiniSeq
Whole genome sequencing of Klebsiella pneumoniae ST11 was performed using an Illumina Miniseq Sequencing System. PMID:31493526
- A small benchtop DNA sequencer which is manufactured by the Illumina corporation with integrated cluster generation, sequencing and data analysis. The sequencer accommodates various flow cell configurations and can produce up to 25M single reads or 50M paired-end reads per run.
+ A small benchtop DNA sequencer which is manufactured by the Illumina corporation with integrated cluster generation, sequencing and data analysis. The sequencer accommodates various flow cell configurations and can produce up to 25M single reads or 50M paired-end reads per run.
PERSON: Bonita Lam
MiniSeq
url:https://www.illumina.com/systems/sequencing-platforms/miniseq.html
@@ -8406,7 +8406,7 @@
- A device that contains blood in a membrane penetrable to mosquitoes, designed to feed mosquitoes without the need for an animal host.
+ A device that contains blood in a membrane penetrable to mosquitoes, designed to feed mosquitoes without the need for an animal host.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1439
@@ -8421,7 +8421,7 @@
assay kit
Glutathione S-Transferase (GST) Assay Kit: https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/product/documents/101/301/cs0410bul.pdf
- A device that consists of reagents and devices that enable the performance of a specific type of assay, which could, in addition, require specific instruments not included in the kit.
+ A device that consists of reagents and devices that enable the performance of a specific type of assay, which could, in addition, require specific instruments not included in the kit.
John Judkins
OBI, VEuPathDB
https://github.com/obi-ontology/obi/issues/1456
@@ -8442,7 +8442,7 @@
Illumina HiSeq 1500
- A DNA sequencer which is manufactured by the Illumina corporation, with a single flow cell. Built upon sequencing by synthesis technology, the machine employs dual surface imaging and offers two high-output options and one rapid-run option.
+ A DNA sequencer which is manufactured by the Illumina corporation, with a single flow cell. Built upon sequencing by synthesis technology, the machine employs dual surface imaging and offers two high-output options and one rapid-run option.
Jain Aluvathingal
Michelle Giglio
Suvarna Nadendla
@@ -8466,7 +8466,7 @@
NextSeq 550
- A DNA sequencer manufactured by the Illumina corporation, which provides the increased flexibility of microarray scanning in addition to sequencing.
+ A DNA sequencer manufactured by the Illumina corporation, which provides the increased flexibility of microarray scanning in addition to sequencing.
Jain Aluvathingal
Michelle Giglio
Suvarna Nadendla
@@ -8489,7 +8489,7 @@
Agilent-026655 Whole Mouse Genome Microarray 4x44K v2
- A DNA microarray manufactured with Agilent 60-mer SurePrint Technology .The SurePrint G3 Mouse Gene Expression 4x44K v2 Microarray provide full coverage of the mouse transcriptome using the latest annotation databases, including long non-coding RNA(lncRNA). Each glass slide is formatted with four high-definition 44K arrays.
+ A DNA microarray manufactured with Agilent 60-mer SurePrint Technology .The SurePrint G3 Mouse Gene Expression 4x44K v2 Microarray provide full coverage of the mouse transcriptome using the latest annotation databases, including long non-coding RNA(lncRNA). Each glass slide is formatted with four high-definition 44K arrays.
Jain Aluvathingal
Michelle Giglio
Suvarna Nadendla
@@ -8512,7 +8512,7 @@
Agilent-030493 SurePrint G3 Mouse Exon 4x180K Microarray
- A DNA microarray manufactured with Agilent 60-mer SurePrint Technology for studying exon-level gene expression changes. The SurePrint G3 Mouse Exon 4x180K Microarray include probes targeting individual exons. Each glass slide formatted with four 180K arrays.
+ A DNA microarray manufactured with Agilent 60-mer SurePrint Technology for studying exon-level gene expression changes. The SurePrint G3 Mouse Exon 4x180K Microarray include probes targeting individual exons. Each glass slide formatted with four 180K arrays.
Jain Aluvathingal
Michelle Giglio
Suvarna Nadendla
@@ -8535,7 +8535,7 @@
Agilent-074809 SurePrint G3 Mouse GE v2 8x60K Microarray
- A DNA microarray manufactured with Agilent 60-mer SurePrint technology which provides comprehensive coverage of genes and transcripts using the latest annotation databases. The SurePrint G3 Mouse Gene Expression 8x60K v2 Microarray features complete coverage of established RefSeq coding transcripts (NM) from the latest build and updated long non-coding RNA (lncRNA) content to ensure relevant research.Each glass slide formatted with eight high-definition 60K arrays.
+ A DNA microarray manufactured with Agilent 60-mer SurePrint technology which provides comprehensive coverage of genes and transcripts using the latest annotation databases. The SurePrint G3 Mouse Gene Expression 8x60K v2 Microarray features complete coverage of established RefSeq coding transcripts (NM) from the latest build and updated long non-coding RNA (lncRNA) content to ensure relevant research.Each glass slide formatted with eight high-definition 60K arrays.
Jain Aluvathingal
Michelle Giglio
Suvarna Nadendla
@@ -8558,7 +8558,7 @@
Affymetrix Mouse Genome 430 2.0 Array
- A DNA microarray manufactured by Affymetrix, which includes complete coverage of the GeneChip Mouse Expression Set 430, for analysis of over 39,000 transcripts and variants from more than 34,000 well-characterized mouse genes and UniGene clusters, on a single array. The sequences for this array were selected from GenBank™, dbEST, and RefSeq., and sequence clusters cretaed from the UniGene database.
+ A DNA microarray manufactured by Affymetrix, which includes complete coverage of the GeneChip Mouse Expression Set 430, for analysis of over 39,000 transcripts and variants from more than 34,000 well-characterized mouse genes and UniGene clusters, on a single array. The sequences for this array were selected from GenBank™, dbEST, and RefSeq., and sequence clusters cretaed from the UniGene database.
Jain Aluvathingal
Michelle Giglio
Suvarna Nadendla
@@ -8582,7 +8582,7 @@
Affymetrix Mouse Genome 430A 2.0 Array
- A DNA microarray manufactured by Affymetrix for gene expression analysis focusing on approximately 14,000 well-characterized genes in the transcribed mouse genome using single-array cartridge. Sequences used in the design of the array were selected from GenBank™, dbEST, and RefSeq. The sequence clusters were created from the UniGene database.
+ A DNA microarray manufactured by Affymetrix for gene expression analysis focusing on approximately 14,000 well-characterized genes in the transcribed mouse genome using single-array cartridge. Sequences used in the design of the array were selected from GenBank™, dbEST, and RefSeq. The sequence clusters were created from the UniGene database.
Jain Aluvathingal
Michelle Giglio
Suvarna Nadendla
@@ -8606,7 +8606,7 @@
Affymetrix Mouse Gene 1.0 ST Array
- A DNA microarray manufactured by Affymetrix, which is a whole-transcript array that includes probes to measure both messenger (mRNA) and long intergenic non-coding RNA transcripts (lincRNA). This whole-transcript array design provides a complete expression profile of mRNA as well as the intermediary lincRNA transcripts that impact the mRNA expression profile.
+ A DNA microarray manufactured by Affymetrix, which is a whole-transcript array that includes probes to measure both messenger (mRNA) and long intergenic non-coding RNA transcripts (lincRNA). This whole-transcript array design provides a complete expression profile of mRNA as well as the intermediary lincRNA transcripts that impact the mRNA expression profile.
Jain Aluvathingal
Michelle Giglio
Suvarna Nadendla
@@ -8630,7 +8630,7 @@
Affymetrix Mouse Gene 2.1 ST Array
- A DNA microarray manufactured by Affymetrix, which is a whole-transcript array that includes probes to measure both messenger (mRNA) and long intergenic non-coding RNA transcripts (lincRNA).To supplement the lincRNA data contained in RefSeq, we used sequence and transcript data from lncRNA db.
+ A DNA microarray manufactured by Affymetrix, which is a whole-transcript array that includes probes to measure both messenger (mRNA) and long intergenic non-coding RNA transcripts (lincRNA).To supplement the lincRNA data contained in RefSeq, we used sequence and transcript data from lncRNA db.
Jain Aluvathingal
Michelle Giglio
Suvarna Nadendla
@@ -8654,7 +8654,7 @@
Affymetrix Rhesus Macaque Genome Array
- A DNA microarray manufactured by Affymetrix,which is a single-labeled high-density oligonucleotide array, designed to study gene expression in the rhesus animal model and to interrogate rhesus transcripts orthologous to the 3' end of human transcripts. The array consists of over 52,000 probe sets representing more than 20,000 genes, and several relevant viral organisms for studying host-disease immune response.
+ A DNA microarray manufactured by Affymetrix,which is a single-labeled high-density oligonucleotide array, designed to study gene expression in the rhesus animal model and to interrogate rhesus transcripts orthologous to the 3' end of human transcripts. The array consists of over 52,000 probe sets representing more than 20,000 genes, and several relevant viral organisms for studying host-disease immune response.
Jain Aluvathingal
Michelle Giglio
Suvarna Nadendla
@@ -8678,7 +8678,7 @@
Affymetrix Human Transcriptome Array 2.0
- A DNA microarray manufactured by Affymetrix, to go beyond gene-level expression profiling to accurately detect all known transcript isoforms produced by a gene. The array design covers >245,000 coding transcripts, >40,000 non-coding transcripts and >339,000 probe sets covering exon-exon junctions, thus ensuring uniform coverage of the transcriptome.
+ A DNA microarray manufactured by Affymetrix, to go beyond gene-level expression profiling to accurately detect all known transcript isoforms produced by a gene. The array design covers >245,000 coding transcripts, >40,000 non-coding transcripts and >339,000 probe sets covering exon-exon junctions, thus ensuring uniform coverage of the transcriptome.
Jain Aluvathingal
Michelle Giglio
Suvarna Nadendla
@@ -8702,7 +8702,7 @@
Affymetrix Human Genome U219 Array
- A DNA microarray manufactured by Affymetrix, which comprises more than 530,000 probes covering more than 36,000 transcripts and variants, which represent more than 20,000 genes mapped through RefSeq or via UniGene annotation. Sequences used in the design of the array were selected from the RefSeq version 36, UniGene database 219, and full-length human mRNAs from GenBank™.
+ A DNA microarray manufactured by Affymetrix, which comprises more than 530,000 probes covering more than 36,000 transcripts and variants, which represent more than 20,000 genes mapped through RefSeq or via UniGene annotation. Sequences used in the design of the array were selected from the RefSeq version 36, UniGene database 219, and full-length human mRNAs from GenBank™.
Jain Aluvathingal
Michelle Giglio
Suvarna Nadendla
@@ -8726,7 +8726,7 @@
Affymetrix Human Gene 2.0 ST Array
- A DNA microarray manufactured by Affymetrix, which provides the most accurate, sensitive, and comprehensive measurement of protein coding (mRNA) and long intergenic non-coding RNA (lincRNA) transcripts. The array design covers >33,500 coding transcripts and >11,000 lincRNA transcripts thus enabling researchers to understand whole-transcriptome gene expression at the gene and exon levels, which allows the study of transcript variants and alternative splicing events.
+ A DNA microarray manufactured by Affymetrix, which provides the most accurate, sensitive, and comprehensive measurement of protein coding (mRNA) and long intergenic non-coding RNA (lincRNA) transcripts. The array design covers >33,500 coding transcripts and >11,000 lincRNA transcripts thus enabling researchers to understand whole-transcriptome gene expression at the gene and exon levels, which allows the study of transcript variants and alternative splicing events.
Jain Aluvathingal
Michelle Giglio
Suvarna Nadendla
@@ -8750,7 +8750,7 @@
Affymetrix Clariom S Assay, Human
- A DNA microarray manufactured by Affymetrix, to obtain a gene-level view of the human transcriptome. The assay design covers >20,000 well-annotated genes, providing researchers with the ability to perform gene-level expression profiling studies, to identify expression biomarkers , and to quickly assess changes in key genes and pathways.
+ A DNA microarray manufactured by Affymetrix, to obtain a gene-level view of the human transcriptome. The assay design covers >20,000 well-annotated genes, providing researchers with the ability to perform gene-level expression profiling studies, to identify expression biomarkers , and to quickly assess changes in key genes and pathways.
Jain Aluvathingal
Michelle Giglio
Suvarna Nadendla
@@ -8773,7 +8773,7 @@
Affymetrix Clariom S Assay, Mouse
- A DNA microarray manufactured by Affymetrix, to obtain a gene-level view of the mouse transcriptome. The assay design covers >20,000 well-annotated genes, providing researchers with the ability to perform gene-level expression profiling studies, to identify expression biomarkers, and to quickly assess changes in key genes and pathways.
+ A DNA microarray manufactured by Affymetrix, to obtain a gene-level view of the mouse transcriptome. The assay design covers >20,000 well-annotated genes, providing researchers with the ability to perform gene-level expression profiling studies, to identify expression biomarkers, and to quickly assess changes in key genes and pathways.
Jain Aluvathingal
Michelle Giglio
Suvarna Nadendla
@@ -8796,7 +8796,7 @@
Illumina HumanHT-12 V4.0 expression beadchip
- An Illumina BeadChip which employs direct-hybridization assay, for whole-genome expression profiling and expression-based quantitative trait loci (eQTL) studies. This BeadChip contains 12 arrays, each featuring more than 48,000 probes, targeting more than 31,000 annotated genes, providing genome-wide coverage of well-characterized genes, gene candidates, and splice variants.
+ An Illumina BeadChip which employs direct-hybridization assay, for whole-genome expression profiling and expression-based quantitative trait loci (eQTL) studies. This BeadChip contains 12 arrays, each featuring more than 48,000 probes, targeting more than 31,000 annotated genes, providing genome-wide coverage of well-characterized genes, gene candidates, and splice variants.
Jain Aluvathingal
Michelle Giglio
Suvarna Nadendla
@@ -8819,7 +8819,7 @@
Illumina MouseRef-8 v2.0 beadchip
- An Illumina BeadChip which employs direct-hybridization assay, for whole-genome expression profiling in the mouse.This Beadchip contains 8 microarrays, featuring more than 25,000 probes per array, derived from the NCBI RefSeq database and supplemented with MEEBO and RIKEN FANTOM2 content.
+ An Illumina BeadChip which employs direct-hybridization assay, for whole-genome expression profiling in the mouse.This Beadchip contains 8 microarrays, featuring more than 25,000 probes per array, derived from the NCBI RefSeq database and supplemented with MEEBO and RIKEN FANTOM2 content.
Jain Aluvathingal
Michelle Giglio
Suvarna Nadendla
@@ -8842,7 +8842,7 @@
Affymetrix Mouse Exon Junction Array
- A DNA microarray manufactured by Affymetrix, used to identify exon-exon junctions associated with alternate splice variants in the mouse transcriptome.
+ A DNA microarray manufactured by Affymetrix, used to identify exon-exon junctions associated with alternate splice variants in the mouse transcriptome.
Jain Aluvathingal
Michelle Giglio
Suvarna Nadendla
@@ -8865,7 +8865,7 @@
Affymetrix Human Exon Junction Array
- A DNA microarray manufactured by Affymetrix, used to identify exon-exon junctions associated with alternate splice variants in the human transcriptome.
+ A DNA microarray manufactured by Affymetrix, used to identify exon-exon junctions associated with alternate splice variants in the human transcriptome.
Jain Aluvathingal
Michelle Giglio
Suvarna Nadendla
@@ -8881,7 +8881,7 @@
- An arthropod trap that is designed to emit a combination of carbon dioxide, heat, water, and oct-1-en-3-ol attractants while simultaneously using suction to trap arthropods. This trap has the same design as the Mosquito Magnet Pro trap but is smaller, is more lightweight, and uses a main line electricity supply instead of propane to power itself. Both use propane to produce the arthropod attractor.
+ An arthropod trap that is designed to emit a combination of carbon dioxide, heat, water, and oct-1-en-3-ol attractants while simultaneously using suction to trap arthropods. This trap has the same design as the Mosquito Magnet Pro trap but is smaller, is more lightweight, and uses a main line electricity supply instead of propane to power itself. Both use propane to produce the arthropod attractor.
VEuPathDB
https://github.com/obi-ontology/obi/issues/1523
Mosquito Magnet Liberty Plus trap
@@ -8899,7 +8899,7 @@
- A resting arthropod trap that consists of a tent inside which an adult cow is tethered to the ground, in order to attract arthropods and collect those that rest on the interior walls of the tent.
+ A resting arthropod trap that consists of a tent inside which an adult cow is tethered to the ground, in order to attract arthropods and collect those that rest on the interior walls of the tent.
John Judkins ORCID:0000-0001-6595-0902
Sarah Kelly
https://github.com/obi-ontology/obi/issues/1602
@@ -8924,7 +8924,7 @@
- An assay kit that is manufactured by InBios International to use ELISA to test for IgM antibodies for Orientia tsutsugamushi strains Karp, Kato, Gilliam, and TA 716, with a protein microarray that has a 96-well plate and the 56-kDa type-specific antigen.
+ An assay kit that is manufactured by InBios International to use ELISA to test for IgM antibodies for Orientia tsutsugamushi strains Karp, Kato, Gilliam, and TA 716, with a protein microarray that has a 96-well plate and the 56-kDa type-specific antigen.
John Judkins ORCID:0000-0001-6595-0902
https://inbios.com/scrub-typhus-detecttm-igm-elisa-kit-intl/
Scrub Typhus Detect IgM ELISA kit
@@ -8948,7 +8948,7 @@
- An assay kit that is manufactured by Abbott to test for IgM antibodies for Dengue with a two-plate protein microarray. One plate contains stabilized Dengue viruses 1 through 4, and the other plate contains anti-human IgM antibody.
+ An assay kit that is manufactured by Abbott to test for IgM antibodies for Dengue with a two-plate protein microarray. One plate contains stabilized Dengue viruses 1 through 4, and the other plate contains anti-human IgM antibody.
John Judkins ORCID:0000-0001-6595-0902
Panbio Dengue IgM capture ELISA kit
@@ -8971,7 +8971,7 @@
- An assay kit that is manufactured by Abbott to detect the NS1 Dengue viral protein with a protein microarray and an anti-NS1 monoclonal antibody.
+ An assay kit that is manufactured by Abbott to detect the NS1 Dengue viral protein with a protein microarray and an anti-NS1 monoclonal antibody.
John Judkins ORCID:0000-0001-6595-0902
Panbio Dengue Early ELISA kit
@@ -8994,7 +8994,7 @@
- A device manufactured by Abbott for rapid detection of human IgM antibodies for Chikungunya virus in blood, using analytical chromatography.
+ A device manufactured by Abbott for rapid detection of human IgM antibodies for Chikungunya virus in blood, using analytical chromatography.
John Judkins ORCID:0000-0001-6595-0902
https://www.indiamart.com/proddetail/abbott-sd-bioline-chikungunya-igm-test-kit-12908515588.html
SD Bioline Chikungunya IgM RDT kit
@@ -9018,7 +9018,7 @@
- An assay kit that is manufactured by Abbott to detect human IgM antibodies for Chikungunya with a protein microarray and ELISA.
+ An assay kit that is manufactured by Abbott to detect human IgM antibodies for Chikungunya with a protein microarray and ELISA.
John Judkins ORCID:0000-0001-6595-0902
SD Bioline Chikungunya IgM capture ELISA kit
@@ -9041,7 +9041,7 @@
- An assay kit that is manufactured by J. Mitra to detect human IgM antibodies for Chikungunya virus with a protein microarray and double-antigen sandwich ELISA.
+ An assay kit that is manufactured by J. Mitra to detect human IgM antibodies for Chikungunya virus with a protein microarray and double-antigen sandwich ELISA.
John Judkins ORCID:0000-0001-6595-0902
Advantage Chikungunya IgM Card kit
@@ -9088,7 +9088,7 @@
- A CDC light trap that uses odorous gas from a human being as an attractant, by pumping it from the room where the human being sleeps into the trap.
+ A CDC light trap that uses odorous gas from a human being as an attractant, by pumping it from the room where the human being sleeps into the trap.
John Judkins ORCID:0000-0001-6595-0902
human odour baited light trap
VEuPathDB
@@ -9102,7 +9102,7 @@
- A resting arthropod trap that consists of a container composed primarily of clay.
+ A resting arthropod trap that consists of a container composed primarily of clay.
John Judkins ORCID:0000-0001-6595-0902
resting clay pot catch
https://github.com/obi-ontology/obi/issues/1651
@@ -9121,7 +9121,7 @@
- A DNA sequencer which is manufactured by the Illumina corporation using sequence-by-synthesis chemistry that fits on a benchtop and uses P1 and P2 flow cells.
+ A DNA sequencer which is manufactured by the Illumina corporation using sequence-by-synthesis chemistry that fits on a benchtop and uses P1 and P2 flow cells.
Sebastian Duesing
NextSeq 1000
https://www.illumina.com/systems/sequencing-platforms/nextseq-1000-2000.html
@@ -9137,7 +9137,7 @@
Illumina Infinium MethylationEPIC v2.0 BeadChip
- An Illumina methylation BeadChip that targets 935,000 methylation sites per sample at single-nucleotide resolution.
+ An Illumina methylation BeadChip that targets 935,000 methylation sites per sample at single-nucleotide resolution.
Sebastian Duesing
https://www.illumina.com/products/by-type/microarray-kits/infinium-methylation-epic.html
https://github.com/obi-ontology/obi/issues/1665
@@ -9158,7 +9158,7 @@
A10-Analyzer
- A A10 is a flow_cytometer_analyser manufactured by Apogee. It uses an arc lamp as a light source, with choices of 75W Xe, 75W Xe/Hg or 100W Hg arc lamps. It has filters and collectors for up to three fluorescent parameters and two scatter parameters. It uses analog electronics. The A10 can be used for measuring the properties of individual cells.
+ A A10 is a flow_cytometer_analyser manufactured by Apogee. It uses an arc lamp as a light source, with choices of 75W Xe, 75W Xe/Hg or 100W Hg arc lamps. It has filters and collectors for up to three fluorescent parameters and two scatter parameters. It uses analog electronics. The A10 can be used for measuring the properties of individual cells.
John Quinn
http://www.apogeeflow.com/flow_cytometry_products.htm
A10-Analyzer
@@ -9172,7 +9172,7 @@
A40-MiniFCM
- A A40-MiniFCM is a flow_cytometer_analyser that allows for the choice of one of four lasers (375nm, 405nm,488nm, 532nm, 635nm), and PMTs and filters for collecting up to four parameters. It uses digital electronics. A military version of this cytometer is available as well. The A40-MiniFCM is geared towards the most demanding applications such as archaea, bacteria and large virus.
+ A A40-MiniFCM is a flow_cytometer_analyser that allows for the choice of one of four lasers (375nm, 405nm,488nm, 532nm, 635nm), and PMTs and filters for collecting up to four parameters. It uses digital electronics. A military version of this cytometer is available as well. The A40-MiniFCM is geared towards the most demanding applications such as archaea, bacteria and large virus.
John Quinn
http://www.apogeeflow.com/flow_cytometry_products.htm
A40-MiniFCM
@@ -9193,7 +9193,7 @@
analog-to-digital converter
The analog to digital converter transformed the analog output from the photomultiplier tube to a digital signal for collection.
- An analog-to-digital_converter is an instrument that converts an infinite resolution analog signal to a finite resolution digital signal.
+ An analog-to-digital_converter is an instrument that converts an infinite resolution analog signal to a finite resolution digital signal.
John Quinn
Melanie Courtot
A-D
@@ -9241,7 +9241,7 @@
flow cytometer analyzer
FACS Calibur, Luminex 100
- An analyser is a flow_cytometer that is used to measure properties of particles (whole cells, nuclei, chromosomes, diatoms, plankton, bacteria, viruses) by moving these particles through a detection chamber. An analyser is used to collect data for analysis.
+ An analyser is a flow_cytometer that is used to measure properties of particles (whole cells, nuclei, chromosomes, diatoms, plankton, bacteria, viruses) by moving these particles through a detection chamber. An analyser is used to collect data for analysis.
John Quinn
http://www.flocyte.com/FRTP/Resources/flow_cytometry_glossary.htm
flow cytometer analyzer
@@ -9256,7 +9256,7 @@
arc lamp
The Jablochkoff Candle
- Arc lamp is a light source that produces light by an electric arc (or voltaic arc). The lamp consists of two electrodes typically made of tungsten which are separated by a gas. The type of lamp is often named by the gas contained in the bulb; including neon, argon, xenon, krypton, sodium, metal halide, and mercury. The electric arc in an arc lamp consists of gas which is initially ionized by a voltage and is therefore electrically conductive. To start an arc lamp, usually a very high voltage is needed to ignite or strike the arc. This requires an electrical circuit sometimes called an igniter, which is part of a larger circuit called the ballast. The ballast supplies a suitable voltage and current to the lamp as its electrical characteristics change with temperature and time. Older cytometers may use arc lamps to irradiate particles at the interrogation point.
+ Arc lamp is a light source that produces light by an electric arc (or voltaic arc). The lamp consists of two electrodes typically made of tungsten which are separated by a gas. The type of lamp is often named by the gas contained in the bulb; including neon, argon, xenon, krypton, sodium, metal halide, and mercury. The electric arc in an arc lamp consists of gas which is initially ionized by a voltage and is therefore electrically conductive. To start an arc lamp, usually a very high voltage is needed to ignite or strike the arc. This requires an electrical circuit sometimes called an igniter, which is part of a larger circuit called the ballast. The ballast supplies a suitable voltage and current to the lamp as its electrical characteristics change with temperature and time. Older cytometers may use arc lamps to irradiate particles at the interrogation point.
John Quinn
http://en.wikipedia.org/wiki/Arc_lamp
arc lamp
@@ -9271,7 +9271,7 @@
argon ion laser
argon ion laser in a cytometer
- An argon-ion laser is an ion laser that uses argon ions as the lasing medium. These lasers are used primarily to emit light at wave lengths of 458 nm, 488 nm or 514.5 nm, though it is possible to use them to emit several wavelengths of blue and green light. Argon-ion lasers can emit light at many different wave lenghts, and excite a number of different flourochromes.
+ An argon-ion laser is an ion laser that uses argon ions as the lasing medium. These lasers are used primarily to emit light at wave lengths of 458 nm, 488 nm or 514.5 nm, though it is possible to use them to emit several wavelengths of blue and green light. Argon-ion lasers can emit light at many different wave lenghts, and excite a number of different flourochromes.
Daniel Schober
John Quinn
http://en.wikipedia.org/wiki/Laser#Gas_lasers
@@ -9287,7 +9287,7 @@
avalanche photodiode
C30644E - InGaAs Avalanche Photodiode
- An avalanche photodiode is typically used to collect photons emitted by forward scatter because it is far less sensitive, and less likely o be burned out, than a PMT. A photodiode with high quantum efficiency and a mechanism for producing gains as high as a few thousand.
+ An avalanche photodiode is typically used to collect photons emitted by forward scatter because it is far less sensitive, and less likely o be burned out, than a PMT. A photodiode with high quantum efficiency and a mechanism for producing gains as high as a few thousand.
John Quinn
Practical Flow Cytometry 4th Edition, Howard Shapiro, ISBN-10: 0471411256, ISBN-13: 978-0471411253
avalanche photodiode
@@ -9301,7 +9301,7 @@
Bactiflow
- A Bactiflow is a flow_cytometer_analyser manufactured by Chemunex SA. It is a cell counter for bacteria and other micro organisms. Bacteria are stained with a fluorochrome and the number of particles that fluoresce are counted. The system uses digital electronics, a single laser and a single detector. An ALS version is available as well - Automatic Labeling System. The Bactiflow is specialized cytometer used exclusively for counting microbes.
+ A Bactiflow is a flow_cytometer_analyser manufactured by Chemunex SA. It is a cell counter for bacteria and other micro organisms. Bacteria are stained with a fluorochrome and the number of particles that fluoresce are counted. The system uses digital electronics, a single laser and a single detector. An ALS version is available as well - Automatic Labeling System. The Bactiflow is specialized cytometer used exclusively for counting microbes.
John Quinn
http://www.chemunex.com/products/chemframe.htm
Bactiflow
@@ -9316,7 +9316,7 @@
band pass filter
530/30 BP filter, 585/42 BP filter
- A band pass filter is an optical filter that passes wavelengths of light within a certain range and rejects (attenuates) frequencies outside that range. The passed wavelengths are indicated in the specifications of the filter and its name. A 480/20 band-pass filter pass light with at wavelengths of 460 to 500 nm and attenuates all others.
+ A band pass filter is an optical filter that passes wavelengths of light within a certain range and rejects (attenuates) frequencies outside that range. The passed wavelengths are indicated in the specifications of the filter and its name. A 480/20 band-pass filter pass light with at wavelengths of 460 to 500 nm and attenuates all others.
Person:John Quinn
http://en.wikipedia.org/wiki/Band_pass_filter
band pass filter
@@ -9331,7 +9331,7 @@
BioSorter1000
BioSorter 1000 at TSRI Flow Cytometry Core Facility
- A BioSorter1000 is a flow_cytometer_sorter manufactured by Union Biometrica. It includes analog electronics, 488/514 nm multi-line Argon-ion laser for fluorescence and a light stabilized 670 nm forward scatter laser for extinction and time-of-flight. It has filters and PMTs for 3 fluorescent parameters and photodiodes for scatter, time of flight, and extinction. The flow cell is quartz cuvette. The BioSorterTM 1000 is an instrument for analyzing and sorting objects from 200-600 microns in diameter.
+ A BioSorter1000 is a flow_cytometer_sorter manufactured by Union Biometrica. It includes analog electronics, 488/514 nm multi-line Argon-ion laser for fluorescence and a light stabilized 670 nm forward scatter laser for extinction and time-of-flight. It has filters and PMTs for 3 fluorescent parameters and photodiodes for scatter, time of flight, and extinction. The flow cell is quartz cuvette. The BioSorterTM 1000 is an instrument for analyzing and sorting objects from 200-600 microns in diameter.
John Quinn
http://www.unionbio.com/products/BioSorter.html
BioSorter1000
@@ -9346,7 +9346,7 @@
BioSorter2000
BioSorter 2000 at TSRI Flow Cytometry Core Facility
- A BioSorter2000 is a sorter manufactured by Union Biometrica. It includes analog electronics, 488/514 nm multi-line Argon-ion laser for fluorescence and a light stabilized 670 nm forward scatter laser for extinction and time-of-flight. It has filters and PMTs for 3 fluorescent parameters and photodiodes for scatter, time of flight, and extinction. The flow cell is quartz cuvette. The BioSorterTM 2000 is an instrument for analyzing and sorting objects from 500 microns to 1.5 millimeters in diameter.
+ A BioSorter2000 is a sorter manufactured by Union Biometrica. It includes analog electronics, 488/514 nm multi-line Argon-ion laser for fluorescence and a light stabilized 670 nm forward scatter laser for extinction and time-of-flight. It has filters and PMTs for 3 fluorescent parameters and photodiodes for scatter, time of flight, and extinction. The flow cell is quartz cuvette. The BioSorterTM 2000 is an instrument for analyzing and sorting objects from 500 microns to 1.5 millimeters in diameter.
John Quinn
http://www.unionbio.com/products/BioSorter.html
BioSorter2000
@@ -9361,7 +9361,7 @@
BioSorter250
BioSorter 250 at TSRI Flow Cytometry Core Facility
- A BioSorter250 is a flow_cytometer_sorter manufactured by Union Biometrica. It includes analog electronics, 488/514 nm multi-line Argon-ion laser for fluorescence and a light stabilized 670 nm forward scatter laser for extinction and time-of-flight. It has filters and PMTs for 3 fluorescent parameters and photodiodes for scatter, time of flight, and extinction. The flow cell is quartz cuvette. The BioSorterTM 250 is an instrument for analyzing and sorting objects from 40-200 microns in diameter.
+ A BioSorter250 is a flow_cytometer_sorter manufactured by Union Biometrica. It includes analog electronics, 488/514 nm multi-line Argon-ion laser for fluorescence and a light stabilized 670 nm forward scatter laser for extinction and time-of-flight. It has filters and PMTs for 3 fluorescent parameters and photodiodes for scatter, time of flight, and extinction. The flow cell is quartz cuvette. The BioSorterTM 250 is an instrument for analyzing and sorting objects from 40-200 microns in diameter.
John Quinn
http://www.unionbio.com/products/BioSorter.html
BioSorter250
@@ -9376,7 +9376,7 @@
BioSorter500
BioSorter 500 at TSRI Flow Cytometry Core Facility
- A BioSorter500 is a flow_cytometer_sorter manufactured by Union Biometrica. It includes analog electronics, 488/514 nm multi-line Argon-ion laser for fluorescence and a light stabilized 670 nm forward scatter laser for extinction and time-of-flight. It has filters and PMTs for 3 fluorescent parameters and photodiodes for scatter, time of flight, and extinction. The flow cell is quartz cuvette. The BioSorterTM 500 is an instrument for analyzing and sorting objects from 100-250 microns in diameter and less than 2mm in length.
+ A BioSorter500 is a flow_cytometer_sorter manufactured by Union Biometrica. It includes analog electronics, 488/514 nm multi-line Argon-ion laser for fluorescence and a light stabilized 670 nm forward scatter laser for extinction and time-of-flight. It has filters and PMTs for 3 fluorescent parameters and photodiodes for scatter, time of flight, and extinction. The flow cell is quartz cuvette. The BioSorterTM 500 is an instrument for analyzing and sorting objects from 100-250 microns in diameter and less than 2mm in length.
John Quinn
http://www.unionbio.com/products/BioSorter.html
BioSorter500
@@ -9390,7 +9390,7 @@
Cell Lab Quanta SC
- A Cell Lab Quanta SC is a flow_cytometer_analyser manufactured by Becman Coulter. It features a mercury arc lamp optimized at 366, 405, and 435 nm, and a 488 nm laser diode. It has filters and PMTs to collect up to 3 fluorescent parameters, and a photodiode for side scatter detection. This cytometer uses Couter-Volume for cell size measurements. The Cell Lab Quanta SC can be used for measuring the properties of individual cells.
+ A Cell Lab Quanta SC is a flow_cytometer_analyser manufactured by Becman Coulter. It features a mercury arc lamp optimized at 366, 405, and 435 nm, and a 488 nm laser diode. It has filters and PMTs to collect up to 3 fluorescent parameters, and a photodiode for side scatter detection. This cytometer uses Couter-Volume for cell size measurements. The Cell Lab Quanta SC can be used for measuring the properties of individual cells.
John Quinn
http://www.beckmancoulter.com/cell-lab
Cell Lab Quanta SC
@@ -9417,7 +9417,7 @@
charge plate
LSR2 charge plate
- Part of the fluidics subsystem. Charge plates are used or sorters. They create an charged electric field when particles deemed to be desired for further analysis are shaken form the piexo electric crystal. The charged particles are drawn toward the charged plate, and the altered drop location causes the particles to fall into a collection tube. Charge plates enable sorting.
+ Part of the fluidics subsystem. Charge plates are used or sorters. They create an charged electric field when particles deemed to be desired for further analysis are shaken form the piexo electric crystal. The charged particles are drawn toward the charged plate, and the altered drop location causes the particles to fall into a collection tube. Charge plates enable sorting.
John Quinn
Practical Flow Cytometry 4th Edition, Howard Shapiro, ISBN-10: 0471411256, ISBN-13: 978-0471411253
charge plate
@@ -9432,7 +9432,7 @@
cell sorter collection tube
LSR2 collection tube
- Part of the fluidics subsystem. The collection tube is a vessel for capturing cells of interest that have been identified by a sorter. The collection tube is the end location of sorted cells.
+ Part of the fluidics subsystem. The collection tube is a vessel for capturing cells of interest that have been identified by a sorter. The collection tube is the end location of sorted cells.
John Quinn
Practical Flow Cytometry 4th Edition, Howard Shapiro, ISBN-10: 0471411256, ISBN-13: 978-0471411253
cell sorter collection tube
@@ -9446,7 +9446,7 @@
Cyan
- A Cyan is a flow_cytometer_analyser manufactured by Dako Cytomation. It features include digital electronics, three lasers: 488 nm, 635 nm, and 405 nm, and filters and collectors for nine fluorescent parameters and two scatter parameters. The Cyan can be used for measuring the properties of individual cells.
+ A Cyan is a flow_cytometer_analyser manufactured by Dako Cytomation. It features include digital electronics, three lasers: 488 nm, 635 nm, and 405 nm, and filters and collectors for nine fluorescent parameters and two scatter parameters. The Cyan can be used for measuring the properties of individual cells.
John Quinn
http://www.dakousa.com/prod_productrelatedinformation?url=gprod_cyan_index.htm
Cyan
@@ -9460,7 +9460,7 @@
CYFlow ML
- A CyFlow_ML is a flow_cytometer_analyser manufactured by Partec. It is a digital machine which uses 4 light sources: triple laser configurations including new powerful 200mW@488nm blue solid state laser + 100W UV lamp for highest resolution DNA analysis, and can collect 16 optical parameters: FSC1, FSC2, SSC, FL1-FL13. Ultracompact high end desktop multilaser Flow Cytometer for all applications in cell analysis and absolute counting.
+ A CyFlow_ML is a flow_cytometer_analyser manufactured by Partec. It is a digital machine which uses 4 light sources: triple laser configurations including new powerful 200mW@488nm blue solid state laser + 100W UV lamp for highest resolution DNA analysis, and can collect 16 optical parameters: FSC1, FSC2, SSC, FL1-FL13. Ultracompact high end desktop multilaser Flow Cytometer for all applications in cell analysis and absolute counting.
John Quinn
http://www.partec.de/products/cyflow-ml.html
CYFlow ML
@@ -9474,7 +9474,7 @@
CyFlow SL
- a flow_cytometer_analyser manufactured by Partec. Its specs are: ultracompact and fully equipped mobile/portable instrument, dimensions [cm]: L 43 x H 16 x D 37, highest stability/robustness and highest precision, 5 optical parameters: FSC, SSC, FL-1, FL-2, FL-3, 20mW@488nm blue solid state laser , other laser light sources optional (UV, violet, green, red), WindowsTM XP FloMax (software for real time data acquisition, data display, and data evaluation), parallel 16 bit digital pulse processing Compact mobile Flow Cytometer for any kind of cell analysis and absolute volumetric counting. The CyFlow_SL allows to analyze forward and side scatter signals in combination with up to 3 fluorescence channels.
+ a flow_cytometer_analyser manufactured by Partec. Its specs are: ultracompact and fully equipped mobile/portable instrument, dimensions [cm]: L 43 x H 16 x D 37, highest stability/robustness and highest precision, 5 optical parameters: FSC, SSC, FL-1, FL-2, FL-3, 20mW@488nm blue solid state laser , other laser light sources optional (UV, violet, green, red), WindowsTM XP FloMax (software for real time data acquisition, data display, and data evaluation), parallel 16 bit digital pulse processing Compact mobile Flow Cytometer for any kind of cell analysis and absolute volumetric counting. The CyFlow_SL allows to analyze forward and side scatter signals in combination with up to 3 fluorescence channels.
John Quinn
http://www.partec.de/products/cyflow.html
CyFlow SL
@@ -9488,7 +9488,7 @@
CyFlow SL3
- A CyFlow_Sl3 is a flow_cytometer_analyser manufactured by Partec. Its specs are: ultracompact and fully equipped mobile/portable instrument, dimensions [cm]: L 43 x H 16 x D 37 , highest stability/robustness and highest precision, 5 optical parameters: FSC, SSC, FL-1, FL-2, FL-3, 20mW@488nm blue solid state laser, other laser light sources optional (UV, violet, green, red), WindowsTM XP FloMax (software for real time data acquisition, data display, and data evaluation), parallel 16 bit digital pulse processing. The CyFlow SL3 is a compact and dedicated portable Flow Cytometer for accurate and affordable cell analysis and true volumetric absolute counting in HIV Monitoring and AIDS patient follow-up by precise and direct CD4 and CD4% measurement.
+ A CyFlow_Sl3 is a flow_cytometer_analyser manufactured by Partec. Its specs are: ultracompact and fully equipped mobile/portable instrument, dimensions [cm]: L 43 x H 16 x D 37 , highest stability/robustness and highest precision, 5 optical parameters: FSC, SSC, FL-1, FL-2, FL-3, 20mW@488nm blue solid state laser, other laser light sources optional (UV, violet, green, red), WindowsTM XP FloMax (software for real time data acquisition, data display, and data evaluation), parallel 16 bit digital pulse processing. The CyFlow SL3 is a compact and dedicated portable Flow Cytometer for accurate and affordable cell analysis and true volumetric absolute counting in HIV Monitoring and AIDS patient follow-up by precise and direct CD4 and CD4% measurement.
John Quinn
http://www.partec.de/products/cyflowsl3.html
CyFlow SL3
@@ -9503,7 +9503,7 @@
CyFlow Space
CyFlow Space at TSRI Flow Cytometry Core Facility
- A CyFlow_Space is a flow_cytometer_sorter manufactured by Partec. Its specs are: 8optical parameters, 6 colours:FSC, SSC, FL1-FL6 , 3laser light sources: 200mW@488nm blue solid state laser 25mW@635nm red diode laser 50mW@405nm violet or 8mW@375nm ultraviolet diode laser _ultracompact desktop high end instrument. Parallel 16bit digital pulse processing. The CyFlow Space is a 6-Colour FCM System and Cell Sorter for Clinical Routine and Research.
+ A CyFlow_Space is a flow_cytometer_sorter manufactured by Partec. Its specs are: 8optical parameters, 6 colours:FSC, SSC, FL1-FL6 , 3laser light sources: 200mW@488nm blue solid state laser 25mW@635nm red diode laser 50mW@405nm violet or 8mW@375nm ultraviolet diode laser _ultracompact desktop high end instrument. Parallel 16bit digital pulse processing. The CyFlow Space is a 6-Colour FCM System and Cell Sorter for Clinical Routine and Research.
John Quinn
http://www.partec.de/products/cyflowspace.html
CyFlow Space
@@ -9524,7 +9524,7 @@
CytoBuoy
CytoBuoy can be used to conduct extended and/or high frequency time series of phytoplankton distribution and abundance on fixed locations
- A flow cytometer analyser which is manufactured by Cyto Buoy Inc. They are the buoy mounted version of the CytoSense, equipped with wireless transmission of control and data files. They are a single laser, multi parameter instrument. Various types of micro-laser are offered; available measuring parameters are forward light scatter, side scatter, and fluorescence (max. 9 colour bands). The current series have 5 parameters.
+ A flow cytometer analyser which is manufactured by Cyto Buoy Inc. They are the buoy mounted version of the CytoSense, equipped with wireless transmission of control and data files. They are a single laser, multi parameter instrument. Various types of micro-laser are offered; available measuring parameters are forward light scatter, side scatter, and fluorescence (max. 9 colour bands). The current series have 5 parameters.
John Quinn, Melanie Courtot
http://www.cytobuoy.com/
CytoBuoy flow cytometer analyzer
@@ -9538,7 +9538,7 @@
CytoSence
- A CytoSense is a flow_cytometer_analyser manufactured by Cyto Buoy Inc. They are a single laser, multi parameter instrument. Various types of micro-laser are offered; available measuring parameters are forward light scatter, side scatter, and fluorescence (max. 9 colour bands). The current series have 5 parameters. The CytoSense is the basic instrument, which can be used for normal laboratory applications, as well as for autonomous monitoring with internal data logging or direct data transmission. The special instrument design and its splashproof housing allow operation on moving platforms and outdoor sites.
+ A CytoSense is a flow_cytometer_analyser manufactured by Cyto Buoy Inc. They are a single laser, multi parameter instrument. Various types of micro-laser are offered; available measuring parameters are forward light scatter, side scatter, and fluorescence (max. 9 colour bands). The current series have 5 parameters. The CytoSense is the basic instrument, which can be used for normal laboratory applications, as well as for autonomous monitoring with internal data logging or direct data transmission. The special instrument design and its splashproof housing allow operation on moving platforms and outdoor sites.
John Quinn
http://www.cytobuoy.com/
CytoSence
@@ -9552,7 +9552,7 @@
CytoSub
- A CytoSub is a flow_cytometer_analyser manufactured by Cyto Buoy Inc. They are a single laser, multi parameter instrument. Various types of micro-laser are offered; available measuring parameters are forward light scatter, side scatter, and fluorescence (max. 9 colour bands). The current series have 5 parameters. The CytoSub is the submersible version equipped with a high pressure sample inlet loop and a high pressure housing to allow underwater operation down to 200 m, lowered on a cable or mounted on a flooded underwater vehicle.
+ A CytoSub is a flow_cytometer_analyser manufactured by Cyto Buoy Inc. They are a single laser, multi parameter instrument. Various types of micro-laser are offered; available measuring parameters are forward light scatter, side scatter, and fluorescence (max. 9 colour bands). The current series have 5 parameters. The CytoSub is the submersible version equipped with a high pressure sample inlet loop and a high pressure housing to allow underwater operation down to 200 m, lowered on a cable or mounted on a flooded underwater vehicle.
John Quinn
http://www.cytobuoy.com/
CytoSub
@@ -9567,7 +9567,7 @@
dichroic filter
Cy3 Dichroic Filter
- A dichroic filter is an optical filter which is used to selectively pass light of a small range of colors while reflecting other colors. A dichroic filter passes the specified range of light whereas a dichroic mirror reflects the specified range of light.
+ A dichroic filter is an optical filter which is used to selectively pass light of a small range of colors while reflecting other colors. A dichroic filter passes the specified range of light whereas a dichroic mirror reflects the specified range of light.
John Quinn
http://en.wikipedia.org/wiki/Dichroic_filter
dichroic filter
@@ -9582,7 +9582,7 @@
dichroic mirror
ViewLux Alexa 594 dichroic mirror
- A dichroic mirror is an optical filter which is used to selectively reflect light of a small range of colors while passing other colors. A dichroic filter passes the specified range of light whereas a dichroic mirror reflects the specified range of light.
+ A dichroic mirror is an optical filter which is used to selectively reflect light of a small range of colors while passing other colors. A dichroic filter passes the specified range of light whereas a dichroic mirror reflects the specified range of light.
John Quinn
http://en.wikipedia.org/wiki/Dichroic_mirror
dichroic mirror
@@ -9603,7 +9603,7 @@
differential pressure gauge
LSR2 differential pressure gauge
- Part of the fluidics subsystem. The differential pressure gauge monitors the difference between sample and sheath fluid pressures in systems where pressure is used to force the sample fluid to flow in the center of the sheath fluid. A differential pressure gauge can be used by the operator to make sure that the sample fluid is at a greater pressure than the sheath fluid, which maintains a core of sample fluid.
+ Part of the fluidics subsystem. The differential pressure gauge monitors the difference between sample and sheath fluid pressures in systems where pressure is used to force the sample fluid to flow in the center of the sheath fluid. A differential pressure gauge can be used by the operator to make sure that the sample fluid is at a greater pressure than the sheath fluid, which maintains a core of sample fluid.
John Quinn
Practical Flow Cytometry 4th Edition, Howard Shapiro, ISBN-10: 0471411256, ISBN-13: 978-0471411253
differential pressure gauge
@@ -9618,7 +9618,7 @@
diode laser
FAX-RS3-H0 diode laser manufactured by Diode Laser Concepts, Inc.
- A diode laser is a laser in which the active medium is a p-n junction semiconductor laser diode, similar to that found in a light-emitting diode. Laser diodes emit at wavelengths from 375 nm to 1800 nm, and wavelengths of over 3 micrometer have been demonstrated. A diode laser can by used to irradiate cells in a flow cytometer.
+ A diode laser is a laser in which the active medium is a p-n junction semiconductor laser diode, similar to that found in a light-emitting diode. Laser diodes emit at wavelengths from 375 nm to 1800 nm, and wavelengths of over 3 micrometer have been demonstrated. A diode laser can by used to irradiate cells in a flow cytometer.
Daniel Schober
John Quinn
diode laser
@@ -9633,7 +9633,7 @@
dye laser
Rhodamine 101 dye laser used to irradiate cells in a flow cytometer.
- A dye laser is a laser in which the lasing medium is a fluorescent dye, usually dissolved in an organic solvent such as ethanol or ethylene glycol. The particular dye used determines the wavelengths the laser can emit. The laser medium is places between two parallel mirrors for light emission amplification.
+ A dye laser is a laser in which the lasing medium is a fluorescent dye, usually dissolved in an organic solvent such as ethanol or ethylene glycol. The particular dye used determines the wavelengths the laser can emit. The laser medium is places between two parallel mirrors for light emission amplification.
Daniel Schober
John Quinn
Practical Flow Cytometry 4th Edition, Howard Shapiro, ISBN-10: 0471411256, ISBN-13: 978-0471411253
@@ -9649,7 +9649,7 @@
FACS Calibur
FACS Calibur at TFL, BCCRC, Vancouver
- The FACS Calibur is one of the most popular cytometers in use for research.
+ The FACS Calibur is one of the most popular cytometers in use for research.
John Quinn
http://www.bdbiosciences.com/immunocytometry_systems/products/display_product.php?keyID=45, 2007-05-11
FACS Calibur
@@ -9663,7 +9663,7 @@
FACS Canto
- A FACS_Canto is a flow_cytometer_analyser manufactured by Becton Dickinson. It features digital electronics, a solid state 488 nm, and a HeNe 633 nm lasers, and filters and PMTs for collecting up to 6 fluorescent parameters. The FACS_Canto is an analyser usually used in clinical applications.
+ A FACS_Canto is a flow_cytometer_analyser manufactured by Becton Dickinson. It features digital electronics, a solid state 488 nm, and a HeNe 633 nm lasers, and filters and PMTs for collecting up to 6 fluorescent parameters. The FACS_Canto is an analyser usually used in clinical applications.
John Quinn
http://www.bdbiosciences.com/pdfs/brochures/23-8742-00.pdf
FACS Canto
@@ -9677,7 +9677,7 @@
FACS Canto2
- A FACS_Canto2 is a flow_cytometer_analyser manufactured by BD. It features digital electronics, two solid state lasers at 488 and 633 nm with the option for a third 405 nm laser, and filters and collectors for measuring up to 8 fluorescent paramters with either the 2 or 3 laser option. The FACS_Canto2 is an analyser usually used in clinical applications.
+ A FACS_Canto2 is a flow_cytometer_analyser manufactured by BD. It features digital electronics, two solid state lasers at 488 and 633 nm with the option for a third 405 nm laser, and filters and collectors for measuring up to 8 fluorescent paramters with either the 2 or 3 laser option. The FACS_Canto2 is an analyser usually used in clinical applications.
John Quinn
http://www.bdbiosciences.com/cgi-bin/literature/view?part_num=23-8786-01
FACS Canto2
@@ -9691,7 +9691,7 @@
FACS Scan
- A FACS_Scan is a flow_cytometer_analyser manufactured by Becton Dickinson. IT features analog electronics, one 488 nm solid state laser, and the filters and PMTs to collect up to three fluorescent parameters The FACS_Scan is usually used for research applications.
+ A FACS_Scan is a flow_cytometer_analyser manufactured by Becton Dickinson. IT features analog electronics, one 488 nm solid state laser, and the filters and PMTs to collect up to three fluorescent parameters The FACS_Scan is usually used for research applications.
John Quinn
http://www.brc.ubc.ca/brc/facs.html
FACS Scan
@@ -9706,7 +9706,7 @@
FACSAria
FACSAria at TSRI Flow Cytometry Core Facility
- A FASCSAria is a flow_cytometer_sorter manufactured by Becton Dickinson. It features digital electronics, a solid state 488 nm blue laser, a solid state 407 nm violet laser, and a HeNe (633 nm) ion laser. The Aria has the filters and PMTs to collect side scatter and 9 fluorescent parameters. The Aria has a photodiode detector for forward scatter collector. The flow cell is Quartz cuvette. The FACSAria is a sorter used to collect and analyse cells using up to 11 parameters.
+ A FASCSAria is a flow_cytometer_sorter manufactured by Becton Dickinson. It features digital electronics, a solid state 488 nm blue laser, a solid state 407 nm violet laser, and a HeNe (633 nm) ion laser. The Aria has the filters and PMTs to collect side scatter and 9 fluorescent parameters. The Aria has a photodiode detector for forward scatter collector. The flow cell is Quartz cuvette. The FACSAria is a sorter used to collect and analyse cells using up to 11 parameters.
John Quinn
http://www.bdbiosciences.com/external_files/is/doc/mkt_lit/brochures/SJ-0003-00Aria.pdf
FACSAria
@@ -9721,7 +9721,7 @@
FACSvantage
FACSvantage at TSRI Flow Cytometry Core Facility
- The FACSvantage is a flow_cytometer_sorter manufactured by Becton Dickinson. It has analog electronics, three lasers (several options are available), and the filters and PMTs to collect 6 fluorescent parameters and side scatter, and a photodiode to collect forward scatter. The FACSvantage can be used to analyse, sort and collect cells.
+ The FACSvantage is a flow_cytometer_sorter manufactured by Becton Dickinson. It has analog electronics, three lasers (several options are available), and the filters and PMTs to collect 6 fluorescent parameters and side scatter, and a photodiode to collect forward scatter. The FACSvantage can be used to analyse, sort and collect cells.
John Quinn
http://www.bdbiosciences.com/features/products/display_product.php?keyID=42
FACSvantage
@@ -9735,7 +9735,7 @@
FC 500
- A FC_500 is a flow_cytometer_analyser manufactured by Beckman Coulter. It features digital electronics, 488 nm and 635 nm lasers, filters and PMTs for 5 fluorescent parameters, a diode for collecting side scatter and a solid state detector for forward scatter. The FC 500 is an analyser usually used for either research or clinical applications.
+ A FC_500 is a flow_cytometer_analyser manufactured by Beckman Coulter. It features digital electronics, 488 nm and 635 nm lasers, filters and PMTs for 5 fluorescent parameters, a diode for collecting side scatter and a solid state detector for forward scatter. The FC 500 is an analyser usually used for either research or clinical applications.
John Quinn
http://www.beckmancoulter.com/products/instrument/flowcytometry/fc500series.asp
FC 500
@@ -9756,7 +9756,7 @@
flow cell
Biofilm Flow Cell
- Aparatus in the fluidic subsystem where the sheath and sample meet. Can be one of several types; jet-in-air, quartz cuvette, or a hybrid of the two. The sample flows through the center of a fluid column of sheath fluid in the flow cell.
+ Aparatus in the fluidic subsystem where the sheath and sample meet. Can be one of several types; jet-in-air, quartz cuvette, or a hybrid of the two. The sample flows through the center of a fluid column of sheath fluid in the flow cell.
Person:John Quinn
flow_cell
http://www.flocyte.com/FRTP/Resources/flow_cytometry_glossary.htm
@@ -9808,7 +9808,7 @@
flow cytometer
FACS Calibur
- A flow_cytometer is an instrument for counting, examining and sorting microscopic particles in suspension. It allows simultaneous multiparametric analysis of the physical and/or chemical characteristics of single cells flowing through an optical and/or electronic detection apparatus. A flow cytometer is an instrument that can be used to quantitatively measure the properties of individual cells in a flowing medium.
+ A flow_cytometer is an instrument for counting, examining and sorting microscopic particles in suspension. It allows simultaneous multiparametric analysis of the physical and/or chemical characteristics of single cells flowing through an optical and/or electronic detection apparatus. A flow cytometer is an instrument that can be used to quantitatively measure the properties of individual cells in a flowing medium.
John Quinn
http://en.wikipedia.org/wiki/Flow_cytometer
flow cytometer
@@ -9835,7 +9835,7 @@
fluid pressure regulator
LSR2 fluid pressure regulator
- Part of the fluidic subsystem. The fluid pressure regulator maintains constant pressure within the sheath and or sample lines by filling the lines with enough gas to push the fluid at the desired rate. The gas is usually air, and less frequently nitrogen. In the sheath line, the gas is pushed into the sheath tank. In the sample line the gas is pushed into the collection tube. Fluid pressure regulators maintain great enough pressure to push sample fluid out of the tube and sheath fluid out of the sheath tank.
+ Part of the fluidic subsystem. The fluid pressure regulator maintains constant pressure within the sheath and or sample lines by filling the lines with enough gas to push the fluid at the desired rate. The gas is usually air, and less frequently nitrogen. In the sheath line, the gas is pushed into the sheath tank. In the sample line the gas is pushed into the collection tube. Fluid pressure regulators maintain great enough pressure to push sample fluid out of the tube and sheath fluid out of the sheath tank.
Person: John Quinn
Practical Flow Cytometry 4th Edition, Howard Shapiro, ISBN-10: 0471411256, ISBN-13: 978-0471411253
fluid pressure regulator
@@ -9850,7 +9850,7 @@
gas laser
helium-neon gas laser used to erradiate cells in a flow cytometer.
- A gas laser is a laser in which the lasing medium is a gas. The laser medium is places between two parallel mirrors for light emission amplification. The gas is excited to emit light via an external light source or an electric current discharging through the gas.
+ A gas laser is a laser in which the lasing medium is a gas. The laser medium is places between two parallel mirrors for light emission amplification. The gas is excited to emit light via an external light source or an electric current discharging through the gas.
Daniel Schober
John Quinn
http://en.wikipedia.org/wiki/Gas_laser
@@ -9865,7 +9865,7 @@
Guava EasyCyte Mini
- A Guava_EasyCyte_Mini is a flow_cytometer_analyser that includes a single 488 nm laser, and filters and PMTs to collect up to 3 fluorescent parameters. It includes a photodiode forward scatter collector and an optional photodiode for side scatter collection.Guava cytometers use aspiration instead of fluid systems to transport cells within the machine. The mini accepts tubes only for inputting cells or beads. The Guava_EasyCyte_Mini cytometer is a small portable cytometer particularly useful for field measurement.
+ A Guava_EasyCyte_Mini is a flow_cytometer_analyser that includes a single 488 nm laser, and filters and PMTs to collect up to 3 fluorescent parameters. It includes a photodiode forward scatter collector and an optional photodiode for side scatter collection.Guava cytometers use aspiration instead of fluid systems to transport cells within the machine. The mini accepts tubes only for inputting cells or beads. The Guava_EasyCyte_Mini cytometer is a small portable cytometer particularly useful for field measurement.
John Quinn
http://www.guavatechnologies.com/main/products/easyCyteMini.cfm
Guava EasyCyte Mini
@@ -9879,7 +9879,7 @@
Guava EasyCyte Plus
- A Guava_EasyCyte_Plus System is a flow_cytometer_analyser that includes a single 488 nm laser, and filters and PMTs to collect up to 4 fluorescent parameters. It includes a photodiode forward scatter collector and an optional photodiode for side scatter collection.Guava cytometers use aspiration instead of fluid systems to transport cells within the machine. The EasyCyte plus accepts 96 well plates as well as tubes. The Guava_EasyCyte_Plus cytometer is a small portable cytometer particularly useful for field measurement.
+ A Guava_EasyCyte_Plus System is a flow_cytometer_analyser that includes a single 488 nm laser, and filters and PMTs to collect up to 4 fluorescent parameters. It includes a photodiode forward scatter collector and an optional photodiode for side scatter collection.Guava cytometers use aspiration instead of fluid systems to transport cells within the machine. The EasyCyte plus accepts 96 well plates as well as tubes. The Guava_EasyCyte_Plus cytometer is a small portable cytometer particularly useful for field measurement.
John Quinn
http://www.guavatechnologies.com/main/products/easycyte-new.cfm
Guava EasyCyte Plus
@@ -9893,7 +9893,7 @@
Guava Personal Cell Analysis
- A Guava_Personal_Cell_Analysis System is a flow_cytometer_analyser that includes a single 532 nm laser, and filters and PMTs to collect up to 2 fluorescent parameters. It includes a photodiode forward scatter collector. Guava cytometers use aspiration instead of fluid systems to transport cells within the machine. The PCA96 uses only tubes to introduce specimen. The Guava PCA cytometer is a small portable cytometer particularly useful for field measurement.
+ A Guava_Personal_Cell_Analysis System is a flow_cytometer_analyser that includes a single 532 nm laser, and filters and PMTs to collect up to 2 fluorescent parameters. It includes a photodiode forward scatter collector. Guava cytometers use aspiration instead of fluid systems to transport cells within the machine. The PCA96 uses only tubes to introduce specimen. The Guava PCA cytometer is a small portable cytometer particularly useful for field measurement.
John Quinn
Guava_PCA
http://www.guavatechnologies.com/main/products/PCA-new.cfm
@@ -9908,7 +9908,7 @@
Guava Personal Cell Analysis-96
- The Guava_Personal_Cell_Analysis-96 Systems is a flow_cytometer_analyser that includes a single 532 nm laser, and filters and PMTs to collect up to 2 fluorescent parameters. It includes a photodiode forward scatter collector. Guava cytometers use aspiration instead of fluid systems to transport cells within the machine. The PCA96 uses either tubes or 96 well plates to introduce specimen. The Guava PCA -96 cytometer is a small portable cytometer particularly useful for field measurement.
+ The Guava_Personal_Cell_Analysis-96 Systems is a flow_cytometer_analyser that includes a single 532 nm laser, and filters and PMTs to collect up to 2 fluorescent parameters. It includes a photodiode forward scatter collector. Guava cytometers use aspiration instead of fluid systems to transport cells within the machine. The PCA96 uses either tubes or 96 well plates to introduce specimen. The Guava PCA -96 cytometer is a small portable cytometer particularly useful for field measurement.
John Quinn
Guava_PCA-96
http://www.guavatechnologies.com/main/products/PCA-96new.cfm
@@ -9924,7 +9924,7 @@
helium cadmium ion laser
KIMMON HeCd 325nm laser
- A helium-cadmium laser is a metal vapor laser that emits wavelengths of 442, 325 and 354 nms. This laser is a metal vapor laser. A helium-cadmium laser can by used to irradiate cells in a flow cytometer.
+ A helium-cadmium laser is a metal vapor laser that emits wavelengths of 442, 325 and 354 nms. This laser is a metal vapor laser. A helium-cadmium laser can by used to irradiate cells in a flow cytometer.
John Quinn
http://en.wikipedia.org/wiki/Laser#Gas_lasers
helium cadmium ion laser
@@ -9939,7 +9939,7 @@
helium neon ion laser
A helium neon laser can by used to irradiate cells in a flow cytometer.
- A helium-neon laser (HeNe) is an ion laser that uses helium and neon gas-ions as lasing medium. HeNe lasers emit at 543 nm and 633 nm most commonly and can also be used at 543, 594, and 611 nm.
+ A helium-neon laser (HeNe) is an ion laser that uses helium and neon gas-ions as lasing medium. HeNe lasers emit at 543 nm and 633 nm most commonly and can also be used at 543, 594, and 611 nm.
Daniel Schober
John Quinn
http://en.wikipedia.org/wiki/Laser#Gas_lasers
@@ -9966,7 +9966,7 @@
Amnis ImageStream
- The ImageStream is a multispectral_imaging_flow_cytometer manufactured by Amnis. Its has digital electronics, a single standard 488 nm solid state laser. In addition an optional 658 nm and your choice of either a 405 nm or 375 nm solid state laser can be added. Information is collected using cameras. The ImageStream system CCD camera produces six images of each cell, including darkfield, brightfield, and up to four fluorescent colors. Each image is used to calculate over 40 features, so a six-image assay results in ~250 morphometric and photometric features per cell. The ImageStream is a flow cytometer that takes pictures of the cells in flow. It has both components, an Image cytometer and a flow cytometer.
+ The ImageStream is a multispectral_imaging_flow_cytometer manufactured by Amnis. Its has digital electronics, a single standard 488 nm solid state laser. In addition an optional 658 nm and your choice of either a 405 nm or 375 nm solid state laser can be added. Information is collected using cameras. The ImageStream system CCD camera produces six images of each cell, including darkfield, brightfield, and up to four fluorescent colors. Each image is used to calculate over 40 features, so a six-image assay results in ~250 morphometric and photometric features per cell. The ImageStream is a flow cytometer that takes pictures of the cells in flow. It has both components, an Image cytometer and a flow cytometer.
It has both components, an Image cytometer and a flow cytometer.
John Quinn
Melanie Courtot
@@ -9982,7 +9982,7 @@
inFlux Analyzer
- The inFlux Analyzer is a flow_cytometer_analyser manufactured by Cytopeia. It is a digital machine, with these laser options: Coherent 70, 90, 300 series water cooled lasers, solid state UV 355nm, Violet 408nm, Violet-Blue 479nm, Blue-488nm, Green-531nm, Red-635nm, Red-647nm. Filters and PMTs are used for all parameters (including forward light scatter), and up to 12 PMTs can be included. The Influx analyser can be used to measure the properties of individual cells.
+ The inFlux Analyzer is a flow_cytometer_analyser manufactured by Cytopeia. It is a digital machine, with these laser options: Coherent 70, 90, 300 series water cooled lasers, solid state UV 355nm, Violet 408nm, Violet-Blue 479nm, Blue-488nm, Green-531nm, Red-635nm, Red-647nm. Filters and PMTs are used for all parameters (including forward light scatter), and up to 12 PMTs can be included. The Influx analyser can be used to measure the properties of individual cells.
John Quinn
http://www.cytopeia.com/analyzer.htm
inFlux Analyzer
@@ -9997,7 +9997,7 @@
Influx Cell Sorter
Influx Cell Sorter at TSRI Flow Cytometry Core Facility
- A Influx Cell Sorter is a flow_cytometer_sorter manufactured by Cytopeia. It is a digital machine, with these laser options: Coherent 70, 90, 300 series water cooled lasers, solid state UV 355nm, Violet 408nm, Violet-Blue 479nm, Blue-488nm, Green-531nm, Red-635nm, Red-647nm. The sorting is multi-way, index, and proportional sorting. Filters and PMTs are used for all parameters (including forward light scatter), and up to 12 PMTs can be included. The Influx cell sorter can be used to measure, sort, and collect ndividual cells.
+ A Influx Cell Sorter is a flow_cytometer_sorter manufactured by Cytopeia. It is a digital machine, with these laser options: Coherent 70, 90, 300 series water cooled lasers, solid state UV 355nm, Violet 408nm, Violet-Blue 479nm, Blue-488nm, Green-531nm, Red-635nm, Red-647nm. The sorting is multi-way, index, and proportional sorting. Filters and PMTs are used for all parameters (including forward light scatter), and up to 12 PMTs can be included. The Influx cell sorter can be used to measure, sort, and collect ndividual cells.
John Quinn
http://www.cytopeia.com/sorter.htm
Influx Cell Sorter
@@ -10012,7 +10012,7 @@
ion laser
2 Watt Lexel 88 Argon Ion laser
- An ion laser is a gas laser which uses an ionized gas as its lasing medium.
+ An ion laser is a gas laser which uses an ionized gas as its lasing medium.
Daniel Schober
John Quinn
http://en.wikipedia.org/wiki/Ion_laser
@@ -10028,7 +10028,7 @@
krypton ion laser
Lexel 95L krypton laser
- A krypton-ion laser is an ion laser that uses krypton as the lasing medium. These lasers can emit at 468, 476, 482, 520, 531, 568, 647 (the most powerful line), and 676 nm all at once. They have much lower gain than argon lasers however.
+ A krypton-ion laser is an ion laser that uses krypton as the lasing medium. These lasers can emit at 468, 476, 482, 520, 531, 568, 647 (the most powerful line), and 676 nm all at once. They have much lower gain than argon lasers however.
Daniel Schober
John Quinn
krypton ion laser
@@ -10043,7 +10043,7 @@
LactoScope C4
LactoScope C4 Automatic Economical
- A LactoScope_C4 is a spectrophotometer with which the composition of milk and milk products is analysed via infrared technology. The LactoScope determines the amount of the constituents fat, protein, lactose and the total solids content with extreme accuracy.
+ A LactoScope_C4 is a spectrophotometer with which the composition of milk and milk products is analysed via infrared technology. The LactoScope determines the amount of the constituents fat, protein, lactose and the total solids content with extreme accuracy.
Josef Spidlen
Melanie Courtot
http://www.aicompanies.com/DeltaCD/lacto_ftir_auto.htm
@@ -10059,7 +10059,7 @@
laser
A laser is the most common way to irradiate a cell in a flow cytometer.
- A laser (acronym for light amplification by the stimulated emission of radiation) is a light source that emits photons of the same characteristics in a coherent beam. A laser uses a solid, liquid or gaseous lasing medium, that contains molecules, of which some atoms have electrons that emit photons of the same frequency when falling back to their normal orbital after excitation (pumping) by external means A laser is the most common way to irradiate a cell in a flow cytometer.
+ A laser (acronym for light amplification by the stimulated emission of radiation) is a light source that emits photons of the same characteristics in a coherent beam. A laser uses a solid, liquid or gaseous lasing medium, that contains molecules, of which some atoms have electrons that emit photons of the same frequency when falling back to their normal orbital after excitation (pumping) by external means A laser is the most common way to irradiate a cell in a flow cytometer.
Daniel Schober
light amplification by the stimulated emission of radiation
John Quinn
@@ -10081,7 +10081,7 @@
light source
- A light source is an optical subsystem that provides light for use in a distant area using a delivery system (e.g., fiber optics). Light sources may include one of a variety of lamps (e.g., xenon, halogen, mercury). Most light sources are operated from line power, but some may be powered from batteries. They are mostly used in endoscopic, microscopic, and other examination and/or in surgical procedures. The light source is part of the optical subsystem. In a flow cytometer the light source directs high intensity light at particles at the interrogation point. The light source in a flow cytometer is usually a laser.
+ A light source is an optical subsystem that provides light for use in a distant area using a delivery system (e.g., fiber optics). Light sources may include one of a variety of lamps (e.g., xenon, halogen, mercury). Most light sources are operated from line power, but some may be powered from batteries. They are mostly used in endoscopic, microscopic, and other examination and/or in surgical procedures. The light source is part of the optical subsystem. In a flow cytometer the light source directs high intensity light at particles at the interrogation point. The light source in a flow cytometer is usually a laser.
Elizabeth M. Goralczyk
John Quinn
Olga Tchuvatkina
@@ -10098,7 +10098,7 @@
logarithmic voltage amplifier
HLVA-100 logarithmic voltage amplifier developed by FEMTO Messtechnik, GmbH
- A logarithmic voltage amplifier is an analog electronic circuit that puts out a voltage or current proportional to the voltage or current at its input, with logarithmic proportionality. In an analog system, the logarithmic voltage amplifier is used to present parameters with a high dynamic range on a more useful scale.
+ A logarithmic voltage amplifier is an analog electronic circuit that puts out a voltage or current proportional to the voltage or current at its input, with logarithmic proportionality. In an analog system, the logarithmic voltage amplifier is used to present parameters with a high dynamic range on a more useful scale.
John Quinn
Practical Flow Cytometry 4th Edition, Howard Shapiro, ISBN-10: 0471411256, ISBN-13: 978-0471411253
logarithmic voltage amplifier
@@ -10113,7 +10113,7 @@
long pass filter
750 LP filter
- A long pass filter is an optical filter that passes high wavelengths of light but attenuates (or reduces) wavelengths lower than the cutoff frequency. A long pass filter with a cutoff of 500 nm would pass all wavelengths greater than 500 nm.
+ A long pass filter is an optical filter that passes high wavelengths of light but attenuates (or reduces) wavelengths lower than the cutoff frequency. A long pass filter with a cutoff of 500 nm would pass all wavelengths greater than 500 nm.
John Quinn
http://en.wikipedia.org/wiki/high-pass_filter
long pass filter
@@ -10128,7 +10128,7 @@
LSR2
LSR2 at TSRI Flow Cytometry Core Facility
- A LSR2 is a sorter manufactured by Becton Dickinson. It features digital electronics, a solid state 488 nm blue laser and optionally can also have any combination of solid state UV (355 nm) and violet (405 nm) lasers and the a HeNe (633 nm) ion laser. The LSR2 has the filters and PMTs to work with 13 fluorescent parameters. The LSR II is one of the most common sorters in use.
+ A LSR2 is a sorter manufactured by Becton Dickinson. It features digital electronics, a solid state 488 nm blue laser and optionally can also have any combination of solid state UV (355 nm) and violet (405 nm) lasers and the a HeNe (633 nm) ion laser. The LSR2 has the filters and PMTs to work with 13 fluorescent parameters. The LSR II is one of the most common sorters in use.
John Quinn
http://www.bdbiosciences.com/external_files/is/doc/mkt_lit/brochures/live/web_enabled/SJ-0142-00LSR2.pdf
LSR2
@@ -10142,7 +10142,7 @@
Luminex 100
- The Luminex 100 is a flow_cytometer_analyser manufactured by Luminex. It is a single laser system (575 nm) with avalanche photodiodes in red and infrared and a single PMT for fluorescence. The flow chamber is a square quartz cuvette.
+ The Luminex 100 is a flow_cytometer_analyser manufactured by Luminex. It is a single laser system (575 nm) with avalanche photodiodes in red and infrared and a single PMT for fluorescence. The flow chamber is a square quartz cuvette.
John Quinn
http://www.luminexcorp.com/products/luminex_100IS.html
Luminex 100
@@ -10156,7 +10156,7 @@
Luminex 200
- A Luminex_200 is a flow_cytometer_analyser manufactured by Luminex. The optical specifications are: Reporter laser: 532 nm, nominal output 10 - 15 mW, maximum 500 mW, frequency-doubled diode; mode of operation, continuous wave (CW). Classification laser: 635 nm, 9.1 __ 6%, maximum output 25 mW, diode; mode of operation, continuous wave (CW) Reporter detector: Photomultiplier tube, detection bandwidth of 565 - 585 nm Classification detector and doublet discriminator: Avalanche photo diodes with temperature compensation
+ A Luminex_200 is a flow_cytometer_analyser manufactured by Luminex. The optical specifications are: Reporter laser: 532 nm, nominal output 10 - 15 mW, maximum 500 mW, frequency-doubled diode; mode of operation, continuous wave (CW). Classification laser: 635 nm, 9.1 __ 6%, maximum output 25 mW, diode; mode of operation, continuous wave (CW) Reporter detector: Photomultiplier tube, detection bandwidth of 565 - 585 nm Classification detector and doublet discriminator: Avalanche photo diodes with temperature compensation
John Quinn
http://www.luminexcorp.com/support/faqs.html
Luminex 200
@@ -10170,7 +10170,7 @@
MACS Quant
- A MACS Quant is a flow_cytometer_analyser manufactured by Miltenyi. It uses digital electronics, and has three lasers of wavelengths 405 nm, 488 nm, and 635 nm. It has filters and detectors to collect 7 fluorescent parameters and 2 scatter parameters. The MACS Quant is an analyser usually used in research applications.
+ A MACS Quant is a flow_cytometer_analyser manufactured by Miltenyi. It uses digital electronics, and has three lasers of wavelengths 405 nm, 488 nm, and 635 nm. It has filters and detectors to collect 7 fluorescent parameters and 2 scatter parameters. The MACS Quant is an analyser usually used in research applications.
John Quinn
http://www.miltenyi.com
MACS Quant
@@ -10185,7 +10185,7 @@
metal vapor laser
Gold vapor laser, Helium-cadmium metal-vapor laser
- A metal vapor laser is a gas laser in which the lasing medium is metal vapor. A metal vapor laser can by used to irradiate cells in a flow cytometer.
+ A metal vapor laser is a gas laser in which the lasing medium is metal vapor. A metal vapor laser can by used to irradiate cells in a flow cytometer.
John Quinn
Practical Flow Cytometry 4th Edition, Howard Shapiro, ISBN-10: 0471411256, ISBN-13: 978-0471411253
metal vapor laser
@@ -10200,7 +10200,7 @@
mixed argon-krypton gas laser
argon-krypton laser in a cytometer
- A mixed argon krypton gas laser is an ion laser in which the lasing medium is a mixture of argon and krypton. A mixed argon-krypton laser can by used to irradiate cells in a flow cytometer.
+ A mixed argon krypton gas laser is an ion laser in which the lasing medium is a mixture of argon and krypton. A mixed argon-krypton laser can by used to irradiate cells in a flow cytometer.
John Quinn
http://www.eio.com/repairfaq/sam/laserarg.htm
mixed argon-krypton gas laser
@@ -10215,7 +10215,7 @@
MoFlo
MoFlo at TSRI Flow Cytometry Core Facility
- A MoFlo is a flow_cytometer_sorter manufactured by Dako Cytomation. It features digital electronics, the option to include several lasers (solid state 488 nm, 635 nm, and a 351 nm diode laser), and has the filtering and collection capacity for up to 10 flouresecent parameters. The MoFlo is an instrument that can be used to both analyze quantitatively and collect cells in a flowing medium.
+ A MoFlo is a flow_cytometer_sorter manufactured by Dako Cytomation. It features digital electronics, the option to include several lasers (solid state 488 nm, 635 nm, and a 351 nm diode laser), and has the filtering and collection capacity for up to 10 flouresecent parameters. The MoFlo is an instrument that can be used to both analyze quantitatively and collect cells in a flowing medium.
John Quinn
http://www.dakousa.com/index/prod_search/prod_groups.htm?productareaid=16
MoFlo
@@ -10230,7 +10230,7 @@
neodymium-YAG laser
Neodymium-YAG Laser in DURIP99 System
- A Neodymium-YAG (yttrium aluminum garnet) laser is a solid state laser in which the lasing medium is a solid rod of crystalline material pumped by a flash lamp or a diode laser. Typical output wavelengths are 355, 532, and 1064 nm. A neodymium-YAG laser can by used to irradiate cells in a flow cytometer.
+ A Neodymium-YAG (yttrium aluminum garnet) laser is a solid state laser in which the lasing medium is a solid rod of crystalline material pumped by a flash lamp or a diode laser. Typical output wavelengths are 355, 532, and 1064 nm. A neodymium-YAG laser can by used to irradiate cells in a flow cytometer.
Daniel Schober
John Quinn
neodymium-YAG laser
@@ -10251,7 +10251,7 @@
obscuration bar
obscuration bar in a flow cytometer
- An obscuration bar is a an optical subsystem which is a strip of metal or other material that serves to block out direct light from the illuminating beam. The obscuration bar prevents the bright light scattered in the forward directions from burning out the collection device.
+ An obscuration bar is a an optical subsystem which is a strip of metal or other material that serves to block out direct light from the illuminating beam. The obscuration bar prevents the bright light scattered in the forward directions from burning out the collection device.
Daniel Schober
Flow Cytometry: First Principles, by Alice Longobardi Givan, ISBN-10: 0471382248, ISBN-13: 978-0471382249
John Quinn
@@ -10273,7 +10273,7 @@
optical filter
720 LP filter, 580/30 BP filter
- An optical filter is an optical subsystem that selectively transmits light having certain properties (often, a particular range of wavelengths, that is, range of colours of light), while blocking the remainder. They are commonly used in photography, in many optical instruments, and to colour stage lighting Optical filters can be arranged to segregate and collect light by wave length.
+ An optical filter is an optical subsystem that selectively transmits light having certain properties (often, a particular range of wavelengths, that is, range of colours of light), while blocking the remainder. They are commonly used in photography, in many optical instruments, and to colour stage lighting Optical filters can be arranged to segregate and collect light by wave length.
John Quinn
http://en.wikipedia.org/wiki/Optical_filter
optical filter
@@ -10306,7 +10306,7 @@
optical subsystem
optical subsystem of a cytometer
- A device or part of a device that deals with the behavior and properties of light and the interaction of light with matter. Commonly optical subsystems consist of an excitation optics and collection optics. The excitation optics of a flow cytometer optical subsystem consist of the laser and lenses that are used to shape and focus the laser beam. The collections optics consist of a collection lens to collect light emitted from the particle laser beam interaction and a system of optical mirrors and filters to route specified wavelengths of the collected light to designated optical detectors. The optical subsystem in a flow cytometer consists of the equipment used to irradiate particles, and collect the light either emitted or scattered by those particles.
+ A device or part of a device that deals with the behavior and properties of light and the interaction of light with matter. Commonly optical subsystems consist of an excitation optics and collection optics. The excitation optics of a flow cytometer optical subsystem consist of the laser and lenses that are used to shape and focus the laser beam. The collections optics consist of a collection lens to collect light emitted from the particle laser beam interaction and a system of optical mirrors and filters to route specified wavelengths of the collected light to designated optical detectors. The optical subsystem in a flow cytometer consists of the equipment used to irradiate particles, and collect the light either emitted or scattered by those particles.
DS: Is 'subsystem' necessary or is 'optical_system' enough. Not sure its graph position since an optical subsystem is not necessarily an instrument, but more likely part of one.
Person: Daniel Schober
John Quinn
@@ -10328,7 +10328,7 @@
photodetector
A photomultiplier tube, a photo diode
- A photodetector is a device used to detect and measure the intensity of radiant energy through photoelectric action. In a cytometer, photodetectors measure either the number of photons of laser light scattered on impact with a cell (for example), or the flourescence emitted by excitation of a fluorescent dye.
+ A photodetector is a device used to detect and measure the intensity of radiant energy through photoelectric action. In a cytometer, photodetectors measure either the number of photons of laser light scattered on impact with a cell (for example), or the flourescence emitted by excitation of a fluorescent dye.
John Quinn
http://einstein.stanford.edu/content/glossary/glossary.html
photodetector
@@ -10343,7 +10343,7 @@
photodiode
Avalanche photodiode
- A photodiode is a semiconductor photodetector used to detect light and generate an electrical current. Typically used in forward scatter (FSC) detection. The photodiode collects the forward light scatter in a cytometer.
+ A photodiode is a semiconductor photodetector used to detect light and generate an electrical current. Typically used in forward scatter (FSC) detection. The photodiode collects the forward light scatter in a cytometer.
John Quinn
http://cyto.mednet.ucla.edu/Protocols/flow.htm
photodiode
@@ -10376,7 +10376,7 @@
photomultiplier tube
R9647 by manufactured by Hamamatsu
- A photomultiplier is a device that is normally in the form of a tube, that uses a photocathode to convert photons into photoelectrons which are then amplified. PMTs are typically used to detect SSC and fluorescent parameters. Cytometers have a PMT for each color they can collect.
+ A photomultiplier is a device that is normally in the form of a tube, that uses a photocathode to convert photons into photoelectrons which are then amplified. PMTs are typically used to detect SSC and fluorescent parameters. Cytometers have a PMT for each color they can collect.
John Quinn
http://cyto.mednet.ucla.edu/Protocols/flow.htm
photomultiplier tube
@@ -10397,7 +10397,7 @@
plate loader
FC 500 plate loader
- Part of the fluidics system. A plate loader positions the wells of a multi-well plate under the aspiration tube is a preset order. A plate loader is used for high throughput applications.
+ Part of the fluidics system. A plate loader positions the wells of a multi-well plate under the aspiration tube is a preset order. A plate loader is used for high throughput applications.
measurement function is not corret as discussed on April 26 dev call. Will add new function such as positioning function. Add to tracker will discuss in the future.
John Quinn
http://www.beckmancoulter.com/literature/Bioresearch/P-10202A.pdf
@@ -10413,7 +10413,7 @@
preamplifier
Built in preamplifier in a Hamamatsu H9656 PMT
- A preamplifier is part of the electronics subsystem. It converts the current output from its associated detector to a voltage. The preamplifier is the first stage in analog electronics signal processing.
+ A preamplifier is part of the electronics subsystem. It converts the current output from its associated detector to a voltage. The preamplifier is the first stage in analog electronics signal processing.
John Quinn
Practical Flow Cytometry 4th Edition, Howard Shapiro, ISBN-10: 0471411256, ISBN-13: 978-0471411253
preamplifier
@@ -10428,7 +10428,7 @@
quartz cuvette flow chamber
CVF-Q-10 flow chamber, CV-Q-10 flow chamber
- A flow cell in which the laser irradiates the cell as it passes through a quartz cuvette. A quartz cuvette flow chamber can be used to allow the laser to irradiate cells.
+ A flow cell in which the laser irradiates the cell as it passes through a quartz cuvette. A quartz cuvette flow chamber can be used to allow the laser to irradiate cells.
John Quinn
http://www.flocyte.com/FRTP/Resources/flow_cytometry_glossary.htm
quartz cuvette flow chamber
@@ -10443,7 +10443,7 @@
Reflection
Reflection at TSRI Flow Cytometry Core Facility
- A Reflection is a sorter manufactured by iCyte. It uses digital signal processing, and can be configured with lasers of the users choice from among these excitation wavelengths: 355, 405,488, 532, 635nm. It accommodates up to 48 traditional PMTs. Options include an acousto-optical tunable filter (AOTF) and 16 channel spectrometer (370 to 730 nm). The various detection components can be uniquely configured across multiple Highly Automated Parallel Sorting (HAPS) modules. The Reflection can be used to analyse, sort, and collect cells.
+ A Reflection is a sorter manufactured by iCyte. It uses digital signal processing, and can be configured with lasers of the users choice from among these excitation wavelengths: 355, 405,488, 532, 635nm. It accommodates up to 48 traditional PMTs. Options include an acousto-optical tunable filter (AOTF) and 16 channel spectrometer (370 to 730 nm). The various detection components can be uniquely configured across multiple Highly Automated Parallel Sorting (HAPS) modules. The Reflection can be used to analyse, sort, and collect cells.
John Quinn
http://www.i-cyt.com/reflection.htm
Reflection
@@ -10458,7 +10458,7 @@
cytometer sample tube
sample tube in a cytometer
- A particle delivery vessel. The cytometer sample tube is a vessel in which the sample is introduced to the cytometer. Frequently the tube is placed on the cytometer in such a manner that a seal is formed between the tube and cytometer, and gas is used to create enough pressure to push the sample out of the tube and into the cytometer.
+ A particle delivery vessel. The cytometer sample tube is a vessel in which the sample is introduced to the cytometer. Frequently the tube is placed on the cytometer in such a manner that a seal is formed between the tube and cytometer, and gas is used to create enough pressure to push the sample out of the tube and into the cytometer.
John Quinn
Practical Flow Cytometry 4th Edition, Howard Shapiro, ISBN-10: 0471411256, ISBN-13: 978-0471411253
cytometer sample tube
@@ -10485,7 +10485,7 @@
sheath tank
LSR2 sheath tank
- Part of the fluidics system. The sheath tank is the vessel that holds the sheath fluid at a constant pressure, allowing for it to be pushed into the flow chamber at a constant rate. The sheath tank holds the pressurized sheath fluid.
+ Part of the fluidics system. The sheath tank is the vessel that holds the sheath fluid at a constant pressure, allowing for it to be pushed into the flow chamber at a constant rate. The sheath tank holds the pressurized sheath fluid.
John Quinn
Practical Flow Cytometry 4th Edition, Howard Shapiro, ISBN-10: 0471411256, ISBN-13: 978-0471411253
sheath tank
@@ -10500,7 +10500,7 @@
short pass filter
620 SP filter
- A short pass filter is an optical filter that passes low wavelengths of light but attenuates (or reduces) wavelengths higher than the cutoff frequency. A short pass filter with a cutoff of 500 nm would pass all wavelengths less than 500 nm.
+ A short pass filter is an optical filter that passes low wavelengths of light but attenuates (or reduces) wavelengths higher than the cutoff frequency. A short pass filter with a cutoff of 500 nm would pass all wavelengths less than 500 nm.
John Quinn
http://en.wikipedia.org/wiki/Low-pass_filter
short pass filter
@@ -10515,7 +10515,7 @@
solid state laser
Solid State Heat Capacity Laser developed at DOE's Lawrence Livermore National Laboratory for the USA Army's Space and Missile Defense Command
- A solid-state laser is a laser that uses a lasing medium that is a solid, rather than a liquid such as dye lasers or a gas such as gas lasers. Semiconductor-based diode lasers are also in the solid state, but are generally considered separately from solid-state lasers. The first laser developed was an optical pumped ruby crystal solid state laser.
+ A solid-state laser is a laser that uses a lasing medium that is a solid, rather than a liquid such as dye lasers or a gas such as gas lasers. Semiconductor-based diode lasers are also in the solid state, but are generally considered separately from solid-state lasers. The first laser developed was an optical pumped ruby crystal solid state laser.
Daniel Schober
http://en.wikipedia.org/wiki/Solid-state_laser
solid state laser
@@ -10529,7 +10529,7 @@
Somacount
- A Somacount is a flow_cytometer_analyser manufactured by Bently Instruments. It is a specialized tool for counting somatic cells in milk by specifically staining them with Ethidium Bromide and counting the cells that fluoresce. It has one laser, and the filters and a PMT for the single parameter. There are three sizes available, the 150, 300, and 500 with the number indicating the maximum number of cells that can be analysed per hour. The Somacount is an example of a very specific use cytometer; it exclusively counts somatic cells in milk.
+ A Somacount is a flow_cytometer_analyser manufactured by Bently Instruments. It is a specialized tool for counting somatic cells in milk by specifically staining them with Ethidium Bromide and counting the cells that fluoresce. It has one laser, and the filters and a PMT for the single parameter. There are three sizes available, the 150, 300, and 500 with the number indicating the maximum number of cells that can be analysed per hour. The Somacount is an example of a very specific use cytometer; it exclusively counts somatic cells in milk.
John Quinn
http://www.bentleyinstruments.com/somacount.html#Anchor-Bentley-49575
Somacount
@@ -10544,7 +10544,7 @@
SomaScope
SomaScope Mark II Automatic Economical
- The SomaScope is an instrument to quantify somatic cells in milk.
+ The SomaScope is an instrument to quantify somatic cells in milk.
Josef Spidlen
http://www.aicompanies.com/DeltaCD/soma_auto_adv.htm, 2007-05-10
SomaScope
@@ -10589,7 +10589,7 @@
flow cytometer sorter
BioSorter2000, LSR2
- A flow_cytometer_sorter is a flow_cytometer that analyzes and separates or sorts particles passing through (based on properties measured during analysis) to collect cells of interest.
+ A flow_cytometer_sorter is a flow_cytometer that analyzes and separates or sorts particles passing through (based on properties measured during analysis) to collect cells of interest.
John Quinn
Melanie Courtot
http://www.flocyte.com/FRTP/Resources/flow_cytometry_glossary.htm
@@ -10617,7 +10617,7 @@
syringe pump
NE-1000 Single Syringe Pump
- Part of the fluidics system. A syringe pump can be used to inject the sample fluid and cells into the sheath fluid in the flow chamber. Syringe pumps are useful for creating stable flow rates.
+ Part of the fluidics system. A syringe pump can be used to inject the sample fluid and cells into the sheath fluid in the flow chamber. Syringe pumps are useful for creating stable flow rates.
Person:John Quinn
http://www.answers.com/topic/syringe, 2007-05-11
syringe pump
@@ -10638,7 +10638,7 @@
voltage amplifier
Linear amplifier, log amplifier, microwave amplifier
- A voltage amplifier is a device that amplifies the voltage signal.
+ A voltage amplifier is a device that amplifies the voltage signal.
Frank Gibson
John Quinn
http://en.wiktionary.org/wiki/amplifier
@@ -10660,7 +10660,7 @@
waste tank
LSR2 waste tank
- Part of the fluidics systems. In analyzers the sheath and sample fluid, once analyzed is dumped into a waste tank. The waste tank is where the fluids passing through the cytometer end up after the analysis is finished.
+ Part of the fluidics systems. In analyzers the sheath and sample fluid, once analyzed is dumped into a waste tank. The waste tank is where the fluids passing through the cytometer end up after the analysis is finished.
Person:John Quinn
Practical Flow Cytometry 4th Edition, Howard Shapiro, ISBN-10: 0471411256, ISBN-13: 978-0471411253
waste tank
@@ -10681,7 +10681,7 @@
DNA sequencer
ABI 377 DNA Sequencer, ABI 310 DNA Sequencer
- A DNA sequencer is an instrument that determines the order of deoxynucleotides in deoxyribonucleic acid sequences.
+ A DNA sequencer is an instrument that determines the order of deoxynucleotides in deoxyribonucleic acid sequences.
Trish Whetzel
MO
DNA sequencer
@@ -10708,7 +10708,7 @@
array scanner
GenePix 4200A, GenePix4000B
- An processed material which acquires images of fluorescence (induced with lasers) from labeled molecules on the surface of the microarray chip
+ An processed material which acquires images of fluorescence (induced with lasers) from labeled molecules on the surface of the microarray chip
Trish Whetzel
GROUP: MGED Ontology
array scanner
@@ -10729,7 +10729,7 @@
arrayer
BioRobotics Microgrid II TAS, Affymetrix GMS 417
- A device which deposits biological material onto a substrate in a defined pattern.
+ A device which deposits biological material onto a substrate in a defined pattern.
Trish Whetzel
MO_697 arrayer
arrayer
@@ -10776,7 +10776,7 @@
centrifuge
- A device with a rapidly rotating container that applies centrifugal force to its contents
+ A device with a rapidly rotating container that applies centrifugal force to its contents
Melanie Courtot
Person: Jennifer Fostel
Trish Whetzel
@@ -10799,7 +10799,7 @@
computer
Apple PowerBook, Dell OptiPlex
- A computer is an instrument which manipulates (stores, retrieves, and processes) data according to a list of instructions.
+ A computer is an instrument which manipulates (stores, retrieves, and processes) data according to a list of instructions.
Melanie Courtot
Trish Whetzel
http://en.wikipedia.org/wiki/Computer
@@ -10821,7 +10821,7 @@
heating block
An instrument used to heat and/or maintain material at a set temperature.
- A heating block is an instrument or part of an instrument which raises or maintains the temperature of a sample to a defined constant temperature during certain parts of an assay
+ A heating block is an instrument or part of an instrument which raises or maintains the temperature of a sample to a defined constant temperature during certain parts of an assay
Daniel Schober
MO
heating block
@@ -10842,7 +10842,7 @@
homogenizer
mortar, blender
- A homogenizer is an instrument for the homogenization of various types of material, such as tissue, plant, food, soil, and many others.
+ A homogenizer is an instrument for the homogenization of various types of material, such as tissue, plant, food, soil, and many others.
Melanie Courtot
Trish Whetzel
http://en.wikipedia.org/wiki/Homogenizer
@@ -10870,7 +10870,7 @@
hybridization chamber
Glass Array Hybridization Cassette
- A device which is used to maintain constant contact of a liquid on an array. This can be either a glass vial or slide.
+ A device which is used to maintain constant contact of a liquid on an array. This can be either a glass vial or slide.
Trish Whetzel
MO_563 hybridization_chamber
hybridization chamber
@@ -10897,7 +10897,7 @@
hybridization station
Labnet Problot12
- A device which is used to maintain the temperature of one or more hybridization_chamber(s) at a defined, constant temperature.
+ A device which is used to maintain the temperature of one or more hybridization_chamber(s) at a defined, constant temperature.
Trish Whetzel
MO_497 hybridization station
hybridization station
@@ -10918,7 +10918,7 @@
liquid handler
Beckman BioMek 2000
- A device that is used for automated liquid transfer and handling.
+ A device that is used for automated liquid transfer and handling.
liquid_handling_instrument
MO_868 liquid_handler
DS: Is this class justified? Its a unnamed class. If so, put a fluidic_system and the fluidic_subsystem as subclasses. TW: This is required by MO. FG & DS: Capture as function. All: Needs to be reviewed, according to query use case. If we keep it its kept as unnamed owl class. The liquid handling class remains but as an undefined class with are unlikely to have children. It is expected that the reasoner would classifiy appropriate classes under this class that meet the have the liquid_handling function relation.
@@ -10947,7 +10947,7 @@
oligonucleotide synthesizer
Automated Multiplex Oligonucleotide Synthesizer
- An instrument used to chemically synthesize oligonucleotides.
+ An instrument used to chemically synthesize oligonucleotides.
Trish Whetzel
MO
oligonucleotide synthesizer
@@ -10968,7 +10968,7 @@
sonicator
Sonicator 3000
- A device that converts a variable electrical current to mechanical vibration of a metallic probe. The device is used for the lysis of cells, the mixing of compounds or solutions, to framgent molecules of DNA, or to create emulsions.
+ A device that converts a variable electrical current to mechanical vibration of a metallic probe. The device is used for the lysis of cells, the mixing of compounds or solutions, to framgent molecules of DNA, or to create emulsions.
Trish Whetzel
MO
sonicator
@@ -10989,7 +10989,7 @@
spectrophotometer
Helios Gamma Spectrophotometer
- A spectrophotometer is an instrument that measures the intensity of light as a function of the color, or more specifically, the wavelength of light, transmitted by a substance.
+ A spectrophotometer is an instrument that measures the intensity of light as a function of the color, or more specifically, the wavelength of light, transmitted by a substance.
Melanie Courtot
Trish Whetzel
MO
@@ -11017,7 +11017,7 @@
thermal cycler
Piko(tm) 96-well Thermal Cycler
- An instrument that is capable of repeatedly altering and maintaining specific temperatures for defined periods of time.
+ An instrument that is capable of repeatedly altering and maintaining specific temperatures for defined periods of time.
Melanie Courtot
Trish Whetzel
DNA_amplifier
@@ -11055,7 +11055,7 @@
vacuum dryer
Model 777 Microarray Oven
- An instrument which removes liquid by the application of negative pressure, i.e. vacuum.
+ An instrument which removes liquid by the application of negative pressure, i.e. vacuum.
Trish Whetzel
MO
vacuum dryer
@@ -11076,7 +11076,7 @@
vortexer
VWR Genie 2
- A vortexer is an instrument that mixes small vials of liquid by creating a rotation of the liquid around its own center. It consists of an electric motor with the drive shaft oriented vertically and attached to a cupped rubber piece mounted slightly off-center. As the motor runs the rubber piece oscillates rapidly in a circular motion. When a test tube or other appropriate container is pressed into the rubber cup (or touched to its edge) the motion is transmitted to the liquid inside and a vortex is created.
+ A vortexer is an instrument that mixes small vials of liquid by creating a rotation of the liquid around its own center. It consists of an electric motor with the drive shaft oriented vertically and attached to a cupped rubber piece mounted slightly off-center. As the motor runs the rubber piece oscillates rapidly in a circular motion. When a test tube or other appropriate container is pressed into the rubber cup (or touched to its edge) the motion is transmitted to the liquid inside and a vortex is created.
Melanie Courtot
Trish Whetzel
vortex_mixer
@@ -11099,7 +11099,7 @@
microarray wash station
ArrayIt(r) Microarray Wash Station
- A device that is used to wash Affymetrix-type arrays.
+ A device that is used to wash Affymetrix-type arrays.
Trish Whetzel
MO_626 wash_station
microarray wash station
@@ -11126,7 +11126,7 @@
temperature control bath
VWR Signature Deep-Chamber Heated Water Bath. A water bath is used for temperatures up to 100 degrees C. An oil bath is employed for temperatures over 100 degrees C.
- A temperature_control_bath is a device that has the function to regulate the temperature of a material, the function to contain fluid and the function to vary and maintain the temperature of the contained fluid. Heat exchange (energy transfer) between the material and the heating element is facilitated via the contained fluid. A temperature_control_bath is composed of a container, a heating element and/or a cooling element and a means to adjust the needed temperature. In most cases also a timer and a means to stir the fluid is provided as well.
+ A temperature_control_bath is a device that has the function to regulate the temperature of a material, the function to contain fluid and the function to vary and maintain the temperature of the contained fluid. Heat exchange (energy transfer) between the material and the heating element is facilitated via the contained fluid. A temperature_control_bath is composed of a container, a heating element and/or a cooling element and a means to adjust the needed temperature. In most cases also a timer and a means to stir the fluid is provided as well.
Alan Ruttenburg
Daniel Schober
Frank Gibson
@@ -11156,7 +11156,7 @@
molecular crosslinker
Stratalinker
- A device that is able to chemically join two or more molecules.
+ A device that is able to chemically join two or more molecules.
AL: if we intend that other ontologies can be used in conjunction with OBI, we shouldn't have such a general term used specifically for chemically joining two or more molecules. I'm sure there are other "crosslinkers" that are on a much different scale in engineering etc. I have moved the original label to be an alternative term, and have renamed the main label accordingly.
Trish Whetzel
molecular crosslinker
@@ -11197,7 +11197,7 @@
image cytometer
The most common current application of image cytometry is for DNA analysis, followed by quantitation of immunohistochemical staining.
- An image_cytometer is an instrument for image-based study or measurement of cells.
+ An image_cytometer is an instrument for image-based study or measurement of cells.
Melanie Courtot
http://web.mit.edu/solab/Research/ImageCytometry.html
image cytometer
@@ -11235,7 +11235,7 @@
cytometer
- A cytometer is an instrument for counting and/or measuring characteristics of cells.
+ A cytometer is an instrument for counting and/or measuring characteristics of cells.
Melanie Courtot
http://medical.merriam-webster.com/medical/cytometer
cytometer
@@ -11262,7 +11262,7 @@
gel tank
CHEF gel box, slab gel box, capillary electrophoresis
- A device which holds a gel and running buffers to allow electrophoresis to be performed. A gel tank has the function to contain and to control the contained environment and transfer energy from an energy supply through the running buffers to the gel matrix and the material with charged molecules in an electric field across a porous matrix or medium with the objective to separate the charged molecules.
+ A device which holds a gel and running buffers to allow electrophoresis to be performed. A gel tank has the function to contain and to control the contained environment and transfer energy from an energy supply through the running buffers to the gel matrix and the material with charged molecules in an electric field across a porous matrix or medium with the objective to separate the charged molecules.
Person:Frank Gibson
Person:Kevin Clancy
electrophoresis box
@@ -11286,7 +11286,7 @@
power supply
A AC/DC transformer that generates the reqired power for an electrophoresis apparatus
- A power supply is an device or part of a device that permits the required application of a defined electrical charge to an instrument. The power supply may permit the defined application of a given amount of current for a defined length of time.
+ A power supply is an device or part of a device that permits the required application of a defined electrical charge to an instrument. The power supply may permit the defined application of a given amount of current for a defined length of time.
Daniel Schober
Frank Gibson
PSU
@@ -11308,7 +11308,7 @@
fluorometer
laser/detector in capillary electrophoresis apparatus, NanoDrop ND-3300
- A fluorometer is an instrument for the detection and measurement of parameters of fluoresence, which in turn are used to identify the presence and amount of specific molecules in the sample.
+ A fluorometer is an instrument for the detection and measurement of parameters of fluoresence, which in turn are used to identify the presence and amount of specific molecules in the sample.
Allyson Lister
Kevin Lister
OBI
@@ -11341,7 +11341,7 @@
multispectral imaging flow cytometer
- A multispectral_imaging_flow_cytometer is an instrument which combines quantitative image analysis and flow cytometry in a single platform. It measures the amount, location and movement of molecules on, in, or between cells, and the location and co-localization of multiple markers on or in cells. It can also quantitate morphologically distinct cell subpopulations.
+ A multispectral_imaging_flow_cytometer is an instrument which combines quantitative image analysis and flow cytometry in a single platform. It measures the amount, location and movement of molecules on, in, or between cells, and the location and co-localization of multiple markers on or in cells. It can also quantitate morphologically distinct cell subpopulations.
Melanie Courtot
MIFC
http://www.amnis.com/
@@ -11357,7 +11357,7 @@
microarray
An affymetrix U133 array is a microarray. Microarrays include 1 and 2-color arrays, custom and commercial arrays (e.g, Affymetrix, Agilent, Nimblegen, Illumina, etc.) for expression profiling, DNA variant detection, protein binding, and other genomic and functional genomic assays.
- A processed material that is made to be used in an analyte assay. It consists of a physical immobilisation matrix in which substances that bind the analyte are placed in regular spatial position.
+ A processed material that is made to be used in an analyte assay. It consists of a physical immobilisation matrix in which substances that bind the analyte are placed in regular spatial position.
Daniel Schober
PERSON: Chris Stoeckert
microarray
@@ -11372,7 +11372,7 @@
DNA microarray
Moran G, Stokes C, Thewes S, Hube B, Coleman DC, Sullivan D (2004). "Comparative genomics using Candida albicans DNA microarrays reveals absence and divergence of virulence-associated genes in Candida dubliniensis". Microbiology 150: 3363-3382. doi:10.1099/mic.0.27221-0. PMID 15470115
- A DNA-microarray is a microarray that is used as a physical 2D immobilisation matrix for DNA sequences. DNA microarray-bound DNA fragments are used as targets for a hybridising probed sample.
+ A DNA-microarray is a microarray that is used as a physical 2D immobilisation matrix for DNA sequences. DNA microarray-bound DNA fragments are used as targets for a hybridising probed sample.
PERSON: Daniel Schober
PERSON: Frank Gibson
DNA Chip
@@ -11390,7 +11390,7 @@
protein microarray
The most common protein microarray is the antibody microarray, where antibodies are spotted onto the protein chip and are used as capture molecules to detect proteins from cell lysate solutions.
- A protein-microarray is a microarray, ususlly a piece of glass, on which different molecules of protein have been affixed at separate locations in an ordered manner. These are used to identify protein-protein or protein-small molecule interactions.
+ A protein-microarray is a microarray, ususlly a piece of glass, on which different molecules of protein have been affixed at separate locations in an ordered manner. These are used to identify protein-protein or protein-small molecule interactions.
Daniel Schober
PERSON: Daniel Schober
protein microarray
@@ -11410,7 +11410,7 @@
droplet sorter
- A droplet sorter is part_of a flow cytometer sorter that converts the carrier fluid stream into individual droplets, and these droplets are directed into separate locations for recovery (enriching the original sample for particles of interest based on qualities determined by gating) or disposal.
+ A droplet sorter is part_of a flow cytometer sorter that converts the carrier fluid stream into individual droplets, and these droplets are directed into separate locations for recovery (enriching the original sample for particles of interest based on qualities determined by gating) or disposal.
OBI Instrument branch
OBI Instrument branch
droplet sorter
@@ -11425,7 +11425,7 @@
water bath
A water bath was used to allow for cell incubation at 38 degree centigrade for 8 hours.
- A water bath is a temperature control bath in which a water acts as contact medium enabling temperature transfer from the heating element or cooling element to the sample. The temperature can be controlled in the 0 to 100 degree centigrade range (under normal pressure).
+ A water bath is a temperature control bath in which a water acts as contact medium enabling temperature transfer from the heating element or cooling element to the sample. The temperature can be controlled in the 0 to 100 degree centigrade range (under normal pressure).
Daniel Schober
PERSON: Daniel Schober
water bath
@@ -11440,7 +11440,7 @@
oil bath
An oil bath was used to allow for fast reaction of two chemical compounds during a 2 hour period.
- An oil bath is a temperature control bath in which oil acts as contact medium for the temperature transfer (from heating or cooling elements to the sample).
+ An oil bath is a temperature control bath in which oil acts as contact medium for the temperature transfer (from heating or cooling elements to the sample).
Daniel Schober
PERSON: Daniel Schober
oil bath
@@ -11461,7 +11461,7 @@
digital-to-analog converter
A digital-to-analog_converter is used to convert a computergenerated discrete signal into a continuous analog one, e.g. a sound.
- A digital-to-analog_converter is an instrument that converts a finite resolution digital signal into an infinite resolution analog signal.
+ A digital-to-analog_converter is an instrument that converts a finite resolution digital signal into an infinite resolution analog signal.
Daniel Schober
PERSON: Daniel Schober
digital-to-analog converter
@@ -11488,7 +11488,7 @@
microtome
PMID: 9974145.Serial sectioning of thick tissue with a novel vibrating blade microtome. Brain Res Brain Res Protoc. 1999 Jan;3(3):302-7.
- A microtome is a mechanical instrument used to cut biological specimens into very thin segments for further treatment (e.g. ISH) and ultimately microscopic or histologic examination. Most microtomes provide cooling facilities (cryo-microtome) and use a steel blade to cut a slice of defined thickness. Some are automatic, and some are driven by hand.
+ A microtome is a mechanical instrument used to cut biological specimens into very thin segments for further treatment (e.g. ISH) and ultimately microscopic or histologic examination. Most microtomes provide cooling facilities (cryo-microtome) and use a steel blade to cut a slice of defined thickness. Some are automatic, and some are driven by hand.
PERSON: Phillippe Rocca-Serra
PERSON: Daniel Schober
microtome
@@ -11515,7 +11515,7 @@
microscope
PMID:18466942. A light and transmission electron microscope study of hepatic portal tracts in the rhesus monkey (Macacus rhesus). Tissue Cell. 2008 May 6
- A microscope is an instrument which magnifies the view on objects (too small to be viewed by the naked eye) under increased resolution. A microscope can be an optical instrument but also and electronic instrument. There are various kind of optical microscopes, e.g confocal microscope, epifluoresence microscope)
+ A microscope is an instrument which magnifies the view on objects (too small to be viewed by the naked eye) under increased resolution. A microscope can be an optical instrument but also and electronic instrument. There are various kind of optical microscopes, e.g confocal microscope, epifluoresence microscope)
PERSON: Phillippe Rocca-Serra
wikipedia
microscope
@@ -11536,7 +11536,7 @@
microscope slide
PMID: 9668975.Microscope slide for enhanced analysis of DNA damage using the comet assay.
- A microscope slide is a device usually made of glass which is used as a solid matrix for (biological) material deposited on its surface and which is compatible for use with a microscope instrument
+ A microscope slide is a device usually made of glass which is used as a solid matrix for (biological) material deposited on its surface and which is compatible for use with a microscope instrument
PERSON: Phillippe Rocca-Serra
OBI biomaterial branch
microscope slide
@@ -11557,7 +11557,7 @@
animal cage
PMID: 18246864.Barthold SW.Effects of cage density on behavior in young adult mice.
- A processed material which has the function to define a bounded habitat which is amenable to keeping animals.
+ A processed material which has the function to define a bounded habitat which is amenable to keeping animals.
PERSON: Phillippe Rocca-Serra
laboratory cage
OBI biomaterial branch
diff --git a/src/ontology/modules/epitope-assays.owl b/src/ontology/modules/epitope-assays.owl
index 15c3a55c..04366946 100644
--- a/src/ontology/modules/epitope-assays.owl
+++ b/src/ontology/modules/epitope-assays.owl
@@ -865,7 +865,7 @@
- An enzyme-linked immunospot assay that detects transforming growth factor-beta production by T cells.
+ An enzyme-linked immunospot assay that detects transforming growth factor-beta production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
TGFb release|ELISPOT
@@ -903,7 +903,7 @@
- A cytometric bead array assay that detects IP-10 production by T cells.
+ A cytometric bead array assay that detects IP-10 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CXCL10/IP-10 release|cytometric bead array
@@ -941,7 +941,7 @@
- A T cell epitope specific cytokine production assay that detects interleukin-27 production by T cells.
+ A T cell epitope specific cytokine production assay that detects interleukin-27 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-27 release|biological activity
@@ -979,7 +979,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects transforming growth factor-beta production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects transforming growth factor-beta production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
TGFb release|RNA/DNA detection
@@ -1017,7 +1017,7 @@
- An enzyme-linked immunospot assay that detects granulocyte macrophage colony stimulating factor production by T cells.
+ An enzyme-linked immunospot assay that detects granulocyte macrophage colony stimulating factor production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
GM-CSF release|ELISPOT
@@ -1055,7 +1055,7 @@
- A T cell epitope specific cytokine production assay that detects interleukin-10 production by T cells.
+ A T cell epitope specific cytokine production assay that detects interleukin-10 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-10 release|biological activity
@@ -1093,7 +1093,7 @@
- A cytometric bead array assay that detects transforming growth factor-beta production by T cells
+ A cytometric bead array assay that detects transforming growth factor-beta production by T cells
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
TGFb release|cytometric bead array
@@ -1131,7 +1131,7 @@
- A flow cytometry assay that detects epitope specific perforin release by T cells.
+ A flow cytometry assay that detects epitope specific perforin release by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
perforin release|intracellular staining
@@ -1169,7 +1169,7 @@
- A reporter cell line analyte detection bioassay that detects interleukin-2 production by T cells.
+ A reporter cell line analyte detection bioassay that detects interleukin-2 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-2 release|bioassay
@@ -1207,7 +1207,7 @@
- A T cell epitope specific cytokine production assay that detects interleukin-22 production by T cells.
+ A T cell epitope specific cytokine production assay that detects interleukin-22 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-22 release|biological activity
@@ -1245,7 +1245,7 @@
- A T cell epitope specific cytokine production assay that detects interleukin-8 production by T cells.
+ A T cell epitope specific cytokine production assay that detects interleukin-8 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-8 release|biological activity
@@ -1283,7 +1283,7 @@
- A reporter cell line analyte detection bioassay that detects interleukin-10 production by T cells.
+ A reporter cell line analyte detection bioassay that detects interleukin-10 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-10 release|bioassay
@@ -1321,7 +1321,7 @@
- An enzyme-linked immunosorbent assay that detects RANTES production by T cells.
+ An enzyme-linked immunosorbent assay that detects RANTES production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL5/RANTES release|ELISA
@@ -1359,7 +1359,7 @@
- A cytometric bead array assay that detects interleukin-1 beta production by T cells.
+ A cytometric bead array assay that detects interleukin-1 beta production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-1b release|cytometric bead array
@@ -1397,7 +1397,7 @@
- An enzyme-linked immunospot assay that detects interleukin-6 production by T cells
+ An enzyme-linked immunospot assay that detects interleukin-6 production by T cells
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-6 release|ELISPOT
@@ -1459,7 +1459,7 @@
- A T cell epitope specific helper activity assay that detects the ability of a T cell epitope to enhance an antibody response.
+ A T cell epitope specific helper activity assay that detects the ability of a T cell epitope to enhance an antibody response.
IEDB
IEDB
antibody help|in vivo assay
@@ -1500,7 +1500,7 @@
- A surface plasmon resonance binding assay that measures the dissociation constant [KD] of an epitope:MHC complex binding with a T cell receptor.
+ A surface plasmon resonance binding assay that measures the dissociation constant [KD] of an epitope:MHC complex binding with a T cell receptor.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
dissociation constant KD|surface plasmon resonance (SPR)|nM
@@ -1538,7 +1538,7 @@
- A T cell epitope specific cytokine production assay that detects interleukin-5 production by T cells.
+ A T cell epitope specific cytokine production assay that detects interleukin-5 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-5 release|biological activity
@@ -1576,7 +1576,7 @@
- An enzyme-linked immunosorbent assay that detects transforming growth factor-beta production by T cells.
+ An enzyme-linked immunosorbent assay that detects transforming growth factor-beta production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
TGFb release|ELISA
@@ -1614,7 +1614,7 @@
- A T cell epitope specific cytokine production assay that detects RANTES production by T cells.
+ A T cell epitope specific cytokine production assay that detects RANTES production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL5/RANTES release|biological activity
@@ -1652,7 +1652,7 @@
- A T cell epitope specific cytokine production assay that detects granulocyte macrophage colony stimulating factor production by T cells.
+ A T cell epitope specific cytokine production assay that detects granulocyte macrophage colony stimulating factor production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
GM-CSF release|biological activity
@@ -1690,7 +1690,7 @@
- An enzyme-linked immunosorbent assay that detects interleukin-22 production by T cells.
+ An enzyme-linked immunosorbent assay that detects interleukin-22 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-22 release|ELISA
@@ -1728,7 +1728,7 @@
- A T cell epitope specific cytokine production assay that detects interleukin-21 production by T cells.
+ A T cell epitope specific cytokine production assay that detects interleukin-21 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-21 release|biological activity
@@ -1766,7 +1766,7 @@
- An enzyme-linked immunosorbent assay that detects interleukin-9 production by T cells.
+ An enzyme-linked immunosorbent assay that detects interleukin-9 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-9 release|ELISA
@@ -1804,7 +1804,7 @@
- A flow cytometry assay that detects interleukin-6 production by T cells.
+ A flow cytometry assay that detects interleukin-6 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-6 release|ICS
@@ -1842,7 +1842,7 @@
- A reporter cell line analyte detection bioassay that detects interleukin-4 production by T cells.
+ A reporter cell line analyte detection bioassay that detects interleukin-4 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-4 release|bioassay
@@ -1880,7 +1880,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects tumor necrosis factor alpha production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects tumor necrosis factor alpha production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
TNFa release|RNA/DNA detection
@@ -1918,7 +1918,7 @@
- A cytometric bead array assay that detects monocyte chemotactic protein-1 production by T cells.
+ A cytometric bead array assay that detects monocyte chemotactic protein-1 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL2/MCP-1 release|cytometric bead array
@@ -1956,7 +1956,7 @@
- An enzyme-linked immunosorbent assay that detects interleukin-23 production by T cells.
+ An enzyme-linked immunosorbent assay that detects interleukin-23 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-23 release|ELISA
@@ -1994,7 +1994,7 @@
- A detection of specific nucleic acids with complementary probes assay that detects epitope specific perforin release by T cells.
+ A detection of specific nucleic acids with complementary probes assay that detects epitope specific perforin release by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
perforin release|RNA/DNA detection
@@ -2032,7 +2032,7 @@
- An enzyme-linked immunosorbent assay that detects tumor necrosis factor superfamily cytokine production by T cells.
+ An enzyme-linked immunosorbent assay that detects tumor necrosis factor superfamily cytokine production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
TNF release|ELISA
@@ -2070,7 +2070,7 @@
- A T cell epitope specific cytokine production assay that detects interleukin-13 production by T cells.
+ A T cell epitope specific cytokine production assay that detects interleukin-13 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-13 release|biological activity
@@ -2108,7 +2108,7 @@
- A T cell epitope specific cytokine production assay that detects interleukin-9 production by T cells.
+ A T cell epitope specific cytokine production assay that detects interleukin-9 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-9 release|biological activity
@@ -2146,7 +2146,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects interleukin-5 production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects interleukin-5 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-5 release|RNA/DNA detection
@@ -2184,7 +2184,7 @@
- An enzyme-linked immunosorbent assay that detects interleukin-3 production by T cells.
+ An enzyme-linked immunosorbent assay that detects interleukin-3 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-3 release|ELISA
@@ -2222,7 +2222,7 @@
- An enzyme-linked immunosorbent assay that detects interleukin-1 alpha production by T cells.
+ An enzyme-linked immunosorbent assay that detects interleukin-1 alpha production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-1a release|ELISA
@@ -2284,7 +2284,7 @@
- A T cell epitope specific helper activity assay that detects the ability of a T cell epitope to enhance a T cell response.
+ A T cell epitope specific helper activity assay that detects the ability of a T cell epitope to enhance a T cell response.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
T cell help|in vivo assay
@@ -2322,7 +2322,7 @@
- A T cell epitope specific cytokine production assay that detects transforming growth factor-beta production by T cells.
+ A T cell epitope specific cytokine production assay that detects transforming growth factor-beta production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
TGFb release|biological activity
@@ -2360,7 +2360,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects interleukin-12 production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects interleukin-12 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-12 release|RNA/DNA detection
@@ -2401,7 +2401,7 @@
- A T cell epitope dependent biological activity assay that detects cytotoxic T cell degranulation.
+ A T cell epitope dependent biological activity assay that detects cytotoxic T cell degranulation.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
degranulation|biological activity
@@ -2439,7 +2439,7 @@
- A reporter cell line analyte detection bioassay that detects transforming growth factor-beta production by T cells.
+ A reporter cell line analyte detection bioassay that detects transforming growth factor-beta production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
TGFb release|bioassay
@@ -2477,7 +2477,7 @@
- An enzyme-linked immunospot assay that detects tumor necrosis factor superfamily cytokine production by T cells.
+ An enzyme-linked immunospot assay that detects tumor necrosis factor superfamily cytokine production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
TNF release|ELISPOT
@@ -2515,7 +2515,7 @@
- A reporter cell line analyte detection bioassay that detects interleukin-5 production by T cells.
+ A reporter cell line analyte detection bioassay that detects interleukin-5 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-5 release|bioassay
@@ -2553,7 +2553,7 @@
- A T cell epitope specific cytokine production assay that detects production of chemokine (C-C motif) ligand 1 by T cells.
+ A T cell epitope specific cytokine production assay that detects production of chemokine (C-C motif) ligand 1 by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL1/TCA-3 release|biological activity
@@ -2591,7 +2591,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects interleukin-2 production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects interleukin-2 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-2 release|RNA/DNA detection
@@ -2629,7 +2629,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects interleukin-22 production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects interleukin-22 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-22 release|RNA/DNA detection
@@ -2667,7 +2667,7 @@
- A T cell epitope specific cytokine production assay that detects interleukin-16 production by T cells.
+ A T cell epitope specific cytokine production assay that detects interleukin-16 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-16 release|biological activity
@@ -2705,7 +2705,7 @@
- An enzyme-linked immunosorbent assay that detects IP-10 production by T cells.
+ An enzyme-linked immunosorbent assay that detects IP-10 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CXCL10/IP-10 release|ELISA
@@ -2743,7 +2743,7 @@
- An enzyme-linked immunosorbent assay that detects interleukin-15 production by T cells.
+ An enzyme-linked immunosorbent assay that detects interleukin-15 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-15 release|ELISA
@@ -2781,7 +2781,7 @@
- A cytometric bead array assay that detects interleukin-12 production by T cells.
+ A cytometric bead array assay that detects interleukin-12 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-12 release|cytometric bead array
@@ -2819,7 +2819,7 @@
- An enzyme-linked immunosorbent assay that detects lymphotoxin A production by T cells.
+ An enzyme-linked immunosorbent assay that detects lymphotoxin A production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
lymphotoxin A/TNFb release|ELISA
@@ -2857,7 +2857,7 @@
- A cytometric bead array assay that detects interleukin-5 production by T cells.
+ A cytometric bead array assay that detects interleukin-5 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-5 release|cytometric bead array
@@ -2895,7 +2895,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects interleukin-17 production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects interleukin-17 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-17 release|RNA/DNA detection
@@ -2933,7 +2933,7 @@
- A T cell epitope specific cytokine production assay that detects interleukin-15 production by T cells.
+ A T cell epitope specific cytokine production assay that detects interleukin-15 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-15 release|biological activity
@@ -2971,7 +2971,7 @@
- A T cell epitope specific cytokine production assay that detects interleukin-17 production by T cells.
+ A T cell epitope specific cytokine production assay that detects interleukin-17 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-17 release|biological activity
@@ -3009,7 +3009,7 @@
- A cytometric bead array assay that detects interleukin-17 production by T cells.
+ A cytometric bead array assay that detects interleukin-17 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-17 release|cytometric bead array
@@ -3047,7 +3047,7 @@
- A cytometric bead array assay that detects interleukin-10 production by T cells.
+ A cytometric bead array assay that detects interleukin-10 production by T cells.
IEDB
IEDB
IL-10 release|cytometric bead array
@@ -3085,7 +3085,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects interleukin-21 production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects interleukin-21 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-21 release|RNA/DNA detection
@@ -3123,7 +3123,7 @@
- A flow cytometry assay that detects interleukin-5 production by T cells.
+ A flow cytometry assay that detects interleukin-5 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-5 release|ICS
@@ -3161,7 +3161,7 @@
- A cytometric bead array assay that detects interleukin-2 production by T cells.
+ A cytometric bead array assay that detects interleukin-2 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-2 release|cytometric bead array
@@ -3199,7 +3199,7 @@
- A reporter cell line analyte detection bioassay that detects interleukin-16 production by T cells.
+ A reporter cell line analyte detection bioassay that detects interleukin-16 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-16 release|bioassay
@@ -3237,7 +3237,7 @@
- An enzyme-linked immunosorbent assay that detects macrophage inflammatory protein-1 alpha production by T cells.
+ An enzyme-linked immunosorbent assay that detects macrophage inflammatory protein-1 alpha production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL3/MIP-1a release|ELISA
@@ -3275,7 +3275,7 @@
- A flow cytometry assay that detects granulocyte macrophage colony stimulating factor production by T cells.
+ A flow cytometry assay that detects granulocyte macrophage colony stimulating factor production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
GM-CSF release|ICS
@@ -3313,7 +3313,7 @@
- A T cell epitope specific cytokine production assay that detects IP-10 production by T cells.
+ A T cell epitope specific cytokine production assay that detects IP-10 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CXCL10/IP-10 release|biological activity
@@ -3351,7 +3351,7 @@
- A flow cytometry assay that detects interleukin-13 production by T cells.
+ A flow cytometry assay that detects interleukin-13 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-13 release|ICS
@@ -3392,7 +3392,7 @@
- A X-ray crystallography 3D molecular structure determination assay that characterizes the 3-dimensional molecular structure of a T cell epitope:MHC:TCR complex.
+ A X-ray crystallography 3D molecular structure determination assay that characterizes the 3-dimensional molecular structure of a T cell epitope:MHC:TCR complex.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
3D structure|x-ray crystallography|angstroms
@@ -3430,7 +3430,7 @@
- An enzyme-linked immunosorbent assay that detects chemokine (C-C motif) ligand 1 production by T cells.
+ An enzyme-linked immunosorbent assay that detects chemokine (C-C motif) ligand 1 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL1/TCA-3 release|ELISA
@@ -3460,7 +3460,7 @@
- A flow cytometry assay that measures the cell-cell binding of an epitope:MHC complex binding with a T cell receptor.
+ A flow cytometry assay that measures the cell-cell binding of an epitope:MHC complex binding with a T cell receptor.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
T cell- APC binding|binding assay
@@ -3498,7 +3498,7 @@
- A reporter cell line analyte detection bioassay that detects interferon-gamma production by T cells.
+ A reporter cell line analyte detection bioassay that detects interferon-gamma production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IFNg release|bioassay
@@ -3536,7 +3536,7 @@
- An enzyme-linked immunospot assay that detects epitope specific granzyme B release by T cells.
+ An enzyme-linked immunospot assay that detects epitope specific granzyme B release by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
granzyme B release|ELISPOT
@@ -3598,7 +3598,7 @@
- An efficacy of T cell epitope intervention experiment that uses a tolerance induction intervention experiment.
+ An efficacy of T cell epitope intervention experiment that uses a tolerance induction intervention experiment.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
tolerance|in vivo assay
@@ -3636,7 +3636,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects RANTES production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects RANTES production by T cells.
IEDB
IEDB
CCL5/RANTES release|RNA/DNA detection
@@ -3674,7 +3674,7 @@
- A cytometric bead array assay that detects interleukin-4 production by T cells
+ A cytometric bead array assay that detects interleukin-4 production by T cells
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-4 release|cytometric bead array
@@ -3712,7 +3712,7 @@
- A T cell epitope specific cytokine production assay that detects lymphotoxin A production by T cells.
+ A T cell epitope specific cytokine production assay that detects lymphotoxin A production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
lymphotoxin A/TNFb release|biological activity
@@ -3750,7 +3750,7 @@
- An enzyme-linked immunosorbent assay that detects chemokine (C-X-C motif) ligand 9 production by T cells.
+ An enzyme-linked immunosorbent assay that detects chemokine (C-X-C motif) ligand 9 production by T cells.
IEDB
IEDB
CXCL9/MIG release|ELISA
@@ -3788,7 +3788,7 @@
- A T cell epitope specific cytokine production assay that detects macrophage inflammatory protein-1 alpha production by T cells.
+ A T cell epitope specific cytokine production assay that detects macrophage inflammatory protein-1 alpha production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL3/MIP-1a release|biological activity
@@ -3826,7 +3826,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects interleukin-4 production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects interleukin-4 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-4 release|RNA/DNA detection
@@ -3864,7 +3864,7 @@
- A reporter cell line analyte detection bioassay that detects granulocyte macrophage colony stimulating factor production by T cells.
+ A reporter cell line analyte detection bioassay that detects granulocyte macrophage colony stimulating factor production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
GM-CSF release|bioassay
@@ -3902,7 +3902,7 @@
- A flow cytometry assay that detects interleukin-21 production by T cells.
+ A flow cytometry assay that detects interleukin-21 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-21 release|ICS
@@ -3940,7 +3940,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects monocyte chemotactic protein-1 production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects monocyte chemotactic protein-1 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL2/MCP-1 release|RNA/DNA detection
@@ -3978,7 +3978,7 @@
- An enzyme-linked immunosorbent assay that detects monocyte chemotactic protein-1 production by T cells.
+ An enzyme-linked immunosorbent assay that detects monocyte chemotactic protein-1 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL2/MCP-1 release|ELISA
@@ -4016,7 +4016,7 @@
- A T cell epitope specific cytokine production assay that detects chemokine (C-C motif) ligand 4 production by T cells.
+ A T cell epitope specific cytokine production assay that detects chemokine (C-C motif) ligand 4 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL4/MIP-1b release|biological activity
@@ -4054,7 +4054,7 @@
- An enzyme-linked immunosorbent assay that detects interleukin-21 production by T cells.
+ An enzyme-linked immunosorbent assay that detects interleukin-21 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-21 release|ELISA
@@ -4116,7 +4116,7 @@
- An efficacy of T cell epitope intervention experiment that detects epitope specific type IV hypersensitivity.
+ An efficacy of T cell epitope intervention experiment that detects epitope specific type IV hypersensitivity.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
type IV hypersensitivity (DTH)|in vivo skin test
@@ -4154,7 +4154,7 @@
- A cytometric bead array assay that detects interleukin-13 production by T cells.
+ A cytometric bead array assay that detects interleukin-13 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-13 release|cytometric bead array
@@ -4192,7 +4192,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects interferon-gamma production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects interferon-gamma production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IFNg release|RNA/DNA detection
@@ -4230,7 +4230,7 @@
- A cytometric bead array assay that detects tumor necrosis factor alpha production by T cells.
+ A cytometric bead array assay that detects tumor necrosis factor alpha production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
TNFa release|cytometric bead array
@@ -4268,7 +4268,7 @@
- An enzyme-linked immunospot assay that detects interleukin-17 production by T cells.
+ An enzyme-linked immunospot assay that detects interleukin-17 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-17 release|ELISPOT
@@ -4306,7 +4306,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects interferon-beta production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects interferon-beta production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IFNb release|RNA/DNA detection
@@ -4344,7 +4344,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects granulocyte macrophage colony stimulating factor production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects granulocyte macrophage colony stimulating factor production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
GM-CSF release|RNA/DNA detection
@@ -4382,7 +4382,7 @@
- An enzyme-linked immunosorbent assay that detects interleukin-8 production by T cells.
+ An enzyme-linked immunosorbent assay that detects interleukin-8 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-8 release|ELISA
@@ -4420,7 +4420,7 @@
- A cytometric bead array assay that detects interleukin-6 production by T cells.
+ A cytometric bead array assay that detects interleukin-6 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-6 release|cytometric bead array
@@ -4458,7 +4458,7 @@
- A T cell epitope specific cytokine production assay that detects interleukin-23 production by T cells.
+ A T cell epitope specific cytokine production assay that detects interleukin-23 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-23 release|biological activity
@@ -4496,7 +4496,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects interleukin-10 production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects interleukin-10 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-10 release|RNA/DNA detection
@@ -4534,7 +4534,7 @@
- A cytometric bead array assay that detects tumor necrosis factor superfamily cytokine production by T cells.
+ A cytometric bead array assay that detects tumor necrosis factor superfamily cytokine production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
TNF release|cytometric bead array
@@ -4572,7 +4572,7 @@
- A flow cytometry assay that detects chemokine (C-C motif) ligand 4 production by T cells.
+ A flow cytometry assay that detects chemokine (C-C motif) ligand 4 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL4/MIP-1b release|ICS
@@ -4610,7 +4610,7 @@
- A flow cytometry assay that detects interleukin-3 production by T cells.
+ A flow cytometry assay that detects interleukin-3 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-3 release|ICS
@@ -4648,7 +4648,7 @@
- An enzyme-linked immunosorbent assay that detects chemokine (C-C motif) ligand 4 production by T cells.
+ An enzyme-linked immunosorbent assay that detects chemokine (C-C motif) ligand 4 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL4/MIP-1b release|ELISA
@@ -4686,7 +4686,7 @@
- A cytometric bead array assay that detects interferon-gamma production by T cells.
+ A cytometric bead array assay that detects interferon-gamma production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IFNg release|cytometric bead array
@@ -4724,7 +4724,7 @@
- A T cell epitope specific cytokine production assay that detects interleukin-18 production by T cells.
+ A T cell epitope specific cytokine production assay that detects interleukin-18 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-18 release|biological activity
@@ -4762,7 +4762,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects interleukin-27 production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects interleukin-27 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-27 release|RNA/DNA detection
@@ -4800,7 +4800,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects IP-10 production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects IP-10 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CXCL10/IP-10 release|RNA/DNA detection
@@ -4838,7 +4838,7 @@
- A reporter cell line analyte detection bioassay that detects interleukin-3 production by T cells.
+ A reporter cell line analyte detection bioassay that detects interleukin-3 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-3 release|bioassay
@@ -4876,7 +4876,7 @@
- A flow cytometry assay that detects tumor necrosis factor superfamily cytokine production by T cells.
+ A flow cytometry assay that detects tumor necrosis factor superfamily cytokine production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
TNF release|ICS
@@ -4914,7 +4914,7 @@
- A T cell epitope specific cytokine production assay that detects interleukin-1 alpha production by T cells.
+ A T cell epitope specific cytokine production assay that detects interleukin-1 alpha production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-1a release|biological activity
@@ -4952,7 +4952,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects interleukin-6 production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects interleukin-6 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-6 release|RNA/DNA detection
@@ -4990,7 +4990,7 @@
- A T cell epitope specific cytokine production assay that detects interferon-beta production by T cells.
+ A T cell epitope specific cytokine production assay that detects interferon-beta production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IFNb release|biological activity
@@ -5028,7 +5028,7 @@
- A T cell epitope specific cytokine production assay that detects interleukin-12 production by T cells.
+ A T cell epitope specific cytokine production assay that detects interleukin-12 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-12 release|biological activity
@@ -5090,7 +5090,7 @@
- An in vivo cell killing assay that measures the killing of antigen presenting cells (APC) by T cells whose TCR recognizes an epitope presented by the APC.
+ An in vivo cell killing assay that measures the killing of antigen presenting cells (APC) by T cells whose TCR recognizes an epitope presented by the APC.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
cytotoxicity|in vivo assay
@@ -5128,7 +5128,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects interleukin-23 production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects interleukin-23 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-23 release|RNA/DNA detection
@@ -5166,7 +5166,7 @@
- A cytometric bead array assay that detects granulocyte colony stimulating factor production by T cells.
+ A cytometric bead array assay that detects granulocyte colony stimulating factor production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
G-CSF release|cytometric bead array
@@ -5204,7 +5204,7 @@
- A T cell epitope specific cytokine production assay that detects tumor necrosis factor superfamily cytokine production by T cells.
+ A T cell epitope specific cytokine production assay that detects tumor necrosis factor superfamily cytokine production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
TNF release|biological activity
@@ -5242,7 +5242,7 @@
- A promoter activity detection by reporter gene assay that detects interleukin-2 production by T cells.
+ A promoter activity detection by reporter gene assay that detects interleukin-2 production by T cells.
IEDB
IEDB
IL-2 release|reporter gene assay
@@ -5280,7 +5280,7 @@
- A cytometric bead array assay that detects macrophage inflammatory protein-1 alpha production by T cells.
+ A cytometric bead array assay that detects macrophage inflammatory protein-1 alpha production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL3/MIP-1a release|cytometric bead array
@@ -5318,7 +5318,7 @@
- A T cell epitope specific cytokine production assay that detects interleukin-3 production by T cells.
+ A T cell epitope specific cytokine production assay that detects interleukin-3 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-3 release|biological activity
@@ -5356,7 +5356,7 @@
- A T cell epitope dependent biological activity assay that detects T cell activation.
+ A T cell epitope dependent biological activity assay that detects T cell activation.
IEDB
IEDB
activation|biological activity
@@ -5394,7 +5394,7 @@
- A cytometric bead array assay that detects RANTES production by T cells.
+ A cytometric bead array assay that detects RANTES production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL5/RANTES release|cytometric bead array
@@ -5432,7 +5432,7 @@
- A reporter cell line analyte detection bioassay that detects interleukin-6 production by T cells.
+ A reporter cell line analyte detection bioassay that detects interleukin-6 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-6 release|bioassay
@@ -5470,7 +5470,7 @@
- A T cell epitope specific cytokine production assay that detects interferon-gamma production by T cells.
+ A T cell epitope specific cytokine production assay that detects interferon-gamma production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IFNg release|biological activity
@@ -5508,7 +5508,7 @@
- An assay of epitope specific tumor necrosis factor alpha production by T cells that detects tumor necrosis factor production.
+ An assay of epitope specific tumor necrosis factor alpha production by T cells that detects tumor necrosis factor production.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
TNFa release|biological activity
@@ -5546,7 +5546,7 @@
- A flow cytometry assay that detects epitope specific granzyme B release by T cells
+ A flow cytometry assay that detects epitope specific granzyme B release by T cells
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
granzyme B release|intracellular staining
@@ -5584,7 +5584,7 @@
- A radio immuno assay that detects interferon-gamma production by T cells.
+ A radio immuno assay that detects interferon-gamma production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IFNg release|radio immuno assay (RIA)
@@ -5622,7 +5622,7 @@
- A T cell epitope specific cytotoxic T cell degranulation assay that detects granzyme B release by T cells.
+ A T cell epitope specific cytotoxic T cell degranulation assay that detects granzyme B release by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
granzyme B release|biological activity
@@ -5660,7 +5660,7 @@
- A flow cytometry assay that detects chemokine (C-X-C motif) ligand 9 production by T cells.
+ A flow cytometry assay that detects chemokine (C-X-C motif) ligand 9 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CXCL9/MIG release|ICS
@@ -5698,7 +5698,7 @@
- An enzyme-linked immunosorbent assay that detects macrophage inflammatory protein-1 gamma production by T cells.
+ An enzyme-linked immunosorbent assay that detects macrophage inflammatory protein-1 gamma production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL9/MIP-1g release|ELISA
@@ -5736,7 +5736,7 @@
- A T cell epitope specific cytokine production assay that detects interleukin-2 production by T cells.
+ A T cell epitope specific cytokine production assay that detects interleukin-2 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-2 release|biological activity
@@ -5774,7 +5774,7 @@
- A T cell epitope specific cytokine production assay that detects interleukin-1 beta production by T cells.
+ A T cell epitope specific cytokine production assay that detects interleukin-1 beta production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-1b release|biological activity
@@ -5812,7 +5812,7 @@
- A T cell epitope specific cytokine production assay that detects interleukin-4 production by T cells.
+ A T cell epitope specific cytokine production assay that detects interleukin-4 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-4 release|biological activity
@@ -5850,7 +5850,7 @@
- A T cell epitope specific cytokine production assay that detects interleukin-6 production by T cells.
+ A T cell epitope specific cytokine production assay that detects interleukin-6 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-6 release|biological activity
@@ -5888,7 +5888,7 @@
- A reporter cell line analyte detection bioassay that detects tumor necrosis factor alpha production by T cells.
+ A reporter cell line analyte detection bioassay that detects tumor necrosis factor alpha production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
TNFa release|bioassay
@@ -5926,7 +5926,7 @@
- A flow cytometry assay that detects lymphotoxin A production by T cells.
+ A flow cytometry assay that detects lymphotoxin A production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
lymphotoxin A/TNFb release|ICS
@@ -5964,7 +5964,7 @@
- An enzyme-linked immunospot assay that detects interleukin-5 production by T cells.
+ An enzyme-linked immunospot assay that detects interleukin-5 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-5 release|ELISPOT
@@ -6002,7 +6002,7 @@
- A T cell epitope specific cytokine production assay that detects macrophage inflammatory protein-1 gamma production by T cells.
+ A T cell epitope specific cytokine production assay that detects macrophage inflammatory protein-1 gamma production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL9/MIP-1g release|biological activity
@@ -6040,7 +6040,7 @@
- A cytometric bead array assay that detects interleukin-8 production by T cells.
+ A cytometric bead array assay that detects interleukin-8 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-8 release|cytometric bead array
@@ -6078,7 +6078,7 @@
- A T cell epitope specific cytokine production assay that detects chemokine (C-X-C motif) ligand 9 production by T cells.
+ A T cell epitope specific cytokine production assay that detects chemokine (C-X-C motif) ligand 9 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CXCL9/MIG release|biological activity
@@ -6116,7 +6116,7 @@
- An enzyme-linked immunosorbent assay that detects epitope specific granzyme B release by T cells.
+ An enzyme-linked immunosorbent assay that detects epitope specific granzyme B release by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
granzyme B release|ELISA
@@ -6154,7 +6154,7 @@
- A T cell epitope specific cytokine production assay that detects monocyte chemotactic protein-1 production by T cells.
+ A T cell epitope specific cytokine production assay that detects monocyte chemotactic protein-1 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL2/MCP-1 release|biological activity
@@ -6192,7 +6192,7 @@
- A flow cytometry assay that detects interleukin-12 production by T cells.
+ A flow cytometry assay that detects interleukin-12 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-12 release|ICS
@@ -6249,7 +6249,7 @@
- An efficacy of T cell epitope intervention experiment that uses a disease exacerbation in vivo intervention experiment.
+ An efficacy of T cell epitope intervention experiment that uses a disease exacerbation in vivo intervention experiment.
IEDB
IEDB
disease exacerbation|in vivo assay
@@ -6275,7 +6275,7 @@
- A MHC ligand processing and presentation assay in which the presence of a specific ligand in an eluate is detected using the response of T cells that are known to be monospecific for that ligand as a readout.
+ A MHC ligand processing and presentation assay in which the presence of a specific ligand in an eluate is detected using the response of T cells that are known to be monospecific for that ligand as a readout.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
ligand presentation|T cell recognition
@@ -6340,7 +6340,7 @@
- An in vivo assay measuring T cell epitope specific protection from tumor challenge using tumor burden.
+ An in vivo assay measuring T cell epitope specific protection from tumor challenge using tumor burden.
IEDB
IEDB
tumor burden after challenge|in vivo assay
@@ -6405,7 +6405,7 @@
- An in vivo assay measuring T cell epitope specific protection from pathogen challenge using pathogen burden.
+ An in vivo assay measuring T cell epitope specific protection from pathogen challenge using pathogen burden.
IEDB
IEDB
pathogen burden after challenge|in vivo assay
@@ -6441,7 +6441,7 @@
- A MHC ligand processing and presentation assay that uses a mass spectrometry assay to identify eluted ligands
+ A MHC ligand processing and presentation assay that uses a mass spectrometry assay to identify eluted ligands
IEDB
IEDB
ligand presentation|mass spectrometry
@@ -6479,7 +6479,7 @@
- A flow cytometry assay that detects transforming growth factor-beta production by T cells.
+ A flow cytometry assay that detects transforming growth factor-beta production by T cells.
IEDB
IEDB
TGFb release|ICS
@@ -6536,7 +6536,7 @@
- A T cell epitope dependent biological activity determination assay that uses an in vivo intervention experiment.
+ A T cell epitope dependent biological activity determination assay that uses an in vivo intervention experiment.
IEDB
IEDB
in vivo activity|biological activity
@@ -6574,7 +6574,7 @@
- A mass spectrometry of MHC ligands assay that identifies eluted ligands from cell bound MHC.
+ A mass spectrometry of MHC ligands assay that identifies eluted ligands from cell bound MHC.
IEDB
IEDB
ligand presentation|cellular MHC/mass spectrometry
@@ -6612,7 +6612,7 @@
- A cytometric bead array assay that detects granulocyte macrophage colony stimulating factor production by T cells.
+ A cytometric bead array assay that detects granulocyte macrophage colony stimulating factor production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
GM-CSF release|cytometric bead array
@@ -6694,7 +6694,7 @@
- An in vivo assay measuring T cell epitope specific protection from other challenge using survival.
+ An in vivo assay measuring T cell epitope specific protection from other challenge using survival.
IEDB
IEDB
survival from challenge|in vivo assay
@@ -6769,7 +6769,7 @@
- A cell bound MHC binding assay that uses a T cell epitope recognition assay.
+ A cell bound MHC binding assay that uses a T cell epitope recognition assay.
IEDB
IEDB
qualitative binding|cellular MHC/T cell inhibition
@@ -6831,7 +6831,7 @@
- A T cell epitope dependent biological activity assay that detects the ability of epitope specific helper T cells to enhance either B cell or T cell adaptive immune response function.
+ A T cell epitope dependent biological activity assay that detects the ability of epitope specific helper T cells to enhance either B cell or T cell adaptive immune response function.
IEDB
IEDB
helper response|in vivo assay
@@ -6869,7 +6869,7 @@
- A flow cytometry assay that detects interleukin-22 production by T cells.
+ A flow cytometry assay that detects interleukin-22 production by T cells.
IEDB
IEDB
IL-22 release|ICS
@@ -6907,7 +6907,7 @@
- A T cell epitope specific cytotoxic T cell degranulation assay that detects perforin release by T cells.
+ A T cell epitope specific cytotoxic T cell degranulation assay that detects perforin release by T cells.
IEDB
IEDB
perforin release|biological activity
@@ -6955,7 +6955,7 @@
- A MHC ligand processing and presentation assay in which an HPL chromatography is run to separate an input mixture of ligands eluted from MHC into fractions. These fractions are tested for recognition by T cells and compared to the recognition of a synthetic ligand that is presumed to be the recognized epitope. Identical HPLC fractionation and T cell recognition patterns confirm that the specific ligand was presented by MHC molecules.
+ A MHC ligand processing and presentation assay in which an HPL chromatography is run to separate an input mixture of ligands eluted from MHC into fractions. These fractions are tested for recognition by T cells and compared to the recognition of a synthetic ligand that is presumed to be the recognized epitope. Identical HPLC fractionation and T cell recognition patterns confirm that the specific ligand was presented by MHC molecules.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
ligand presentation|coelution
@@ -7022,7 +7022,7 @@
- An efficacy of T cell epitope intervention experiment that detects a decrease in disease.
+ An efficacy of T cell epitope intervention experiment that detects a decrease in disease.
IEDB
IEDB
decreased disease|in vivo assay
@@ -7052,7 +7052,7 @@
- A MHC ligand processing and presentation assay that uses Edman degradation to identify the eluted ligands
+ A MHC ligand processing and presentation assay that uses Edman degradation to identify the eluted ligands
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
ligand presentation|Edman degradation
@@ -7078,7 +7078,7 @@
- A mass spectrometry of MHC ligands that identifies eluted ligands from secreted MHC.
+ A mass spectrometry of MHC ligands that identifies eluted ligands from secreted MHC.
IEDB
IEDB
ligand presentation|secreted MHC/mass spectrometry
@@ -7116,7 +7116,7 @@
- A cytometric bead array assay that detects interleukin-17A production by T cells.
+ A cytometric bead array assay that detects interleukin-17A production by T cells.
IEDB
IEDB
IL-17A release|cytometric bead array
@@ -7178,7 +7178,7 @@
- A radioactivity detection assay that detects loss of binding of a known reference ligand to purified-MHC due to competition by the ligand under investigation.
+ A radioactivity detection assay that detects loss of binding of a known reference ligand to purified-MHC due to competition by the ligand under investigation.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
qualitative binding|purified MHC/competitive/radioactivity
@@ -7233,7 +7233,7 @@
- A radioactivity detection assay that measures half maximal effective concentration (EC50) to detect the direct binding of a cell-lysate-MHC molecule with a ligand.
+ A radioactivity detection assay that measures half maximal effective concentration (EC50) to detect the direct binding of a cell-lysate-MHC molecule with a ligand.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
half maximal effective concentration (EC50)|lysate MHC/direct/radioactivity|nM
@@ -7302,7 +7302,7 @@
- A radioactivity detection assay that measures half maximal inhibitory concentration (IC50) to detect the loss of binding of a known reference ligand to cell-bound-MHC due to competition by the ligand under investigation.
+ A radioactivity detection assay that measures half maximal inhibitory concentration (IC50) to detect the loss of binding of a known reference ligand to cell-bound-MHC due to competition by the ligand under investigation.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
half maximal inhibitory concentration (IC50)|cellular MHC/competitive/radioactivity|nM
@@ -7348,7 +7348,7 @@
- A fluorescence detection assay that detects direct binding of a cell-lysate-MHC molecule with a ligand.
+ A fluorescence detection assay that detects direct binding of a cell-lysate-MHC molecule with a ligand.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
qualitative binding|lysate MHC/direct/fluorescence
@@ -7417,7 +7417,7 @@
- A fluorescence detection assay that measures half maximal inhibitory concentration (IC50) to detect the loss of binding of a known reference ligand to cell-bound-MHC due to competition by the ligand under investigation.
+ A fluorescence detection assay that measures half maximal inhibitory concentration (IC50) to detect the loss of binding of a known reference ligand to cell-bound-MHC due to competition by the ligand under investigation.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
half maximal inhibitory concentration (IC50)|cellular MHC/competitive/fluorescence|nM
@@ -7455,7 +7455,7 @@
- An enzyme-linked immunosorbent assay that detects granulocyte colony stimulating factor production by T cells.
+ An enzyme-linked immunosorbent assay that detects granulocyte colony stimulating factor production by T cells.
IEDB
IEDB
G-CSF release|ELISA
@@ -7493,7 +7493,7 @@
- A cytometric bead array assay that detects interleukin-17F production by T cells.
+ A cytometric bead array assay that detects interleukin-17F production by T cells.
IEDB
IEDB
IL-17F release|cytometric bead array
@@ -7548,7 +7548,7 @@
- A fluorescence detection assay that measures equilibrium association constant (KA) to detect the direct binding of a cell-bound-MHC molecule with a ligand.
+ A fluorescence detection assay that measures equilibrium association constant (KA) to detect the direct binding of a cell-bound-MHC molecule with a ligand.
IEDB
IEDB
association constant KA|cellular MHC/direct/fluorescence|1/M
@@ -7603,7 +7603,7 @@
- A fluorescence detection assay that measures half life to detect the direct binding of a purified-MHC molecule with a ligand.
+ A fluorescence detection assay that measures half life to detect the direct binding of a purified-MHC molecule with a ligand.
IEDB
IEDB
half life|purified MHC/direct/fluorescence|min
@@ -7641,7 +7641,7 @@
- A cytometric bead array assay that detects interleukin-9 production by T cells.
+ A cytometric bead array assay that detects interleukin-9 production by T cells.
IEDB
IEDB
IL-9 release|cytometric bead array
@@ -7703,7 +7703,7 @@
- A fluorescence detection assay that detects loss of binding of a known reference ligand to purified-MHC due to competition by the ligand under investigation.
+ A fluorescence detection assay that detects loss of binding of a known reference ligand to purified-MHC due to competition by the ligand under investigation.
IEDB
IEDB
qualitative binding|purified MHC/competitive/fluorescence
@@ -7778,7 +7778,7 @@
- A fluorescence detection assay that measures equilibrium dissociation constant (KD) to detect the loss of binding of a known reference ligand to purified-MHC due to competition by the ligand under investigation.
+ A fluorescence detection assay that measures equilibrium dissociation constant (KD) to detect the loss of binding of a known reference ligand to purified-MHC due to competition by the ligand under investigation.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
dissociation constant KD|purified MHC/competitive/fluorescence|nM
@@ -7847,7 +7847,7 @@
- A fluorescence detection assay that measures equilibrium dissociation constant (KD) to detect the loss of binding of a known reference ligand to cell-bound-MHC due to competition by the ligand under investigation.
+ A fluorescence detection assay that measures equilibrium dissociation constant (KD) to detect the loss of binding of a known reference ligand to cell-bound-MHC due to competition by the ligand under investigation.
IEDB
IEDB
dissociation constant KD|cellular MHC/competitive/fluorescence|nM
@@ -7902,7 +7902,7 @@
- A fluorescence detection assay measuring binding on rate (kon) to detect direct binding of a purified-MHC:ligand complex.
+ A fluorescence detection assay measuring binding on rate (kon) to detect direct binding of a purified-MHC:ligand complex.
IEDB
IEDB
on rate|purified MHC/direct/fluorescence|nM^-1s^-1
@@ -7940,7 +7940,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects interleukin-13 production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects interleukin-13 production by T cells.
IEDB
IEDB
IL-13 release|RNA/DNA detection
@@ -7995,7 +7995,7 @@
- A fluorescence detection assay that measures equilibrium dissociation constant (KD) to detect direct binding of a purified-MHC molecule with a ligand and provides EC50 values determined under assay conditions where the EC50 approximates a KD value.
+ A fluorescence detection assay that measures equilibrium dissociation constant (KD) to detect direct binding of a purified-MHC molecule with a ligand and provides EC50 values determined under assay conditions where the EC50 approximates a KD value.
IEDB
IEDB
dissociation constant KD (~EC50)|purified MHC/direct/fluorescence|nM
@@ -8064,7 +8064,7 @@
- A radioactivity detection assay that measures equilibrium dissociation constant (KD) to detect the loss of binding of a known reference ligand to cell-lysate-MHC due to competition by the ligand under investigation.
+ A radioactivity detection assay that measures equilibrium dissociation constant (KD) to detect the loss of binding of a known reference ligand to cell-lysate-MHC due to competition by the ligand under investigation.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
dissociation constant KD|lysate MHC/competitive/radioactivity|nM
@@ -8102,7 +8102,7 @@
- A flow cytometry assay that detects macrophage inflammatory protein-1 alpha production by T cells.
+ A flow cytometry assay that detects macrophage inflammatory protein-1 alpha production by T cells.
IEDB
IEDB
CCL3/MIP-1a release|ICS
@@ -8177,7 +8177,7 @@
- A radioactivity detection assay that measures equilibrium dissociation constant (KD) to detect the loss of binding of a known reference ligand to cell-bound-MHC due to competition by the ligand under investigation.
+ A radioactivity detection assay that measures equilibrium dissociation constant (KD) to detect the loss of binding of a known reference ligand to cell-bound-MHC due to competition by the ligand under investigation.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
dissociation constant KD|cellular MHC/competitive/radioactivity|nM
@@ -8223,7 +8223,7 @@
- A qualitative binding assay that detects the binding of a cell-bound-MHC molecule with a ligand.
+ A qualitative binding assay that detects the binding of a cell-bound-MHC molecule with a ligand.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
qualitative binding|cellular MHC
@@ -8261,7 +8261,7 @@
- A flow cytometry assay that detects tumor necrosis factor (ligand) superfamily member 11 production by T cells.
+ A flow cytometry assay that detects tumor necrosis factor (ligand) superfamily member 11 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
TNFSF11/RANKL release|ICS
@@ -8293,7 +8293,7 @@
- A MHC:ligand binding assay that measures a binding constant.
+ A MHC:ligand binding assay that measures a binding constant.
IEDB
IEDB
binding constant|binding assay
@@ -8339,7 +8339,7 @@
- A qualitative binding assay that detects the binding of a purified-MHC molecule with a ligand.
+ A qualitative binding assay that detects the binding of a purified-MHC molecule with a ligand.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
qualitative binding|purified MHC
@@ -8385,7 +8385,7 @@
- A radioactivity detection assay that detects direct binding of a cell-lysate-MHC molecule with a ligand.
+ A radioactivity detection assay that detects direct binding of a cell-lysate-MHC molecule with a ligand.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
qualitative binding|lysate MHC/direct/radioactivity
@@ -8440,7 +8440,7 @@
- A radioactivity detection assay that measures half life to detect the direct binding of a cell-bound-MHC molecule with a ligand.
+ A radioactivity detection assay that measures half life to detect the direct binding of a cell-bound-MHC molecule with a ligand.
IEDB
IEDB
half life|cellular MHC/direct/radioactivity|min
@@ -8495,7 +8495,7 @@
- A fluorescence detection assay that measures half life to detect the direct binding of a cell-bound-MHC molecule with a ligand.
+ A fluorescence detection assay that measures half life to detect the direct binding of a cell-bound-MHC molecule with a ligand.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
half life|cellular MHC/direct/fluorescence|min
@@ -8550,7 +8550,7 @@
- A fluorescence detection assay that measures half maximal effective concentration (EC50) to detect direct binding of a cell-bound-MHC molecule with a ligand.
+ A fluorescence detection assay that measures half maximal effective concentration (EC50) to detect direct binding of a cell-bound-MHC molecule with a ligand.
IEDB
IEDB
half maximal effective concentration (EC50)|cellular MHC/direct/fluorescence|nM
@@ -8588,7 +8588,7 @@
- A flow cytometry assay that detects interleukin-17F production by T cells.
+ A flow cytometry assay that detects interleukin-17F production by T cells.
IEDB
IEDB
IL-17F release|ICS
@@ -8657,7 +8657,7 @@
- A radioactivity detection assay that measures equilibrium dissociation constant (KD) to detect the loss of binding of a known reference ligand to purified-MHC due to competition by the ligand under investigation and provides IC50 values determined under assay conditions where the IC50 approximates a KD value.
+ A radioactivity detection assay that measures equilibrium dissociation constant (KD) to detect the loss of binding of a known reference ligand to purified-MHC due to competition by the ligand under investigation and provides IC50 values determined under assay conditions where the IC50 approximates a KD value.
IEDB
IEDB
dissociation constant KD (~IC50)|purified MHC/competitive/radioactivity|nM
@@ -8712,7 +8712,7 @@
- A radioactivity detection assay that measures half life to detect the direct binding of a cell-lysate-MHC molecule with a ligand.
+ A radioactivity detection assay that measures half life to detect the direct binding of a cell-lysate-MHC molecule with a ligand.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
half life|lysate MHC/direct/radioactivity|min
@@ -8773,7 +8773,7 @@
- A radioactivity detection assay that measures binding off rate [koff] to detect direct binding of a cell-lysate-MHC molecule with a ligand.
+ A radioactivity detection assay that measures binding off rate [koff] to detect direct binding of a cell-lysate-MHC molecule with a ligand.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
off rate|lysate MHC/direct/radioactivity|1/s
@@ -8842,7 +8842,7 @@
- A radioactivity detection assay that measures half maximal inhibitory concentration (IC50) to detect the loss of binding of a known reference ligand to purified-MHC due to competition by the ligand under investigation.
+ A radioactivity detection assay that measures half maximal inhibitory concentration (IC50) to detect the loss of binding of a known reference ligand to purified-MHC due to competition by the ligand under investigation.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
half maximal inhibitory concentration (IC50)|purified MHC/competitive/radioactivity|nM
@@ -8897,7 +8897,7 @@
- A fluorescence detection assay that measures binding off rate [koff] to detect direct binding of a purified-MHC molecule with a ligand.
+ A fluorescence detection assay that measures binding off rate [koff] to detect direct binding of a purified-MHC molecule with a ligand.
IEDB
IEDB
off rate|purified MHC/direct/fluorescence|1/s
@@ -8935,7 +8935,7 @@
- A T cell epitope specific cytokine production assay that detects vascular endothelial growth factor production by T cells.
+ A T cell epitope specific cytokine production assay that detects vascular endothelial growth factor production by T cells.
IEDB
IEDB
VEGF release|biological activity
@@ -8979,7 +8979,7 @@
- A cytometric bead array assay that detects interleukin-22 production by T cells.
+ A cytometric bead array assay that detects interleukin-22 production by T cells.
IEDB
IEDB
IL-22 release|cytometric bead array
@@ -9017,7 +9017,7 @@
- An enzyme-linked immunosorbent assay that detects vascular endothelial growth factor production by T cells.
+ An enzyme-linked immunosorbent assay that detects vascular endothelial growth factor production by T cells.
IEDB
IEDB
VEGF release|ELISA
@@ -9063,7 +9063,7 @@
- A qualitative binding assay that detects the binding of a cell-lysate-MHC molecule with a ligand.
+ A qualitative binding assay that detects the binding of a cell-lysate-MHC molecule with a ligand.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
qualitative binding|lysate MHC
@@ -9121,7 +9121,7 @@
- A phage display binding assay that detects direct binding of a purified-MHC molecule with a ligand.
+ A phage display binding assay that detects direct binding of a purified-MHC molecule with a ligand.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
qualitative binding|purified MHC/direct/phage display
@@ -9159,7 +9159,7 @@
- A cytometric bead array assay that detects interleukin-7 production by T cells.
+ A cytometric bead array assay that detects interleukin-7 production by T cells.
IEDB
IEDB
IL-7 release|cytometric bead array
@@ -9214,7 +9214,7 @@
- A radioactivity detection assay that measures half life to detect the direct binding of a purified-MHC molecule with a ligand.
+ A radioactivity detection assay that measures half life to detect the direct binding of a purified-MHC molecule with a ligand.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
half life|purified MHC/direct/radioactivity|min
@@ -9252,7 +9252,7 @@
- A T cell epitope specific cytokine production assay that detects interleukin-7 production by T cells.
+ A T cell epitope specific cytokine production assay that detects interleukin-7 production by T cells.
IEDB
IEDB
IL-7 release|biological activity
@@ -9290,7 +9290,7 @@
- A flow cytometry assay that detects interleukin-17A production by T cells.
+ A flow cytometry assay that detects interleukin-17A production by T cells.
IEDB
IEDB
IL-17A release|ICS
@@ -9336,7 +9336,7 @@
- A fluorescence detection assay that detects direct binding of a purified-MHC molecule with a ligand.
+ A fluorescence detection assay that detects direct binding of a purified-MHC molecule with a ligand.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
qualitative binding|purified MHC/direct/fluorescence
@@ -9391,7 +9391,7 @@
- A fluorescence detection assay that measures half maximal effective concentration (EC50) to detect direct binding of a purified-MHC molecule with a ligand.
+ A fluorescence detection assay that measures half maximal effective concentration (EC50) to detect direct binding of a purified-MHC molecule with a ligand.
IEDB
IEDB
half maximal effective concentration (EC50)|purified MHC/direct/fluorescence|nM
@@ -9453,7 +9453,7 @@
- A fluorescence detection assay that detects loss of binding of a known reference ligand to cell-bound-MHC due to competition by the ligand under investigation.
+ A fluorescence detection assay that detects loss of binding of a known reference ligand to cell-bound-MHC due to competition by the ligand under investigation.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
qualitative binding|cellular MHC/competitive/fluorescence
@@ -9508,7 +9508,7 @@
- A X-ray crystallography 3D molecular structure determination assay that characterizes the 3-dimensional molecular structure of a MHC:ligand complex.
+ A X-ray crystallography 3D molecular structure determination assay that characterizes the 3-dimensional molecular structure of a MHC:ligand complex.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
3D structure|x-ray crystallography|angstroms
@@ -9588,7 +9588,7 @@
- A cell bound MHC ligand binding half maximal inhibitory concentration (IC50) determination assay that uses a T cell epitope recognition assay to measure ligand binding.
+ A cell bound MHC ligand binding half maximal inhibitory concentration (IC50) determination assay that uses a T cell epitope recognition assay to measure ligand binding.
IEDB
IEDB
half maximal inhibitory concentration (IC50)|cellular MHC/T cell inhibition|nM
@@ -9650,7 +9650,7 @@
- A radioactivity detection assay that detects loss of binding of a known reference ligand to cell-bound-MHC due to competition by the ligand under investigation.
+ A radioactivity detection assay that detects loss of binding of a known reference ligand to cell-bound-MHC due to competition by the ligand under investigation.
IEDB
IEDB
qualitative binding|cellular MHC/competitive/radioactivity
@@ -9688,7 +9688,7 @@
- A T cell epitope specific cytokine production assay that detects granulocyte colony stimulating factor production by T cells.
+ A T cell epitope specific cytokine production assay that detects granulocyte colony stimulating factor production by T cells.
IEDB
IEDB
G-CSF release|biological activity
@@ -9726,7 +9726,7 @@
- A cytometric bead array assay that detects interleukin-21 production by T cells.
+ A cytometric bead array assay that detects interleukin-21 production by T cells.
IEDB
IEDB
IL-21 release|cytometric bead array
@@ -9772,7 +9772,7 @@
- A radioactivity detection assay that detects direct binding of a cell-bound-MHC molecule with a ligand.
+ A radioactivity detection assay that detects direct binding of a cell-bound-MHC molecule with a ligand.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
qualitative binding|cellular MHC/direct/radioactivity
@@ -9833,7 +9833,7 @@
- A fluorescence detection assay that measures the 50% dissociation of binding temperature of a purified-MHC molecule with a ligand.
+ A fluorescence detection assay that measures the 50% dissociation of binding temperature of a purified-MHC molecule with a ligand.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
50% dissociation temperature|purified MHC/direct/fluorescence|°C
@@ -9885,7 +9885,7 @@
- A fluorescence detection assay that detects direct binding of a cell-bound-MHC molecule with a ligand.
+ A fluorescence detection assay that detects direct binding of a cell-bound-MHC molecule with a ligand.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
qualitative binding|cellular MHC/direct/fluorescence
@@ -9923,7 +9923,7 @@
- An assay of epitope specific tumor necrosis factor (ligand) superfamily member 11 production by T cells that detects tumor necrosis factor production.
+ An assay of epitope specific tumor necrosis factor (ligand) superfamily member 11 production by T cells that detects tumor necrosis factor production.
IEDB
IEDB
TNFSF11/RANKL release|biological activity
@@ -9969,7 +9969,7 @@
- A radioactivity detection assay that detects direct binding of a purified-MHC molecule with a ligand.
+ A radioactivity detection assay that detects direct binding of a purified-MHC molecule with a ligand.
IEDB
IEDB
qualitative binding|purified MHC/direct/radioactivity
@@ -10007,7 +10007,7 @@
- A flow cytometry assay that detects interleukin-8 production by T cells.
+ A flow cytometry assay that detects interleukin-8 production by T cells.
IEDB
IEDB
IL-8 release|ICS
@@ -10045,7 +10045,7 @@
- A cytometric bead array assay that detects interleukin-23 production by T cells.
+ A cytometric bead array assay that detects interleukin-23 production by T cells.
IEDB
IEDB
IL-23 release|cytometric bead array
@@ -10114,7 +10114,7 @@
- A fluorescence detection assay that measures half maximal inhibitory concentration (IC50) to detect the loss of binding of a known reference ligand to purified-MHC due to competition by the ligand under investigation.
+ A fluorescence detection assay that measures half maximal inhibitory concentration (IC50) to detect the loss of binding of a known reference ligand to purified-MHC due to competition by the ligand under investigation.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
half maximal inhibitory concentration (IC50)|purified MHC/competitive/fluorescence|nM
@@ -10201,7 +10201,7 @@
- A B cell epitope equilibrium dissociation constant (KD) assay that provides IC50 values determined under assay conditions where the IC50 approximates a KD value using a B cell epitope antigen inhibition of binding assay.
+ A B cell epitope equilibrium dissociation constant (KD) assay that provides IC50 values determined under assay conditions where the IC50 approximates a KD value using a B cell epitope antigen inhibition of binding assay.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
dissociation constant KD|inhibition by antigen (~ IC50)|nM
@@ -10253,7 +10253,7 @@
- A B cell epitope specific activation of additional immune response assay that detects histamine release in vitro.
+ A B cell epitope specific activation of additional immune response assay that detects histamine release in vitro.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
histamine release|biological activity
@@ -10287,7 +10287,7 @@
- A B cell epitope dependent biological activity determination assay that detects antigen activation.
+ A B cell epitope dependent biological activity determination assay that detects antigen activation.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
antigen activation|biological activity
@@ -10339,7 +10339,7 @@
- A B cell epitope specific activation of additional immune response assay that detects complement-dependent cytotoxicity in vitro .
+ A B cell epitope specific activation of additional immune response assay that detects complement-dependent cytotoxicity in vitro .
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
complement-dependent cytotoxicity|biological activity
@@ -10391,7 +10391,7 @@
- A B cell epitope specific activation of additional immune response assay that detects antibody-dependent cellular cytotoxicity in vitro.
+ A B cell epitope specific activation of additional immune response assay that detects antibody-dependent cellular cytotoxicity in vitro.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
antibody-dependent cellular cytotoxicity|biological activity
@@ -10425,7 +10425,7 @@
- A B cell epitope dependent biological activity determination assay that detects neutralization of the antigen.
+ A B cell epitope dependent biological activity determination assay that detects neutralization of the antigen.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
neutralization |biological activity
@@ -10477,7 +10477,7 @@
- A B cell epitope specific activation of additional immune response assay that detects opsonization in vitro .
+ A B cell epitope specific activation of additional immune response assay that detects opsonization in vitro .
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
opsonization|biological activity
@@ -10509,7 +10509,7 @@
- A calorimetric binding assay that detects the binding of an antigen with an antibody.
+ A calorimetric binding assay that detects the binding of an antigen with an antibody.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
qualitative binding|calorimetry
@@ -10541,7 +10541,7 @@
- An electron-microscopy 3D molecular structure determination assay that characterizes the 3-dimensional molecular structrue of a B cell epitope:antibody complex
+ An electron-microscopy 3D molecular structure determination assay that characterizes the 3-dimensional molecular structrue of a B cell epitope:antibody complex
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
3D structure|electron microscopy
@@ -10573,7 +10573,7 @@
- A nuclear magnetic resonance 3D molecular structure determination assay that characterizes the 3-dimensional structure of a B cell epitope:antibody complex.
+ A nuclear magnetic resonance 3D molecular structure determination assay that characterizes the 3-dimensional structure of a B cell epitope:antibody complex.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
3D structure|nuclear magnetic resonance (NMR)
@@ -10605,7 +10605,7 @@
- A cross-blocking assay that detects the binding of an antigen with an antibody.
+ A cross-blocking assay that detects the binding of an antigen with an antibody.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
qualitative binding|cross blocking
@@ -10637,7 +10637,7 @@
- A radio immuno assay that detects the binding of an antigen with an antibody.
+ A radio immuno assay that detects the binding of an antigen with an antibody.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
qualitative binding|radio immuno assay (RIA)
@@ -10669,7 +10669,7 @@
- An immunoblot assay that detects the binding of an antigen with an antibody.
+ An immunoblot assay that detects the binding of an antigen with an antibody.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
qualitative binding|western blot
@@ -10701,7 +10701,7 @@
- A surface plasmon resonance binding assay that detects the binding of an antigen with an antibody.
+ A surface plasmon resonance binding assay that detects the binding of an antigen with an antibody.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
qualitative binding|surface plasmon resonance (SPR)
@@ -10733,7 +10733,7 @@
- An immuno staining assay that detects the binding of an antigen with an antibody.
+ An immuno staining assay that detects the binding of an antigen with an antibody.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
qualitative binding|immuno staining
@@ -10765,7 +10765,7 @@
- An immunoprecipitation assay that detects the binding of an antigen with an antibody.
+ An immunoprecipitation assay that detects the binding of an antigen with an antibody.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
qualitative binding|immunoprecipitation
@@ -10797,7 +10797,7 @@
- A mass spectrometry assay that detects the binding of an antigen with an antibody.
+ A mass spectrometry assay that detects the binding of an antigen with an antibody.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
qualitative binding|mass spectrometry
@@ -10829,7 +10829,7 @@
- A phage display binding assay that detects the binding of an antigen with an antibody.
+ A phage display binding assay that detects the binding of an antigen with an antibody.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
qualitative binding|phage display
@@ -10861,7 +10861,7 @@
- An electron microscopy imaging assay that detects the binding of an antigen with an antibody.
+ An electron microscopy imaging assay that detects the binding of an antigen with an antibody.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
qualitative binding|electron microscopy
@@ -10893,7 +10893,7 @@
- An enzyme-linked immunosorbent assay that detects the binding of an antigen with an antibody.
+ An enzyme-linked immunosorbent assay that detects the binding of an antigen with an antibody.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
qualitative binding|ELISA
@@ -10925,7 +10925,7 @@
- An enzyme-linked immunospot assay that detects the binding of an antigen with an antibody.
+ An enzyme-linked immunospot assay that detects the binding of an antigen with an antibody.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
qualitative binding|ELISPOT
@@ -10957,7 +10957,7 @@
- A flow cytometry assay that detects the binding of an antigen with an antibody.
+ A flow cytometry assay that detects the binding of an antigen with an antibody.
IEDB
IEDB
qualitative binding|flow cytometry
@@ -10995,7 +10995,7 @@
- A flow cytometry assay that detects epitope specific granzyme A release by T cells.
+ A flow cytometry assay that detects epitope specific granzyme A release by T cells.
IEDB
IEDB
granzyme A release|intracellular staining
@@ -11027,7 +11027,7 @@
- An analytical chromatography assay that detects the binding of an antigen with an antibody.
+ An analytical chromatography assay that detects the binding of an antigen with an antibody.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
qualitative binding|chromatography
@@ -11070,7 +11070,7 @@
- A B cell epitope qualitative binding to antibody assay that uses a nuclear magnetic resonance assay.
+ A B cell epitope qualitative binding to antibody assay that uses a nuclear magnetic resonance assay.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
qualitative binding|nuclear magnetic resonance (NMR)
@@ -11108,7 +11108,7 @@
- An enzyme-linked immunosorbent assay that detects epitope specific granulysin release by T cells.
+ An enzyme-linked immunosorbent assay that detects epitope specific granulysin release by T cells.
IEDB
IEDB
granulysin release|ELISA
@@ -11146,7 +11146,7 @@
- A flow cytometry assay that detects epitope specific granulysin release by T cells.
+ A flow cytometry assay that detects epitope specific granulysin release by T cells.
IEDB
IEDB
granulysin release|intracellular staining
@@ -11201,7 +11201,7 @@
- A fluorescence detection assay that measures binding off rate [koff] to detect direct binding of a cell-bound-MHC molecule with a ligand.
+ A fluorescence detection assay that measures binding off rate [koff] to detect direct binding of a cell-bound-MHC molecule with a ligand.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
off rate|cellular MHC/direct/fluorescence|1/s
@@ -11256,7 +11256,7 @@
- A fluorescence detection assay that measures binding on rate (kon) to detect direct binding of a cell-bound-MHC molecule with a ligand.
+ A fluorescence detection assay that measures binding on rate (kon) to detect direct binding of a cell-bound-MHC molecule with a ligand.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
on rate|cellular MHC/direct/fluorescence|nM^-1s^-1
@@ -11325,7 +11325,7 @@
- A fluorescence detection assay that measures equilibrium dissociation constant (KD) to detect the loss of binding of a known reference ligand to purified-MHC due to competition by the ligand under investigation and provides IC50 values determined under assay conditions where the IC50 approximates a KD value.
+ A fluorescence detection assay that measures equilibrium dissociation constant (KD) to detect the loss of binding of a known reference ligand to purified-MHC due to competition by the ligand under investigation and provides IC50 values determined under assay conditions where the IC50 approximates a KD value.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
dissociation constant KD (~IC50)|purified MHC/competitive/fluorescence|nM
@@ -11363,7 +11363,7 @@
- An enzyme-linked immunosorbent assay that detects interleukin-17A production by T cells.
+ An enzyme-linked immunosorbent assay that detects interleukin-17A production by T cells.
IEDB
IEDB
IL-17A release|ELISA
@@ -11401,7 +11401,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects interleukin-7 production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects interleukin-7 production by T cells.
IEDB
IEDB
IL-7 release|RNA/DNA detection
@@ -11456,7 +11456,7 @@
- An efficacy of B cell epitope intervention experiment that uses a epitope protection experiment based on reduction of fertility.
+ An efficacy of B cell epitope intervention experiment that uses a epitope protection experiment based on reduction of fertility.
PERSON:Randi Vita, James Overton, Bjoern Peters
IEDB
protection from fertility|in vivo assay
@@ -11518,7 +11518,7 @@
- An efficacy of B cell epitope intervention experiment that uses a tolerance induction intervention experiment.
+ An efficacy of B cell epitope intervention experiment that uses a tolerance induction intervention experiment.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
tolerance|in vivo assay
@@ -11580,7 +11580,7 @@
- An efficacy of B cell epitope intervention experiment that detects a hypersensitivity response by monitoring skin reactions.
+ An efficacy of B cell epitope intervention experiment that detects a hypersensitivity response by monitoring skin reactions.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
hypersensitivity|in vivo assay
@@ -11632,7 +11632,7 @@
- A B cell epitope specific activation of additional immune response assay that detects agglutination in vitro.
+ A B cell epitope specific activation of additional immune response assay that detects agglutination in vitro.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
agglutination|biological activity
@@ -11708,7 +11708,7 @@
- An in vivo assay measuring B cell epitope specific protection from other challenge using survival.
+ An in vivo assay measuring B cell epitope specific protection from other challenge using survival.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
survival from challenge|in vivo assay
@@ -11769,7 +11769,7 @@
- An efficacy of B cell epitope intervention experiment that detects a decrease in disease.
+ An efficacy of B cell epitope intervention experiment that detects a decrease in disease.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
decreased disease|in vivo assay
@@ -11826,7 +11826,7 @@
- A B cell epitope dependent biological activity determination assay that uses an in vivo intervention experiment.
+ A B cell epitope dependent biological activity determination assay that uses an in vivo intervention experiment.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
in vivo activity|biological activity
@@ -11884,7 +11884,7 @@
- A B cell epitope qualitative binding to antibody assay that measures the ability of an antigen to inhibit antibody binding to a known ligand.
+ A B cell epitope qualitative binding to antibody assay that measures the ability of an antigen to inhibit antibody binding to a known ligand.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
qualitative binding|inhibition by antigen
@@ -11922,7 +11922,7 @@
- An assay that detects the binding of an antigen with an antibody, and produces a qualitative measurement of the binding as an output.
+ An assay that detects the binding of an antigen with an antibody, and produces a qualitative measurement of the binding as an output.
IEDB
IEDB
qualitative binding|binding assay
@@ -11969,7 +11969,7 @@
- A B cell epitope dependent biological activity determination assay that detects secondary in vitro activity.
+ A B cell epitope dependent biological activity determination assay that detects secondary in vitro activity.
IEDB
IEDB
secondary in vitro activity|biological activity
@@ -12014,7 +12014,7 @@
- A B cell epitope dependent biological activity determination assay that detects inhibition of the antibody's activity by the antigen.
+ A B cell epitope dependent biological activity determination assay that detects inhibition of the antibody's activity by the antigen.
IEDB
IEDB
antibody activity inhibition|biological activity
@@ -12047,7 +12047,7 @@
- A B cell epitope assay that measures the immune response process resulting from the binding of an antibody receptor to epitope or recognition of the epitope.
+ A B cell epitope assay that measures the immune response process resulting from the binding of an antibody receptor to epitope or recognition of the epitope.
IEDB
IEDB
biological activity|any method
@@ -12088,7 +12088,7 @@
- A B cell epitope binding constant determination assay that measures the dissociation constant KD.
+ A B cell epitope binding constant determination assay that measures the dissociation constant KD.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
dissociation constant KD|binding assay|nM
@@ -12120,7 +12120,7 @@
- A B cell epitope recognition assay that quantitavely characterizes the binding of an antibody / BCR with a ligand by determining a binding constant.
+ A B cell epitope recognition assay that quantitavely characterizes the binding of an antibody / BCR with a ligand by determining a binding constant.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
binding constant|binding assay
@@ -12177,7 +12177,7 @@
- An efficacy of B cell epitope intervention experiment that uses a epitope protection experiment.
+ An efficacy of B cell epitope intervention experiment that uses a epitope protection experiment.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
protection from challenge|in vivo assay
@@ -12234,7 +12234,7 @@
- An efficacy of B cell epitope intervention experiment that uses a disease exacerbation in vivo intervention experiment.
+ An efficacy of B cell epitope intervention experiment that uses a disease exacerbation in vivo intervention experiment.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
disease exacerbation|in vivo assay
@@ -12275,7 +12275,7 @@
- A B cell epitope binding constant determination assay that measures the on rate.
+ A B cell epitope binding constant determination assay that measures the on rate.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
on rate|binding assay|M^-1s^-1
@@ -12316,7 +12316,7 @@
- A B cell epitope binding constant determination assay that measures the association constant KA.
+ A B cell epitope binding constant determination assay that measures the association constant KA.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
association constant KA|binding assay|1/nM
@@ -12348,7 +12348,7 @@
- A 3D structure determination of bound molecular complex assay that characterizes the 3-dimensional structure of an antigen:antobody complex.
+ A 3D structure determination of bound molecular complex assay that characterizes the 3-dimensional structure of an antigen:antobody complex.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
3D structure|any method
@@ -12389,7 +12389,7 @@
- A B cell epitope binding constant determination assay that measures the off rate.
+ A B cell epitope binding constant determination assay that measures the off rate.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
off rate|binding assay|1/s
@@ -12421,7 +12421,7 @@
- A viral hemagglutination inhibition assay that detects the binding of an antigen with an antibody.
+ A viral hemagglutination inhibition assay that detects the binding of an antigen with an antibody.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
qualitative binding| hemagglutination inhibition
@@ -12453,7 +12453,7 @@
- A fluorescence quenching assay that detects the binding of an antigen with an antibody.
+ A fluorescence quenching assay that detects the binding of an antigen with an antibody.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
qualitative binding|quenching
@@ -12494,7 +12494,7 @@
- A radio immuno assay that measures the dissociation constant [KD] of an antigen binding with an antibody.
+ A radio immuno assay that measures the dissociation constant [KD] of an antigen binding with an antibody.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
dissociation constant KD|radio immuno assay (RIA)|nM
@@ -12535,7 +12535,7 @@
- An enzyme-linked immunosorbent assay that measures the dissociation constant [KD] of an antigen binding with an antibody.
+ An enzyme-linked immunosorbent assay that measures the dissociation constant [KD] of an antigen binding with an antibody.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
dissociation constant KD|ELISA|nM
@@ -12576,7 +12576,7 @@
- A fluorescence quenching assay that measures the dissociation constant [KD] of an antigen binding with an antibody.
+ A fluorescence quenching assay that measures the dissociation constant [KD] of an antigen binding with an antibody.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
dissociation constant KD|quenching|nM
@@ -12617,7 +12617,7 @@
- A surface plasmon resonance binding assay that measures the association constant [KA] of an antigen binding with an antibody.
+ A surface plasmon resonance binding assay that measures the association constant [KA] of an antigen binding with an antibody.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
association constant KA|surface plasmon resonance (SPR)|1/nM
@@ -12658,7 +12658,7 @@
- A surface plasmon resonance binding assay that measures the dissociation constant [KD] of an antigen binding with an antibody.
+ A surface plasmon resonance binding assay that measures the dissociation constant [KD] of an antigen binding with an antibody.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
dissociation constant KD|surface plasmon resonance (SPR)|nM
@@ -12699,7 +12699,7 @@
- A fluorescence quenching assay that measures the association constant [KA] of an antigen binding with an antibody.
+ A fluorescence quenching assay that measures the association constant [KA] of an antigen binding with an antibody.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
association constant KA|quenching|1/nM
@@ -12740,7 +12740,7 @@
- A calorimetric binding assay that measures the association constant [KA] of an antigen binding with an antibody.
+ A calorimetric binding assay that measures the association constant [KA] of an antigen binding with an antibody.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
association constant KA|calorimetry|1/nM
@@ -12781,7 +12781,7 @@
- A calorimetric binding assay that measures the dissociation constant [KD] of an antigen binding with an antibody.
+ A calorimetric binding assay that measures the dissociation constant [KD] of an antigen binding with an antibody.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
dissociation constant KD|calorimetry|nM
@@ -12822,7 +12822,7 @@
- An enzyme-linked immunosorbent assay that measures the association constant [KA] of an antigen binding with an antibody.
+ An enzyme-linked immunosorbent assay that measures the association constant [KA] of an antigen binding with an antibody.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
association constant KA|ELISA|1/nM
@@ -12863,7 +12863,7 @@
- A radio immuno assay that measures the association constant [KA] of an antigen binding with an antibody.
+ A radio immuno assay that measures the association constant [KA] of an antigen binding with an antibody.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
association constant KA|radio immuno assay (RIA)|1/nM
@@ -12904,7 +12904,7 @@
- A X-ray crystallography 3D molecular structure determination assay that characterizes the 3-dimensional molecular structrue of a B cell epitope:antibody complex.
+ A X-ray crystallography 3D molecular structure determination assay that characterizes the 3-dimensional molecular structrue of a B cell epitope:antibody complex.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
3D structure|x-ray crystallography|angstroms
@@ -12945,7 +12945,7 @@
- A surface plasmon resonance binding assay that measures the off rate [koff] of an antigen binding with an antibody.
+ A surface plasmon resonance binding assay that measures the off rate [koff] of an antigen binding with an antibody.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
off rate|surface plasmon resonance (SPR)|1/s
@@ -12986,7 +12986,7 @@
- A fluorescence quenching assay that measures the off rate [koff] of an antigen binding with an antibody.
+ A fluorescence quenching assay that measures the off rate [koff] of an antigen binding with an antibody.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
off rate|quenching|1/s
@@ -13027,7 +13027,7 @@
- A surface plasmon resonance binding assay that measures the on rate [kon] of an antigen binding with an antibody.
+ A surface plasmon resonance binding assay that measures the on rate [kon] of an antigen binding with an antibody.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
on rate|surface plasmon resonance (SPR)|M^-1s^-1
@@ -13068,7 +13068,7 @@
- A fluorescence quenching assay that measures the on rate [kon] of an antigen binding with an antibody.
+ A fluorescence quenching assay that measures the on rate [kon] of an antigen binding with an antibody.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
on rate|quenching|M^-1s^-1
@@ -13106,7 +13106,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects interleukin-1 beta production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects interleukin-1 beta production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-1b release|RNA/DNA detection
@@ -13144,7 +13144,7 @@
- A flow cytometry assay that detects interleukin-1 alpha production by T cells.
+ A flow cytometry assay that detects interleukin-1 alpha production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-1a release|ICS
@@ -13182,7 +13182,7 @@
- An enzyme-linked immunospot assay that detects interleukin-1 alpha production by T cells.
+ An enzyme-linked immunospot assay that detects interleukin-1 alpha production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-1a release|ELISPOT
@@ -13220,7 +13220,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects interleukin-1 alpha production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects interleukin-1 alpha production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-1a release|RNA/DNA detection
@@ -13258,7 +13258,7 @@
- A cytometric bead array assay that detects interleukin-1 alpha production by T cells.
+ A cytometric bead array assay that detects interleukin-1 alpha production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-1a release|cytometric bead array
@@ -13296,7 +13296,7 @@
- An enzyme-linked immunospot assay that detects interferon-beta production by T cells.
+ An enzyme-linked immunospot assay that detects interferon-beta production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IFNb release|ELISPOT
@@ -13334,7 +13334,7 @@
- A flow cytometry assay that detects interferon-beta production by T cells.
+ A flow cytometry assay that detects interferon-beta production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IFNb release|ICS
@@ -13372,7 +13372,7 @@
- A flow cytometry assay that detects granulocyte colony stimulating factor production by T cells.
+ A flow cytometry assay that detects granulocyte colony stimulating factor production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
G-CSF release|ICS
@@ -13410,7 +13410,7 @@
- An enzyme-linked immunosorbent assay that detects interferon-beta production by T cells.
+ An enzyme-linked immunosorbent assay that detects interferon-beta production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IFNb release|ELISA
@@ -13448,7 +13448,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects granulocyte colony stimulating factor production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects granulocyte colony stimulating factor production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
G-CSF release|RNA/DNA detection
@@ -13486,7 +13486,7 @@
- An enzyme-linked immunospot assay that detects granulocyte colony stimulating factor production by T cells.
+ An enzyme-linked immunospot assay that detects granulocyte colony stimulating factor production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
G-CSF release|ELISPOT
@@ -13524,7 +13524,7 @@
- A cytometric bead array assay that detects chemokine (C-X-C motif) ligand 9 production by T cells.
+ A cytometric bead array assay that detects chemokine (C-X-C motif) ligand 9 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CXCL9/MIG release|cytometric bead array
@@ -13562,7 +13562,7 @@
- An enzyme-linked immunospot assay that detects chemokine (C-X-C motif) ligand 9 production by T cells.
+ An enzyme-linked immunospot assay that detects chemokine (C-X-C motif) ligand 9 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CXCL9/MIG release|ELISPOT
@@ -13600,7 +13600,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects chemokine (C-X-C motif) ligand 9 production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects chemokine (C-X-C motif) ligand 9 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CXCL9/MIG release|RNA/DNA detection
@@ -13638,7 +13638,7 @@
- An enzyme-linked immunospot assay that detects chemokine (C-C motif) ligand 4 production by T cells.
+ An enzyme-linked immunospot assay that detects chemokine (C-C motif) ligand 4 production by T cells.
IEDB
IEDB
CCL4/MIP-1b release|ELISPOT
@@ -13676,7 +13676,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects chemokine (C-X-C motif) ligand 12 production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects chemokine (C-X-C motif) ligand 12 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CXCL12/SDF-1 release|RNA/DNA detection
@@ -13714,7 +13714,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects chemokine (C-X-C motif) ligand 13 production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects chemokine (C-X-C motif) ligand 13 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CXCL13/BLC release|RNA/DNA detection
@@ -13752,7 +13752,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects chemokine (C-X-C motif) ligand 16 production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects chemokine (C-X-C motif) ligand 16 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CXCL16 release|RNA/DNA detection
@@ -13790,7 +13790,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects chemokine (C-C motif) ligand 21 production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects chemokine (C-C motif) ligand 21 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL21/SLC release|RNA/DNA detection
@@ -13828,7 +13828,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects chemokine (C-C motif) ligand 22 production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects chemokine (C-C motif) ligand 22 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL22/MDC release|RNA/DNA detection
@@ -13866,7 +13866,7 @@
- A cytometric bead array assay that detects chemokine (C-C motif) ligand 4 production by T cells.
+ A cytometric bead array assay that detects chemokine (C-C motif) ligand 4 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL4/MIP-1b release|cytometric bead array
@@ -13904,7 +13904,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects chemokine (C-C motif) ligand 4 production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects chemokine (C-C motif) ligand 4 production by T cells.
IEDB
IEDB
CCL4/MIP-1b release|RNA/DNA detection
@@ -13942,7 +13942,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects vascular endothelial growth factor production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects vascular endothelial growth factor production by T cells.
IEDB
IEDB
VEGF release|RNA/DNA detection
@@ -13980,7 +13980,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects chemokine (C-C motif) ligand 19 production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects chemokine (C-C motif) ligand 19 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL19/MIP-3b release|RNA/DNA detection
@@ -14018,7 +14018,7 @@
- A flow cytometry assay that detects chemokine (C-C motif) ligand 1 production by T cells.
+ A flow cytometry assay that detects chemokine (C-C motif) ligand 1 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL1/TCA-3 release|ICS
@@ -14056,7 +14056,7 @@
- A flow cytometry assay that detects vascular endothelial growth factor production by T cells.
+ A flow cytometry assay that detects vascular endothelial growth factor production by T cells.
IEDB
IEDB
VEGF release|ICS
@@ -14094,7 +14094,7 @@
- An enzyme-linked immunospot assay that detects vascular endothelial growth factor production by T cells.
+ An enzyme-linked immunospot assay that detects vascular endothelial growth factor production by T cells.
IEDB
IEDB
VEGF release|ELISPOT
@@ -14132,7 +14132,7 @@
- An assay of epitope specific interleukin-17 production by T cells that detects interleukin-17F production.
+ An assay of epitope specific interleukin-17 production by T cells that detects interleukin-17F production.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-17F release|biological activity
@@ -14170,7 +14170,7 @@
- An assay of epitope specific interleukin-17 production by T cells that detects interleukin-17A production.
+ An assay of epitope specific interleukin-17 production by T cells that detects interleukin-17A production.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-17A release|biological activity
@@ -14208,7 +14208,7 @@
- A T cell epitope specific cytokine production assay that detects chemokine (C-C motif) ligand 21 production by T cells.
+ A T cell epitope specific cytokine production assay that detects chemokine (C-C motif) ligand 21 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL21/SLC release|biological activity
@@ -14246,7 +14246,7 @@
- A T cell epitope specific cytokine production assay that detects chemokine (C-C motif) ligand 19 production by T cells.
+ A T cell epitope specific cytokine production assay that detects chemokine (C-C motif) ligand 19 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL19/MIP-3b release|biological activity
@@ -14284,7 +14284,7 @@
- A T cell epitope specific cytokine production assay that detects chemokine (C-X-C motif) ligand 12 production by T cells.
+ A T cell epitope specific cytokine production assay that detects chemokine (C-X-C motif) ligand 12 production by T cells.
IEDB
IEDB
CXCL12/SDF-1 release|biological activity
@@ -14322,7 +14322,7 @@
- A T cell epitope specific cytokine production assay that detects chemokine (C-C motif) ligand 22 production by T cells.
+ A T cell epitope specific cytokine production assay that detects chemokine (C-C motif) ligand 22 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL22/MDC release|biological activity
@@ -14360,7 +14360,7 @@
- A T cell epitope specific cytokine production assay that detects chemokine (C-X-C motif) ligand 16 production by T cells.
+ A T cell epitope specific cytokine production assay that detects chemokine (C-X-C motif) ligand 16 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CXCL16 release|biological activity
@@ -14398,7 +14398,7 @@
- A T cell epitope specific cytokine production assay that detects chemokine (C-X-C motif) ligand 13 production by T cells.
+ A T cell epitope specific cytokine production assay that detects chemokine (C-X-C motif) ligand 13 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CXCL13/BLC release|biological activity
@@ -14436,7 +14436,7 @@
- An enzyme-linked immunospot assay that detects macrophage inflammatory protein-1 alpha production by T cells.
+ An enzyme-linked immunospot assay that detects macrophage inflammatory protein-1 alpha production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL3/MIP-1a release|ELISPOT
@@ -14474,7 +14474,7 @@
- A cytometric bead array assay that detects macrophage inflammatory protein-1 gamma production by T cells.
+ A cytometric bead array assay that detects macrophage inflammatory protein-1 gamma production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL9/MIP-1g release|cytometric bead array
@@ -14512,7 +14512,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects macrophage inflammatory protein-1 gamma production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects macrophage inflammatory protein-1 gamma production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL9/MIP-1g release|RNA/DNA detection
@@ -14550,7 +14550,7 @@
- A flow cytometry assay that detects monocyte chemotactic protein-1 production by T cells.
+ A flow cytometry assay that detects monocyte chemotactic protein-1 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL2/MCP-1 release|ICS
@@ -14588,7 +14588,7 @@
- An enzyme-linked immunospot assay that detects monocyte chemotactic protein-1 production by T cells.
+ An enzyme-linked immunospot assay that detects monocyte chemotactic protein-1 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL2/MCP-1 release|ELISPOT
@@ -14626,7 +14626,7 @@
- A flow cytometry assay that detects macrophage inflammatory protein-1 gamma production by T cells.
+ A flow cytometry assay that detects macrophage inflammatory protein-1 gamma production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL9/MIP-1g release|ICS
@@ -14664,7 +14664,7 @@
- An enzyme-linked immunospot assay that detects inflammatory protein-1 gamma production by T cells.
+ An enzyme-linked immunospot assay that detects inflammatory protein-1 gamma production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL9/MIP-1g release|ELISPOT
@@ -14702,7 +14702,7 @@
- A cytometric bead array assay that detects vascular endothelial growth factor production by T cells.
+ A cytometric bead array assay that detects vascular endothelial growth factor production by T cells.
IEDB
IEDB
VEGF release|cytometric bead array
@@ -14740,7 +14740,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects tumor necrosis factor superfamily cytokine production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects tumor necrosis factor superfamily cytokine production by T cells.
IEDB
IEDB
TNF release|RNA/DNA detection
@@ -14778,7 +14778,7 @@
- A flow cytometry assay that detects RANTES production by T cells.
+ A flow cytometry assay that detects RANTES production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL5/RANTES release|ICS
@@ -14816,7 +14816,7 @@
- An enzyme-linked immunospot assay that detects RANTES production by T cells.
+ An enzyme-linked immunospot assay that detects RANTES production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL5/RANTES release|ELISPOT
@@ -14854,7 +14854,7 @@
- An enzyme-linked immunospot assay that detects lymphotoxin A production by T cells.
+ An enzyme-linked immunospot assay that detects lymphotoxin A production by T cells.
IEDB
IEDB
lymphotoxin A/TNFb release|ELISPOT
@@ -14892,7 +14892,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects macrophage inflammatory protein-1 alpha production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects macrophage inflammatory protein-1 alpha production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL3/MIP-1a release|RNA/DNA detection
@@ -14930,7 +14930,7 @@
- A cytometric bead array assay that detects lymphotoxin A production by T cells.
+ A cytometric bead array assay that detects lymphotoxin A production by T cells.
IEDB
IEDB
lymphotoxin A/TNFb release|cytometric bead array
@@ -14968,7 +14968,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects lymphotoxin A production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects lymphotoxin A production by T cells.
IEDB
IEDB
lymphotoxin A/TNFb release|RNA/DNA detection
@@ -15006,7 +15006,7 @@
- An enzyme-linked immunospot assay that detects IP-10 production by T cells.
+ An enzyme-linked immunospot assay that detects IP-10 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CXCL10/IP-10 release|ELISPOT
@@ -15044,7 +15044,7 @@
- A flow cytometry assay that detects IP-10 production by T cells.
+ A flow cytometry assay that detects IP-10 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CXCL10/IP-10 release|ICS
@@ -15082,7 +15082,7 @@
- An enzyme-linked immunospot assay that detects interleukin-9 production by T cells.
+ An enzyme-linked immunospot assay that detects interleukin-9 production by T cells.
IEDB
IEDB
IL-9 release|ELISPOT
@@ -15120,7 +15120,7 @@
- A flow cytometry assay that detects interleukin-9 production by T cells.
+ A flow cytometry assay that detects interleukin-9 production by T cells.
IEDB
IEDB
IL-9 release|ICS
@@ -15158,7 +15158,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects interleukin-9 production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects interleukin-9 production by T cells.
IEDB
IEDB
IL-9 release|RNA/DNA detection
@@ -15196,7 +15196,7 @@
- An enzyme-linked immunospot assay that detects interleukin-8 production by T cells.
+ An enzyme-linked immunospot assay that detects interleukin-8 production by T cells.
IEDB
IEDB
IL-8 release|ELISPOT
@@ -15234,7 +15234,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects interleukin-8 production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects interleukin-8 production by T cells.
IEDB
IEDB
IL-8 release|RNA/DNA detection
@@ -15272,7 +15272,7 @@
- An enzyme-linked immunospot assay that detects interleukin-3 production by T cells.
+ An enzyme-linked immunospot assay that detects interleukin-3 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-3 release|ELISPOT
@@ -15310,7 +15310,7 @@
- An enzyme-linked immunosorbent assay that detects interleukin-7 production by T cells.
+ An enzyme-linked immunosorbent assay that detects interleukin-7 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-7 release|ELISA
@@ -15348,7 +15348,7 @@
- An enzyme-linked immunospot assay that detects interleukin-7 production by T cells.
+ An enzyme-linked immunospot assay that detects interleukin-7 production by T cells.
IEDB
IEDB
IL-7 release|ELISPOT
@@ -15386,7 +15386,7 @@
- A flow cytometry assay that detects interleukin-7 production by T cells.
+ A flow cytometry assay that detects interleukin-7 production by T cells.
IEDB
IEDB
IL-7 release|ICS
@@ -15424,7 +15424,7 @@
- A flow cytometry assay that detects interleukin-27 production by T cells.
+ A flow cytometry assay that detects interleukin-27 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-27 release|ICS
@@ -15462,7 +15462,7 @@
- A cytometric bead array assay that detects interleukin-3 production by T cells.
+ A cytometric bead array assay that detects interleukin-3 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-3 release|cytometric bead array
@@ -15500,7 +15500,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects interleukin-3 production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects interleukin-3 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-3 release|RNA/DNA detection
@@ -15538,7 +15538,7 @@
- A T cell epitope specific cytotoxic T cell degranulation assay that detects granzyme A release by T cells.
+ A T cell epitope specific cytotoxic T cell degranulation assay that detects granzyme A release by T cells.
IEDB
IEDB
granzyme A release|biological activity
@@ -15576,7 +15576,7 @@
- A T cell epitope specific cytotoxic T cell degranulation assay that detects granulysin release by T cells.
+ A T cell epitope specific cytotoxic T cell degranulation assay that detects granulysin release by T cells.
IEDB
IEDB
granulysin release|biological activity
@@ -15614,7 +15614,7 @@
- A cytometric bead array assay that detects interleukin-27 production by T cells.
+ A cytometric bead array assay that detects interleukin-27 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-27 release|cytometric bead array
@@ -15652,7 +15652,7 @@
- A flow cytometry assay that detects interleukin-23 production by T cells.
+ A flow cytometry assay that detects interleukin-23 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-23 release|ICS
@@ -15690,7 +15690,7 @@
- An enzyme-linked immunospot assay that detects interleukin-27 production by T cells.
+ An enzyme-linked immunospot assay that detects interleukin-27 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-27 release|ELISPOT
@@ -15728,7 +15728,7 @@
- An enzyme-linked immunosorbent assay that detects interleukin-27 production by T cells.
+ An enzyme-linked immunosorbent assay that detects interleukin-27 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-27 release|ELISA
@@ -15766,7 +15766,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects interleukin-18 production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects interleukin-18 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-18 release|RNA/DNA detection
@@ -15804,7 +15804,7 @@
- An enzyme-linked immunospot assay that detects interleukin-18 production by T cells.
+ An enzyme-linked immunospot assay that detects interleukin-18 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-18 release|ELISPOT
@@ -15842,7 +15842,7 @@
- An enzyme-linked immunospot assay that detects interleukin-22 production by T cells.
+ An enzyme-linked immunospot assay that detects interleukin-22 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-22 release|ELISPOT
@@ -15880,7 +15880,7 @@
- An enzyme-linked immunospot assay that detects interleukin-23 production by T cells.
+ An enzyme-linked immunospot assay that detects interleukin-23 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-23 release|ELISPOT
@@ -15918,7 +15918,7 @@
- A flow cytometry assay that detects interleukin-18 production by T cells.
+ A flow cytometry assay that detects interleukin-18 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-18 release|ICS
@@ -15956,7 +15956,7 @@
- An enzyme-linked immunospot assay that detects interleukin-21 production by T cells.
+ An enzyme-linked immunospot assay that detects interleukin-21 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-21 release|ELISPOT
@@ -15994,7 +15994,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects chemokine (C-C motif) ligand 1 production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects chemokine (C-C motif) ligand 1 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL1/TCA-3 release|RNA/DNA detection
@@ -16032,7 +16032,7 @@
- A cytometric bead array assay that detects chemokine (C-C motif) ligand 1 production by T cells.
+ A cytometric bead array assay that detects chemokine (C-C motif) ligand 1 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL1/TCA-3 release|cytometric bead array
@@ -16070,7 +16070,7 @@
- An enzyme-linked immunospot assay that detects chemokine (C-C motif) ligand 1 production by T cells.
+ An enzyme-linked immunospot assay that detects chemokine (C-C motif) ligand 1 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
CCL1/TCA-3 release|ELISPOT
@@ -16108,7 +16108,7 @@
- An enzyme-linked immunospot assay that detects interleukin-17F production by T cells.
+ An enzyme-linked immunospot assay that detects interleukin-17F production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-17F release|ELISPOT
@@ -16146,7 +16146,7 @@
- An enzyme-linked immunosorbent assay that detects interleukin-17F production by T cells.
+ An enzyme-linked immunosorbent assay that detects interleukin-17F production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-17F release|ELISA
@@ -16184,7 +16184,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects interleukin-17F production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects interleukin-17F production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-17F release|RNA/DNA detection
@@ -16222,7 +16222,7 @@
- An enzyme-linked immunospot assay that detects interleukin-17A production by T cells.
+ An enzyme-linked immunospot assay that detects interleukin-17A production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-17A release|ELISPOT
@@ -16260,7 +16260,7 @@
- A cytometric bead array assay that detects interleukin-18 production by T cells.
+ A cytometric bead array assay that detects interleukin-18 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-18 release|cytometric bead array
@@ -16298,7 +16298,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects interleukin-16 production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects interleukin-16 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-16 release|RNA/DNA detection
@@ -16336,7 +16336,7 @@
- An enzyme-linked immunosorbent assay that detects interleukin-16 production by T cells.
+ An enzyme-linked immunosorbent assay that detects interleukin-16 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-16 release|ELISA
@@ -16374,7 +16374,7 @@
- An enzyme-linked immunospot assay that detects interleukin-16 production by T cells.
+ An enzyme-linked immunospot assay that detects interleukin-16 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-16 release|ELISPOT
@@ -16412,7 +16412,7 @@
- A flow cytometry assay that detects interleukin-16 production by T cells.
+ A flow cytometry assay that detects interleukin-16 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-16 release|ICS
@@ -16450,7 +16450,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects interleukin-17A production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects interleukin-17A production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-17A release|RNA/DNA detection
@@ -16488,7 +16488,7 @@
- A flow cytometry assay that detects interleukin-1 beta production by T cells.
+ A flow cytometry assay that detects interleukin-1 beta production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-1b release|ICS
@@ -16526,7 +16526,7 @@
- An enzyme-linked immunospot assay that detects interleukin-1 beta production by T cells.
+ An enzyme-linked immunospot assay that detects interleukin-1 beta production by T cells.
IEDB
IEDB
IL-1b release|ELISPOT
@@ -16564,7 +16564,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects interleukin-15 production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects interleukin-15 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-15 release|RNA/DNA detection
@@ -16602,7 +16602,7 @@
- An enzyme-linked immunospot assay that detects interleukin-12 production by T cells.
+ An enzyme-linked immunospot assay that detects interleukin-12 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-12 release|ELISPOT
@@ -16640,7 +16640,7 @@
- A flow cytometry assay that detects interleukin-15 production by T cells.
+ A flow cytometry assay that detects interleukin-15 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-15 release|ICS
@@ -16678,7 +16678,7 @@
- An enzyme-linked immunospot assay that detects interleukin-15 production by T cells.
+ An enzyme-linked immunospot assay that detects interleukin-15 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-15 release|ELISPOT
@@ -16755,7 +16755,7 @@
- A MHC binding constant determination assay measuring equilibrium association constant (KA).
+ A MHC binding constant determination assay measuring equilibrium association constant (KA).
IEDB
IEDB
association constant KA|binding assay|1/M
@@ -16796,7 +16796,7 @@
- A MHC binding constant determination assay measuring equilibrium dissociation constant (KD).
+ A MHC binding constant determination assay measuring equilibrium dissociation constant (KD).
IEDB
IEDB
dissociation constant KD|binding assay|nM
@@ -16865,7 +16865,7 @@
- A radioactivity detection assay that measures equilibrium dissociation constant (KD) to detect the loss of binding of a known reference ligand to purified-MHC due to competition by the ligand under investigation.
+ A radioactivity detection assay that measures equilibrium dissociation constant (KD) to detect the loss of binding of a known reference ligand to purified-MHC due to competition by the ligand under investigation.
IEDB
IEDB
dissociation constant KD|purified MHC/direct/radioactivity|nM
@@ -16897,7 +16897,7 @@
- A MHC binding constant determination assay measuring half life of binding.
+ A MHC binding constant determination assay measuring half life of binding.
IEDB
IEDB
half life|binding assay|min
@@ -16938,7 +16938,7 @@
- A MHC binding constant determination assay measuring half maximal effective concentration (EC50).
+ A MHC binding constant determination assay measuring half maximal effective concentration (EC50).
IEDB
IEDB
half maximal effective concentration (EC50)|binding assay|nM
@@ -16970,7 +16970,7 @@
- A MHC binding constant determination assay measuring half maximal inhibitory concentration (IC50).
+ A MHC binding constant determination assay measuring half maximal inhibitory concentration (IC50).
IEDB
IEDB
half maximal inhibitory concentration (IC50)|binding assay|nM
@@ -17011,7 +17011,7 @@
- A MHC binding constant determination assay measuring binding off rate measurement data item (koff).
+ A MHC binding constant determination assay measuring binding off rate measurement data item (koff).
IEDB
IEDB
off rate|binding assay|1/s
@@ -17043,7 +17043,7 @@
- A MHC binding constant determination assay measuring binding on rate (kon).
+ A MHC binding constant determination assay measuring binding on rate (kon).
IEDB
IEDB
on rate|binding assay|nM^-1s^-1
@@ -17084,7 +17084,7 @@
- An analytical chromatography assay that measures the association constant [KA] of an antigen binding with an antibody.
+ An analytical chromatography assay that measures the association constant [KA] of an antigen binding with an antibody.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
association constant KA|chromatography|1/nM
@@ -17125,7 +17125,7 @@
- An analytical chromatography assay that measures the dissociation constant [KD] of an antigen binding with an antibody.
+ An analytical chromatography assay that measures the dissociation constant [KD] of an antigen binding with an antibody.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
dissociation constant KD|chromatography|nM
@@ -17157,7 +17157,7 @@
- A hydrogen/deuterium exchange footprinting assay that detects the binding of an antigen with an antibody.
+ A hydrogen/deuterium exchange footprinting assay that detects the binding of an antigen with an antibody.
PERSON:Randi Vita, James Overton, Bjoern Peters
IEDB
qualitative binding|hydrogen/deuterium exchange footprinting assay
@@ -17189,7 +17189,7 @@
- A immunohistochemistry assay that detects the binding of an antigen with an antibody.
+ A immunohistochemistry assay that detects the binding of an antigen with an antibody.
IEDB
IEDB
qualitative binding|immunohistochemistry
@@ -17221,7 +17221,7 @@
- A 3D structure determination of bound molecular complex assay that characterizes the 3-dimensional structure of a T cell epitope:MHC:TCR complex.
+ A 3D structure determination of bound molecular complex assay that characterizes the 3-dimensional structure of a T cell epitope:MHC:TCR complex.
IEDB
IEDB
3D structure|any method
@@ -17253,7 +17253,7 @@
- A 3D structure determination of bound molecular complex assay that characterizes the 3-dimensional structure of a MHC:ligand complex.
+ A 3D structure determination of bound molecular complex assay that characterizes the 3-dimensional structure of a MHC:ligand complex.
IEDB
IEDB
3D structure|any method
@@ -17318,7 +17318,7 @@
- An in vivo assay measuring B cell epitope specific protection from pathogen challenge using pathogen burden.
+ An in vivo assay measuring B cell epitope specific protection from pathogen challenge using pathogen burden.
IEDB
IEDB
pathogen burden after challenge|in vivo assay
@@ -17383,7 +17383,7 @@
- An in vivo assay measuring B cell epitope specific protection from tumor challenge using tumor burden.
+ An in vivo assay measuring B cell epitope specific protection from tumor challenge using tumor burden.
IEDB
IEDB
tumor burden after challenge|in vivo assay
@@ -17415,7 +17415,7 @@
- A microarray assay that detects the binding of an antigen with an antibody.
+ A microarray assay that detects the binding of an antigen with an antibody.
IEDB
IEDB
qualitative binding|microarray
@@ -17467,7 +17467,7 @@
- A B cell epitope equilibrium dissociation constant (KD) determination assay that uses a nuclear magnetic resonance assay.
+ A B cell epitope equilibrium dissociation constant (KD) determination assay that uses a nuclear magnetic resonance assay.
IEDB
IEDB
dissociation constant KD|nuclear magnetic resonance (NMR)|nM
@@ -17500,7 +17500,7 @@
- A T cell epitope recognition assay that measures the immune response process resulting from the binding of a T cell receptor to epitope or the recongition of the epitope.
+ A T cell epitope recognition assay that measures the immune response process resulting from the binding of a T cell receptor to epitope or the recongition of the epitope.
IEDB
IEDB
biological activity|any method
@@ -17538,7 +17538,7 @@
- A T cell epitope specific cytokine production assay that detects production of chemokine (C-C motif) ligand 17 production by T cells.
+ A T cell epitope specific cytokine production assay that detects production of chemokine (C-C motif) ligand 17 production by T cells.
IEDB
IEDB
CCL17/TARC release|biological activity
@@ -17576,7 +17576,7 @@
- A T cell epitope specific cytokine production assay that detects macrophage migration inhibitory factor (MIF) production by T cells.
+ A T cell epitope specific cytokine production assay that detects macrophage migration inhibitory factor (MIF) production by T cells.
IEDB
IEDB
MIF release|biological activity
@@ -17614,7 +17614,7 @@
- A T cell epitope specific cytokine production assay that detects oncostatin M production by T cells.
+ A T cell epitope specific cytokine production assay that detects oncostatin M production by T cells.
IEDB
IEDB
oncostatin M release|biological activity
@@ -17646,7 +17646,7 @@
- A T cell epitope recognition assay that quantitavely characterizes the binding of a TCR with a ligand by determining a binding constant.
+ A T cell epitope recognition assay that quantitavely characterizes the binding of a TCR with a ligand by determining a binding constant.
IEDB
IEDB
binding constant|binding assay
@@ -17684,7 +17684,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects chemokine (C-C motif) ligand 17 production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects chemokine (C-C motif) ligand 17 production by T cells.
IEDB
IEDB
CCL17/TARC release|RNA/DNA detection
@@ -17722,7 +17722,7 @@
- A cytometric bead array assay that detects chemokine (C-C motif) ligand 22 production by T cells.
+ A cytometric bead array assay that detects chemokine (C-C motif) ligand 22 production by T cells.
IEDB
IEDB
CCL22/MDC release|cytometric bead array
@@ -17774,7 +17774,7 @@
- An in vitro cell killing assay that measures the killing of antigen presenting cells (APC) by T cells whose TCR recognizes an epitope presented by the APC.
+ An in vitro cell killing assay that measures the killing of antigen presenting cells (APC) by T cells whose TCR recognizes an epitope presented by the APC.
IEDB
IEDB
cytotoxicity|in vitro assay
@@ -17812,7 +17812,7 @@
- A cytometric bead array assay that detects epitope specific granzyme A release by T cells.
+ A cytometric bead array assay that detects epitope specific granzyme A release by T cells.
IEDB
IEDB
granzyme A release|cytometric bead array
@@ -17850,7 +17850,7 @@
- A detection of specific nucleic acids with complementary probes assay that detects epitope specific granzyme A release by T cells.
+ A detection of specific nucleic acids with complementary probes assay that detects epitope specific granzyme A release by T cells.
IEDB
IEDB
granzyme A release|RNA/DNA detection
@@ -17888,7 +17888,7 @@
- A cytometric bead array assay that detects epitope specific granzyme B release by T cells.
+ A cytometric bead array assay that detects epitope specific granzyme B release by T cells.
IEDB
IEDB
granzyme B release|cytometric bead array
@@ -17926,7 +17926,7 @@
- A detection of specific nucleic acids with complementary probes assay that detects epitope specific granzyme B release by T cells
+ A detection of specific nucleic acids with complementary probes assay that detects epitope specific granzyme B release by T cells
IEDB
IEDB
granzyme B release|RNA/DNA detection
@@ -17964,7 +17964,7 @@
- A cytometric bead array assay that detects macrophage migration inhibitory factor (MIF) production by T cells.
+ A cytometric bead array assay that detects macrophage migration inhibitory factor (MIF) production by T cells.
IEDB
IEDB
MIF release|cytometric bead array
@@ -18002,7 +18002,7 @@
- A cytometric bead array assay that detects oncostatin M production by T cells.
+ A cytometric bead array assay that detects oncostatin M production by T cells.
IEDB
IEDB
oncostatin M release|cytometric bead array
@@ -18040,7 +18040,7 @@
- An enzyme-linked immunospot assay that detects epitope specific perforin release by T cells.
+ An enzyme-linked immunospot assay that detects epitope specific perforin release by T cells.
IEDB
IEDB
perforin release|ELISPOT
@@ -18102,7 +18102,7 @@
- A T cell epitope specific proliferation assay that is performed in vivo.
+ A T cell epitope specific proliferation assay that is performed in vivo.
IEDB
IEDB
proliferation|in vivo assay
@@ -18154,7 +18154,7 @@
- A T cell epitope specific proliferation assay that is performed on cells in vitro.
+ A T cell epitope specific proliferation assay that is performed on cells in vitro.
IEDB
IEDB
proliferation|in vitro assay
@@ -18186,7 +18186,7 @@
- An assay that detects the binding of a MHC molecule with a ligand, and produces a qualitative measurement of the binding as an output.
+ An assay that detects the binding of a MHC molecule with a ligand, and produces a qualitative measurement of the binding as an output.
IEDB
IEDB
qualitative binding|binding assay
@@ -18243,7 +18243,7 @@
- An efficacy of T cell epitope intervention experiment that uses a epitope protection experiment.
+ An efficacy of T cell epitope intervention experiment that uses a epitope protection experiment.
IEDB
IEDB
protection from challenge|in vivo assay
@@ -18288,7 +18288,7 @@
- T cell epitope dependent biological activity assay that detects suppression of an in vitro response.
+ T cell epitope dependent biological activity assay that detects suppression of an in vitro response.
PERSON:Randi Vita, James Overton, Bjoern Peters
IEDB
suppression|in vitro assay
@@ -18323,7 +18323,7 @@
- An immune epitope assay that characterizes the structrue of a MHC-ligand complex, or detects the processing and presentation of a ligand by an antigen presenting cell, or the binding of a ligand to an MHC molecule.
+ An immune epitope assay that characterizes the structrue of a MHC-ligand complex, or detects the processing and presentation of a ligand by an antigen presenting cell, or the binding of a ligand to an MHC molecule.
IEDB
IEDB
MHC ligand assay|any method
@@ -18375,7 +18375,7 @@
- A CFSE assay that detects T cell epitope specific proliferation in vitro.
+ A CFSE assay that detects T cell epitope specific proliferation in vitro.
IEDB
IEDB
proliferation|CFSE
@@ -18416,7 +18416,7 @@
- A T cell epitope binding constant determination assay that measures the dissociation constant KD.
+ A T cell epitope binding constant determination assay that measures the dissociation constant KD.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
dissociation constant KD|binding assay|nM
@@ -18457,7 +18457,7 @@
- A T cell epitope binding constant determination assay that measures the on rate.
+ A T cell epitope binding constant determination assay that measures the on rate.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
on rate|binding assay|M^-1s^-1
@@ -18498,7 +18498,7 @@
- A T cell epitope binding constant determination assay that measures the off rate.
+ A T cell epitope binding constant determination assay that measures the off rate.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
off rate|binding assay|1/s
@@ -18539,7 +18539,7 @@
- A T cell epitope binding constant determination assay that measures the association constant KA.
+ A T cell epitope binding constant determination assay that measures the association constant KA.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
association constant KA|binding assay|1/nM
@@ -18571,7 +18571,7 @@
- A small-angle scattering 3D molecular structure determination assay that characterizes the 3-dimensional molecular structure of a B cell epitope:antibody complex
+ A small-angle scattering 3D molecular structure determination assay that characterizes the 3-dimensional molecular structure of a B cell epitope:antibody complex
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
3D structure|small-angle scattering assay
@@ -18612,7 +18612,7 @@
- A bio-layer interferometry assay that measures the on rate of an antigen with an antibody.
+ A bio-layer interferometry assay that measures the on rate of an antigen with an antibody.
IEDB
IEDB
on rate|bio-layer interferometry assay|M^-1s^-1
@@ -18653,7 +18653,7 @@
- A bio-layer interferometry assay that measures the off rate of an antigen with an antibody.
+ A bio-layer interferometry assay that measures the off rate of an antigen with an antibody.
IEDB
IEDB
off rate|bio-layer interferometry assay|1/s
@@ -18685,7 +18685,7 @@
- A bio-layer interferometry assay that detects the binding of an antigen with an antibody.
+ A bio-layer interferometry assay that detects the binding of an antigen with an antibody.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
qualitative binding|bio-layer interferometry assay
@@ -18726,7 +18726,7 @@
- A bio-layer interferometry assay that measures the dissociation constant [KD] of an antigen with an antibody.
+ A bio-layer interferometry assay that measures the dissociation constant [KD] of an antigen with an antibody.
IEDB
IEDB
dissociation constant KD|bio-layer interferometry assay|nM
@@ -18782,7 +18782,7 @@
- A cytometric bead array assay that detects chemokine (C-C motif) ligand 20 production by T cells.
+ A cytometric bead array assay that detects chemokine (C-C motif) ligand 20 production by T cells.
PERSON:Randi Vita, James Overton, Bjoern Peters
IEDB
CCL20/MIP-3a release|cytometric bead array
@@ -18820,7 +18820,7 @@
- A T cell epitope specific cytokine production assay that detects chemokine (C-C motif) ligand 20 production by T cells.
+ A T cell epitope specific cytokine production assay that detects chemokine (C-C motif) ligand 20 production by T cells.
PERSON:Randi Vita, James Overton, Bjoern Peters
IEDB
CCL20/MIP-3a release|biological activity
@@ -18864,7 +18864,7 @@
- A footprinting assay that detects the binding of an antigen with an antibody.
+ A footprinting assay that detects the binding of an antigen with an antibody.
PERSON:Randi Vita, James Overton, Bjoern Peters
IEDB
qualitative binding|footprinting assay
@@ -18896,7 +18896,7 @@
- A hydroxyl-radical footprinting assay that detects the binding of an antigen with an antibody.
+ A hydroxyl-radical footprinting assay that detects the binding of an antigen with an antibody.
PERSON:Randi Vita, James Overton, Bjoern Peters
IEDB
qualitative binding|hydroxyl-radical footprinting assay
@@ -18934,7 +18934,7 @@
- An enzyme-linked immunosorbent assay that detects interferon-alpha production by T cells.
+ An enzyme-linked immunosorbent assay that detects interferon-alpha production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IFNa release|ELISA
@@ -18972,7 +18972,7 @@
- A T cell epitope specific cytokine production assay that detects interferon-alpha production by T cells.
+ A T cell epitope specific cytokine production assay that detects interferon-alpha production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IFNa release|biological activity
@@ -19033,7 +19033,7 @@
- An efficacy of B cell epitope intervention experiment that uses a disease exacerbation in vivo intervention experiment after adoptive transfer of epitope specific antibodies or B cells.
+ An efficacy of B cell epitope intervention experiment that uses a disease exacerbation in vivo intervention experiment after adoptive transfer of epitope specific antibodies or B cells.
IEDB
IEDB
disease exacerbation after adoptive transfer|in vivo assay
@@ -19101,7 +19101,7 @@
- An efficacy of T cell epitope intervention experiment that detects a decrease in disease after adoptive transfer of epitope specfic T cells.
+ An efficacy of T cell epitope intervention experiment that detects a decrease in disease after adoptive transfer of epitope specfic T cells.
IEDB
IEDB
decreased disease after adoptive transfer|in vivo assay
@@ -19169,7 +19169,7 @@
- An efficacy of B cell epitope intervention experiment that detects a decrease in disease after adoptive transfer of epitope specific antibodies or B cells.
+ An efficacy of B cell epitope intervention experiment that detects a decrease in disease after adoptive transfer of epitope specific antibodies or B cells.
IEDB
IEDB
decreased disease after adoptive transfer|in vivo assay
@@ -19230,7 +19230,7 @@
- An efficacy of T cell epitope intervention experiment that uses a epitope protection experiment after adoptive transfer of epitope specfic T cells.
+ An efficacy of T cell epitope intervention experiment that uses a epitope protection experiment after adoptive transfer of epitope specfic T cells.
IEDB
IEDB
protection from challenge after adoptive transfer|in vivo assay
@@ -19291,7 +19291,7 @@
- An efficacy of B cell epitope intervention experiment that uses a epitope protection experiment after adoptive transfer of epitope specific antibodies or B cells.
+ An efficacy of B cell epitope intervention experiment that uses a epitope protection experiment after adoptive transfer of epitope specific antibodies or B cells.
IEDB
IEDB
protection from challenge after adoptive transfer|in vivo assay
@@ -19365,7 +19365,7 @@
- An in vivo assay measuring T cell epitope specific protection from pathogen challenge resulting from the adoptive transfer of epitope specific antibodies or B cells using pathogen burden.
+ An in vivo assay measuring T cell epitope specific protection from pathogen challenge resulting from the adoptive transfer of epitope specific antibodies or B cells using pathogen burden.
IEDB
IEDB
pathogen burden after challenge after adoptive transfer|in vivo assay
@@ -19439,7 +19439,7 @@
- An in vivo assay measuring B cell epitope specific protection from pathogen challenge resulting from the adoptive transfer of epitope specific antibodies or B cells using pathogen burden.
+ An in vivo assay measuring B cell epitope specific protection from pathogen challenge resulting from the adoptive transfer of epitope specific antibodies or B cells using pathogen burden.
IEDB
IEDB
pathogen burden after challenge after adoptive transfer|in vivo assay
@@ -19524,7 +19524,7 @@
- An in vivo assay measuring T cell epitope specific protection from other challenge resulting from the adoptive transfer of epitope specific T cells using survival.
+ An in vivo assay measuring T cell epitope specific protection from other challenge resulting from the adoptive transfer of epitope specific T cells using survival.
IEDB
IEDB
survival from other challenge after adoptive transfer|in vivo assay
@@ -19609,7 +19609,7 @@
- An in vivo assay measuring B cell epitope specific protection from other challenge resulting from the adoptive transfer of epitope specific antibodies or B cells using survival.
+ An in vivo assay measuring B cell epitope specific protection from other challenge resulting from the adoptive transfer of epitope specific antibodies or B cells using survival.
IEDB
IEDB
survival from other challenge after adoptive transfer|in vivo assay
@@ -19683,7 +19683,7 @@
- An in vivo assay measuring T cell epitope specific protection from tumor challenge resulting from the adoptive transfer of epitope specific T cells using tumor burden.
+ An in vivo assay measuring T cell epitope specific protection from tumor challenge resulting from the adoptive transfer of epitope specific T cells using tumor burden.
IEDB
IEDB
tumor burden after challenge after adoptive transfer|in vivo assay
@@ -19757,7 +19757,7 @@
- An in vivo assay measuring B cell epitope specific protection from tumor challenge resulting from the adoptive transfer of epitope specific antibodies or B cells using tumor burden.
+ An in vivo assay measuring B cell epitope specific protection from tumor challenge resulting from the adoptive transfer of epitope specific antibodies or B cells using tumor burden.
IEDB
IEDB
tumor burden after challenge after adoptive transfer|in vivo assay
@@ -19823,7 +19823,7 @@
- An efficacy of T cell epitope intervention experiment that uses a tolerance induction intervention experiment after adoptive transfer of epitope specfic T cells.
+ An efficacy of T cell epitope intervention experiment that uses a tolerance induction intervention experiment after adoptive transfer of epitope specfic T cells.
IEDB
IEDB
tolerance after adoptive transfer|in vivo assay
@@ -19889,7 +19889,7 @@
- An efficacy of B cell epitope intervention experiment that uses a tolerance induction intervention experiment after adoptive transfer of epitope specific antibodies or B cells.
+ An efficacy of B cell epitope intervention experiment that uses a tolerance induction intervention experiment after adoptive transfer of epitope specific antibodies or B cells.
IEDB
IEDB
tolerance after adoptive transfer|in vivo assay
@@ -19927,7 +19927,7 @@
- A cytometric bead array assay that detects interleukin-15 production by T cells.
+ A cytometric bead array assay that detects interleukin-15 production by T cells.
IEDB
IEDB
IL-15 release|cytometric bead array
@@ -19965,7 +19965,7 @@
- A cytometric bead array assay that detects interleukin-16 production by T cells.
+ A cytometric bead array assay that detects interleukin-16 production by T cells.
IEDB
IEDB
IL-16 release|cytometric bead array
@@ -20031,7 +20031,7 @@
- An efficacy of B cell epitope intervention experiment that detects a hypersensitivity response by monitoring skin reactions after adoptive transfer of epitope specific antibodies or B cells.
+ An efficacy of B cell epitope intervention experiment that detects a hypersensitivity response by monitoring skin reactions after adoptive transfer of epitope specific antibodies or B cells.
IEDB
IEDB
hypersensitivity after adoptive transfer|in vivo assay
@@ -20097,7 +20097,7 @@
- An efficacy of T cell epitope intervention experiment that detects epitope specific type IV hypersensitivity after adoptive transfer of epitope specfic T cells.
+ An efficacy of T cell epitope intervention experiment that detects epitope specific type IV hypersensitivity after adoptive transfer of epitope specfic T cells.
IEDB
IEDB
type IV hypersensitivity (DTH) after adoptive transfer|in vivo skin test
@@ -20163,7 +20163,7 @@
- A T cell epitope specific proliferation assay that is performed in vivo after adoptive transfer of epitope specfic T cells.
+ A T cell epitope specific proliferation assay that is performed in vivo after adoptive transfer of epitope specfic T cells.
IEDB
IEDB
proliferation after adoptive transfer|in vivo assay
@@ -20229,7 +20229,7 @@
- A T cell epitope specific helper activity assay that detects the ability of a T cell epitope to enhance an antibody response after adoptive transfer of epitope specfic T cells.
+ A T cell epitope specific helper activity assay that detects the ability of a T cell epitope to enhance an antibody response after adoptive transfer of epitope specfic T cells.
IEDB
IEDB
antibody help after adoptive transfer|in vivo assay
@@ -20295,7 +20295,7 @@
- A T cell epitope specific helper activity assay that detects the ability of a T cell epitope to enhance a T cell response after adoptive transfer of epitope specfic T cells.
+ A T cell epitope specific helper activity assay that detects the ability of a T cell epitope to enhance a T cell response after adoptive transfer of epitope specfic T cells.
IEDB
IEDB
T cell help after adoptive transfer|in vivo assay
@@ -20361,7 +20361,7 @@
- An in vivo cell killing assay that detects the killing of an antigen presenting cell (APC) by a T cell whose TCR recognizes an epitope presented by the APC after adoptive transfer of epitope specific T cells.
+ An in vivo cell killing assay that detects the killing of an antigen presenting cell (APC) by a T cell whose TCR recognizes an epitope presented by the APC after adoptive transfer of epitope specific T cells.
IEDB
IEDB
cytotoxicity after adoptive transfer|in vivo assay
@@ -20399,7 +20399,7 @@
- An enzyme-linked immunosorbent assay that detects epitope specific perforin release by T cells.
+ An enzyme-linked immunosorbent assay that detects epitope specific perforin release by T cells.
IEDB
IEDB
perforin release|ELISA
@@ -20460,7 +20460,7 @@
- An efficacy of T cell epitope intervention experiment that is performed after adoptive transfer of epitope specfic T cells.
+ An efficacy of T cell epitope intervention experiment that is performed after adoptive transfer of epitope specfic T cells.
IEDB
IEDB
in vivo response after adoptive transfer|in vivo assay
@@ -20521,7 +20521,7 @@
- An efficacy of B cell epitope intervention experiment that is performed after adoptive transfer of epitope specific antibodies or B cells.
+ An efficacy of B cell epitope intervention experiment that is performed after adoptive transfer of epitope specific antibodies or B cells.
IEDB
IEDB
in vivo response after adoptive transfer|in vivo assay
@@ -20582,7 +20582,7 @@
- An efficacy of T cell epitope intervention experiment that uses a disease exacerbation in vivo intervention experiment after adoptive transfer of epitope specfic T cells.
+ An efficacy of T cell epitope intervention experiment that uses a disease exacerbation in vivo intervention experiment after adoptive transfer of epitope specfic T cells.
IEDB
IEDB
disease exacerbation after adoptive transfer|in vivo assay
@@ -20651,7 +20651,7 @@
- An immune epitope assay that characterizes the structrue of an antibody-epitope complex, or measures the binding of an antibody receptor to epitope, or the immune response process resulting from such a binding event or the recognition of the epitope.
+ An immune epitope assay that characterizes the structrue of an antibody-epitope complex, or measures the binding of an antibody receptor to epitope, or the immune response process resulting from such a binding event or the recognition of the epitope.
IEDB
IEDB
B cell assay|any method
@@ -20690,7 +20690,7 @@
- An immune epitope assay that characterizes the structrue of an epitope-T cell receptor complex, or measures the binding of a T cell receptor to epitope, or the immune response process resulting from such a binding event or the recognition of the epitope.
+ An immune epitope assay that characterizes the structrue of an epitope-T cell receptor complex, or measures the binding of a T cell receptor to epitope, or the immune response process resulting from such a binding event or the recognition of the epitope.
IEDB
IEDB
T cell assay|any method
@@ -20746,7 +20746,7 @@
- An assay that detects the binding of a MHC molecule with a ligand, and produces a quantitative measurement of the binding as an output.
+ An assay that detects the binding of a MHC molecule with a ligand, and produces a quantitative measurement of the binding as an output.
IEDB
IEDB
quantitative binding|binding assay
@@ -20778,7 +20778,7 @@
- An assay that detects the binding of an antigen with an antibody, and produces a quantitative measurement of the binding as an output.
+ An assay that detects the binding of an antigen with an antibody, and produces a quantitative measurement of the binding as an output.
IEDB
IEDB
quantitative binding|binding assay
@@ -20810,7 +20810,7 @@
- An assay that detects the binding of a MHC:epitope complex with a T cell receptor, and produces a quantitative measurement of the binding as an output.
+ An assay that detects the binding of a MHC:epitope complex with a T cell receptor, and produces a quantitative measurement of the binding as an output.
IEDB
IEDB
quantitative binding|binding assay
@@ -20848,7 +20848,7 @@
- A cytometric bead array assay that detects epitope specific granulysin release by T cells.
+ A cytometric bead array assay that detects epitope specific granulysin release by T cells.
IEDB
IEDB
granulysin release|cytometric bead array
@@ -20886,7 +20886,7 @@
- A cytometric bead array assay that detects epitope specific perforin release by T cells.
+ A cytometric bead array assay that detects epitope specific perforin release by T cells.
IEDB
IEDB
perforin release|cytometric bead array
@@ -20924,7 +20924,7 @@
- A T cell epitope specific cytokine production assay that detects amphiregulin production by T cells.
+ A T cell epitope specific cytokine production assay that detects amphiregulin production by T cells.
IEDB
IEDB
amphiregulin release|biological activity
@@ -20962,7 +20962,7 @@
- An enzyme-linked immunosorbent assay that detects amphiregulin production by T cells.
+ An enzyme-linked immunosorbent assay that detects amphiregulin production by T cells.
IEDB
IEDB
amphiregulin release|ELISA
@@ -21000,7 +21000,7 @@
Next-generation high-density peptide microarrays measuring antibody responses to overlapping peptides: PMID:25922409.
- A B cell epitope assay that measures the binding of an antibody receptor to an epitope using a high throughput multiplexed assay.
+ A B cell epitope assay that measures the binding of an antibody receptor to an epitope using a high throughput multiplexed assay.
IEDB
IEDB
antibody binding|High throughput multiplexed assay
@@ -21014,7 +21014,7 @@
Adaptive Biotech multiplexed TCR sequencing assays: PMID:32793919.
- A T cell epitope assay that measures the binding of T cell receptor to an epitope using a high throughput multiplexed assay.
+ A T cell epitope assay that measures the binding of T cell receptor to an epitope using a high throughput multiplexed assay.
IEDB
IEDB
T cell binding|High throughput multiplexed assay
@@ -21028,7 +21028,7 @@
Peptide microarray with fluorescence detection for millions of MHC binding measurements: PMID: 33705522.
- A MHC ligand assay that detects the binding of a ligand to an MHC molecule using a high throughput multiplexed assay.
+ A MHC ligand assay that detects the binding of a ligand to an MHC molecule using a high throughput multiplexed assay.
IEDB
IEDB
MHC binding|High throughput multiplexed assay
@@ -21042,7 +21042,7 @@
Mass spectrometry identified 35,367 and 28,132 HLA-class I ligands witth a false discovery rate: PMID: 29789417.
- A MHC ligand assay that determines what ligands are processed and loaded onto MHC molecules by eluting ligands and identifying them using a high throughput multiplexed assay.
+ A MHC ligand assay that determines what ligands are processed and loaded onto MHC molecules by eluting ligands and identifying them using a high throughput multiplexed assay.
IEDB
IEDB
ligand presentation|High throughput multiplexed assay
@@ -21086,7 +21086,7 @@
- A T cell epitope specific cytokine production assay that detects lymphotactin production by T cells.
+ A T cell epitope specific cytokine production assay that detects lymphotactin production by T cells.
IEDB
IEDB
lymphotactin release|biological activity
@@ -21124,7 +21124,7 @@
- An enzyme-linked immunosorbent assay that detects lymphotactin production by T cells.
+ An enzyme-linked immunosorbent assay that detects lymphotactin production by T cells.
IEDB
IEDB
lymphotactin release|ELISA
@@ -21219,7 +21219,7 @@
- An in vivo assay measuring T cell epitope specific protection from pathogen challenge.
+ An in vivo assay measuring T cell epitope specific protection from pathogen challenge.
IEDB
IEDB
protection from pathogen challenge|in vivo assay
@@ -21284,7 +21284,7 @@
- An in vivo assay measuring T cell epitope specific protection from tumor challenge.
+ An in vivo assay measuring T cell epitope specific protection from tumor challenge.
IEDB
IEDB
protection from tumor challenge|in vivo assay
@@ -21360,7 +21360,7 @@
- An in vivo assay measuring T cell epitope specific protection from a challenge other than pathogen, infection, or tumor.
+ An in vivo assay measuring T cell epitope specific protection from a challenge other than pathogen, infection, or tumor.
IEDB
IEDB
protection from other challenge|in vivo assay
@@ -21425,7 +21425,7 @@
- An in vivo assay measuring T cell epitope specific protection from tumor challenge using survival.
+ An in vivo assay measuring T cell epitope specific protection from tumor challenge using survival.
IEDB
IEDB
survival from tumor challenge|in vivo assay
@@ -21490,7 +21490,7 @@
- An in vivo assay measuring T cell epitope specific protection from pathogen challenge using survival.
+ An in vivo assay measuring T cell epitope specific protection from pathogen challenge using survival.
IEDB
IEDB
survival from pathogen challenge|in vivo assay
@@ -21555,7 +21555,7 @@
- An in vivo assay measuring B cell epitope specific protection from pathogen challenge.
+ An in vivo assay measuring B cell epitope specific protection from pathogen challenge.
IEDB
IEDB
protection from pathogen challenge|in vivo assay
@@ -21620,7 +21620,7 @@
- An in vivo assay measuring B cell epitope specific protection from tumor challenge.
+ An in vivo assay measuring B cell epitope specific protection from tumor challenge.
IEDB
IEDB
protection from tumor challenge|in vivo assay
@@ -21696,7 +21696,7 @@
- An in vivo assay measuring B cell epitope specific protection from a challenge other than pathogen, infection, or tumor.
+ An in vivo assay measuring B cell epitope specific protection from a challenge other than pathogen, infection, or tumor.
IEDB
IEDB
protection from other challenge|in vivo assay
@@ -21761,7 +21761,7 @@
- An in vivo assay measuring B cell epitope specific protection from pathogen challenge using survival.
+ An in vivo assay measuring B cell epitope specific protection from pathogen challenge using survival.
IEDB
IEDB
survival from pathogen challenge|in vivo assay
@@ -21826,7 +21826,7 @@
- An in vivo assay measuring B cell epitope specific protection from tumor challenge using survival.
+ An in vivo assay measuring B cell epitope specific protection from tumor challenge using survival.
IEDB
IEDB
survival from tumor challenge|in vivo assay
@@ -21891,7 +21891,7 @@
- An in vivo assay measuring a T cell epitope specific protection from a pathogen challenge after adoptive transfer of epitope specific antibodies or B cells.
+ An in vivo assay measuring a T cell epitope specific protection from a pathogen challenge after adoptive transfer of epitope specific antibodies or B cells.
IEDB
IEDB
protection from pathogen challenge after adoptive transfer|in vivo assay
@@ -21965,7 +21965,7 @@
- An in vivo assay measuring T cell epitope specific protection from pathogen challenge resulting from the adoptive transfer of epitope specific T cells using survival.
+ An in vivo assay measuring T cell epitope specific protection from pathogen challenge resulting from the adoptive transfer of epitope specific T cells using survival.
IEDB
IEDB
survival after pathogen challenge after adoptive transfer|in vivo assay
@@ -22030,7 +22030,7 @@
- An in vivo assay measuring a T cell epitope specific protection from a tumor challenge after adoptive transfer of epitope specific T cells.
+ An in vivo assay measuring a T cell epitope specific protection from a tumor challenge after adoptive transfer of epitope specific T cells.
IEDB
IEDB
protection from tumor challenge after adoptive transfer|in vivo assay
@@ -22104,7 +22104,7 @@
- An in vivo assay measuring T cell epitope specific protection from tumor challenge resulting from the adoptive transfer of epitope specific T cells using survival.
+ An in vivo assay measuring T cell epitope specific protection from tumor challenge resulting from the adoptive transfer of epitope specific T cells using survival.
IEDB
IEDB
survival after tumor challenge after adoptive transfer|in vivo assay
@@ -22180,7 +22180,7 @@
- An in vivo assay measuring a T cell epitope specific protection from other challenge after adoptive transfer of epitope specific T cells.
+ An in vivo assay measuring a T cell epitope specific protection from other challenge after adoptive transfer of epitope specific T cells.
IEDB
IEDB
protection from other challenge after adoptive transfer|in vivo assay
@@ -22245,7 +22245,7 @@
- An in vivo assay measuring a B cell epitope specific protection from a pathogen challenge after adoptive transfer of epitope specific antibodies or B cells.
+ An in vivo assay measuring a B cell epitope specific protection from a pathogen challenge after adoptive transfer of epitope specific antibodies or B cells.
IEDB
IEDB
protection from pathogen challenge after adoptive transfer|in vivo assay
@@ -22319,7 +22319,7 @@
- An in vivo assay measuring B cell epitope specific protection from pathogen challenge resulting from the adoptive transfer of epitope specific antibodies or B cells using survival.
+ An in vivo assay measuring B cell epitope specific protection from pathogen challenge resulting from the adoptive transfer of epitope specific antibodies or B cells using survival.
IEDB
IEDB
survival after pathogen challenge after adoptive transfer|in vivo assay
@@ -22384,7 +22384,7 @@
- An in vivo assay measuring a B cell epitope specific protection from a tumor challenge after adoptive transfer of epitope specific antibodies or B cells.
+ An in vivo assay measuring a B cell epitope specific protection from a tumor challenge after adoptive transfer of epitope specific antibodies or B cells.
IEDB
IEDB
protection from tumor challenge after adoptive transfer|in vivo assay
@@ -22458,7 +22458,7 @@
- An in vivo assay measuring B cell epitope specific protection from tumor challenge resulting from the adoptive transfer of epitope specific antibodies or B cells using survival.
+ An in vivo assay measuring B cell epitope specific protection from tumor challenge resulting from the adoptive transfer of epitope specific antibodies or B cells using survival.
IEDB
IEDB
survival after tumor challenge after adoptive transfer|in vivo assay
@@ -22534,7 +22534,7 @@
- An in vivo assay measuring a B cell epitope specific protection from other challenge after adoptive transfer of epitope specific antibodies or B cells.
+ An in vivo assay measuring a B cell epitope specific protection from other challenge after adoptive transfer of epitope specific antibodies or B cells.
IEDB
IEDB
protection from other challenge after adoptive transfer|in vivo assay
@@ -22572,7 +22572,7 @@
- A T cell epitope specific cytokine production assay that detects interleukin-25 production by T cells.
+ A T cell epitope specific cytokine production assay that detects interleukin-25 production by T cells.
IEDB
IEDB
IL-25 release|biological activity
@@ -22610,7 +22610,7 @@
- A detection of specific nucleic acid polymers with complementary probes that detects interleukin-25 production by T cells.
+ A detection of specific nucleic acid polymers with complementary probes that detects interleukin-25 production by T cells.
IEDB
IEDB
IL-25 release|RNA/DNA detection
@@ -22648,7 +22648,7 @@
- A flow cytometry assay that detects interleukin-25 production by T cells.
+ A flow cytometry assay that detects interleukin-25 production by T cells.
IEDB
IEDB
IL-25 release|ICS
@@ -22686,7 +22686,7 @@
- An enzyme-linked immunosorbent assay that detects interleukin-25 production by T cells.
+ An enzyme-linked immunosorbent assay that detects interleukin-25 production by T cells.
IEDB
IEDB
IL-25 release|ELISA
@@ -22724,7 +22724,7 @@
- A reporter cell line analyte detection bioassay that detects tumor necrosis factor superfamily cytokine production by T cells.
+ A reporter cell line analyte detection bioassay that detects tumor necrosis factor superfamily cytokine production by T cells.
IEDB
IEDB
TNF release|bioassay
@@ -22772,7 +22772,7 @@
quartz crystal microbalance measuring the dissociation constant [KD] of a B cell epitope:antibody complex
- A quartz crystal microbalance assay that measures the dissociation constant [KD] of an antigen binding with an antibody.
+ A quartz crystal microbalance assay that measures the dissociation constant [KD] of an antigen binding with an antibody.
Bjoern Peters
Randi Vita
Sebastian Duesing
@@ -22807,7 +22807,7 @@
- An electron-microscopy 3D molecular structure determination assay that characterizes the 3-dimensional molecular structrue of a T cell epitope:MHC:TCR complex.
+ An electron-microscopy 3D molecular structure determination assay that characterizes the 3-dimensional molecular structrue of a T cell epitope:MHC:TCR complex.
PERSON:Randi Vita, Sebastian Duesing, Bjoern Peters
IEDB
3D structure|electron microscopy
@@ -22839,7 +22839,7 @@
- An electron-microscopy 3D molecular structure determination assay that characterizes the 3-dimensional molecular structrue of a MHC:ligand complex.
+ An electron-microscopy 3D molecular structure determination assay that characterizes the 3-dimensional molecular structrue of a MHC:ligand complex.
PERSON:Randi Vita, Sebastian Duesing, Bjoern Peters
IEDB
3D structure|electron microscopy
@@ -22889,7 +22889,7 @@
- An enzyme-linked immunospot assay that detects interleukin-2 production by T cells.
+ An enzyme-linked immunospot assay that detects interleukin-2 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-2 release|ELISPOT
@@ -22921,7 +22921,7 @@
- A T cell epitope assay that measures the binding of T cell receptor to an epitope.
+ A T cell epitope assay that measures the binding of T cell receptor to an epitope.
IEDB
IEDB
T cell binding|any method
@@ -22965,7 +22965,7 @@
- An enzyme-linked immunospot assay that detects interferon-gamma production by T cells.
+ An enzyme-linked immunospot assay that detects interferon-gamma production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IFNg release|ELISPOT
@@ -22997,7 +22997,7 @@
- An assay that detects the binding of a MHC:epitope complex with a T cell receptor, and produces a qualitative measurement of the binding as an output.
+ An assay that detects the binding of a MHC:epitope complex with a T cell receptor, and produces a qualitative measurement of the binding as an output.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
qualitative binding|binding assay
@@ -23049,7 +23049,7 @@
- A MHC ligand assay that determines what ligands are processed and loaded onto MHC molecules by eluting ligands and identifying them.
+ A MHC ligand assay that determines what ligands are processed and loaded onto MHC molecules by eluting ligands and identifying them.
IEDB
IEDB
ligand presentation|any method
@@ -23081,7 +23081,7 @@
- A MHC ligand assay that detects the binding of a ligand to an MHC molecule.
+ A MHC ligand assay that detects the binding of a ligand to an MHC molecule.
IEDB
IEDB
MHC binding|any method
@@ -23113,7 +23113,7 @@
- A B cell epitope assay that measures the binding of an antibody receptor to an epitope.
+ A B cell epitope assay that measures the binding of an antibody receptor to an epitope.
IEDB
IEDB
antibody binding|any method
@@ -23172,7 +23172,7 @@
- An assay that detects the binding of an epitope to an adaptive immune receptor, or an immune process resulting from such a binding event, or characterizes the structrue of the complex resulting from such a binding event.
+ An assay that detects the binding of an epitope to an adaptive immune receptor, or an immune process resulting from such a binding event, or characterizes the structrue of the complex resulting from such a binding event.
IEDB
IEDB
immune epitope assay
@@ -23210,7 +23210,7 @@
- A T cell epitope assay that detects cytokine production by T cells.
+ A T cell epitope assay that detects cytokine production by T cells.
IEDB
IEDB
cytokine release|biological activity
@@ -23248,7 +23248,7 @@
- A T cell epitope dependent biological activity assay that detects the killing of an antigen presenting cell (APC) by a T cell whose TCR recognizes an epitope presented by the APC.
+ A T cell epitope dependent biological activity assay that detects the killing of an antigen presenting cell (APC) by a T cell whose TCR recognizes an epitope presented by the APC.
IEDB
IEDB
cytotoxicity|biological activity
@@ -23286,7 +23286,7 @@
- A T cell epitope dependent biological activity assay that detects T cell proliferation.
+ A T cell epitope dependent biological activity assay that detects T cell proliferation.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
proliferation|biological activity
@@ -23338,7 +23338,7 @@
- A chromium release assay that detects the killing of an antigen presenting cell (APC) by a T cell whose TCR recognizes an epitope presented by the APC.
+ A chromium release assay that detects the killing of an antigen presenting cell (APC) by a T cell whose TCR recognizes an epitope presented by the APC.
IEDB
IEDB
cytotoxicity|51 chromium
@@ -23376,7 +23376,7 @@
- An enzyme-linked immunosorbent assay that detects interferon-gamma production by T cells.
+ An enzyme-linked immunosorbent assay that detects interferon-gamma production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IFNg release|ELISA
@@ -23414,7 +23414,7 @@
- An enzyme-linked immunosorbent assay that detects interleukin-2 production by T cells.
+ An enzyme-linked immunosorbent assay that detects interleukin-2 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-2 release|ELISA
@@ -23452,7 +23452,7 @@
- An enzyme-linked immunosorbent assay that detects interleukin-4 production by T cells.
+ An enzyme-linked immunosorbent assay that detects interleukin-4 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-4 release|ELISA
@@ -23490,7 +23490,7 @@
- An enzyme-linked immunosorbent assay that detects interleukin-5 production by T cells.
+ An enzyme-linked immunosorbent assay that detects interleukin-5 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-5 release|ELISA
@@ -23528,7 +23528,7 @@
- An enzyme-linked immunosorbent assay that detects tumor necrosis factor alpha production by T cells.
+ An enzyme-linked immunosorbent assay that detects tumor necrosis factor alpha production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
TNFa release|ELISA
@@ -23566,7 +23566,7 @@
- An enzyme-linked immunosorbent assay that detects interleukin-10 production by T cells.
+ An enzyme-linked immunosorbent assay that detects interleukin-10 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-10 release|ELISA
@@ -23604,7 +23604,7 @@
- An enzyme-linked immunosorbent assay that detects granulocyte macrophage colony stimulating factor production by T cells.
+ An enzyme-linked immunosorbent assay that detects granulocyte macrophage colony stimulating factor production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
GM-CSF release|ELISA
@@ -23642,7 +23642,7 @@
- An enzyme-linked immunosorbent assay that detects interleukin-6 production by T cells.
+ An enzyme-linked immunosorbent assay that detects interleukin-6 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-6 release|ELISA
@@ -23680,7 +23680,7 @@
- An enzyme-linked immunosorbent assay that detects interleukin-13 production by T cells.
+ An enzyme-linked immunosorbent assay that detects interleukin-13 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-13 release|ELISA
@@ -23718,7 +23718,7 @@
- An enzyme-linked immunosorbent assay that detects interleukin-12 production by T cells.
+ An enzyme-linked immunosorbent assay that detects interleukin-12 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-12 release|ELISA
@@ -23756,7 +23756,7 @@
- An enzyme-linked immunosorbent assay that detects interleukin-1 beta production by T cells.
+ An enzyme-linked immunosorbent assay that detects interleukin-1 beta production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-1b release|ELISA
@@ -23794,7 +23794,7 @@
- An enzyme-linked immunosorbent assay that detects interleukin-17 production by T cells.
+ An enzyme-linked immunosorbent assay that detects interleukin-17 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-17 release|ELISA
@@ -23832,7 +23832,7 @@
- An enzyme-linked immunosorbent assay that detects interleukin-18 production by T cells.
+ An enzyme-linked immunosorbent assay that detects interleukin-18 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-18 release|ELISA
@@ -23870,7 +23870,7 @@
- An enzyme-linked immunospot assay that detects interleukin-4 production by T cells.
+ An enzyme-linked immunospot assay that detects interleukin-4 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-4 release|ELISPOT
@@ -23908,7 +23908,7 @@
- An enzyme-linked immunospot assay that detects tumor necrosis factor alpha production by T cells
+ An enzyme-linked immunospot assay that detects tumor necrosis factor alpha production by T cells
IEDB
IEDB
TNFa release|ELISPOT
@@ -23946,7 +23946,7 @@
- An enzyme-linked immunospot assay that detects interleukin-10 production by T cells.
+ An enzyme-linked immunospot assay that detects interleukin-10 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-10 release|ELISPOT
@@ -23984,7 +23984,7 @@
- An enzyme-linked immunospot assay that detects interleukin-13 production by T cells.
+ An enzyme-linked immunospot assay that detects interleukin-13 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-13 release|ELISPOT
@@ -24022,7 +24022,7 @@
- A flow cytometry assay that detects interferon-gamma production by T cells.
+ A flow cytometry assay that detects interferon-gamma production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IFNg release|ICS
@@ -24060,7 +24060,7 @@
- A flow cytometry assay that detects interleukin-2 production by T cells.
+ A flow cytometry assay that detects interleukin-2 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-2 release|ICS
@@ -24098,7 +24098,7 @@
- A flow cytometry assay that detects tumor necrosis factor alpha production by T cells.
+ A flow cytometry assay that detects tumor necrosis factor alpha production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
TNFa release|ICS
@@ -24136,7 +24136,7 @@
- A flow cytometry assay that detects interleukin-4 production by T cells.
+ A flow cytometry assay that detects interleukin-4 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-4 release|ICS
@@ -24174,7 +24174,7 @@
- A flow cytometry assay that detects interleukin-10 production by T cells.
+ A flow cytometry assay that detects interleukin-10 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-10 release|ICS
@@ -24212,7 +24212,7 @@
- A flow cytometry assay that detects interleukin-17 production by T cells.
+ A flow cytometry assay that detects interleukin-17 production by T cells.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
IL-17 release|ICS
@@ -24266,7 +24266,7 @@
- A MHC tetramer/multimer assay that measures the binding of an epitope:MHC complex binding with a T cell receptor.
+ A MHC tetramer/multimer assay that measures the binding of an epitope:MHC complex binding with a T cell receptor.
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB
qualitative binding|multimer/tetramer
@@ -24318,7 +24318,7 @@
- A tritiated thymidine incorporation assay that detects T cell epitope specific proliferation in vitro.
+ A tritiated thymidine incorporation assay that detects T cell epitope specific proliferation in vitro.
IEDB
IEDB
proliferation|3H-thymidine
@@ -24370,7 +24370,7 @@
- A BrdU incorporation assay that detects T cell epitope specific proliferation in vitro.
+ A BrdU incorporation assay that detects T cell epitope specific proliferation in vitro.
IEDB
IEDB
proliferation|BrdU
diff --git a/src/ontology/modules/medical-history.owl b/src/ontology/modules/medical-history.owl
index 8d4bf194..a3f717cf 100644
--- a/src/ontology/modules/medical-history.owl
+++ b/src/ontology/modules/medical-history.owl
@@ -97,7 +97,7 @@
- A clinical history in which there is a diagnosis of cancer.
+ A clinical history in which there is a diagnosis of cancer.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -110,7 +110,7 @@
- A clinical history in which there was no diagnosis of cancer.
+ A clinical history in which there was no diagnosis of cancer.
Chris Stoeckert, Helena Ellis
clinical history of no cancer
NCI BBRB, OBIB
@@ -124,7 +124,7 @@
- A clinical history in which it is not known whether there was a diagnosis of cancer.
+ A clinical history in which it is not known whether there was a diagnosis of cancer.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -137,7 +137,7 @@
- A diagnosis that is an assertion that a patient who is the subject of a diagnostic process has cancer.
+ A diagnosis that is an assertion that a patient who is the subject of a diagnostic process has cancer.
Chris Stoeckert, Helena Ellis
cancer diagnosis
OBIB
@@ -151,7 +151,7 @@
- A clinical history in which there is a diagnosis of cancer in a blood relative.
+ A clinical history in which there is a diagnosis of cancer in a blood relative.
Chris Stoeckert, Helena Ellis
family history of cancer
NCI BBRB, OBIB
@@ -165,7 +165,7 @@
- A clinical history in which there is a diagnosis of cancer in the female sibling of a parent.
+ A clinical history in which there is a diagnosis of cancer in the female sibling of a parent.
Chris Stoeckert, Helena Ellis
OBIB
NCI BBRB
@@ -178,7 +178,7 @@
- A clinical history in which there is a diagnosis of cancer in a male sibling.
+ A clinical history in which there is a diagnosis of cancer in a male sibling.
Chris Stoeckert, Helena Ellis
OBIB
NCI BBRB
@@ -191,7 +191,7 @@
- A clinical history in which there is a diagnosis of cancer in a person's female child.
+ A clinical history in which there is a diagnosis of cancer in a person's female child.
Chris Stoeckert, Helena Ellis
OBIB
NCI BBRB
@@ -204,7 +204,7 @@
- A clinical history in which there is a diagnosis of cancer in a male parent.
+ A clinical history in which there is a diagnosis of cancer in a male parent.
Chris Stoeckert, Helena Ellis
OBIB
NCI BBRB
@@ -217,7 +217,7 @@
- A clinical history in which there is a diagnosis of cancer in a female parent.
+ A clinical history in which there is a diagnosis of cancer in a female parent.
Chris Stoeckert, Helena Ellis
OBIB
NCI BBRB
@@ -230,7 +230,7 @@
- A clinical history in which there is a diagnosis of cancer in a female sibling.
+ A clinical history in which there is a diagnosis of cancer in a female sibling.
Chris Stoeckert, Helena Ellis
OBIB
NCI BBRB
@@ -243,7 +243,7 @@
- A clinical history in which there is a diagnosis of cancer in a person's male child.
+ A clinical history in which there is a diagnosis of cancer in a person's male child.
Chris Stoeckert, Helena Ellis
OBIB
NCI BBRB
@@ -256,7 +256,7 @@
- A clinical history in which there is a diagnosis of cancer in a male sibling of a parent.
+ A clinical history in which there is a diagnosis of cancer in a male sibling of a parent.
Chris Stoeckert, Helena Ellis
OBIB
NCI BBRB
@@ -269,7 +269,7 @@
- A clinical history in which there is a diagnosis of cancer in a female parent of a parent.
+ A clinical history in which there is a diagnosis of cancer in a female parent of a parent.
Chris Stoeckert, Helena Ellis
OBIB
NCI BBRB
@@ -282,7 +282,7 @@
- A clinical history in which there is a diagnosis of cancer in a male parent of a parent.
+ A clinical history in which there is a diagnosis of cancer in a male parent of a parent.
Chris Stoeckert, Helena Ellis
OBIB
NCI BBRB
@@ -295,7 +295,7 @@
- A clinical history in which there is a diagnosis of cancer in a male child of a sibling.
+ A clinical history in which there is a diagnosis of cancer in a male child of a sibling.
Chris Stoeckert, Helena Ellis
OBIB
NCI BBRB
@@ -308,7 +308,7 @@
- A clinical history in which there is a diagnosis of cancer in a female child of a sibling.
+ A clinical history in which there is a diagnosis of cancer in a female child of a sibling.
Chris Stoeckert, Helena Ellis
OBIB
NCI BBRB
@@ -321,7 +321,7 @@
- A diagnosis that is an assertion that a patient who is the subject of a diagnostic process has an infectious disease.
+ A diagnosis that is an assertion that a patient who is the subject of a diagnostic process has an infectious disease.
Chris Stoeckert, Helena Ellis
OBIB
NCI BBRB
@@ -334,7 +334,7 @@
- A diagnosis of infectious disease caused by the hepatitis B virus.
+ A diagnosis of infectious disease caused by the hepatitis B virus.
Chris Stoeckert, Helena Ellis
OBIB
NCI BBRB
@@ -347,7 +347,7 @@
- A diagnosis of infectious disease caused by the hepatitis C virus.
+ A diagnosis of infectious disease caused by the hepatitis C virus.
Chris Stoeckert, Helena Ellis
OBIB
NCI BBRB
@@ -360,7 +360,7 @@
- A diagnosis of infectious disease caused by the human immunodeficiency virus (1 or 2).
+ A diagnosis of infectious disease caused by the human immunodeficiency virus (1 or 2).
Chris Stoeckert, Helena Ellis
OBIB
NCI BBRB
@@ -373,7 +373,7 @@
- A clinical history in which there is repeated reactive screening assays for human immunodeficiency virus (1 or 2) antibodies regardless of the results of supplemental assays.
+ A clinical history in which there is repeated reactive screening assays for human immunodeficiency virus (1 or 2) antibodies regardless of the results of supplemental assays.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -386,7 +386,7 @@
- A clinical history in which there has been second hand exposure to tobacco smoking.
+ A clinical history in which there has been second hand exposure to tobacco smoking.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -399,7 +399,7 @@
- An exposure to second hand smoke that occurred in the (patient's) household when the person was a child.
+ An exposure to second hand smoke that occurred in the (patient's) household when the person was a child.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -412,7 +412,7 @@
- An exposure to second hand smoke in person's current household.
+ An exposure to second hand smoke in person's current household.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -425,7 +425,7 @@
- A clinical history in which a female has had a pregnancy.
+ A clinical history in which a female has had a pregnancy.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -438,7 +438,7 @@
- A measurement datum of the total number of pregnancies a woman has had.
+ A measurement datum of the total number of pregnancies a woman has had.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -451,7 +451,7 @@
- A measurement datum of the total number of live births a female has had.
+ A measurement datum of the total number of live births a female has had.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -464,7 +464,7 @@
- An age measurement datum performed on a female when her first biological child was born.
+ An age measurement datum performed on a female when her first biological child was born.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -477,7 +477,7 @@
- A clinical history in which a woman has had gynecologic surgery in the past.
+ A clinical history in which a woman has had gynecologic surgery in the past.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -490,7 +490,7 @@
- A gynecologic surgery history in which a woman has had a hysterectomy.
+ A gynecologic surgery history in which a woman has had a hysterectomy.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -503,7 +503,7 @@
- A gynecologic surgery history in which a woman has had a unilateral oophorectomy.
+ A gynecologic surgery history in which a woman has had a unilateral oophorectomy.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -516,7 +516,7 @@
- A gynecologic surgery history in which a woman has not had either a hysterectomy or an oophorectomy.
+ A gynecologic surgery history in which a woman has not had either a hysterectomy or an oophorectomy.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -529,7 +529,7 @@
- An information content entity that indicates whether a woman has ever used oral contraceptives in order to block ovulation and prevent the occurrence of pregnancy.
+ An information content entity that indicates whether a woman has ever used oral contraceptives in order to block ovulation and prevent the occurrence of pregnancy.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -542,7 +542,7 @@
- A hormonal birth control use history that indicates an individual has previously been a hormonal birth control user but is not a current user.
+ A hormonal birth control use history that indicates an individual has previously been a hormonal birth control user but is not a current user.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -555,7 +555,7 @@
- A hormonal birth control use history that indicates an individual is currently a hormonal birth control user.
+ A hormonal birth control use history that indicates an individual is currently a hormonal birth control user.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -568,7 +568,7 @@
- A hormonal birth control use history that indicates an individual has not ever been a hormonal birth control user.
+ A hormonal birth control use history that indicates an individual has not ever been a hormonal birth control user.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -581,7 +581,7 @@
- A clinical history in which an individual has had hormonal replacement therapy in the past.
+ A clinical history in which an individual has had hormonal replacement therapy in the past.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -594,7 +594,7 @@
- A processed material used for delivery of hormones in hormone replacement therapy.
+ A processed material used for delivery of hormones in hormone replacement therapy.
Chris Stoeckert, Helena Ellis
form of hormone replacement therapy
NCI BBRB, OBIB
@@ -608,7 +608,7 @@
- A delivery form for hormonal replacement therapy that is a pill for oral administration.
+ A delivery form for hormonal replacement therapy that is a pill for oral administration.
Chris Stoeckert, Helena Ellis
OBIB
NCI BBRB
@@ -621,7 +621,7 @@
- A delivery form for hormonal replacement therapy that is a patch for transdermal administration.
+ A delivery form for hormonal replacement therapy that is a patch for transdermal administration.
Chris Stoeckert, Helena Ellis
OBIB
NCI BBRB
@@ -634,7 +634,7 @@
- A delivery form for hormonal replacement therapy that is a cream for transdermal administration.
+ A delivery form for hormonal replacement therapy that is a cream for transdermal administration.
Chris Stoeckert, Helena Ellis
OBIB
NCI BBRB
@@ -647,7 +647,7 @@
- An information content entity that indicates the state of a female's cessation of menstruation.
+ An information content entity that indicates the state of a female's cessation of menstruation.
Chris Stoeckert, Helena Ellis
OBIB
NCI BBRB
@@ -660,7 +660,7 @@
- A menopausal status that is neither pre- nor post-menopausal.
+ A menopausal status that is neither pre- nor post-menopausal.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -673,7 +673,7 @@
- A menopausal status indicating that less than 6 months has passed since the last menstrual period and there has not been prior bilateral oophorectomy and not on estrogen replacement.
+ A menopausal status indicating that less than 6 months has passed since the last menstrual period and there has not been prior bilateral oophorectomy and not on estrogen replacement.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -686,7 +686,7 @@
- A menopausal status indicating that it has been 6-12 months since last menstrual period.
+ A menopausal status indicating that it has been 6-12 months since last menstrual period.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -699,7 +699,7 @@
- A menopausal status indicating that it has been more than 12 months since the last menstrual period with no prior hysterectomy or that there has been a prior bilateral oophorectomy.
+ A menopausal status indicating that it has been more than 12 months since the last menstrual period with no prior hysterectomy or that there has been a prior bilateral oophorectomy.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -712,7 +712,7 @@
- An information content entity that indicates the exposure of an individual to carcinogens in the workplace or environment.
+ An information content entity that indicates the exposure of an individual to carcinogens in the workplace or environment.
Chris Stoeckert, Helena Ellis
OBIB
NCI BBRB
@@ -725,7 +725,7 @@
- An exposure to environmental and workplace carcinogens history where the carcinogen is arsenic.
+ An exposure to environmental and workplace carcinogens history where the carcinogen is arsenic.
Chris Stoeckert, Helena Ellis
OBIB
NCI BBRB
@@ -738,7 +738,7 @@
- An exposure to environmental and workplace carcinogens history where the carcinogen is asbestos.
+ An exposure to environmental and workplace carcinogens history where the carcinogen is asbestos.
Chris Stoeckert, Helena Ellis
OBIB
NCI BBRB
@@ -751,7 +751,7 @@
- An exposure to environmental and workplace carcinogens history where the carcinogen is diesel exhaust.
+ An exposure to environmental and workplace carcinogens history where the carcinogen is diesel exhaust.
Chris Stoeckert, Helena Ellis
OBIB
NCI BBRB
@@ -764,7 +764,7 @@
- An exposure to environmental and workplace carcinogens history where the carcinogen is chromium.
+ An exposure to environmental and workplace carcinogens history where the carcinogen is chromium.
Chris Stoeckert, Helena Ellis
OBIB
NCI BBRB
@@ -777,7 +777,7 @@
- An exposure to environmental and workplace carcinogens history where the carcinogen is silica.
+ An exposure to environmental and workplace carcinogens history where the carcinogen is silica.
Chris Stoeckert, Helena Ellis
OBIB
NCI BBRB
@@ -790,7 +790,7 @@
- An information content entity that indicates whether or not an entity has met a specific requirement in order to take part in a given process.
+ An information content entity that indicates whether or not an entity has met a specific requirement in order to take part in a given process.
Chris Stoeckert, Helena Ellis
eligibility criterion met
NCI BBRB, OBIB
@@ -804,7 +804,7 @@
- An information content entity that indicates whether or not an entity has met all specific requirements in order to take part in a given process.
+ An information content entity that indicates whether or not an entity has met all specific requirements in order to take part in a given process.
Chris Stoeckert, Helena Ellis
all eligibility criteria met
NCI BBRB, OBIB
@@ -818,7 +818,7 @@
- An inclusion criterion that uses the age of majority for a state or institution, where one is generally considered to be an adult, which if met, makes an individual suitable for a given task or participation in a given process.
+ An inclusion criterion that uses the age of majority for a state or institution, where one is generally considered to be an adult, which if met, makes an individual suitable for a given task or participation in a given process.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -831,7 +831,7 @@
- An exclusion criterion that defines whether chemotherapy was received or is being received for a previous or current cancer, which when met, makes an individual unsuitable for a given task or participation in a given process
+ An exclusion criterion that defines whether chemotherapy was received or is being received for a previous or current cancer, which when met, makes an individual unsuitable for a given task or participation in a given process
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -844,7 +844,7 @@
- An exclusion criterion that defines whether radiation was received or is being received for a previous or current cancer, which when met, makes an individual unsuitable for a given task or participation in a given process
+ An exclusion criterion that defines whether radiation was received or is being received for a previous or current cancer, which when met, makes an individual unsuitable for a given task or participation in a given process
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -858,7 +858,7 @@
An exclusion criterion defined by the pathologist is defined as whether the individual received chemotherapy within the last two years.
- An exclusion criterion that defines whether chemotherapy was received within a certain timeframe, which when met, makes an individual unsuitable for a given task or participation in a given process.
+ An exclusion criterion that defines whether chemotherapy was received within a certain timeframe, which when met, makes an individual unsuitable for a given task or participation in a given process.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -872,7 +872,7 @@
An exclusion criterion defined by the pathologist is defined as whether the individual received radiation therapy within the last two years.
- An exclusion criterion that defines whether radiation was received within a certain timeframe, which when met, makes an individual unsuitable for a given task or participation in a given process.
+ An exclusion criterion that defines whether radiation was received within a certain timeframe, which when met, makes an individual unsuitable for a given task or participation in a given process.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -886,7 +886,7 @@
An important inclusion criterion is for for the individual to have a BMI between 18.5 and 35.0
- An inclusion criterion that defines and states a Body Mass Index range, which if met, makes an individual suitable for a given task or participation in a given process.
+ An inclusion criterion that defines and states a Body Mass Index range, which if met, makes an individual suitable for a given task or participation in a given process.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -900,7 +900,7 @@
An exclusion criterion that is defined by whether the specimen donor received a whole blood transfusion within 48 hours prior to death.
- An exclusion criterion that is defined by whether the specimen donor received a whole blood transfusion within a specified time frame prior to death, which if met, makes a specimen donor unsuitable for a given task or participation in a given process.
+ An exclusion criterion that is defined by whether the specimen donor received a whole blood transfusion within a specified time frame prior to death, which if met, makes a specimen donor unsuitable for a given task or participation in a given process.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -913,7 +913,7 @@
- An exclusion criterion defined as whether an individual has ever been diagnosed with metastatic cancer (cancer that spread beyond the initial site such as to other organs like brain bone or liver), which if met, makes the individual unsuitable for a given task or participation in a given process.
+ An exclusion criterion defined as whether an individual has ever been diagnosed with metastatic cancer (cancer that spread beyond the initial site such as to other organs like brain bone or liver), which if met, makes the individual unsuitable for a given task or participation in a given process.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -927,7 +927,7 @@
Donor eligibility based on history of intravenous drug abuse in the last 5 years.
- An exclusion criterion defined as when an individual has a history of intravenous drug abuse for a specific timeframe, which if met, makes the individual unsuitable for a given task or participation in a given process.
+ An exclusion criterion defined as when an individual has a history of intravenous drug abuse for a specific timeframe, which if met, makes the individual unsuitable for a given task or participation in a given process.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -941,7 +941,7 @@
Donor eligibility based on whether the donor has a history of sex with someone who has been diagnosed or at risk for HIV/AIDS and/or HCV and/or HBV in the last 5 years.
- An exclusion criterion defined as whether an individual has a history of sex with someone who has been diagnosed or at risk for a blood borne infections disease in a specified time frame, which if met, makes the individual unsuitable for a given task or participation in a given process.
+ An exclusion criterion defined as whether an individual has a history of sex with someone who has been diagnosed or at risk for a blood borne infections disease in a specified time frame, which if met, makes the individual unsuitable for a given task or participation in a given process.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -955,7 +955,7 @@
Donor eligibility based on whether the donor has a history of sex with someone who has used intravenous drugs in the last 5 years.
- An exclusion criterion defined as whether an individual has a history of sex with someone who has used intravenous drugs in a specified time frame, which if met, makes the individual unsuitable for a given task or participation in a given process.
+ An exclusion criterion defined as whether an individual has a history of sex with someone who has used intravenous drugs in a specified time frame, which if met, makes the individual unsuitable for a given task or participation in a given process.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -968,7 +968,7 @@
- An exclusion criterion defined as whether an individual has a history of repeatedly reactive screening assays for HIV-1 or HIV-2 antibody regardless of the results of supplemental assays, which if met, makes the individual unsuitable for a given task or participation in a given process.
+ An exclusion criterion defined as whether an individual has a history of repeatedly reactive screening assays for HIV-1 or HIV-2 antibody regardless of the results of supplemental assays, which if met, makes the individual unsuitable for a given task or participation in a given process.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
@@ -982,7 +982,7 @@
Donor eligibility based on whether the donor has been exposed to HIV/AIDS.
- An exclusion criterion defined as whether an individual has been exposed to a blood borne infections disease through needle sticks and/or contact with non-intact skin and/or contact with open wounds and/or contact with mucous membranes, which if met, makes the individual unsuitable for a given task or participation in a given process.
+ An exclusion criterion defined as whether an individual has been exposed to a blood borne infections disease through needle sticks and/or contact with non-intact skin and/or contact with open wounds and/or contact with mucous membranes, which if met, makes the individual unsuitable for a given task or participation in a given process.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBIB
NCI BBRB
diff --git a/src/ontology/modules/obsolete.owl b/src/ontology/modules/obsolete.owl
index d1a15197..3aeb9954 100644
--- a/src/ontology/modules/obsolete.owl
+++ b/src/ontology/modules/obsolete.owl
@@ -110,7 +110,7 @@
- A platform is an object_aggregate that is the set of instruments and software needed to perform a process. definition_source: OBI.
+ A platform is an object_aggregate that is the set of instruments and software needed to perform a process. definition_source: OBI.
OBI Instrument branch
OBI Instrument branch
@@ -126,7 +126,7 @@
Rat 1A; first enrolled patient to receive treatment
- First subject treated role is a study subject role borne by the subject realized in the application of the process specified in intervention study design with no previous study subject realizing the role prior in the study
+ First subject treated role is a study subject role borne by the subject realized in the application of the process specified in intervention study design with no previous study subject realizing the role prior in the study
Role Branch
OBI
@@ -143,7 +143,7 @@
1983 Sci. Amer. Jan. 58/2 Plasmids are routinely used as vectors for introducing foreign DNA into bacteria.
Some epidemiological aspects and vector role of tick infestation on layers in the Faisalabad district (Pakistan). http://journals.cambridge.org/action/displayAbstract;jsessionid=0373164489D00868AEEF2C556EB4FD29.tomcat1?fromPage=online&aid=624280
- a biological vector role is a material to be added role that is realized by the process of transmitting material to the organism that is the target of the transmission.
+ a biological vector role is a material to be added role that is realized by the process of transmitting material to the organism that is the target of the transmission.
GROUP: Role Branch
OBI and Wikipedia
@@ -158,7 +158,7 @@
- Label role is a role which inheres in a material entity and which is realized in a detection of label assay
+ Label role is a role which inheres in a material entity and which is realized in a detection of label assay
Role Branch
label
OBI
@@ -176,7 +176,7 @@
Escaped rat; human who moved to another city. Rat which escapes part way through a study; a human study participant who moved to another city before the study was completed (and stopped participating in the study)
- Dropout is a study subject role borne by an entity realized by a process of leaving the study earlier than the protocol specified and where the bearer of the dropout role had been borne study subject role prior to bearing dropout role.
+ Dropout is a study subject role borne by an entity realized by a process of leaving the study earlier than the protocol specified and where the bearer of the dropout role had been borne study subject role prior to bearing dropout role.
Role Branch
OBI
@@ -191,7 +191,7 @@
- a worker role of providing medical care either within or outside the study timeline
+ a worker role of providing medical care either within or outside the study timeline
Person:Jennifer Fostel
health care provider
@@ -208,7 +208,7 @@
115 patients received ipilimumab and blinded medication
Inert pill shaped like aspirin tablet
- Is a role which inheres in a material entity which is manufactured to be similar in appearance to a test material entity in e.g. a clinical trial to prevent participants from detecting which is the active and inactive substance
+ Is a role which inheres in a material entity which is manufactured to be similar in appearance to a test material entity in e.g. a clinical trial to prevent participants from detecting which is the active and inactive substance
Jennifer Fostel
Person:Helen Parkinson
@@ -223,7 +223,7 @@
- Place holder class, Utility class to gather the defined classes
+ Place holder class, Utility class to gather the defined classes
Susanna Sansone
OBI Biomaterial derived
@@ -239,7 +239,7 @@
Patterns of benzylpiperazine/trifluoromethylphenylpiperazine party pill use and adverse effects in a population sample in New Zealand. Drug Alcohol Rev. 2008 Mar 31:1-7. PMID: 18608458
- A sample population is an object aggregate that is selected from the population, e.g. the fish in the net that were sampled from the lake, the people that responded to the call for volunteers.
+ A sample population is an object aggregate that is selected from the population, e.g. the fish in the net that were sampled from the lake, the people that responded to the call for volunteers.
PERSON: Jennifer Fostel
PERSON: Philippe Rocca-Serra
recruited population
@@ -257,7 +257,7 @@
Enrollment of patients in a study. Short-term outcome of neuropsychiatric events in systemic lupus erythematosus upon enrollment into an international inception cohort study. Arthritis Rheum. 2008 May 15;59(5):721-9. PMID: 18438902
- enrollment is a process of identifying a set of objects for further use in an investigation based on a set of criteria or rules
+ enrollment is a process of identifying a set of objects for further use in an investigation based on a set of criteria or rules
Bjoern Peters
IEDB
@@ -272,7 +272,7 @@
- is the serous membrane that forms the lining of the abdominal cavity
+ is the serous membrane that forms the lining of the abdominal cavity
obsolete_peritoneum
true
@@ -302,7 +302,7 @@
A trypsinized suspension of cells
- A material entity that has undergone a process of digestion with trypsin
+ A material entity that has undergone a process of digestion with trypsin
Person:Bjoern Peters
obsolete_trypsinized material
@@ -317,7 +317,7 @@
Alan Ruttenberg's heart
- The heart is a muscular organ found in all vertebrates that is responsible for pumping blood throughout the blood vessels by repeated, rhythmic contractions
+ The heart is a muscular organ found in all vertebrates that is responsible for pumping blood throughout the blood vessels by repeated, rhythmic contractions
Person:Bjoern Peters
http://en.wikipedia.org/wiki/Heart
@@ -333,7 +333,7 @@
DNA cleavage assay for the identification of topoisomerase I inhibitors. Nat Protoc. 2008;3(11):1736-50. PMID: 18927559
- a process by which the identity (what a thing is) of a material entity is established within a certain confidence interval
+ a process by which the identity (what a thing is) of a material entity is established within a certain confidence interval
Philippe Rocca-Serra
obsolete_identification
@@ -348,7 +348,7 @@
example of subclass: normalized data set - A normalized data set is a data set that is produced as the output of a normalization data transformation.
- This is only a placeholder for defined classes, as are its siblings _defined_material and _defined protocol application. Its children should be defined classes constructed as output of a process.
+ This is only a placeholder for defined classes, as are its siblings _defined_material and _defined protocol application. Its children should be defined classes constructed as output of a process.
PERSON: Alan Ruttenberg
PERSON: James Malone
PERSON: Melanie Courtot
@@ -365,7 +365,7 @@
the phosphate concentration should be 0.1M
- A concentration is a relational quality that inheres in a material entity towards molecular scattered aggregate that is part of it by virtue of some ratio of masses of the two or the counts of the grains of the two or volume occupied by the larger material entity.
+ A concentration is a relational quality that inheres in a material entity towards molecular scattered aggregate that is part of it by virtue of some ratio of masses of the two or the counts of the grains of the two or volume occupied by the larger material entity.
PERSON: Alan Ruttenberg
Discussion in Karslruhe, Oct 2008, with, among others, Alan Rector, Stefan Schulz, Marijke Keet, Melanie Courtot, and Alan Ruttenberg.
@@ -381,7 +381,7 @@
Permeabilizing T cells and staining them with fluorescent labeled anti-IFN-gamma antibodies
- The measurement of cytokines within the cytoplasm of a cell by permeabilizing the cell membrane to allow entry of specific antibodies, and counting the stained cells using a flow cytometer.
+ The measurement of cytokines within the cytoplasm of a cell by permeabilizing the cell membrane to allow entry of specific antibodies, and counting the stained cells using a flow cytometer.
IEDB
ICCS
ICS
@@ -401,7 +401,7 @@
Measuring T cells that are specific for the SYFPEITHI peptide when presented by the murine MHC molecule H-2 Kd by staining them with a tetramer of peptide loaded MHC complexes.
- An MHC multimer assay is an assay that detects T cells capable of binding the MHC:ligand complexes present in the multimer. The multimer is fluorescently labelled. The T cells bound to multimers are counted in a flow cytometer
+ An MHC multimer assay is an assay that detects T cells capable of binding the MHC:ligand complexes present in the multimer. The multimer is fluorescently labelled. The T cells bound to multimers are counted in a flow cytometer
IEDB
MHC tetramer assay
IEDB
@@ -419,7 +419,7 @@
- Study result is an information content entity that is a specified data output of a study.
+ Study result is an information content entity that is a specified data output of a study.
GROUP: OBI
obsolete_study result
@@ -433,7 +433,7 @@
- A DNA ligase is an enzyme that covalently joins two compatible pieces of DNA through the cleavage of an ATP molecule
+ A DNA ligase is an enzyme that covalently joins two compatible pieces of DNA through the cleavage of an ATP molecule
Kevin Clancy, Bjoern Peters
ligase
@@ -464,7 +464,7 @@
SIINFEKL' is the primary structure of a peptide
- The primary structure of a protein that is completely defined by the set of its amino acid residue parts and the linear order induced by the peptide bonds that hold them together
+ The primary structure of a protein that is completely defined by the set of its amino acid residue parts and the linear order induced by the peptide bonds that hold them together
Person:Bjoern Peters
obsolete_primary structure of protein
@@ -477,7 +477,7 @@
- A quality inhering in a molecule that is completely defined by the linear sequence of a set of residues which are connected by directional, linear bonds
+ A quality inhering in a molecule that is completely defined by the linear sequence of a set of residues which are connected by directional, linear bonds
Person:Bjoern Peters
obsolete_primary structure of sequence macromolecule
@@ -492,7 +492,7 @@
human ethics approval was obtained from the Southern Tasmania Health & Medical Human Research Ethics Committee and the Royal Hobart Hospital Research Ethics Committee [pmid:19696660]
- A medical organization at which sick or injured people are given clinical care
+ A medical organization at which sick or injured people are given clinical care
Person:Alan Ruttenberg
Person:Helen Parkinson
modified from the wording of the wordnet definition; http://www.golovchenko.org/cgi-bin/wnsearch?q=hospital#2n
@@ -521,7 +521,7 @@
- An assay in which the presence of a material inside a cell is measured by permeabilizing the cell membrane to allow entry of specific antibodies, and counting the stained cells using a flow cytometer.
+ An assay in which the presence of a material inside a cell is measured by permeabilizing the cell membrane to allow entry of specific antibodies, and counting the stained cells using a flow cytometer.
intracellular staining
@@ -548,7 +548,7 @@
EBI provides training on databases and tools and has a training service provider role
- a service provider role which is realized by a servicer provider organization performing some training
+ a service provider role which is realized by a servicer provider organization performing some training
PERSON:Helen Parkinson
OBI
@@ -564,7 +564,7 @@
A person or organization who provides access to a DNA sequencer.
- a service provider role which is realized by a servicer provider organization performing access to some material
+ a service provider role which is realized by a servicer provider organization performing access to some material
PERSON:Helen Parkinson
OBI
@@ -601,7 +601,7 @@
- a processed material created to have a function and which requires electrical power to execute
+ a processed material created to have a function and which requires electrical power to execute
obsolete_electrically powered device
true
@@ -626,7 +626,7 @@
DNA sequencing of a sample by a core lab which returns data to the consumer
- a service provider role which is realized by a servicer provider organization performing a protocol execution
+ a service provider role which is realized by a servicer provider organization performing a protocol execution
PERSON:Helen Parkinson
obsolete_protocol service provider role
@@ -640,7 +640,7 @@
- A training process with the objective to provide a trainee with the skill to run DNA sequencing experiments
+ A training process with the objective to provide a trainee with the skill to run DNA sequencing experiments
obsolete_DNA sequencing training service
true
@@ -666,7 +666,7 @@
Diagnosing that a patient has pneumonia based on information on measurements of temperature, sound of breathing, and patient complaining about a headache.
- The interpretation of the information available about bodily features (clinical picture) of a patient resulting in a diagnosis
+ The interpretation of the information available about bodily features (clinical picture) of a patient resulting in a diagnosis
https://github.com/obi-ontology/obi/issues/623
obsolete performing a diagnosis
@@ -680,7 +680,7 @@
- A binding assay where the specified output determines if two or more material entities do or do not have the disposition to form a complex above a threshold level of significance. The threshold can be defined through detection limits of the instrument, the use of experimental controls that establish what is considered significant binding, or a predefined cutoff based on what binding is considered significant in a certain context.
+ A binding assay where the specified output determines if two or more material entities do or do not have the disposition to form a complex above a threshold level of significance. The threshold can be defined through detection limits of the instrument, the use of experimental controls that establish what is considered significant binding, or a predefined cutoff based on what binding is considered significant in a certain context.
PERSON: Bjoern Peters, Randi Vita, Jason Greenbaum
obsolete_qualitative binding detection assay
@@ -694,7 +694,7 @@
- A specimen fixation function is a function that holds or fastens an entity in a fixed position.
+ A specimen fixation function is a function that holds or fastens an entity in a fixed position.
EAGLE-I
obsolete_specimen fixation function
@@ -708,7 +708,7 @@
- An intracellular material detection by flow cytometry assay that measures epitope specific cytotoxic T cell degranulation
+ An intracellular material detection by flow cytometry assay that measures epitope specific cytotoxic T cell degranulation
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB (QTT)
@@ -726,7 +726,7 @@
Using proliferation of a T cell line specific for SIINFEKL in response to material eluted from a cell as evidence that SIINFEKL was presented by MHC on that cell.
- An assay that identifies an MHC ligand using a T cell response assay as a readout
+ An assay that identifies an MHC ligand using a T cell response assay as a readout
PERSON: Randi Vita, Bjoern Peters
IEDB
@@ -743,7 +743,7 @@
- An assay that measures the affinity of a ligand to a MHC in a cell lysate preparation and that quantifies the affinity with a binding constant.
+ An assay that measures the affinity of a ligand to a MHC in a cell lysate preparation and that quantifies the affinity with a binding constant.
PERSON: Bjoern Peters
IEDB
@@ -758,7 +758,7 @@
- An assay that measures the affinity of a ligand to MHC moleculs bound to the cell surface and that quantifies the affinity with a binding constant.
+ An assay that measures the affinity of a ligand to MHC moleculs bound to the cell surface and that quantifies the affinity with a binding constant.
PERSON: Bjoern Peters
IEDB
@@ -773,7 +773,7 @@
- competitive inhibition of binding assay measuring MHC ligand binding by radioactivity detection using MHC derived from a cell lysate
+ competitive inhibition of binding assay measuring MHC ligand binding by radioactivity detection using MHC derived from a cell lysate
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB (QTT)
@@ -790,7 +790,7 @@
- An assay that measures the affinity of a ligand to a purified MHC complex preparation and that quantifies the affinity with a binding constant.
+ An assay that measures the affinity of a ligand to a purified MHC complex preparation and that quantifies the affinity with a binding constant.
PERSON: Bjoern Peters
IEDB
@@ -805,7 +805,7 @@
- direct binding assay measuring MHC ligand binding using MHC derived from a cell
+ direct binding assay measuring MHC ligand binding using MHC derived from a cell
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB (QTT)
@@ -821,7 +821,7 @@
- direct binding assay measuring MHC ligand binding using MHC derived from a purified MHC molecule preparation
+ direct binding assay measuring MHC ligand binding using MHC derived from a purified MHC molecule preparation
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB (QTT)
@@ -837,7 +837,7 @@
- A direct binding assay using a assay
+ A direct binding assay using a assay
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB (QTT)
@@ -853,7 +853,7 @@
- A competitive inhibition of binding assay using a assay
+ A competitive inhibition of binding assay using a assay
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB (QTT)
@@ -869,7 +869,7 @@
- A X-ray crystallography assay measuring epitope specfic antibody binding event in angstroms
+ A X-ray crystallography assay measuring epitope specfic antibody binding event in angstroms
PERSON:Randi Vita, Jason Greenbaum, Bjoern Peters
IEDB (QTT)
@@ -887,7 +887,7 @@
Tissue, organ, system, sperm, blood or body location (arm).
- An anatomical entity is a material entity that is part of a multicellular organism, and which is large enough so that it forms an identifiable structure in the organism. Specifically, it excludes granular parts of the organism, such as atoms, molecules, cells, which can be removed from the organism without affecting it. It is defined as the union of 'multi-tissue structure', 'body substance' and 'portion of tissue'
+ An anatomical entity is a material entity that is part of a multicellular organism, and which is large enough so that it forms an identifiable structure in the organism. Specifically, it excludes granular parts of the organism, such as atoms, molecules, cells, which can be removed from the organism without affecting it. It is defined as the union of 'multi-tissue structure', 'body substance' and 'portion of tissue'
Bjoern Peters
Philippe Rocca-Serra
Tina Boussard
@@ -905,7 +905,7 @@
a single Hela cell
- a cell derived from a multicellular organism that has the potential to replicate indefinitely
+ a cell derived from a multicellular organism that has the potential to replicate indefinitely
PERSON: Bjoern Peters
GROUP: OBI Biomaterial Branch
@@ -921,7 +921,7 @@
the peptide with sequence SIINFEKL, which is eluted from a cell expressing hen egg lysozyme
- A material entity which is derived from a protein
+ A material entity which is derived from a protein
PERSON: Bjoern Peters
GROUP: IEDB
@@ -936,7 +936,7 @@
- A material entity that represents generations of a primary culture.
+ A material entity that represents generations of a primary culture.
PERSON: Susanna Sansone
GROUP: OBI Biomaterial Branch
@@ -951,7 +951,7 @@
- A cell line that is expected to be capable of indefinite propagation in an vitro culture.
+ A cell line that is expected to be capable of indefinite propagation in an vitro culture.
PERSON:Matthew Brush
immortal cell line sample
permanent cell line
@@ -971,7 +971,7 @@
A split of HeLa cells in active culture, or stored in frozen aliquots. Populations of HEK 293 cells used in experiments such as those documented in Changes in ultrastructure and endogenous ionic channels activity during culture of HEK 293 cell line. Eur J Pharmacol. 2007 Jul 12;567(1-2):10-8. PMID: 17482592.
He, Tong-Chuan, et al. Identification of c-MYC as a target of the APC pathway. Science 281.5382 (1998): 1509-1512. - To evaluate the transcriptional effects of APC, we studied a human colorectal cancer cell line (HT29-APC) containing a zinc-inducible APC gene and a control cell line (HT29–β-Gal) containing an analogous inducible lacZ gene. Note that common usage in the literature is often of the form a human colorectal cancer cell line, as seen above. But such references to studies in a line refer to the fact that discrete populations of cells that are input into culturing or experiments, not an entire lineage of cells. It is these discrete populations that we refer to as 'cell lines'.
- A secondary cultured cell population that represents a genetically stable and homogenous population of cultured cells that shares a common propagation history (ie has been successively passaged together in culture).
+ A secondary cultured cell population that represents a genetically stable and homogenous population of cultured cells that shares a common propagation history (ie has been successively passaged together in culture).
PERSON:Matthew Brush
cell line sample
OBI-CLO Alignment Working Group (Spring 2013)
@@ -988,7 +988,7 @@
- A macromolecule is a molecule of high relative molecular mass, the structure of which essentially comprises the multiple repetition of units derived, actually or conceptually, from molecules of low relative molecular mass.
+ A macromolecule is a molecule of high relative molecular mass, the structure of which essentially comprises the multiple repetition of units derived, actually or conceptually, from molecules of low relative molecular mass.
James Malone
Philippe Rocca-Serra
TERM: CHEBI:33839
@@ -1005,7 +1005,7 @@
A precursor ion is selected in the first stage, allowed to fragment and then all resultant masses are scanned in the second mass analyzer and detected in the detector that is positioned after the second mass analyzer. This experiment is commonly performed to identify transitions used for quantification by tandem MS.
- Tandem mass spectrometry is a data transformation that uses two or more analyzers separated by a region in which ions can be induced to fragment by transfer of energy (frequently by collision with other molecules.
+ Tandem mass spectrometry is a data transformation that uses two or more analyzers separated by a region in which ions can be induced to fragment by transfer of energy (frequently by collision with other molecules.
PERSON: James Malone
PERSON: Tina Boussard
PERSON: Tina Boussard
@@ -1022,7 +1022,7 @@
PMID: 18037794. Magn Reson Med Sci. 2007;6(3):139-46. Imaging of a large collection of human embryo using a super-parallel MR microscope.[the Orsay Museum has a nice collection of Impressionnist paintings]
- a collection is a bfo:aggregate object, that is a set of material object of the same kind
+ a collection is a bfo:aggregate object, that is a set of material object of the same kind
PERSON: Susanna Sansone
ensemble
group
@@ -1041,7 +1041,7 @@
PMID: 2104732. Caudate lobe of the liver: anatomy, embryology, and pathology. AJR Am J Roentgenol. 1990 Jan;154(1):87-93.
- liver is an anatomical entity which constituent are mainly hepatocytes, which has a function of detoxification, hematopoietic center, glucose and fat metabolism management. liver is only found in animals , all Vertebrates and some families of invertebrates
+ liver is an anatomical entity which constituent are mainly hepatocytes, which has a function of detoxification, hematopoietic center, glucose and fat metabolism management. liver is only found in animals , all Vertebrates and some families of invertebrates
PERSON: Philippe Rocca-Serra
GROUP: OBI Biomaterial Branch
@@ -1057,7 +1057,7 @@
PMID: 18435934.Fatty acid composition of adipose tissue and blood in humans and its use as a biomarker of dietary intake.Prog Lipid Res. 2008 Apr 4.
- adipose tissue is a tissue which main constituents are adipocytes. adipose tissue can be classified base on its location (site) but also based on adipocyte subtypes (brown or white) which reflect functional differences and is only found in animals, Vertebrates or invertebrates.
+ adipose tissue is a tissue which main constituents are adipocytes. adipose tissue can be classified base on its location (site) but also based on adipocyte subtypes (brown or white) which reflect functional differences and is only found in animals, Vertebrates or invertebrates.
PERSON: Philippe Rocca-Serra
GROUP: OBI Biomaterial derived
@@ -1073,7 +1073,7 @@
PMID: 18566411.Activation of the JAK/STAT-1 Signaling Pathway by IFN-{gamma} Can Down-Regulate Functional Expression of the MHC Class I-Related Neonatal Fc Receptor for IgG.J Immunol. 2008 Jul 1;181(1):449-63.
- a process by which a material entity status is modified and conferred a capability of reacting (this sounds like a circular definition , hugh!)
+ a process by which a material entity status is modified and conferred a capability of reacting (this sounds like a circular definition , hugh!)
Philippe Rocca-Serra
OBI-Branch
@@ -1088,7 +1088,7 @@
- A protocol application during which a series of tests are made of a patient leading to determination of disease state, or condition.
+ A protocol application during which a series of tests are made of a patient leading to determination of disease state, or condition.
PlanAndPlannedProcess Branch
clinical diagnosis
OBI branch derived
@@ -1105,7 +1105,7 @@
- Place holder class, see editor note
+ Place holder class, see editor note
PlanAndPlannedProcess Branch
OBI branch derived
@@ -1120,7 +1120,7 @@
- An occurrence of disease is a process involving pathologic changes within an organism
+ An occurrence of disease is a process involving pathologic changes within an organism
IEDB
IEDB
@@ -1135,7 +1135,7 @@
- placeholder to be imported from disease ontology
+ placeholder to be imported from disease ontology
IEDB
IEDB
@@ -1150,7 +1150,7 @@
- A transmembrane glycoprotein that serves as a co-receptor for the T cell receptor.
+ A transmembrane glycoprotein that serves as a co-receptor for the T cell receptor.
CD8
https://github.com/obi-ontology/obi/issues/353
@@ -1165,7 +1165,7 @@
- A reagent role inhering in a molecular entity intended to associate with some molecular target to serve as a proxy for the presence, abundance, or location of this target in a detection of molecular label assay.
+ A reagent role inhering in a molecular entity intended to associate with some molecular target to serve as a proxy for the presence, abundance, or location of this target in a detection of molecular label assay.
Group: OBI
molecular tracer role
OBI developer call, 3-12-12
@@ -1181,7 +1181,7 @@
- A molecular reagent intended to associate with some molecular target to serve as a proxy for the presence, abundance, or location of this target in a detection of molecular label assay
+ A molecular reagent intended to associate with some molecular target to serve as a proxy for the presence, abundance, or location of this target in a detection of molecular label assay
Group: OBI
molecular tracer
OBI developer call, 3-12-12
diff --git a/src/ontology/modules/organizations.owl b/src/ontology/modules/organizations.owl
index d424f7f6..b4cce305 100644
--- a/src/ontology/modules/organizations.owl
+++ b/src/ontology/modules/organizations.owl
@@ -123,7 +123,7 @@
Affymetrix
Affymetrix supplied microarray
- An organization which supplies technology, tools and protocols for use in high throughput applications
+ An organization which supplies technology, tools and protocols for use in high throughput applications
Affymetrix
@@ -505,7 +505,7 @@
Nimblegen
- An organization that focuses on manufacturing target enrichment probe pools for DNA sequencing.
+ An organization that focuses on manufacturing target enrichment probe pools for DNA sequencing.
Person: Jie Zheng
Nimblegen
@@ -517,7 +517,7 @@
Pacific Biosciences
- An organization that supplies tools for studying the synthesis and regulation of DNA, RNA and protein. It developed a powerful technology platform called single molecule real-time (SMRT) technology which enables real-time analysis of biomolecules with single molecule resolution.
+ An organization that supplies tools for studying the synthesis and regulation of DNA, RNA and protein. It developed a powerful technology platform called single molecule real-time (SMRT) technology which enables real-time analysis of biomolecules with single molecule resolution.
Person: Jie Zheng
Pacific Biosciences
@@ -529,7 +529,7 @@
NanoString Technologies
- An organization that supplies life science tools for translational research and molecular diagnostics based on a novel digital molecular barcoding technology. The NanoString platform can provide simple, multiplexed digital profiling of single molecules.
+ An organization that supplies life science tools for translational research and molecular diagnostics based on a novel digital molecular barcoding technology. The NanoString platform can provide simple, multiplexed digital profiling of single molecules.
NanoString Technologies
@@ -540,7 +540,7 @@
Thermo Fisher Scientific
- An organization that is an American multinational, biotechnology product development company, created in 2006 by the merger of Thermo Electron and Fisher Scientific.
+ An organization that is an American multinational, biotechnology product development company, created in 2006 by the merger of Thermo Electron and Fisher Scientific.
Chris Stoeckert, Helena Ellis
https://en.wikipedia.org/wiki/Thermo_Fisher_Scientific
Thermo Fisher Scientific
@@ -553,7 +553,7 @@
Oxford Nanopore Technologies
- An organization that is developing and selling nanopore sequencing products and is based in the UK.
+ An organization that is developing and selling nanopore sequencing products and is based in the UK.
James A. Overton
https://en.wikipedia.org/wiki/Oxford_Nanopore_Technologies
Oxford Nanopore Technologies
@@ -566,7 +566,7 @@
BioGents
- An organization that manufactures mosquito traps and other mosquito control products.
+ An organization that manufactures mosquito traps and other mosquito control products.
John Judkins
WEB:https://eu.biogents.com/about-biogents/
BioGents
@@ -579,7 +579,7 @@
Abbott
- A manufacturer of rapid point-of-care assay devices.
+ A manufacturer of rapid point-of-care assay devices.
John Judkins ORCID:0000-0001-6595-0902
WEB:https://www.globalpointofcare.abbott/en/about.html
https://github.com/obi-ontology/obi/issues/1456
@@ -593,7 +593,7 @@
J. Mitra
- A manufacturer of in vitro diagnostic assay kits in India.
+ A manufacturer of in vitro diagnostic assay kits in India.
John Judkins ORCID:0000-0001-6595-0902
WEB:https://jmitra.co.in/about-us/
https://github.com/obi-ontology/obi/issues/1456
@@ -607,7 +607,7 @@
InBios
- A manufacturer that specializes in in vitro diagnostic devices designed to test for infectious diseases.
+ A manufacturer that specializes in in vitro diagnostic devices designed to test for infectious diseases.
John Judkins ORCID:0000-0001-6595-0902
WEB:https://inbios.com/about/
https://github.com/obi-ontology/obi/issues/1456
diff --git a/src/ontology/modules/physical-examination.owl b/src/ontology/modules/physical-examination.owl
index c07186b4..0839b7c0 100644
--- a/src/ontology/modules/physical-examination.owl
+++ b/src/ontology/modules/physical-examination.owl
@@ -156,7 +156,7 @@
- A physical examination of an organism's ability to perform functional activities.
+ A physical examination of an organism's ability to perform functional activities.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -191,7 +191,7 @@
- An observational assessment of the loss of facial muscle tissue due to inactivity or disease.
+ An observational assessment of the loss of facial muscle tissue due to inactivity or disease.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -226,7 +226,7 @@
- An observational assessment of the loss of muscle tissue related to tongue movement due to inactivity or disease.
+ An observational assessment of the loss of muscle tissue related to tongue movement due to inactivity or disease.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -261,7 +261,7 @@
- A functional assessment of an individual's ability to cough forcefully.
+ A functional assessment of an individual's ability to cough forcefully.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -296,7 +296,7 @@
- A functional assessment of an individual's ability to understandably repeat spoken sentences.
+ A functional assessment of an individual's ability to understandably repeat spoken sentences.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -331,7 +331,7 @@
- A functional assessment of an individual's ability to touch index fingers together in front of the sternum without oscillation for a specified duration of time
+ A functional assessment of an individual's ability to touch index fingers together in front of the sternum without oscillation for a specified duration of time
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -366,7 +366,7 @@
- A functional assessment of an individual's ability to touch their own nose and then touch an examiners finger in front of them and then touch their own nose once more.
+ A functional assessment of an individual's ability to touch their own nose and then touch an examiners finger in front of them and then touch their own nose once more.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -401,7 +401,7 @@
- A functional assessment of an individual's ability to accurately touch a moving target with their finger and then touch their own chin a number of times in a row.
+ A functional assessment of an individual's ability to accurately touch a moving target with their finger and then touch their own chin a number of times in a row.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -436,7 +436,7 @@
- A functional assessment of an individual's ability to alternate the forearm between pronation and suppination as quickly as possible during a specified duration of time
+ A functional assessment of an individual's ability to alternate the forearm between pronation and suppination as quickly as possible during a specified duration of time
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -471,7 +471,7 @@
- A functional assessment of an individual's ability to touch their finger-tip to thumb as many times as possible during a specified duration of time.
+ A functional assessment of an individual's ability to touch their finger-tip to thumb as many times as possible during a specified duration of time.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -506,7 +506,7 @@
- A functional assessment of an individual's ability to slide their heel back and forth along their contralateral tibia from the patella to the ankle with the contralateral leg extended.
+ A functional assessment of an individual's ability to slide their heel back and forth along their contralateral tibia from the patella to the ankle with the contralateral leg extended.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -541,7 +541,7 @@
- A functional assessment of an individual's ability to tap their heel to the midpoint of the contralateral shin a number of times.
+ A functional assessment of an individual's ability to tap their heel to the midpoint of the contralateral shin a number of times.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -576,7 +576,7 @@
- An observational assesment of an individual's muscle tissue loss due to inactivity or disease.
+ An observational assesment of an individual's muscle tissue loss due to inactivity or disease.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -611,7 +611,7 @@
- A functional assessment of an individual's ability to perform muscle movement to overcome gravity or physical resistence.
+ A functional assessment of an individual's ability to perform muscle movement to overcome gravity or physical resistence.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -646,7 +646,7 @@
- A functional assessment of an individual's ability to sense vibration.
+ A functional assessment of an individual's ability to sense vibration.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -681,7 +681,7 @@
- A functional assessment of an individual's ability to sense the position of a finger or toe that has been manipulated by minimal random movements.
+ A functional assessment of an individual's ability to sense the position of a finger or toe that has been manipulated by minimal random movements.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -716,7 +716,7 @@
- A functional assessment of an individual's muscle contraction when a muscle is triggered by a signal from a muscle spindle in response to a stimulus applied to a specific trigger point on the body.
+ A functional assessment of an individual's muscle contraction when a muscle is triggered by a signal from a muscle spindle in response to a stimulus applied to a specific trigger point on the body.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -740,7 +740,7 @@
- The functional assessment of an individual's ability to maintain balance, posture or upright stability.
+ The functional assessment of an individual's ability to maintain balance, posture or upright stability.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -764,7 +764,7 @@
- A limits of stability assessment designed to assess an individual's ability to maintain unsupported posture while sitting over a given time period.
+ A limits of stability assessment designed to assess an individual's ability to maintain unsupported posture while sitting over a given time period.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -788,7 +788,7 @@
- A limits of stability assessment designed to assess an individual's ability to maintain a stable stance with feet 20 cm apart.
+ A limits of stability assessment designed to assess an individual's ability to maintain a stable stance with feet 20 cm apart.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -812,7 +812,7 @@
- A limits of stability assessment designed to assess an individual's ability to maintain a stable stance with their eyes closed.
+ A limits of stability assessment designed to assess an individual's ability to maintain a stable stance with their eyes closed.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -836,7 +836,7 @@
- A limits of stability assessment designed to assess an individual's ability to maintain a stable stance with feet together.
+ A limits of stability assessment designed to assess an individual's ability to maintain a stable stance with feet together.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -860,7 +860,7 @@
- A limits of stability assessment designed to assess an individual's ability to maintain a stable stance with feet together and eyes closed.
+ A limits of stability assessment designed to assess an individual's ability to maintain a stable stance with feet together and eyes closed.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -884,7 +884,7 @@
- A limits of stability assessment designed to assess an individual's ability to maintain a stable stance with feet in tandem placement.
+ A limits of stability assessment designed to assess an individual's ability to maintain a stable stance with feet in tandem placement.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -908,7 +908,7 @@
- A limits of stability assessment designed to assess an individual's ability to maintain a stable stance on one foot.
+ A limits of stability assessment designed to assess an individual's ability to maintain a stable stance on one foot.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -932,7 +932,7 @@
- A limits of stability assessment designed to assess an individual's ability to maintain balance while walking in a straight line placing steps in tandem.
+ A limits of stability assessment designed to assess an individual's ability to maintain balance while walking in a straight line placing steps in tandem.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -956,7 +956,7 @@
- A limits of stability assessment designed to assess an individual's manner or pattern of walking.
+ A limits of stability assessment designed to assess an individual's manner or pattern of walking.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -980,7 +980,7 @@
- A functional assessment of an individual's lower cranial nerve function via proxy of facial muscle performance.
+ A functional assessment of an individual's lower cranial nerve function via proxy of facial muscle performance.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -1004,7 +1004,7 @@
- A functional assessment of an individual's ability to articulate spoken words.
+ A functional assessment of an individual's ability to articulate spoken words.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -1028,7 +1028,7 @@
- A functional assessment of an individual's ability to coordinate limb movement.
+ A functional assessment of an individual's ability to coordinate limb movement.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -1052,7 +1052,7 @@
- A limb coordination assessment designed to assess an individual's ability to coordinate upper limb movement.
+ A limb coordination assessment designed to assess an individual's ability to coordinate upper limb movement.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -1076,7 +1076,7 @@
- A limb coordination assessment designed to assess an individual's ability to coordinate lower limb movement.
+ A limb coordination assessment designed to assess an individual's ability to coordinate lower limb movement.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -1100,7 +1100,7 @@
- A functional assesment of an individual's nerve performance. Specifically the nerves connecting the sensory and motor structures with the central nervous system.
+ A functional assesment of an individual's nerve performance. Specifically the nerves connecting the sensory and motor structures with the central nervous system.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -1124,7 +1124,7 @@
- A functional assessment of an individual's ability to maintain upright body posture.
+ A functional assessment of an individual's ability to maintain upright body posture.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -1159,7 +1159,7 @@
- A deep tendon reflex assessment of an individual's reaction to stimulus applied to a knee joint.
+ A deep tendon reflex assessment of an individual's reaction to stimulus applied to a knee joint.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -1172,7 +1172,7 @@
- A physical examination of an organism through visual assesment.
+ A physical examination of an organism through visual assesment.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -1207,7 +1207,7 @@
- A deep tendon reflex assessment of an individual's reaction to stimulus applied to an ankle joint.
+ A deep tendon reflex assessment of an individual's reaction to stimulus applied to an ankle joint.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -1242,7 +1242,7 @@
- A deep tendon reflex assessment of an individual's reaction to stimulus applied to a tendon of biceps brachii.
+ A deep tendon reflex assessment of an individual's reaction to stimulus applied to a tendon of biceps brachii.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
@@ -1277,7 +1277,7 @@
- A deep tendon reflex assessment of an individual's reaction to stimulus applied to a brachioradialis.
+ A deep tendon reflex assessment of an individual's reaction to stimulus applied to a brachioradialis.
Daniel Olson, ORCID: 0000-0002-8134-1207
Critical Path Institute
https://github.com/obi-ontology/obi/issues/1637
diff --git a/src/ontology/modules/sample-collection.owl b/src/ontology/modules/sample-collection.owl
index b62e6e6b..ffafea91 100644
--- a/src/ontology/modules/sample-collection.owl
+++ b/src/ontology/modules/sample-collection.owl
@@ -73,7 +73,7 @@
- A live arthropod specimen collection process in which the arthropods are in the adult stage.
+ A live arthropod specimen collection process in which the arthropods are in the adult stage.
John Judkins
collection of adults
MIRO:30000052
@@ -87,7 +87,7 @@
- An arthropod specimen collection by aspiration that occurs while the arthropod is biting an animal.
+ An arthropod specimen collection by aspiration that occurs while the arthropod is biting an animal.
John Judkins
animal biting catch
MIRO:30000012
@@ -101,7 +101,7 @@
- An animal-biting arthropod specimen collection by aspiration that occurs outside a building.
+ An animal-biting arthropod specimen collection by aspiration that occurs outside a building.
John Judkins
animal biting catch - outdoors
MIRO:30000014
@@ -115,7 +115,7 @@
- An arthropod specimen collection process that has the objective of collecting mosquitoes from an aquatic environment.
+ An arthropod specimen collection process that has the objective of collecting mosquitoes from an aquatic environment.
John Judkins
aquatic environment catch
MIRO:30000048
@@ -129,7 +129,7 @@
- An arthropod specimen collection by aspiration that catches specimens resting inside an animal house.
+ An arthropod specimen collection by aspiration that catches specimens resting inside an animal house.
John Judkins
animal shed resting catch
MIRO:30000027
@@ -143,7 +143,7 @@
- An arthropod resting outdoors specimen collection by aspiration that occurs while the arthropod rests on a processed material such as a wall or furniture.
+ An arthropod resting outdoors specimen collection by aspiration that occurs while the arthropod rests on a processed material such as a wall or furniture.
John Judkins
outdoors shelter catch - artificial
MIRO:30000026
@@ -157,7 +157,7 @@
- An arthropod resting outdoors specimen collection by aspiration that occurs while the arthropod rests on an unprocessed material such as a plant.
+ An arthropod resting outdoors specimen collection by aspiration that occurs while the arthropod rests on an unprocessed material such as a plant.
John Judkins
outdoors shelter catch - natural
MIRO:30000025
@@ -171,7 +171,7 @@
- An animal-biting arthropod specimen collection by aspiration that occurs while the arthropod is resting outside a building during a period of inactivity.
+ An animal-biting arthropod specimen collection by aspiration that occurs while the arthropod is resting outside a building during a period of inactivity.
John Judkins
outdoors shelter catch
MIRO:30000024
@@ -185,7 +185,7 @@
- A live arthropod specimen collection process that involves the use of an aspirator, a device which draws an arthropod by suction into a container.
+ A live arthropod specimen collection process that involves the use of an aspirator, a device which draws an arthropod by suction into a container.
John Judkins
catch by aspiration
MIRO:30000043
@@ -199,7 +199,7 @@
- A specimen collection process that has the objective of collecting arthropods as specimens.
+ A specimen collection process that has the objective of collecting arthropods as specimens.
John Judkins
collection of arthropods
field population catch
@@ -214,7 +214,7 @@
- An arthropod specimen collection by aspiration that occurs while the arthropod is biting a human.
+ An arthropod specimen collection by aspiration that occurs while the arthropod is biting a human.
John Judkins
man biting catch
MIRO:30000017
@@ -228,7 +228,7 @@
- An arthropod specimen collection by aspiration that occurs while the arthropod is biting a human inside a building.
+ An arthropod specimen collection by aspiration that occurs while the arthropod is biting a human inside a building.
John Judkins
man biting catch - indoors
MIRO:30000019
@@ -242,7 +242,7 @@
- An arthropod specimen collection by aspiration designed to catch specimens that are in the process of biting a human outside a building.
+ An arthropod specimen collection by aspiration designed to catch specimens that are in the process of biting a human outside a building.
John Judkins
man biting catch - outdoors
MIRO:30000018
@@ -256,7 +256,7 @@
- A knockdown arthropod specimen collection process in which the pesticide is pyrethrum.
+ A knockdown arthropod specimen collection process in which the pesticide is pyrethrum.
John Judkins
pyrethrum spray catch
MIRO:30000023
@@ -270,7 +270,7 @@
- An arthropod specimen collection process that involves exposing arthropods to pesticide, then collecting them once they become dead or immobilized.
+ An arthropod specimen collection process that involves exposing arthropods to pesticide, then collecting them once they become dead or immobilized.
John Judkins
knockdown collection
IRO:0000014
@@ -284,7 +284,7 @@
- An arthropod specimen collection process meant to collect live specimens.
+ An arthropod specimen collection process meant to collect live specimens.
John Judkins
catch of live specimens
MIRO:30000044
@@ -299,7 +299,7 @@
- An arthropod specimen collection process in which the arthropods are in the embryo stage.
+ An arthropod specimen collection process in which the arthropods are in the embryo stage.
VEuPath
collection of eggs
MIRO:30000049
@@ -313,7 +313,7 @@
- An arthropod specimen collection process in which the arthropods are in the larval stage.
+ An arthropod specimen collection process in which the arthropods are in the larval stage.
VEuPath
collection of larvae
MIRO:30000022
@@ -327,7 +327,7 @@
- An arthropod specimen collection process in which the arthropods are in the pupal stage.
+ An arthropod specimen collection process in which the arthropods are in the pupal stage.
VEuPath
collection of pupae
MIRO:30000050
diff --git a/src/ontology/modules/sequence-analysis.owl b/src/ontology/modules/sequence-analysis.owl
index af3f709a..3f7cac1d 100644
--- a/src/ontology/modules/sequence-analysis.owl
+++ b/src/ontology/modules/sequence-analysis.owl
@@ -126,7 +126,7 @@
- A data transformation in which adapter sequences at the end of a molecular sequence are cut (removed).
+ A data transformation in which adapter sequences at the end of a molecular sequence are cut (removed).
Dan Berrios
Dan Berrios
adapter-sequence trimming
@@ -138,7 +138,7 @@
- A data transformation in which data contained in 2 or more files are merged into a single file.
+ A data transformation in which data contained in 2 or more files are merged into a single file.
Dan Berrios
Dan Berrios
file merge
@@ -162,7 +162,7 @@
- A data transformation in which one or more sequences (reads) are positioned on a reference sequence template (often a reference set of genes), according to the genetic base-pairing paradigm.
+ A data transformation in which one or more sequences (reads) are positioned on a reference sequence template (often a reference set of genes), according to the genetic base-pairing paradigm.
Dan Berrios
Dan Berrios
sequence alignment
@@ -186,7 +186,7 @@
- The counting of features (typically, genes) within aligned sequence data, and organization of these counts into one or more tables.
+ The counting of features (typically, genes) within aligned sequence data, and organization of these counts into one or more tables.
Dan Berrios
Dan Berrios
sequence data feature count tabulation
@@ -208,7 +208,7 @@
- The results of a data transformation of sequence data in which (e.g., low quality) read bases are removed, to achieve some specific objective.
+ The results of a data transformation of sequence data in which (e.g., low quality) read bases are removed, to achieve some specific objective.
Dan Berrios
Dan Berrios
trimmed sequence data
@@ -220,7 +220,7 @@
- Nucleotide sequences of molecules that are ligated to assay samples prior to sequencing of these samples; these sequences are provided by assay kit manufacturers and typically used to combine sequencing of multiple samples in one assay run.
+ Nucleotide sequences of molecules that are ligated to assay samples prior to sequencing of these samples; these sequences are provided by assay kit manufacturers and typically used to combine sequencing of multiple samples in one assay run.
Dan Berrios
Dan Berrios
adapter sequence data
@@ -232,7 +232,7 @@
- The results of a data transformation of sequence data in which reference subsequences corresponding to ligated library adapters are removed.
+ The results of a data transformation of sequence data in which reference subsequences corresponding to ligated library adapters are removed.
Dan Berrios
Dan Berrios
adapter-trimmed sequence data
@@ -244,7 +244,7 @@
- The results of a sequence alignment.
+ The results of a sequence alignment.
Dan Berrios
Dan Berrios
aligned sequence data
@@ -262,7 +262,7 @@
- The results of a data transformation of sequence data in which files containing aligned sequence data are merged together
+ The results of a data transformation of sequence data in which files containing aligned sequence data are merged together
Dan Berrios
Dan Berrios
merged aligned sequence data
@@ -274,7 +274,7 @@
- The results of a sequence data feature count tabulation.
+ The results of a sequence data feature count tabulation.
Dan Berrios
Dan Berrios
sequence library feature count data
@@ -292,7 +292,7 @@
- The results of a DNA methylation profiling assay
+ The results of a DNA methylation profiling assay
DNA methylation profiling data
@@ -302,7 +302,7 @@
- The results of a differential expression analysis.
+ The results of a differential expression analysis.
differential expression analysis data
@@ -312,7 +312,7 @@
- A data transformation in which subsequences of a molecular sequence are cut (removed).
+ A data transformation in which subsequences of a molecular sequence are cut (removed).
sequence trimming
@@ -322,7 +322,7 @@
- Sequence data in which an identifier subsequence has been used to categorize each reads by source.
+ Sequence data in which an identifier subsequence has been used to categorize each reads by source.
Dan Berrios
Dan Berrios
demultiplexed sequence data
@@ -334,7 +334,7 @@
- Sequence data from a sequence library generated from at least two different sources, where each read in the sequence data includes base calls from a multiplex identifier sequence that can be used to trace the source of the read to its source.
+ Sequence data from a sequence library generated from at least two different sources, where each read in the sequence data includes base calls from a multiplex identifier sequence that can be used to trace the source of the read to its source.
Dan Berrios
Dan Berrios
multiplexed sequence data
@@ -347,7 +347,7 @@
When a new genome is sequenced, the start sites of proteins are identified by comparing the new sequence to that of a reference sequence in a database. The first amino acid of a protein sequence being analyzed is the input protein sequence start site.
- The position of the first amino acid in a protein sequence being analyzed (input protein sequence).
+ The position of the first amino acid in a protein sequence being analyzed (input protein sequence).
Emma Griffiths
input protein start
query protein start site
@@ -362,7 +362,7 @@
When a new genome is sequenced, the termination sites of proteins are identified by comparing the new sequence to that of a reference sequence in a database. The last amino acid of a protein sequence being analyzed is the input protein sequence stop site.
- The position of the last amino acid in a protein sequence being analyzed (input protein sequence).
+ The position of the last amino acid in a protein sequence being analyzed (input protein sequence).
Emma Griffiths
input protein stop
query protein stop site
@@ -377,7 +377,7 @@
When a new genome is sequenced, the start sites of genes are identified by comparing the new sequence to that of a reference sequence in a database. The first nucelotide of a gene sequence being analyzed is the input gene sequence start site.
- The position of the first nucleotide in a gene sequence being analyzed (input gene sequence).
+ The position of the first nucleotide in a gene sequence being analyzed (input gene sequence).
Emma Griffiths
input gene start
query gene start site
@@ -392,7 +392,7 @@
When a new genome is sequenced, the termination sites of genes are identified by comparing the new sequence to that of a reference sequence in a database. The last nucelotide of a gene sequence being analyzed is the input gene sequence stop site.
- The position of the last nucelotide in a gene sequence being analyzed (input gene sequence).
+ The position of the last nucelotide in a gene sequence being analyzed (input gene sequence).
Emma Griffiths
input gene stop
query gene stop site
@@ -407,7 +407,7 @@
When a new genome is sequenced, the start sites of proteins are identified by comparing the new sequence to that of a reference sequence in a database. The first amino acid of a protein sequence being used for comparison is the reference protein sequence start site.
- The position of the first amino acid in a reference protein sequence (sequence being used for comparison).
+ The position of the first amino acid in a reference protein sequence (sequence being used for comparison).
Emma Griffiths
reference protein start
subject protein start site
@@ -422,7 +422,7 @@
When a new genome is sequenced, the termination sites of proteins are identified by comparing the new sequence to that of a reference sequence in a database. The last amino acid of a protein sequence used for comparison is the reference protein sequence stop site.
- The position of the last amino acid in a reference protein sequence (sequence being used for comparison).
+ The position of the last amino acid in a reference protein sequence (sequence being used for comparison).
Emma Griffiths
reference protein stop
subject protein stop site
@@ -437,7 +437,7 @@
When a new genome is sequenced, the start sites of genes are identified by comparing the new sequence to that of a reference sequence in a database. The first nucelotide of a gene sequence used for comparison is the reference gene sequence start site.
- The position of the first nucleotide in a reference gene sequence (sequence being used for comparison).
+ The position of the first nucleotide in a reference gene sequence (sequence being used for comparison).
Emma Griffiths
reference gene start
subject gene start site
@@ -452,7 +452,7 @@
When a new genome is sequenced, the termination sites of genes are identified by comparing the new sequence to that of a reference sequence in a database. The last nucelotide of a gene sequence used for comparison is the reference gene sequence stop site.
- The position of the last nucelotide in a reference sequence (sequence being used for comparison).
+ The position of the last nucelotide in a reference sequence (sequence being used for comparison).
Emma Griffiths
reference gene stop
subject gene stop site
@@ -466,7 +466,7 @@
- A sequence datum that is the specified output of a read mapping and is the ratio of the count of mapped reads to the total count of reads.
+ A sequence datum that is the specified output of a read mapping and is the ratio of the count of mapped reads to the total count of reads.
John Judkins
VEuPathDB
proportion mapped reads
diff --git a/src/ontology/modules/specimen-assay-data.owl b/src/ontology/modules/specimen-assay-data.owl
index 6599ce13..102001a4 100644
--- a/src/ontology/modules/specimen-assay-data.owl
+++ b/src/ontology/modules/specimen-assay-data.owl
@@ -208,7 +208,7 @@
- A data item that is the specified output of a blood assay.
+ A data item that is the specified output of a blood assay.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -231,7 +231,7 @@
- An organism detection datum that is the specified output of a blood microbiology assay.
+ An organism detection datum that is the specified output of a blood microbiology assay.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -254,7 +254,7 @@
- A data item that is the specified output of a feces assay.
+ A data item that is the specified output of a feces assay.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -277,7 +277,7 @@
- An organism detection datum that is the specified output of a feces microbiology assay.
+ An organism detection datum that is the specified output of a feces microbiology assay.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -300,7 +300,7 @@
- A data item that is the specified output of a urine assay.
+ A data item that is the specified output of a urine assay.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -323,7 +323,7 @@
- An organism detection datum that is the specified output of a urine microbiology assay.
+ An organism detection datum that is the specified output of a urine microbiology assay.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -346,7 +346,7 @@
- A data item that is the specified output of a induced sputum assay.
+ A data item that is the specified output of a induced sputum assay.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -369,7 +369,7 @@
- An organism detection datum that is the specified output of an induced sputum microbiology assay.
+ An organism detection datum that is the specified output of an induced sputum microbiology assay.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -392,7 +392,7 @@
- A data item that is the specified output of a cerebrospinal fluid assay.
+ A data item that is the specified output of a cerebrospinal fluid assay.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -415,7 +415,7 @@
- An organism detection datum that is the specified output of a cerebrospinal fluid microbiology assay.
+ An organism detection datum that is the specified output of a cerebrospinal fluid microbiology assay.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -438,7 +438,7 @@
- An organism detection datum that is the specified output of an endotracheal aspirate assay.
+ An organism detection datum that is the specified output of an endotracheal aspirate assay.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -461,7 +461,7 @@
- An organism detection datum that is the specified output of an endotracheal tube aspirate microbiology assay.
+ An organism detection datum that is the specified output of an endotracheal tube aspirate microbiology assay.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -484,7 +484,7 @@
- An organism detection datum that is the specified output of a lung microbiology assay.
+ An organism detection datum that is the specified output of a lung microbiology assay.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -507,7 +507,7 @@
- An organism detection datum that is the specified output of a nasopharyngeal or oropharyngeal swab microbiology assay.
+ An organism detection datum that is the specified output of a nasopharyngeal or oropharyngeal swab microbiology assay.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -530,7 +530,7 @@
- An organism detection datum that is the specified output of a pleural fluid microbiology assay.
+ An organism detection datum that is the specified output of a pleural fluid microbiology assay.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -553,7 +553,7 @@
- A data item that is the specified output of an umbilical cord blood assay.
+ A data item that is the specified output of an umbilical cord blood assay.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -576,7 +576,7 @@
- An organism detection datum that is the specified output of an umbilical cord blood microbiology assay.
+ An organism detection datum that is the specified output of an umbilical cord blood microbiology assay.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -599,7 +599,7 @@
- A blood microbiology datum that is about bacteria.
+ A blood microbiology datum that is about bacteria.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -622,7 +622,7 @@
- A blood microbiology datum that is about a virus.
+ A blood microbiology datum that is about a virus.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -645,7 +645,7 @@
- A blood microbiology datum that is about eukaryota.
+ A blood microbiology datum that is about eukaryota.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -668,7 +668,7 @@
- A feces microbiology datum that is about bacteria.
+ A feces microbiology datum that is about bacteria.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -691,7 +691,7 @@
- A feces microbiology datum that is about eukaryota.
+ A feces microbiology datum that is about eukaryota.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -714,7 +714,7 @@
- A feces microbiology datum that is about a virus.
+ A feces microbiology datum that is about a virus.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -737,7 +737,7 @@
- A urine microbiology datum that is about eukaryota.
+ A urine microbiology datum that is about eukaryota.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -760,7 +760,7 @@
- An induced sputum microbiology datum that is about bacteria.
+ An induced sputum microbiology datum that is about bacteria.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -783,7 +783,7 @@
- An induced sputum microbiology datum that is about eukaryota.
+ An induced sputum microbiology datum that is about eukaryota.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -806,7 +806,7 @@
- An induced sputum microbiology datum that is about a virus.
+ An induced sputum microbiology datum that is about a virus.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -829,7 +829,7 @@
- An endotracheal tube aspirate microbiology datum that is about bacteria.
+ An endotracheal tube aspirate microbiology datum that is about bacteria.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -852,7 +852,7 @@
- A lung microbiology datum that is about bacteria.
+ A lung microbiology datum that is about bacteria.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -875,7 +875,7 @@
- A lung microbiology datum that is about eukaryota.
+ A lung microbiology datum that is about eukaryota.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -898,7 +898,7 @@
- A lung microbiology datum that is about a virus.
+ A lung microbiology datum that is about a virus.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -921,7 +921,7 @@
- A nasopharyngeal or oropharyngeal swab microbiology datum that is about bacteria.
+ A nasopharyngeal or oropharyngeal swab microbiology datum that is about bacteria.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -944,7 +944,7 @@
- A nasopharyngeal or oropharyngeal swab microbiology datum that is about eukaryota.
+ A nasopharyngeal or oropharyngeal swab microbiology datum that is about eukaryota.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -967,7 +967,7 @@
- A nasopharyngeal or oropharyngeal swab microbiology datum that is about a virus.
+ A nasopharyngeal or oropharyngeal swab microbiology datum that is about a virus.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -990,7 +990,7 @@
- A pleural fluid microbiology datum that is about bacteria.
+ A pleural fluid microbiology datum that is about bacteria.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -1013,7 +1013,7 @@
- A pleural fluid microbiology datum that is about eukaryota.
+ A pleural fluid microbiology datum that is about eukaryota.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -1036,7 +1036,7 @@
- A pleural fluid microbiology datum that is about a virus.
+ A pleural fluid microbiology datum that is about a virus.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -1059,7 +1059,7 @@
- An umbilical cord blood microbiology datum that is about eukaryota.
+ An umbilical cord blood microbiology datum that is about eukaryota.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1428
@@ -1112,7 +1112,7 @@
- A data item that is the specified output of a milk assay.
+ A data item that is the specified output of a milk assay.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1515
@@ -1141,7 +1141,7 @@
- An organism detection datum that is the specified output of a placental blood microbiology assay.
+ An organism detection datum that is the specified output of a placental blood microbiology assay.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1297
@@ -1164,7 +1164,7 @@
- A placental blood microbiology datum that is about eukaryota.
+ A placental blood microbiology datum that is about eukaryota.
John Judkins
VEuPathDB
https://github.com/obi-ontology/obi/issues/1297
@@ -1187,7 +1187,7 @@
- A data item that is the specified output of an antigen specific antibodies assay.
+ A data item that is the specified output of an antigen specific antibodies assay.
John Judkins ORCID:0000-0001-6595-0902
VEuPathDB
https://github.com/obi-ontology/obi/issues/1526
@@ -1210,7 +1210,7 @@
- An antigen specific antibodies assay datum that is the specified output of an antigen specific antibodies in blood assay.
+ An antigen specific antibodies assay datum that is the specified output of an antigen specific antibodies in blood assay.
John Judkins ORCID:0000-0001-6595-0902
VEuPathDB
https://github.com/obi-ontology/obi/issues/1526
@@ -1233,7 +1233,7 @@
- An antigen specific antibodies assay datum that is the specified output of an antigen specific antibodies in milk assay.
+ An antigen specific antibodies assay datum that is the specified output of an antigen specific antibodies in milk assay.
John Judkins ORCID:0000-0001-6595-0902
VEuPathDB
https://github.com/obi-ontology/obi/issues/1526
@@ -1262,7 +1262,7 @@
- An organism detection datum that is the specified output of a skin of body microbiology assay.
+ An organism detection datum that is the specified output of a skin of body microbiology assay.
John Judkins ORCID:0000-0001-6595-0902
VEuPathDB
https://github.com/obi-ontology/obi/issues/1680
@@ -1291,7 +1291,7 @@
- An organism detection datum that is the specified output of a bone marrow microbiology assay.
+ An organism detection datum that is the specified output of a bone marrow microbiology assay.
John Judkins ORCID:0000-0001-6595-0902
VEuPathDB
https://github.com/obi-ontology/obi/issues/1680
@@ -1320,7 +1320,7 @@
- An organism detection datum that is the specified output of a nasal aspirate microbiology assay.
+ An organism detection datum that is the specified output of a nasal aspirate microbiology assay.
John Judkins ORCID:0000-0001-6595-0902
VEuPathDB
https://github.com/obi-ontology/obi/issues/1680
diff --git a/src/ontology/modules/study-designs.owl b/src/ontology/modules/study-designs.owl
index d343f396..d5a544de 100644
--- a/src/ontology/modules/study-designs.owl
+++ b/src/ontology/modules/study-designs.owl
@@ -257,7 +257,7 @@
intervention design
PMID: 18208636.Br J Nutr. 2008 Jan 22;:1-11.Effect of vitamin D supplementation on bone and vitamin D status among Pakistani immigrants in Denmark: a randomised double-blinded placebo-controlled intervention study.
- An intervention design is a study design in which a controlled process applied to the subjects (the intervention) serves as the independent variable manipulated by the experimentalist. The treatment (perturbation or intervention) defined can be defined as a combination of values taken by independent variable manipulated by the experimentalists are applied to the recruited subjects assigned (possibly by applying specific methods) to treatment groups. The specificity of intervention design is the fact that independent variables are being manipulated and a response of the biological system is evaluated via response variables as monitored by possibly a series of assays.
+ An intervention design is a study design in which a controlled process applied to the subjects (the intervention) serves as the independent variable manipulated by the experimentalist. The treatment (perturbation or intervention) defined can be defined as a combination of values taken by independent variable manipulated by the experimentalists are applied to the recruited subjects assigned (possibly by applying specific methods) to treatment groups. The specificity of intervention design is the fact that independent variables are being manipulated and a response of the biological system is evaluated via response variables as monitored by possibly a series of assays.
Philppe Rocca-Serra
OBI branch derived
intervention design
@@ -366,7 +366,7 @@
compound treatment design
- an intervention design in which the treatment is the administration of a compound
+ an intervention design in which the treatment is the administration of a compound
This is meant to include all kinds of material administrations, including vaccinations, chemical compounds etc.
PERSON: Bjoern Peters
MO_555 compound_treatment_design
@@ -425,7 +425,7 @@
growth condition intervention design
- A study design in which the independent variable is the environmental condition in which the specimen is growing
+ A study design in which the independent variable is the environmental condition in which the specimen is growing
PERSON: Bjoern Peters
MO_588 growth_condition_design
growth condition intervention design
@@ -457,7 +457,7 @@
validation by reverse transcription PCR design
- a study design in which checks the accuracy or the quality of the result of an assay by comparing with reverse transcription PCR results
+ a study design in which checks the accuracy or the quality of the result of an assay by comparing with reverse transcription PCR results
PERSON: Chris Stoeckert, Jie Zheng
MO_986 reverse_transcription_PCR_quality_control
validation by reverse transcription PCR design
@@ -471,7 +471,7 @@
validation by real time PCR design
- a study design in which the accuracy or the quality of the result of an assay is checked by comparing with real time PCR results
+ a study design in which the accuracy or the quality of the result of an assay is checked by comparing with real time PCR results
PERSON: Chris Stoeckert, Jie Zheng
MO_434 real_time_PCR_quality_control
validation by real time PCR design
@@ -517,7 +517,7 @@
operator variation design
- A study design that assesses the operator performance and relation to data consistency and quality.
+ A study design that assesses the operator performance and relation to data consistency and quality.
Person: Chris Stoeckert, Jie Zheng
MO_519 operator_variation_design
operator variation design
@@ -537,7 +537,7 @@
comparative genome hybridization by array design
- A study design that detects genomic copy number variations using microarray technology.
+ A study design that detects genomic copy number variations using microarray technology.
Person: Chris Stoeckert, Jie Zheng
MO_856 comparative_genome_hybridization_design
comparative genome hybridization by array design
@@ -550,7 +550,7 @@
- A study design that is conducted entirely in a living organism, e.g. a compound treatment in a mouse model.
+ A study design that is conducted entirely in a living organism, e.g. a compound treatment in a mouse model.
Person: Chris Stoeckert, Jie Zheng
MO_454 in_vivo_design
in vivo design
@@ -564,7 +564,7 @@
genotyping by high throughput sequencing design
- A study design that classifies an individual or group of individuals on the basis of alleles, haplotypes, SNPs using high througput sequencing techniques.
+ A study design that classifies an individual or group of individuals on the basis of alleles, haplotypes, SNPs using high througput sequencing techniques.
Person: Chris Stoeckert, Jie Zheng
MO_560 genotyping_design
genotyping by high throughput sequencing design
@@ -584,7 +584,7 @@
innate behavior design
- A study design in which the innate behavior of the organism is examined, e.g. path finding in bees.
+ A study design in which the innate behavior of the organism is examined, e.g. path finding in bees.
Person: Chris Stoeckert, Jie Zheng
MO_355 innate_behavior_design
innate behavior design
@@ -620,7 +620,7 @@
cell component comparison design
- A study design that compares samples from different cell components.
+ A study design that compares samples from different cell components.
Person: Chris Stoeckert, Jie Zheng
MO_1019 cell_component_comparison_design
cell component comparison design
@@ -634,7 +634,7 @@
ex vivo design
- A study design where all or part of an organism is removed and studied in vitro, e.g. part of a mouse is removed and cultured in vitro. A cell culture with an established cell line is an in vitro experiment.
+ A study design where all or part of an organism is removed and studied in vitro, e.g. part of a mouse is removed and cultured in vitro. A cell culture with an established cell line is an in vitro experiment.
Person: Chris Stoeckert, Jie Zheng
MO_808 ex_vivo_design
ex vivo design
@@ -670,7 +670,7 @@
normalization testing design
- A study design that tests different normalization procedures.
+ A study design that tests different normalization procedures.
Person: Chris Stoeckert, Jie Zheng
MO_729 normalization_testing_design
normalization testing design
@@ -690,7 +690,7 @@
environmental history design
- A study design in which some aspect of the organism's environmental history is studied, such as exposure to teratogen, radiation, climate etc.
+ A study design in which some aspect of the organism's environmental history is studied, such as exposure to teratogen, radiation, climate etc.
Person: Chris Stoeckert, Jie Zheng
MO_698 environmental_history_design
environmental history design
@@ -715,7 +715,7 @@
- A study design in which sequencing technology (e.g. Solexa/454) is used to generate RNA sequence, analyse the transcibed regions of the genome, and/or to quantitate transcript abundance
+ A study design in which sequencing technology (e.g. Solexa/454) is used to generate RNA sequence, analyse the transcibed regions of the genome, and/or to quantitate transcript abundance
Person: Chris Stoeckert, Jie Zheng
Group: ArrayExpress production team
transcription profiling by high throughput sequencing design
@@ -751,7 +751,7 @@
array platform variation design
- A study design in which the array platform is compared, e.g. Agilent versus Affymetrix.
+ A study design in which the array platform is compared, e.g. Agilent versus Affymetrix.
Person: Chris Stoeckert, Jie Zheng
MO_899 array_platform_variation_design
array platform variation design
@@ -777,7 +777,7 @@
ChIP-seq design
- A study design which aims to identify protein and DNA interactions using a combination of chromatin immunoprecipitation and high throughput sequencing. Massively parallel sequence analyses are used in conjunction with whole-genome sequence databases to analyze the interaction pattern of any protein with DNA, or the pattern of any epigenetic chromatin modifications.
+ A study design which aims to identify protein and DNA interactions using a combination of chromatin immunoprecipitation and high throughput sequencing. Massively parallel sequence analyses are used in conjunction with whole-genome sequence databases to analyze the interaction pattern of any protein with DNA, or the pattern of any epigenetic chromatin modifications.
Person: Chris Stoeckert, Jie Zheng
http://en.wikipedia.org/wiki/Chip-Sequencing
ChIP-seq design
@@ -797,7 +797,7 @@
translational bias design
- A study design that characterizes the association of transcripts and translation machinery.
+ A study design that characterizes the association of transcripts and translation machinery.
Person: Chris Stoeckert, Jie Zheng
MO_939 translational_bias_design
translational bias design
@@ -817,7 +817,7 @@
DNA methylation profiling by array design
- A study design in which the methylation state of DNA is determined and is compared between samples using array technology.
+ A study design in which the methylation state of DNA is determined and is compared between samples using array technology.
Person: Chris Stoeckert, Jie Zheng
GROUP: ArrayExpress production team
DNA methylation profiling by array design
@@ -831,7 +831,7 @@
in vitro design
- A study design that is done in a test tube or a culture dish, e.g. A bacterial invasion assay in an established cell culture.
+ A study design that is done in a test tube or a culture dish, e.g. A bacterial invasion assay in an established cell culture.
Person: Chris Stoeckert, Jie Zheng
MO_347 in_vitro_design
in vitro design
@@ -851,7 +851,7 @@
RNAi profiling by array design
- A study design in which experiment double stranded RNA is synthesized with a sequence complementary to a gene(s) of interest and introduced into a cell or organism, where it is recognized as exogenous genetic material and activates the RNAi pathway resulting in knockdown of the transcripts and providing a means to study downstream changes in gene expression.
+ A study design in which experiment double stranded RNA is synthesized with a sequence complementary to a gene(s) of interest and introduced into a cell or organism, where it is recognized as exogenous genetic material and activates the RNAi pathway resulting in knockdown of the transcripts and providing a means to study downstream changes in gene expression.
Person: Chris Stoeckert, Jie Zheng
Group: ArrayExpress production team
RNAi profiling by array design
@@ -871,7 +871,7 @@
transcription profiling by array design
- A study design that identifies forms and abundance of transcripts in the genome using microarray technology.
+ A study design that identifies forms and abundance of transcripts in the genome using microarray technology.
Person: Chris Stoeckert, Jie Zheng
MO_533 transcript_identification_design
transcription profiling by array design
@@ -907,7 +907,7 @@
disease state design
- A study design in which the pathological condition of a part, organ, or system of an organism is studied. The etiology may be from infection, genetic defect, or environmental stress.
+ A study design in which the pathological condition of a part, organ, or system of an organism is studied. The etiology may be from infection, genetic defect, or environmental stress.
Person: Chris Stoeckert, Jie Zheng
MO_902 disease_state_design
disease state design
@@ -937,7 +937,7 @@
RNA stability design
- A study design that examines the stability and/or decay of RNA transcripts.
+ A study design that examines the stability and/or decay of RNA transcripts.
Person: Chris Stoeckert, Jie Zheng
MO_553 RNA_stability_design
RNA stability design
@@ -973,7 +973,7 @@
species comparison design
- A study design that assays differences between distinct species.
+ A study design that assays differences between distinct species.
Person: Chris Stoeckert, Jie Zheng
MO_675 species_design
species comparison design
@@ -993,7 +993,7 @@
transcription profiling by RT-PCR design
- A study design which aims to examine the transcriptome of a biological sample by reverse transcription PCR (RT-PCR).
+ A study design which aims to examine the transcriptome of a biological sample by reverse transcription PCR (RT-PCR).
Person: Chris Stoeckert, Jie Zheng
Group: ArrayExpress production team
transcription profiling by RT-PCR design
@@ -1013,7 +1013,7 @@
microRNA profiling by array design
- A study design in which a microRNA array is used to analyse the microRNA component of the transcriptome.
+ A study design in which a microRNA array is used to analyse the microRNA component of the transcriptome.
Person: Chris Stoeckert, Jie Zheng
Group: ArrayExpress production team
microRNA profiling by array design
@@ -1053,7 +1053,7 @@
organism development design
- A study design that assays events associated with development. Development applies to organism(s) acquiring a mature state.
+ A study design that assays events associated with development. Development applies to organism(s) acquiring a mature state.
Person: Chris Stoeckert, Jie Zheng
MO_892 development_or_differentiation_design
organism development design
@@ -1073,7 +1073,7 @@
family history design
- A study design in which the family history such as traits, characteristics, susceptibility to disease is studied.
+ A study design in which the family history such as traits, characteristics, susceptibility to disease is studied.
Person: Chris Stoeckert, Jie Zheng
MO_544 family_history_design
family history design
@@ -1093,7 +1093,7 @@
quality control testing design
- A study design in which some aspects of the experiment is quality controlled for the purposes of quality assurance.
+ A study design in which some aspects of the experiment is quality controlled for the purposes of quality assurance.
Person: Chris Stoeckert, Jie Zheng
MO_981 quality_control_testing_design
quality control testing design
@@ -1123,7 +1123,7 @@
clinical history design
- A study design that the organism's clinical history of diagnosis, treatments, e.g. vaccinations, surgery etc. is studied.
+ A study design that the organism's clinical history of diagnosis, treatments, e.g. vaccinations, surgery etc. is studied.
Person: Chris Stoeckert, Jie Zheng
MO_832 clinical_history_design
clinical history design
@@ -1159,7 +1159,7 @@
post-transcriptional modification design
- A study design in which a modification of the transcriptome, proteome (not genome) is made, for example RNAi, antibody targeting.
+ A study design in which a modification of the transcriptome, proteome (not genome) is made, for example RNAi, antibody targeting.
post transcription modification design? or more clear RNAi design / antibody targeting design? need to check the use cases
Person: Chris Stoeckert, Jie Zheng
MO_392 cellular_modification_design
@@ -1190,7 +1190,7 @@
cellular process design
- A study design that aims to study the processes that are carried out at the cellular level, but are not necessarily restricted to a single cell. For example, cell communication occurs among more than one cell, but occurs at the cellular level.
+ A study design that aims to study the processes that are carried out at the cellular level, but are not necessarily restricted to a single cell. For example, cell communication occurs among more than one cell, but occurs at the cellular level.
Person: Chris Stoeckert, Jie Zheng
MO_810 cellular_process_design
cellular process design
@@ -1210,7 +1210,7 @@
injury design
- A study design in which the response of an organism(s) to injury or damage is studied.
+ A study design in which the response of an organism(s) to injury or damage is studied.
Person: Chris Stoeckert, Jie Zheng
MO_726 injury_design
injury design
@@ -1258,7 +1258,7 @@
organism status comparison design
- A study design that compares samples from live and dead organisms.
+ A study design that compares samples from live and dead organisms.
Person: Chris Stoeckert, Jie Zheng
MO_841 organism_status_design
organism status comparison design
@@ -1272,7 +1272,7 @@
genotyping by array design
- A study design that classifies an individual or group of individuals on the basis of alleles, haplotypes, SNPs using microarray technology.
+ A study design that classifies an individual or group of individuals on the basis of alleles, haplotypes, SNPs using microarray technology.
Person: Chris Stoeckert, Jie Zheng
MO_560 genotyping_design
genotyping by array design
@@ -1318,7 +1318,7 @@
stimulus or stress design
- A study design in which the response of an organism(s) to the stress or stimulus is studied, e.g. osmotic stress, heat shock, radiation exposure, behavioral treatment etc.
+ A study design in which the response of an organism(s) to the stress or stimulus is studied, e.g. osmotic stress, heat shock, radiation exposure, behavioral treatment etc.
Person: Chris Stoeckert, Jie Zheng
MO_568 stimulus_or_stress_design
stimulus or stress design
@@ -1344,7 +1344,7 @@
protocol optimization design
- A study design where different protocols or protocol parameters are compared aims to find an optimized protocol
+ A study design where different protocols or protocol parameters are compared aims to find an optimized protocol
Person: Chris Stoeckert, Jie Zheng
MO_934 optimization_design
protocol optimization design
@@ -1380,7 +1380,7 @@
ChIP-chip design
- A study design which aims to identify protein binding sites in genomic DNA by a combination of chromatin immunoprecipitation and DNA microarray (chip) assays.
+ A study design which aims to identify protein binding sites in genomic DNA by a combination of chromatin immunoprecipitation and DNA microarray (chip) assays.
Person: Chris Stoeckert, Jie Zheng
ChIP-on-chip design
MO_933 binding_site_identification_design
@@ -1407,7 +1407,7 @@
imprinting design
- A study design where differences in genetic imprinting of maternally- and paternally-inherited chromosomes (e.g., due to in vivo differences in chemical modification and/or chromatin structure) are compared.
+ A study design where differences in genetic imprinting of maternally- and paternally-inherited chromosomes (e.g., due to in vivo differences in chemical modification and/or chromatin structure) are compared.
Person: Chris Stoeckert, Jie Zheng
MO_914 imprinting_design
imprinting design
@@ -1437,7 +1437,7 @@
cell cycle design
- A study design that assays events that occur in relation to the cell cycle, which is the period between the formation of a cell, by division of its mother cell and the time when the cell itself divides to form two daughter cells.
+ A study design that assays events that occur in relation to the cell cycle, which is the period between the formation of a cell, by division of its mother cell and the time when the cell itself divides to form two daughter cells.
Person: Chris Stoeckert, Jie Zheng
MO_822 cell_cycle_design
cell cycle design
@@ -1457,7 +1457,7 @@
translation profiling design
- A study design in which surface-bound, translationally competent ribosome complexes are used to generate a translation profile for mRNA, where mRNA may be a single molecular species, or a combination of species, including complex mixtures such as those found in the set of mRNAs isolated from a cell or tissue. One or more components of the surface-bound ribosome complex may be labeled at specific positions to permit analysis of multiple or single molecules for determination of ribosomal conformational changes and translation kinetics. Translation profiles are used as the basis for comparison of an mRNA or set of mRNA species. The translation profile can be used to determine such characteristics as kinetics of initiation, kinetic of elongation, identity of the polypeptide product, and the like. Analysis of translation profiles may be used to determine differential gene expression, optimization of mRNA sequences for expression, screening drug candidates for an effect on translation.
+ A study design in which surface-bound, translationally competent ribosome complexes are used to generate a translation profile for mRNA, where mRNA may be a single molecular species, or a combination of species, including complex mixtures such as those found in the set of mRNAs isolated from a cell or tissue. One or more components of the surface-bound ribosome complex may be labeled at specific positions to permit analysis of multiple or single molecules for determination of ribosomal conformational changes and translation kinetics. Translation profiles are used as the basis for comparison of an mRNA or set of mRNA species. The translation profile can be used to determine such characteristics as kinetics of initiation, kinetic of elongation, identity of the polypeptide product, and the like. Analysis of translation profiles may be used to determine differential gene expression, optimization of mRNA sequences for expression, screening drug candidates for an effect on translation.
Person: Chris Stoeckert, Jie Zheng
Group: ArrayExpress production team
translation profiling design
@@ -1493,7 +1493,7 @@
cell type comparison design
- A study design that compares cells of different type, for example different cell lines.
+ A study design that compares cells of different type, for example different cell lines.
Person: Chris Stoeckert, Jie Zheng
MO_764 cell_type_comparison_design
cell type comparison design
@@ -1507,7 +1507,7 @@
ChIP-chip by tiling array design
- A study design which aims to identify protein binding sites in genomic DNA by a combination of chromatin immunoprecipitation and tiling microarray (chip) assays.
+ A study design which aims to identify protein binding sites in genomic DNA by a combination of chromatin immunoprecipitation and tiling microarray (chip) assays.
Person: Chris Stoeckert, Jie Zheng
Group: ArrayExpress production team
ChIP-chip by tiling array design
@@ -1576,7 +1576,7 @@
dose response design
- A study design that examines the relationship between the size of the administered dose and the extent of the response.
+ A study design that examines the relationship between the size of the administered dose and the extent of the response.
Person: Chris Stoeckert, Jie Zheng
MO_485 dose_response_design
dose response design
@@ -1612,7 +1612,7 @@
organism part comparison design
- A study design that compares tissues, regions, organs within or between organisms
+ A study design that compares tissues, regions, organs within or between organisms
Person: Chris Stoeckert, Jie Zheng
MO_953 organism_part_comparison_design
organism part comparison design
@@ -1632,7 +1632,7 @@
protein binding site identification design
- A study design that investigates protein binding sites on nucleic acids.
+ A study design that investigates protein binding sites on nucleic acids.
Person: Chris Stoeckert, Jie Zheng
MO_933 binding_site_identification_design
protein binding site identification design
@@ -1668,7 +1668,7 @@
sex comparison design
- A study design that assays differences associated with an organism's sex, gender or mating type.
+ A study design that assays differences associated with an organism's sex, gender or mating type.
Person: Chris Stoeckert, Jie Zheng
MO_575 sex_design
sex comparison design
@@ -1688,7 +1688,7 @@
transcription profiling by tiling array design
- A study design in which gene expression on a genome-wide basis is evaluated, without bias toward coding or noncoding regions, using tiling arrays containing oligonucleotides that are either overlapping or spaced at regular intervals.
+ A study design in which gene expression on a genome-wide basis is evaluated, without bias toward coding or noncoding regions, using tiling arrays containing oligonucleotides that are either overlapping or spaced at regular intervals.
Person: Chris Stoeckert, Jie Zheng
MO_507 tiling_path_design
transcription profiling by tiling array design
@@ -1718,7 +1718,7 @@
cell differentiation design
- A study design that assays events associated with cell development or differentiation.
+ A study design that assays events associated with cell development or differentiation.
Person: Chris Stoeckert, Jie Zheng
MO_892 development_or_differentiation_design
cell differentiation design
@@ -1732,7 +1732,7 @@
transcription profiling design
- A study design that identifies forms and abundance of transcripts in the genome.
+ A study design that identifies forms and abundance of transcripts in the genome.
Person: Chris Stoeckert, Jie Zheng
MO_533 transcript_identification_design
transcription profiling design
@@ -1752,7 +1752,7 @@
operon identification design
- A study design that identifies locations and members of operons in a genome.
+ A study design that identifies locations and members of operons in a genome.
Person: Chris Stoeckert, Jie Zheng
MO_772 operon_identification_design
operon identification design
@@ -1772,7 +1772,7 @@
DNA methylation profiling by high throughput sequencing design
- A study design in which the methylation state of DNA is determined and is compared between samples using high throughput sequencing technology.
+ A study design in which the methylation state of DNA is determined and is compared between samples using high throughput sequencing technology.
Person: Chris Stoeckert, Jie Zheng
GROUP: ArrayExpress production team
DNA methylation profiling by high throughput sequencing design
@@ -1786,7 +1786,7 @@
all pairs design
- A study design in which all specimens are compared to every other specimen.
+ A study design in which all specimens are compared to every other specimen.
Person: Chris Stoeckert, Jie Zheng
MO_565 all_pairs
all pairs design
@@ -1805,7 +1805,7 @@
- A study design in which proteins in a sample are detected, quantified or otherwise analysed, through an array-based technology.
+ A study design in which proteins in a sample are detected, quantified or otherwise analysed, through an array-based technology.
Person: Chris Stoeckert, Jie Zheng, Dan Berrios
Group: ArrayExpress production team
https://github.com/obi-ontology/obi/issues/854
@@ -1826,7 +1826,7 @@
genotyping design
- A study design that classifies an individual or group of individuals on the basis of alleles, haplotypes, SNPs.
+ A study design that classifies an individual or group of individuals on the basis of alleles, haplotypes, SNPs.
Person: Chris Stoeckert, Jie Zheng
MO_560 genotyping_design
genotyping design
@@ -1862,7 +1862,7 @@
individual genetic characteristics comparison design
- A study design where genotype, haplotype, or other individual genetic characteristics are compared.
+ A study design where genotype, haplotype, or other individual genetic characteristics are compared.
Person: Chris Stoeckert, Jie Zheng
MO_527 individual_genetic_characteristics_design
individual genetic characteristics comparison design
@@ -1882,7 +1882,7 @@
pathogenicity design
- A study design in which an infective agent such as a bacterium, virus, protozoan, fungus etc. infects a host organism(s) and the infective agent is assayed.
+ A study design in which an infective agent such as a bacterium, virus, protozoan, fungus etc. infects a host organism(s) and the infective agent is assayed.
Person: Chris Stoeckert, Jie Zheng
MO_807 pathogenicity_design
pathogenicity design
@@ -1925,7 +1925,7 @@
genetic modification design
- A study design in which an organism(s) is studied that has had genetic material removed, rearranged, mutagenized or added, such as in a knock out.
+ A study design in which an organism(s) is studied that has had genetic material removed, rearranged, mutagenized or added, such as in a knock out.
Person: Chris Stoeckert, Jie Zheng
MO_447 genetic_modification_design
genetic modification design
@@ -1961,7 +1961,7 @@
strain comparison design
- A study design that assays differences between multiple strains, cultivars, serovars, isolates, lines from organisms of a single species.
+ A study design that assays differences between multiple strains, cultivars, serovars, isolates, lines from organisms of a single species.
Person: Chris Stoeckert, Jie Zheng
MO_462 strain_or_line_design
strain comparison design
@@ -2000,7 +2000,7 @@
- A study design that aims to compare different types of hardware for performance, reproducibility, accuracy and precision.
+ A study design that aims to compare different types of hardware for performance, reproducibility, accuracy and precision.
Person: Jie Zheng
MO_734 hardware_variation_design
hardware testing design
@@ -2016,7 +2016,7 @@
Red blood cell transfusion in patients with traumatic brain injury: a systematic review protocol. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4090399/
The effect of moderate gestational alcohol consumption during pregnancy on speech and language outcomes in children: a systematic review. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3892059/
- A study design for identifying in the literature prior studies of a pre-determined phenomenon or set of related phenomena according to certain criteria, extracting findings from these studies, and summarizing these findings and/or attempting to draw new conclusions from them which were not justified by any of the individual, prior studies. Many systematic reviews also assess the quality of the studies so reviewed.
+ A study design for identifying in the literature prior studies of a pre-determined phenomenon or set of related phenomena according to certain criteria, extracting findings from these studies, and summarizing these findings and/or attempting to draw new conclusions from them which were not justified by any of the individual, prior studies. Many systematic reviews also assess the quality of the studies so reviewed.
PERSON: Bill Hogan
systematic review study design
@@ -2045,7 +2045,7 @@
decision analysis study design
- a study design that has a decision analysis objective specification as part
+ a study design that has a decision analysis objective specification as part
PERSON: Bill Hogan
PERSON: Bill Hogan
decision analysis study design
@@ -2057,7 +2057,7 @@
- A study design in which proteins in a sample are detected, quantified or otherwise analysed.
+ A study design in which proteins in a sample are detected, quantified or otherwise analysed.
Dan Berrios
OBI:0001441
proteomic profiling design
@@ -2075,7 +2075,7 @@
- A study design that investigates the features of interaction between molecules.
+ A study design that investigates the features of interaction between molecules.
Rebecca Jackson
person:RCT
molecular interaction identification design
@@ -2087,7 +2087,7 @@
- A molecular interaction identification design that investigates the co-occurence and correlation of two or more molecules.
+ A molecular interaction identification design that investigates the co-occurence and correlation of two or more molecules.
Rebecca Jackson
url:https://en.wikipedia.org/wiki/Colocalization
colocalization identification design
@@ -2115,7 +2115,7 @@
- A molecular interaction identification design that investigates a phenotype that is the result of two or more genetic perturbations, and is not explained by the individual genetic perturbations alone.
+ A molecular interaction identification design that investigates a phenotype that is the result of two or more genetic perturbations, and is not explained by the individual genetic perturbations alone.
Rebecca Jackson
MI:0208
genetic interaction identification design
@@ -2127,7 +2127,7 @@
- A molecular interaction identification design that investigates a relationship that is the result of intermediate steps between two or more molecules that are not necessarily in direct contact with each other.
+ A molecular interaction identification design that investigates a relationship that is the result of intermediate steps between two or more molecules that are not necessarily in direct contact with each other.
Rebecca Jackson
MI:2286
functional association identification design
@@ -2155,7 +2155,7 @@
- A molecular interaction identification design that investigates the influence of molecules, which are in direct contact, on one another.
+ A molecular interaction identification design that investigates the influence of molecules, which are in direct contact, on one another.
Rebecca Jackson
molecular binding identification design
MI:0407
@@ -2168,7 +2168,7 @@
- A direct interaction identification design that investigations a biological reaction on a molecule which has been triggered by an enzyme.
+ A direct interaction identification design that investigations a biological reaction on a molecule which has been triggered by an enzyme.
Rebecca Jackson
MI:0414
enzymatic reaction identification design
@@ -2180,7 +2180,7 @@
- A molecular interaction identification design that investigates intra-molecular interactions between two or more regions of a single molecule.
+ A molecular interaction identification design that investigates intra-molecular interactions between two or more regions of a single molecule.
Rebecca Jackson
MI:1126
self interaction identification design
@@ -2193,7 +2193,7 @@
The LucKi Birth Cohort Study was designed and started in 2006 to follow children from birth into adulthood on a wide range of determinants, disorders, and diseases.
- A cohort study design for which the subjects are followed from the time of birth usually including information about gestation and follow up.
+ A cohort study design for which the subjects are followed from the time of birth usually including information about gestation and follow up.
MIABIS
MIABIS contributors
birth cohort study design
@@ -2206,7 +2206,7 @@
A study of the symptoms experienced by patients who have been diagnosed with multiple sclerosis employs a disease specific study design.
- A study design for which material and information is collected from subjects that have already developed a particular disease.
+ A study design for which material and information is collected from subjects that have already developed a particular disease.
MIABIS
MIABIS contributors
disease specific study design
@@ -2218,7 +2218,7 @@
- A study design that entails the creation of two types of roles, such that each participant under investigation bears one or the other. What distinguishes the two types of roles is an 'outcome', which is associated with participants that have the case role but not associated with participants that have the control role. A case-control study examines the hypothesis that the presence of the outcome in case participants is associated with an 'exposure' that is not associated with control participants.
+ A study design that entails the creation of two types of roles, such that each participant under investigation bears one or the other. What distinguishes the two types of roles is an 'outcome', which is associated with participants that have the case role but not associated with participants that have the control role. A case-control study examines the hypothesis that the presence of the outcome in case participants is associated with an 'exposure' that is not associated with control participants.
John Judkins, Bjoern Peters
Wikipedia, OBI
case-control study design
@@ -2233,7 +2233,7 @@
case series study design
PMID: 22213493
- A study design that samples only subjects who have experienced a particular event (outcome or exposure). Such a design, in contrast to a cohort study, does not permit calculation of absolute risk as non-case subjects are not included.
+ A study design that samples only subjects who have experienced a particular event (outcome or exposure). Such a design, in contrast to a cohort study, does not permit calculation of absolute risk as non-case subjects are not included.
http://orcid.org/0000-0002-8844-9165
https://www.ncbi.nlm.nih.gov/pubmed/22213493
case series design
@@ -2246,7 +2246,7 @@
population based design
- A study design where the selection of the individuals that are included into the study are intended to be representative of all individuals in the a priori defined specific population and is done at the population level or among the population groups, generally to find the cause, incidence or spread of the disease or to see the response to the treatment, nutrition or environment.
+ A study design where the selection of the individuals that are included into the study are intended to be representative of all individuals in the a priori defined specific population and is done at the population level or among the population groups, generally to find the cause, incidence or spread of the disease or to see the response to the treatment, nutrition or environment.
Chris Stoeckert
https://link.springer.com/referenceworkentry/10.1007%2F978-1-4419-1005-9_45, EFO_0001430 population based design
https://github.com/obi-ontology/obi/issues/1090
@@ -2259,7 +2259,7 @@
- A study design that is executed primarily on a computer.
+ A study design that is executed primarily on a computer.
Hector Guzman-Orozco
https://en.wikipedia.org/wiki/In_silico
https://github.com/obi-ontology/obi/issues/1430
@@ -2275,7 +2275,7 @@
ring trial design
https://eco-fab.org/about-ecofab-initiative/
- A study design with the objective of establishing the reproducibility of an experimental approach by performing experiments in different laboratories under the same conditions and comparing the experimental outcomes.
+ A study design with the objective of establishing the reproducibility of an experimental approach by performing experiments in different laboratories under the same conditions and comparing the experimental outcomes.
Bjoern Peters
Sebastian Duesing
https://github.com/obi-ontology/obi/issues/1768
@@ -2304,7 +2304,7 @@
sequential design
PMID: 17710740.Pharm Stat. 2007 Aug 20.Sequential design approaches for bioequivalence studies with crossover designs.
- Any design in which the decision as to whether to enroll the next patient, pair of patients, or block of patients is determined by whether the cumulative treatment difference for all previous patients is within specified limits. Enrollment is continued if the difference does not exceed the limits. It is terminated if it does
+ Any design in which the decision as to whether to enroll the next patient, pair of patients, or block of patients is determined by whether the cumulative treatment difference for all previous patients is within specified limits. Enrollment is continued if the difference does not exceed the limits. It is terminated if it does
Philippe Rocca-Serra
MUSC
Provenance: OCI
@@ -2320,7 +2320,7 @@
observation design
PMID: 12387964.Lancet. 2002 Oct 12;360(9340):1144-9.Deficiency of antibacterial peptides in patients with morbus Kostmann: an observation study.
- observation design is a study design in which subjects are monitored in the absence of any active intervention by experimentalists.
+ observation design is a study design in which subjects are monitored in the absence of any active intervention by experimentalists.
Philippe Rocca-Serra
OBI branch derived
observation design
@@ -2341,7 +2341,7 @@
clinical study design
PMID: 17655677.J Cardiovasc Electrophysiol. 2007 Aug;18(9):965-71.Biventricular versus right ventricular pacing in patients with AV block (BLOCK HF): clinical study design and rationale.
- Plan for the precise procedure to be followed in a clinical trial, including planned and actual timing of events, choice of control group, method of allocating treatments, blinding methods; assigns a subject to pass through one or more epochs in the course of a trial. Specific design elements, e.g., crossover, parallel; dose-escalation [Modified from Pocock, Clinical Trials: A Practical Approach]
+ Plan for the precise procedure to be followed in a clinical trial, including planned and actual timing of events, choice of control group, method of allocating treatments, blinding methods; assigns a subject to pass through one or more epochs in the course of a trial. Specific design elements, e.g., crossover, parallel; dose-escalation [Modified from Pocock, Clinical Trials: A Practical Approach]
The definition needs to be extended to other things than simply patients
PlanAndPlannedProcess Branch
Clinical Research Glossary Version 4.0 CDICS glossary group
@@ -2357,7 +2357,7 @@
repeated measure design
PMID: 10959922.J Biopharm Stat. 2000 Aug;10(3):433-45.Equivalence in test assay method comparisons for the repeated-measure, matched-pair design in medical device studies: statistical considerations.
- a study design which use the same individuals and exposure them to a set of conditions. The effect of order and practice can be confounding factor in such designs
+ a study design which use the same individuals and exposure them to a set of conditions. The effect of order and practice can be confounding factor in such designs
PlanAndPlannedProcess Branch
http://www.holah.karoo.net/experimentaldesigns.htm
repeated measure design
@@ -2372,7 +2372,7 @@
cross over design
PMID: 17601993-Objective: HIV-infected patients with lipodystrophy (HIV-lipodystrophy) are insulin resistant and have elevated plasma free fatty acid (FFA) concentrations. We aimed to explore the mechanisms underlying FFA-induced insulin resistance in patients with HIV-lipodystrophy. Research Design and Methods: Using a randomized placebo-controlled cross-over design, we studied the effects of an overnight acipimox-induced suppression of FFA on glucose and FFA metabolism by using stable isotope labelled tracer techniques during basal conditions and a two-stage euglycemic, hyperinsulinemic clamp (20 mU insulin/m(2)/min; 50 mU insulin/m(2)/min) in nine patients with nondiabetic HIV-lipodystrophy. All patients received antiretroviral therapy. Biopsies from the vastus lateralis muscle were obtained during each stage of the clamp. Results: Acipimox treatment reduced basal FFA rate of appearance by 68.9% (52.6%-79.5%) and decreased plasma FFA concentration by 51.6 % (42.0%-58.9%), (both, P < 0.0001). Endogenous glucose production was not influenced by acipimox. During the clamp the increase in glucose-uptake was significantly greater after acipimox treatment compared to placebo (acipimox: 26.85 (18.09-39.86) vs placebo: 20.30 (13.67-30.13) mumol/kg/min; P < 0.01). Insulin increased phosphorylation of Akt (Thr(308)) and GSK-3beta (Ser(9)), decreased phosphorylation of glycogen synthase (GS) site 3a+b and increased GS-activity (I-form) in skeletal muscle (P < 0.01). Acipimox decreased phosphorylation of GS (site 3a+b) (P < 0.02) and increased GS-activity (P < 0.01) in muscle. Conclusion: The present study provides direct evidence that suppression of lipolysis in patients with HIV-lipodystrophy improves insulin-stimulated peripheral glucose-uptake. The increased glucose-uptake may in part be explained by increased dephosphorylation of GS (site 3a+b) resulting in increased GS activity.
- a repeated measure design which ensures that experimental units receive, in sequence, the treatment (or the control), and then, after a specified time interval (aka *wash-out periods*), switch to the control (or treatment). In this design, subjects (patients in human context) serve as their own controls, and randomization may be used to determine the ordering which a subject receives the treatment and control
+ a repeated measure design which ensures that experimental units receive, in sequence, the treatment (or the control), and then, after a specified time interval (aka *wash-out periods*), switch to the control (or treatment). In this design, subjects (patients in human context) serve as their own controls, and randomization may be used to determine the ordering which a subject receives the treatment and control
Philippe Rocca-Serra
(source: http://www.sbu.se/Filer/Content0/publikationer/1/literaturesearching_1993/glossary.html)
cross over design
@@ -2386,7 +2386,7 @@
n-to-1 design
- N-of-1 design is a cross-over design in which the same patient is repeatedly randomised to receive either the experimental treatment or its control (Senn, 1993).
+ N-of-1 design is a cross-over design in which the same patient is repeatedly randomised to receive either the experimental treatment or its control (Senn, 1993).
Philippe Rocca-Serra
Adapted from http://www.childrens-mercy.org/stats/definitions/crossover.htm and source:http://symptomresearch.nih.gov/chapter_6/sec1/csss1pg1.htm)
n-to-1 design
@@ -2401,7 +2401,7 @@
matched pairs design
PMID: 17288613-BSTRACT: BACKGROUND: Physicians in Canadian emergency departments (EDs) annually treat 185,000 alert and stable trauma victims who are at risk for cervical spine (C-spine) injury. However, only 0.9% of these patients have suffered a cervical spine fracture. Current use of radiography is not efficient. The Canadian C-Spine Rule is designed to allow physicians to be more selective and accurate in ordering C-spine radiography, and to rapidly clear the C-spine without the need for radiography in many patients. The goal of this phase III study is to evaluate the effectiveness of an active strategy to implement the Canadian C-Spine Rule into physician practice. Specific objectives are to: 1) determine clinical impact, 2) determine sustainability, 3) evaluate performance, and 4) conduct an economic evaluation. METHODS: We propose a matched-pair cluster design study that compares outcomes during three consecutive 12-months before, after, and decay periods at six pairs of intervention and control sites. These 12 hospital ED sites will be stratified as teaching or community hospitals, matched according to baseline C-spine radiography ordering rates, and then allocated within each pair to either intervention or control groups. During the after period at the intervention sites, simple and inexpensive strategies will be employed to actively implement the Canadian C-Spine Rule. The following outcomes will be assessed: 1) measures of clinical impact, 2) performance of the Canadian C-Spine Rule, and 3) economic measures. During the 12-month decay period, implementation strategies will continue, allowing us to evaluate the sustainability of the effect. We estimate a sample size of 4,800 patients in each period in order to have adequate power to evaluate the main outcomes. DISCUSSION: Phase I successfully derived the Canadian C-Spine Rule and phase II confirmed the accuracy and safety of the rule, hence, the potential for physicians to improve care. What remains unknown is the actual change in clinical behaviors that can be affected by implementation of the Canadian C-Spine Rule, and whether implementation can be achieved with simple and inexpensive measures. We believe that the Canadian C-Spine Rule has the potential to significantly reduce health care costs and improve the efficiency of patient flow in busy Canadian EDs.
- A matched pair design is a study design which use groups of individuals associated (hence matched) to each other based on a set of criteria, one member going to one treatment, the other member receiving the other treatment.
+ A matched pair design is a study design which use groups of individuals associated (hence matched) to each other based on a set of criteria, one member going to one treatment, the other member receiving the other treatment.
Philippe Rocca-Serra
http://www.holah.karoo.net/experimentaldesigns.htm
matched pairs design
@@ -2416,7 +2416,7 @@
parallel group design
PMID: 17408389-Purpose: Proliferative vitreoretinopathy (PVR) is the most important reason for blindness following retinal detachment. Presently, vitreous tamponades such as gas or silicone oil cannot contact the lower part of the retina. A heavier-than-water tamponade displaces the inflammatory and PVR-stimulating environment from the inferior area of the retina. The Heavy Silicone Oil versus Standard Silicone Oil Study (HSO Study) is designed to answer the question of whether a heavier-than-water tamponade improves the prognosis of eyes with PVR of the lower retina. Methods: The HSO Study is a multicentre, randomized, prospective controlled clinical trial comparing two endotamponades within a two-arm parallel group design. Patients with inferiorly and posteriorly located PVR are randomized to either heavy silicone oil or standard silicone oil as a tamponading agent. Three hundred and fifty consecutive patients are recruited per group. After intraoperative re-attachment, patients are randomized to either standard silicone oil (1000 cSt or 5000 cSt) or Densiron((R)) as a tamponading agent. The main endpoint criteria are complete retinal attachment at 12 months and change of visual acuity (VA) 12 months postoperatively compared with the preoperative VA. Secondary endpoints include complete retinal attachment before endotamponade removal, quality of life analysis and the number of retina affecting re-operation within 1 year of follow-up. Results: The design and early recruitment phase of the study are described. Conclusions: The results of this study will uncover whether or not heavy silicone oil improves the prognosis of eyes with PVR.
- A parallel group design or independent measure design is a study design which uses unique experimental unit each experimental group, in other word no two individuals are shared between experimental groups, hence also known as parallel group design. Subjects of a treatment group receive a unique combination of independent variable values making up a treatment
+ A parallel group design or independent measure design is a study design which uses unique experimental unit each experimental group, in other word no two individuals are shared between experimental groups, hence also known as parallel group design. Subjects of a treatment group receive a unique combination of independent variable values making up a treatment
Philippe Rocca-Serra
independent measure design
http://www.holah.karoo.net/experimentaldesigns.htm
@@ -2432,7 +2432,7 @@
randomized complete block design
http://www.stats.gla.ac.uk/steps/glossary/anova.html,(A researcher is carrying out a study of the effectiveness of four different skin creams for the treatment of a certain skin disease. He has eighty subjects and plans to divide them into 4 treatment groups of twenty subjects each. Using a randomised blocks& design, the subjects are assessed and put in blocks of four according to how severe their skin condition is; the four most severe cases are the first block, the next four most severe cases are the second block, and so on to the twentieth block. The four &members of each block are then randomly assigned, one to each of the four treatment groups. http://www.stats.gla.ac.uk/steps/glossary/anova.html#rbd))
- A randomized complete block design is_a study design which assigns randomly treatments to block. The number of units per block equals the number of treatment so each block receives each treatment exactly once (hence the qualifier 'complete'). The design was originally devised from field trials used in agronomy and agriculture. The analysis assumes that there is no interaction between block and treatment. The method was then used in other settings So The randomised complete block design is a design in which the subjects are matched according to a variable which the experimenter wishes to control. The subjects are put into groups (blocks) of the same size as the number of treatments. The members of each block are then randomly assigned to different treatment groups.
+ A randomized complete block design is_a study design which assigns randomly treatments to block. The number of units per block equals the number of treatment so each block receives each treatment exactly once (hence the qualifier 'complete'). The design was originally devised from field trials used in agronomy and agriculture. The analysis assumes that there is no interaction between block and treatment. The method was then used in other settings So The randomised complete block design is a design in which the subjects are matched according to a variable which the experimenter wishes to control. The subjects are put into groups (blocks) of the same size as the number of treatments. The members of each block are then randomly assigned to different treatment groups.
Philippe Rocca-Serra
http://www.tufts.edu/~gdallal/ranblock.htm
randomized complete block design
@@ -2447,7 +2447,7 @@
balanced incomplete block design
PMID: 7622388.Health Educ Q. 1995 May;22(2):201-10.Balanced incomplete block design: description, case study, and implications for practice.
- balanced incomplete block design is a kind of factorial design where all treatment pairs occur together within a block an equal number ?? times. ??ii' is the number of times treatment i occurs with i'
+ balanced incomplete block design is a kind of factorial design where all treatment pairs occur together within a block an equal number ?? times. ??ii' is the number of times treatment i occurs with i'
Philippe Rocca-Serra
http://en.wikipedia.org/wiki/Block_design and http://www.stat.psu.edu/~jglenn/stat503/05_factorial/02_factorial_IBD.html
balanced incomplete block design
@@ -2462,7 +2462,7 @@
loop design
PMID: 12933549
- A loop experiment design is where labeled extracts are compared in consecutive pairs. synonym: circular design
+ A loop experiment design is where labeled extracts are compared in consecutive pairs. synonym: circular design
Philippe Rocca-Serra on behalf of MO
MO_912
loop design
@@ -2477,7 +2477,7 @@
reference design
PMID: 12933549
- A reference experiment design type is where all samples are compared to a common reference.
+ A reference experiment design type is where all samples are compared to a common reference.
Philippe Rocca-Serra on behalf of MO
MO_699
reference design
@@ -2492,7 +2492,7 @@
latin square design
PMID: 17582121-Our objective was to examine the effects of dietary cation-anion difference (DCAD) with different concentrations of dietary crude protein (CP) on performance and acid-base status in early lactation cows. Six lactating Holstein cows averaging 44 d in milk were used in a 6 x 6 Latin square design with a 2 x 3 factorial arrangement of treatments: DCAD of -3, 22, or 47 milliequivalents (Na + K - Cl - S)/100 g of dry matter (DM), and 16 or 19% CP on a DM basis. Linear increases with DCAD occurred in DM intake, milk fat percentage, 4% fat-corrected milk production, milk true protein, milk lactose, and milk solids-not-fat. Milk production itself was unaffected by DCAD. Jugular venous blood pH, base excess and HCO3(-) concentration, and urine pH increased, but jugular venous blood Cl- concentration, urine titratable acidity, and net acid excretion decreased linearly with increasing DCAD. An elevated ratio of coccygeal venous plasma essential AA to nonessential AA with increasing DCAD indicated that N metabolism in the rumen was affected, probably resulting in more microbial protein flowing to the small intestine. Cows fed 16% CP had lower urea N in milk than cows fed 19% CP; the same was true for urea N in coccygeal venous plasma and urine. Dry matter intake, milk production, milk composition, and acid-base status did not differ between the 16 and 19% CP treatments. It was concluded that DCAD affected DM intake and performance of dairy cows in early lactation. Feeding 16% dietary CP to cows in early lactation, compared with 19% CP, maintained lactation performance while reducing urea N excretion in milk and urine.
- Latin square design is_a study design which allows in its simpler form controlling 2 levels of nuisance variables (also known as blocking variables).he 2 nuisance factors are divided into a tabular grid with the property that each row and each column receive each treatment exactly once.
+ Latin square design is_a study design which allows in its simpler form controlling 2 levels of nuisance variables (also known as blocking variables).he 2 nuisance factors are divided into a tabular grid with the property that each row and each column receive each treatment exactly once.
Philippe Rocca-Serra
Adapted from: http://www.itl.nist.gov/div898/handbook/pri/section3/pri3321.htm and
latin square design
@@ -2507,7 +2507,7 @@
graeco latin square design
PMID: 6846242-Beaton et al (Am J Clin Nutr 1979;32:2546-59) reported on the partitioning of variance in 1-day dietary data for the intake of energy, protein, total carbohydrate, total fat, classes of fatty acids, cholesterol, and alcohol. Using the same food intake data and the expanded National Heart, Lung and Blood Institute food composition data base, these analyses of sources of variance have been expanded to include classes of carbohydrate, vitamin A, vitamin C, thiamin, riboflavin, niacin, calcium, iron, total ash, caffeine, and crude fiber. The analyses relate to observed intakes (replicated six times) of 30 adult males and 30 adult females obtained under a paired Graeco-Latin square design with sequence of interview, interviewer, and day of the week as determinants. Neither sequence nor interviewer made consistent contribution to variance. In females, day of the week had a significant effect for several nutrients. The major partitioning of variance was between interindividual variation (between subjects) and intraindividual variation (within subjects) which included both true day-to-day variation in intake and methodological variation. For all except caffeine, the intraindividual variability of 1-day data was larger than the interindividual variability. For vitamin A, almost all of the variance was associated with day-to-day variability. One day data provide a very inadequate estimate of usual intake of individuals. In the design of nutrition studies it is critical that the intended use of dietary data be a major consideration in deciding on methodology. There is no ideal dietary method. There may be preferred methods for particular purposes.
- Greco-Latin square design is a study design which relates to Latin square design
+ Greco-Latin square design is a study design which relates to Latin square design
Philippe Rocca-Serra
Adapted from: http://www.itl.nist.gov/div898/handbook/pri/section3/pri3321.htm and
only 2 articles in pubmed ->probably irrelevant
@@ -2522,7 +2522,7 @@
hyper graeco latin square design
- PRS to do
+ PRS to do
Philippe Rocca-Serra
Adapted from: http://www.itl.nist.gov/div898/handbook/pri/section3/pri3321.htm and
no example found in pubmed->not in use in the community
@@ -2537,7 +2537,7 @@
PMID: 17582121-Our objective was to examine the effects of dietary cation-anion difference (DCAD) with different concentrations of dietary crude protein (CP) on performance and acid-base status in early lactation cows. Six lactating Holstein cows averaging 44 d in milk were used in a 6 x 6 Latin square design with a 2 x 3 factorial arrangement of treatments: DCAD of -3, 22, or 47 milliequivalents (Na + K - Cl - S)/100 g of dry matter (DM), and 16 or 19% CP on a DM basis. Linear increases with DCAD occurred in DM intake, milk fat percentage, 4% fat-corrected milk production, milk true protein, milk lactose, and milk solids-not-fat. Milk production itself was unaffected by DCAD. Jugular venous blood pH, base excess and HCO3(-) concentration, and urine pH increased, but jugular venous blood Cl- concentration, urine titratable acidity, and net acid excretion decreased linearly with increasing DCAD. An elevated ratio of coccygeal venous plasma essential AA to nonessential AA with increasing DCAD indicated that N metabolism in the rumen was affected, probably resulting in more microbial protein flowing to the small intestine. Cows fed 16% CP had lower urea N in milk than cows fed 19% CP; the same was true for urea N in coccygeal venous plasma and urine. Dry matter intake, milk production, milk composition, and acid-base status did not differ between the 16 and 19% CP treatments. It was concluded that DCAD affected DM intake and performance of dairy cows in early lactation. Feeding 16% dietary CP to cows in early lactation, compared with 19% CP, maintained lactation performance while reducing urea N excretion in milk and urine.
- factorial design is_a study design which is used to evaluate two or more factors simultaneously. The treatments are combinations of levels of the factors. The advantages of factorial designs over one-factor-at-a-time experiments is that they are more efficient and they allow interactions to be detected. In statistics, a factorial design experiment is an experiment whose design consists of two or more factors, each with discrete possible values or levels, and whose experimental units take on all possible combinations of these levels across all such factors. Such an experiment allows studying the effect of each factor on the response variable, as well as the effects of interactions between factors on the response variable.
+ factorial design is_a study design which is used to evaluate two or more factors simultaneously. The treatments are combinations of levels of the factors. The advantages of factorial designs over one-factor-at-a-time experiments is that they are more efficient and they allow interactions to be detected. In statistics, a factorial design experiment is an experiment whose design consists of two or more factors, each with discrete possible values or levels, and whose experimental units take on all possible combinations of these levels across all such factors. Such an experiment allows studying the effect of each factor on the response variable, as well as the effects of interactions between factors on the response variable.
Philippe Rocca-Serra
http://www.stats.gla.ac.uk/steps/glossary/anova.html#facdes And from wikipedia (01/03/2007): http://en.wikipedia.org/wiki/Factorial_experiment)
factorial design
@@ -2552,7 +2552,7 @@
2x2 factorial design
PMID: 17561240-The present experiment evaluates the effects of intermittent exposure to a social stimulus on ethanol and water drinking in rats. Four groups of rats were arranged in a 2x2 factorial design with 2 levels of Social procedure (Intermittent Social vs Continuous Social) and 2 levels of sipper Liquid (Ethanol vs Water). Intermittent Social groups received 35 trials per session. Each trial consisted of the insertion of the sipper tube for 10 s followed by lifting of the guillotine door for 15 s. The guillotine door separated the experimental rat from the conspecific rat in the wire mesh cage during the 60 s inter-trial interval. The Continuous Social groups received similar procedures except that the guillotine door was raised during the entire duration of the session. For the Ethanol groups, the concentrations of ethanol in the sipper [3, 4, 6, 8, 10, 12, 14, and 16% (vol/vol)] increased across sessions, while the Water groups received 0% ethanol (water) in the sipper throughout the experiment. Both Social procedures induced more intake of ethanol than water. The Intermittent Social procedure induced more ethanol intake at the two highest ethanol concentration blocks (10-12% and 14-16%) than the Continuous Social procedure, but this effect was not observed with water. Effects of social stimulation on ethanol drinking are discussed.
- a factorial design which has 2 experimental factors (aka independent variables) and 2 factor levels per experimental factors
+ a factorial design which has 2 experimental factors (aka independent variables) and 2 factor levels per experimental factors
Philippe Rocca-Serra
PMID: 17561240
2x2 factorial design
@@ -2566,7 +2566,7 @@
fractional factorial design
- A fractional factorial design is_a study design in which only an adequately chosen fraction of the treatment combinations required for the complete factorial experiment is selected to be run
+ A fractional factorial design is_a study design in which only an adequately chosen fraction of the treatment combinations required for the complete factorial experiment is selected to be run
Philippe Rocca-Serra
http://www.itl.nist.gov/div898/handbook/pri/section3/pri334.htm From ASQC (1983) Glossary & Tables for Statistical Quality Control
fractional factorial design
@@ -2581,7 +2581,7 @@
dye swap design
PMID: 17411393-Dye-specific bias effects, commonly observed in the two-color microarray platform, are normally corrected using the dye swap design. This design, however, is relatively expensive and labor-intensive. We propose a self-self hybridization design as an alternative to the dye swap design. In this design, the treated and control samples are labeled with Cy5 and Cy3 (or Cy3 and Cy5), respectively, without dye swap, along with a set of self-self hybridizations on the control sample. We compare this design with the dye swap design through investigation of mouse primary hepatocytes treated with three peroxisome proliferator-activated receptor-alpha (PPARalpha) agonists at three dose levels. Using Agilent's Whole Mouse Genome microarray, differentially expressed genes (DEG) were determined for both the self-self hybridization and dye swap designs. The DEG concordance between the two designs was over 80% across each dose treatment and chemical. Furthermore, 90% of DEG-associated biological pathways were in common between the designs, indicating that biological interpretations would be consistent. The reduced labor and expense for the self-self hybridization design make it an efficient substitute for the dye swap design. For example, in larger toxicogenomic studies, only about half the chips are required for the self-self hybridization design compared to that needed in the dye swap design.
- An experiment design type where the label orientations are reversed. exact synonym: flip dye, dye flip
+ An experiment design type where the label orientations are reversed. exact synonym: flip dye, dye flip
Philippe Rocca-Serra on behalf of MO
MO_858
dye swap design
@@ -2595,7 +2595,7 @@
replicate design
- A replicate experimental design type is where a series of replicates are performed to evaluate reproducibility or as a pilot study to determine the appropriate number of replicates for a subsequent experiments.
+ A replicate experimental design type is where a series of replicates are performed to evaluate reproducibility or as a pilot study to determine the appropriate number of replicates for a subsequent experiments.
Philippe Rocca-Serra on behalf of MO
MO_885
replicate design
@@ -2610,7 +2610,7 @@
self vs self design
PMID: 17411393-Dye-specific bias effects, commonly observed in the two-color microarray platform, are normally corrected using the dye swap design. This design, however, is relatively expensive and labor-intensive. We propose a self-self hybridization design as an alternative to the dye swap design. In this design, the treated and control samples are labeled with Cy5 and Cy3 (or Cy3 and Cy5), respectively, without dye swap, along with a set of self-self hybridizations on the control sample. We compare this design with the dye swap design through investigation of mouse primary hepatocytes treated with three peroxisome proliferator-activated receptor-alpha (PPARalpha) agonists at three dose levels. Using Agilent's Whole Mouse Genome microarray, differentially expressed genes (DEG) were determined for both the self-self hybridization and dye swap designs. The DEG concordance between the two designs was over 80% across each dose treatment and chemical. Furthermore, 90% of DEG-associated biological pathways were in common between the designs, indicating that biological interpretations would be consistent. The reduced labor and expense for the self-self hybridization design make it an efficient substitute for the dye swap design. For example, in larger toxicogenomic studies, only about half the chips are required for the self-self hybridization design compared to that needed in the dye swap design.
- A study design that investigates variance and error estimates in the experimental system, and is where the same extract is compared.
+ A study design that investigates variance and error estimates in the experimental system, and is where the same extract is compared.
Philippe Rocca-Serra on behalf of MO
MO_490
self vs self design
@@ -2625,7 +2625,7 @@
time series design
PMID: 14744830-Microarrays are powerful tools for surveying the expression levels of many thousands of genes simultaneously. They belong to the new genomics technologies which have important applications in the biological, agricultural and pharmaceutical sciences. There are myriad sources of uncertainty in microarray experiments, and rigorous experimental design is essential for fully realizing the potential of these valuable resources. Two questions frequently asked by biologists on the brink of conducting cDNA or two-colour, spotted microarray experiments are 'Which mRNA samples should be competitively hybridized together on the same slide?' and 'How many times should each slide be replicated?' Early experience has shown that whilst the field of classical experimental design has much to offer this emerging multi-disciplinary area, new approaches which accommodate features specific to the microarray context are needed. In this paper, we propose optimal designs for factorial and time course experiments, which are special designs arising quite frequently in microarray experimentation. Our criterion for optimality is statistical efficiency based on a new notion of admissible designs; our approach enables efficient designs to be selected subject to the information available on the effects of most interest to biologists, the number of arrays available for the experiment, and other resource or practical constraints, including limitations on the amount of mRNA probe. We show that our designs are superior to both the popular reference designs, which are highly inefficient, and to designs incorporating all possible direct pairwise comparisons. Moreover, our proposed designs represent a substantial practical improvement over classical experimental designs which work in terms of standard interactions and main effects. The latter do not provide a basis for meaningful inference on the effects of most interest to biologists, nor make the most efficient use of valuable and limited resources.
- Groups of assays that are related as part of a time series.
+ Groups of assays that are related as part of a time series.
Philippe Rocca-Serra on behalf of MO
MO_887
time series design
diff --git a/src/ontology/modules/value-specifications.owl b/src/ontology/modules/value-specifications.owl
index eb0ea9a3..57e71d3c 100644
--- a/src/ontology/modules/value-specifications.owl
+++ b/src/ontology/modules/value-specifications.owl
@@ -104,7 +104,7 @@
cannot be assessed, not applicable, unknown
- An information content entity that provides an explanation why a data item is not provided.
+ An information content entity that provides an explanation why a data item is not provided.
Chris Stoeckert, Helena Ellis
OBI
NCI BBRB
@@ -117,7 +117,7 @@
- A reason for lack of data item that is the negative output of a determination if assay will provide reliable results.
+ A reason for lack of data item that is the negative output of a determination if assay will provide reliable results.
Chris Stoeckert, Helena Ellis
cannot be assessed
OBI
@@ -131,7 +131,7 @@
- A planned process that is used to assess whether an assay will provide reliable results based on the conditions or qualities of the inputs, devices, and other participants of the assay.
+ A planned process that is used to assess whether an assay will provide reliable results based on the conditions or qualities of the inputs, devices, and other participants of the assay.
Chris Stoeckert, Helena Ellis
OBI
NCI BBRB
@@ -145,7 +145,7 @@
AJCC 7th edition GX: cannot be assessed.
- A cannot be assessed determination for histologic tumor grade.
+ A cannot be assessed determination for histologic tumor grade.
Chris Stoeckert, Helena Ellis
OBI
NCI BBRB
@@ -159,7 +159,7 @@
AJCC 7th edition pTX: cannot be assessed.
- A cannot be assessed determination for pathologic primary tumor staging.
+ A cannot be assessed determination for pathologic primary tumor staging.
Chris Stoeckert, Helena Ellis
OBI
NCI BBRB
@@ -173,7 +173,7 @@
AJCC 7th edition pNX: cannot be assessed.
- A cannot be assessed determination of pathologic staging of lymph nodes.
+ A cannot be assessed determination of pathologic staging of lymph nodes.
Chris Stoeckert, Helena Ellis
OBI
NCI BBRB
@@ -188,7 +188,7 @@
G1:Well differentiated
G4: Undifferentiated
- A categorical value specification that is a histologic grade assigned to a tumor slide specimen according to the American Joint Committee on Cancer (AJCC) 7th Edition grading system.
+ A categorical value specification that is a histologic grade assigned to a tumor slide specimen according to the American Joint Committee on Cancer (AJCC) 7th Edition grading system.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBI
NCI BBRB
@@ -201,7 +201,7 @@
- A categorical value specification that is a histologic grade assigned to a tumor slide specimen according to the Fuhrman Nuclear Grading System.
+ A categorical value specification that is a histologic grade assigned to a tumor slide specimen according to the Fuhrman Nuclear Grading System.
Chris Stoeckert, Helena Ellis
Histologic Grade (Fuhrman Nuclear Grading System)
NCI BBRB, OBI
@@ -215,7 +215,7 @@
- A categorical value specification that is a histologic grade assigned to a ovarian tumor.
+ A categorical value specification that is a histologic grade assigned to a ovarian tumor.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBI
NCI BBRB
@@ -228,7 +228,7 @@
- A histologic grade for ovarian tumor that is from a two-tier histological classification of tumors.
+ A histologic grade for ovarian tumor that is from a two-tier histological classification of tumors.
Chris Stoeckert, Helena Ellis
NCI BBRB, OBI
NCI BBRB
@@ -241,7 +241,7 @@
- A histologic grade for ovarian tumor that is from a histological classification by the World Health Organization (WHO).
+ A histologic grade for ovarian tumor that is from a histological classification by the World Health Organization (WHO).
Chris Stoeckert, Helena Ellis
NCI BBRB, OBI
NCI BBRB
@@ -254,7 +254,7 @@
- A categorical value specification that is a pathologic finding about one or more characteristics of colorectal cancer following the rules of the TNM American Joint Committee on Cancer (AJCC) version 7 classification system as they pertain to staging of the primary tumor. TNM pathologic primary tumor findings are based on clinical findings supplemented by histopathologic examination of one or more tissue specimens acquired during surgery.
+ A categorical value specification that is a pathologic finding about one or more characteristics of colorectal cancer following the rules of the TNM American Joint Committee on Cancer (AJCC) version 7 classification system as they pertain to staging of the primary tumor. TNM pathologic primary tumor findings are based on clinical findings supplemented by histopathologic examination of one or more tissue specimens acquired during surgery.
Chris Stoeckert, Helena Ellis
pT: Pathologic spread colorectal primary tumor (AJCC 7th Edition)
NCI BBRB, OBI
@@ -268,7 +268,7 @@
- A categorical value specification that is a pathologic finding about one or more characteristics of lung cancer following the rules of the TNM American Joint Committee on Cancer (AJCC) version 7 classification system as they pertain to staging of the primary tumor. TNM pathologic primary tumor findings are based on clinical findings supplemented by histopathologic examination of one or more tissue specimens acquired during surgery.
+ A categorical value specification that is a pathologic finding about one or more characteristics of lung cancer following the rules of the TNM American Joint Committee on Cancer (AJCC) version 7 classification system as they pertain to staging of the primary tumor. TNM pathologic primary tumor findings are based on clinical findings supplemented by histopathologic examination of one or more tissue specimens acquired during surgery.
Chris Stoeckert, Helena Ellis
pT: Pathologic spread lung primary tumor (AJCC 7th Edition)
NCI BBRB, OBI
@@ -282,7 +282,7 @@
- A categorical value specification that is a pathologic finding about one or more characteristics of renal cancer following the rules of the TNM AJCC v7 classification system as they pertain to staging of the primary tumor. TNM pathologic primary tumor findings are based on clinical findings supplemented by histopathologic examination of one or more tissue specimens acquired during surgery.
+ A categorical value specification that is a pathologic finding about one or more characteristics of renal cancer following the rules of the TNM AJCC v7 classification system as they pertain to staging of the primary tumor. TNM pathologic primary tumor findings are based on clinical findings supplemented by histopathologic examination of one or more tissue specimens acquired during surgery.
Chris Stoeckert, Helena Ellis
pT: Pathologic spread kidney primary tumor (AJCC 7th Edition)
NCI BBRB, OBI
@@ -296,7 +296,7 @@
- A categorical value specification that is a pathologic finding about one or more characteristics of ovarian cancer following the rules of the TNM AJCC v7 classification system as they pertain to staging of the primary tumor. TNM pathologic primary tumor findings are based on clinical findings supplemented by histopathologic examination of one or more tissue specimens acquired during surgery.
+ A categorical value specification that is a pathologic finding about one or more characteristics of ovarian cancer following the rules of the TNM AJCC v7 classification system as they pertain to staging of the primary tumor. TNM pathologic primary tumor findings are based on clinical findings supplemented by histopathologic examination of one or more tissue specimens acquired during surgery.
Chris Stoeckert, Helena Ellis
pT: Pathologic spread ovarian primary tumor (AJCC 7th Edition)
NCI BBRB, OBI
@@ -310,7 +310,7 @@
- A categorical value specification that is a pathologic finding about one or more characteristics of colorectal cancer following the rules of the TNM AJCC v7 classification system as they pertain to staging of regional lymph nodes.
+ A categorical value specification that is a pathologic finding about one or more characteristics of colorectal cancer following the rules of the TNM AJCC v7 classification system as they pertain to staging of regional lymph nodes.
Chris Stoeckert, Helena Ellis
pN: Pathologic spread colon lymph nodes (AJCC 7th Edition)
NCI BBRB, OBI
@@ -324,7 +324,7 @@
- A categorical value specification that is a pathologic finding about one or more characteristics of lung cancer following the rules of the TNM AJCC v7 classification system as they pertain to staging of regional lymph nodes.
+ A categorical value specification that is a pathologic finding about one or more characteristics of lung cancer following the rules of the TNM AJCC v7 classification system as they pertain to staging of regional lymph nodes.
Chris Stoeckert, Helena Ellis
pN: Pathologic spread colon lymph nodes (AJCC 7th Edition)
NCI BBRB, OBI
@@ -338,7 +338,7 @@
- A categorical value specification that is a pathologic finding about one or more characteristics of renal cancer following the rules of the TNM AJCC v7 classification system as they pertain to staging of regional lymph nodes.
+ A categorical value specification that is a pathologic finding about one or more characteristics of renal cancer following the rules of the TNM AJCC v7 classification system as they pertain to staging of regional lymph nodes.
Chris Stoeckert, Helena Ellis
pN: Pathologic spread kidney lymph nodes (AJCC 7th Edition)
NCI BBRB, OBI
@@ -352,7 +352,7 @@
- A categorical value specification that is a pathologic finding about one or more characteristics of ovarian cancer following the rules of the TNM AJCC v7 classification system as they pertain to staging of regional lymph nodes.
+ A categorical value specification that is a pathologic finding about one or more characteristics of ovarian cancer following the rules of the TNM AJCC v7 classification system as they pertain to staging of regional lymph nodes.
Chris Stoeckert, Helena Ellis
pN: Pathologic spread ovarian lymph nodes (AJCC 7th Edition)
NCI BBRB, OBI
@@ -366,7 +366,7 @@
- A categorical value specification that is a pathologic finding about one or more characteristics of colon cancer following the rules of the TNM AJCC v7 classification system as they pertain to distant metastases. TNM pathologic distant metastasis findings are based on clinical findings supplemented by histopathologic examination of one or more tissue specimens acquired during surgery.
+ A categorical value specification that is a pathologic finding about one or more characteristics of colon cancer following the rules of the TNM AJCC v7 classification system as they pertain to distant metastases. TNM pathologic distant metastasis findings are based on clinical findings supplemented by histopathologic examination of one or more tissue specimens acquired during surgery.
Chris Stoeckert, Helena Ellis
M: colon distant metastases (AJCC 7th Edition)
NCI BBRB, OBI
@@ -380,7 +380,7 @@
- A categorical value specification that is a pathologic finding about one or more characteristics of lung cancer following the rules of the TNM AJCC v7 classification system as they pertain to distant metastases. TNM pathologic distant metastasis findings are based on clinical findings supplemented by histopathologic examination of one or more tissue specimens acquired during surgery.
+ A categorical value specification that is a pathologic finding about one or more characteristics of lung cancer following the rules of the TNM AJCC v7 classification system as they pertain to distant metastases. TNM pathologic distant metastasis findings are based on clinical findings supplemented by histopathologic examination of one or more tissue specimens acquired during surgery.
Chris Stoeckert, Helena Ellis
M: lung distant metastases (AJCC 7th Edition)
NCI BBRB, OBI
@@ -394,7 +394,7 @@
- A categorical value specification that is a pathologic finding about one or more characteristics of renal cancer following the rules of the TNM AJCC v7 classification system as they pertain to distant metastases. TNM pathologic distant metastasis findings are based on clinical findings supplemented by histopathologic examination of one or more tissue specimens acquired during surgery.
+ A categorical value specification that is a pathologic finding about one or more characteristics of renal cancer following the rules of the TNM AJCC v7 classification system as they pertain to distant metastases. TNM pathologic distant metastasis findings are based on clinical findings supplemented by histopathologic examination of one or more tissue specimens acquired during surgery.
Chris Stoeckert, Helena Ellis
M: kidney distant Metastases (AJCC 7th Edition)
NCI BBRB, OBI
@@ -408,7 +408,7 @@
- A categorical value specification that is a pathologic finding about one or more characteristics of ovarian cancer following the rules of the TNM AJCC v7 classification system as they pertain to distant metastases. TNM pathologic distant metastasis findings are based on clinical findings supplemented by histopathologic examination of one or more tissue specimens acquired during surgery.
+ A categorical value specification that is a pathologic finding about one or more characteristics of ovarian cancer following the rules of the TNM AJCC v7 classification system as they pertain to distant metastases. TNM pathologic distant metastasis findings are based on clinical findings supplemented by histopathologic examination of one or more tissue specimens acquired during surgery.
Chris Stoeckert, Helena Ellis
M: ovarian distant metastases (AJCC 7th Edition)
NCI BBRB, OBI
@@ -422,7 +422,7 @@
- A categorical value specification that is an assessment of the stage of a cancer according to the American Joint Committee on Cancer (AJCC) v7 staging systems.
+ A categorical value specification that is an assessment of the stage of a cancer according to the American Joint Committee on Cancer (AJCC) v7 staging systems.
Chris Stoeckert, Helena Ellis
Clinical tumor stage group (AJCC 7th Edition)
NCI BBRB, OBI
@@ -436,7 +436,7 @@
- A categorical value specification that is an assessment of the stage of a gynecologic cancer according to the International Federation of Gynecology and Obstetrics (FIGO) staging systems.
+ A categorical value specification that is an assessment of the stage of a gynecologic cancer according to the International Federation of Gynecology and Obstetrics (FIGO) staging systems.
Chris Stoeckert, Helena Ellis
Clinical FIGO stage
NCI BBRB, OBI
@@ -450,7 +450,7 @@
- A categorical value specification that is a pathologic finding about one or more characteristics of ovarian cancer following the rules of the FIGO classification system.
+ A categorical value specification that is a pathologic finding about one or more characteristics of ovarian cancer following the rules of the FIGO classification system.
Chris Stoeckert, Helena Ellis
Pathologic Tumor Stage Grouping for ovarian cancer (FIGO)
NCI BBRB, OBI
@@ -464,7 +464,7 @@
- A categorical value specification that is an assessment of a participant's performance status (general well-being and activities of daily life).
+ A categorical value specification that is an assessment of a participant's performance status (general well-being and activities of daily life).
Chris Stoeckert, Helena Ellis
Performance Status Scale
https://en.wikipedia.org/wiki/Performance_status
@@ -478,7 +478,7 @@
- A performance status value specification designed by the Eastern Cooperative Oncology Group to assess disease progression and its affect on the daily living abilities of the patient.
+ A performance status value specification designed by the Eastern Cooperative Oncology Group to assess disease progression and its affect on the daily living abilities of the patient.
Chris Stoeckert, Helena Ellis
ECOG score
NCI BBRB, OBI
@@ -492,7 +492,7 @@
- A performance status value specification designed for classifying patients 16 years of age or older by their functional impairment.
+ A performance status value specification designed for classifying patients 16 years of age or older by their functional impairment.
Chris Stoeckert, Helena Ellis
Karnofsky Score
NCI BBRB, OBI
@@ -506,7 +506,7 @@
- A scalar value specification that specifies the point in time that a human participant under investigation self-administers a medication material
+ A scalar value specification that specifies the point in time that a human participant under investigation self-administers a medication material
John Judkins
medication timepoint
OBI
@@ -520,7 +520,7 @@
- A scalar value specification that specifies the value of the quantity of a material entity administered to an organism as a treatment
+ A scalar value specification that specifies the value of the quantity of a material entity administered to an organism as a treatment
John Judkins
medication dose
OBI
@@ -535,7 +535,7 @@
hypertension grade
- A categorical value specification that indicates the severity of hypertension.
+ A categorical value specification that indicates the severity of hypertension.
Bjoern Peters
Randi Vita
Sebastian Duesing
@@ -559,7 +559,7 @@
- A histologic grade according to AJCC 7th edition indicating that the tumor cells and the organization of the tumor tissue appear close to normal.
+ A histologic grade according to AJCC 7th edition indicating that the tumor cells and the organization of the tumor tissue appear close to normal.
Chris Stoeckert, Helena Ellis
G1
https://www.cancer.gov/about-cancer/diagnosis-staging/prognosis/tumor-grade-fact-sheet
@@ -573,7 +573,7 @@
- A histologic grade according to AJCC 7th edition indicating that the tumor cells are moderately differentiated and reflect an intermediate grade.
+ A histologic grade according to AJCC 7th edition indicating that the tumor cells are moderately differentiated and reflect an intermediate grade.
Chris Stoeckert, Helena Ellis
G2
https://www.cancer.gov/about-cancer/diagnosis-staging/prognosis/tumor-grade-fact-sheet
@@ -587,7 +587,7 @@
- A histologic grade according to AJCC 7th edition indicating that the tumor cells are poorly differentiated and do not look like normal cells and tissue.
+ A histologic grade according to AJCC 7th edition indicating that the tumor cells are poorly differentiated and do not look like normal cells and tissue.
Chris Stoeckert, Helena Ellis
G3
https://www.cancer.gov/about-cancer/diagnosis-staging/prognosis/tumor-grade-fact-sheet
@@ -601,7 +601,7 @@
- A histologic grade according to AJCC 7th edition indicating that the tumor cells are undifferentiated and do not look like normal cells and tissue.
+ A histologic grade according to AJCC 7th edition indicating that the tumor cells are undifferentiated and do not look like normal cells and tissue.
Chris Stoeckert, Helena Ellis
G4
https://www.cancer.gov/about-cancer/diagnosis-staging/prognosis/tumor-grade-fact-sheet
@@ -615,7 +615,7 @@
- A histologic grade according to the Fuhrman Nuclear Grading System indicating that nuclei are round, uniform, approximately 10um and that nucleoli are inconspicuous or absent.
+ A histologic grade according to the Fuhrman Nuclear Grading System indicating that nuclei are round, uniform, approximately 10um and that nucleoli are inconspicuous or absent.
Chris Stoeckert, Helena Ellis
Grade 1
NCI BBRB, OBI
@@ -629,7 +629,7 @@
- A histologic grade according to the Fuhrman Nuclear Grading System indicating that nuclei are slightly irregular, approximately 15um and nucleoli are evident.
+ A histologic grade according to the Fuhrman Nuclear Grading System indicating that nuclei are slightly irregular, approximately 15um and nucleoli are evident.
Chris Stoeckert, Helena Ellis
Grade 2
NCI BBRB, OBI
@@ -643,7 +643,7 @@
- A histologic grade according to the Fuhrman Nuclear Grading System indicating that nuclei are very irregular, approximately 20um and nucleoli large and prominent.
+ A histologic grade according to the Fuhrman Nuclear Grading System indicating that nuclei are very irregular, approximately 20um and nucleoli large and prominent.
Chris Stoeckert, Helena Ellis
Grade 3
NCI BBRB, OBI
@@ -657,7 +657,7 @@
- A histologic grade according to the Fuhrman Nuclear Grading System indicating that nuclei arei bizarre and multilobulated, 20um or greater and nucleoli are prominent and chromatin clumped.
+ A histologic grade according to the Fuhrman Nuclear Grading System indicating that nuclei arei bizarre and multilobulated, 20um or greater and nucleoli are prominent and chromatin clumped.
Chris Stoeckert, Helena Ellis
Grade 4
NCI BBRB, OBI
@@ -671,7 +671,7 @@
- A histologic grade for ovarian tumor according to a two-tier grading system indicating that the tumor is low grade.
+ A histologic grade for ovarian tumor according to a two-tier grading system indicating that the tumor is low grade.
Chris Stoeckert, Helena Ellis
Low grade
NCI BBRB, OBI
@@ -685,7 +685,7 @@
- A histologic grade for ovarian tumor according to a two-tier grading system indicating that the tumor is high grade.
+ A histologic grade for ovarian tumor according to a two-tier grading system indicating that the tumor is high grade.
Chris Stoeckert, Helena Ellis
High grade
NCI BBRB, OBI
@@ -699,7 +699,7 @@
- A histologic grade for ovarian tumor according to the World Health Organization indicating that the tumor is well differentiated.
+ A histologic grade for ovarian tumor according to the World Health Organization indicating that the tumor is well differentiated.
Chris Stoeckert, Helena Ellis
G1
NCI BBRB, OBI
@@ -713,7 +713,7 @@
- A histologic grade for ovarian tumor according to the World Health Organization indicating that the tumor is moderately differentiated.
+ A histologic grade for ovarian tumor according to the World Health Organization indicating that the tumor is moderately differentiated.
Chris Stoeckert, Helena Ellis
G2
NCI BBRB, OBI
@@ -727,7 +727,7 @@
- A histologic grade for ovarian tumor according to the World Health Organization indicating that the tumor is poorly differentiated.
+ A histologic grade for ovarian tumor according to the World Health Organization indicating that the tumor is poorly differentiated.
Chris Stoeckert, Helena Ellis
G3
NCI BBRB, OBI
@@ -741,7 +741,7 @@
- A histologic grade for ovarian tumor according to the World Health Organization indicating that the tumor is undifferentiated.
+ A histologic grade for ovarian tumor according to the World Health Organization indicating that the tumor is undifferentiated.
Chris Stoeckert, Helena Ellis
G4
NCI BBRB, OBI
@@ -755,7 +755,7 @@
- A pathologic primary tumor stage for colon and rectum according to AJCC 7th edition indicating that there is no evidence of primary tumor.
+ A pathologic primary tumor stage for colon and rectum according to AJCC 7th edition indicating that there is no evidence of primary tumor.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/colon/path_t/
NCI BBRB
@@ -768,7 +768,7 @@
- A pathologic primary tumor stage for colon and rectum according to AJCC 7th edition indicating carcinoma in situ (intraepithelial or invasion of lamina propria).
+ A pathologic primary tumor stage for colon and rectum according to AJCC 7th edition indicating carcinoma in situ (intraepithelial or invasion of lamina propria).
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/colon/path_t/
NCI BBRB
@@ -781,7 +781,7 @@
- A pathologic primary tumor stage for colon and rectum according to AJCC 7th edition indicating that the tumor invades submucosa.
+ A pathologic primary tumor stage for colon and rectum according to AJCC 7th edition indicating that the tumor invades submucosa.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/colon/path_t/
NCI BBRB
@@ -794,7 +794,7 @@
- A pathologic primary tumor stage for colon and rectum according to AJCC 7th edition indicating that the tumor invades muscularis propria.
+ A pathologic primary tumor stage for colon and rectum according to AJCC 7th edition indicating that the tumor invades muscularis propria.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/colon/path_t/
NCI BBRB
@@ -807,7 +807,7 @@
- A pathologic primary tumor stage for colon and rectum according to AJCC 7th edition indicating that the tumor invades subserosa or into non-peritionealized pericolic or perirectal tissues.
+ A pathologic primary tumor stage for colon and rectum according to AJCC 7th edition indicating that the tumor invades subserosa or into non-peritionealized pericolic or perirectal tissues.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/colon/path_t/
NCI BBRB
@@ -820,7 +820,7 @@
- A pathologic primary tumor stage for colon and rectum according to AJCC 7th edition indicating that the tumor perforates visceral peritoneum.
+ A pathologic primary tumor stage for colon and rectum according to AJCC 7th edition indicating that the tumor perforates visceral peritoneum.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/colon/path_t/
NCI BBRB
@@ -833,7 +833,7 @@
- A pathologic primary tumor stage for colon and rectum according to AJCC 7th edition indicating that the tumor directly invades other organs or structures.
+ A pathologic primary tumor stage for colon and rectum according to AJCC 7th edition indicating that the tumor directly invades other organs or structures.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/colon/path_t/
NCI BBRB
@@ -846,7 +846,7 @@
- A pathologic primary tumor stage for lung according to AJCC 7th edition indicating that there is no evidence of primary tumor.
+ A pathologic primary tumor stage for lung according to AJCC 7th edition indicating that there is no evidence of primary tumor.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/lung/path_t/
NCI BBRB
@@ -859,7 +859,7 @@
- A pathologic primary tumor stage for lung according to AJCC 7th edition indicating carcinoma in situ.
+ A pathologic primary tumor stage for lung according to AJCC 7th edition indicating carcinoma in situ.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/lung/path_t/
NCI BBRB
@@ -872,7 +872,7 @@
- A pathologic primary tumor stage for lung according to AJCC 7th edition indicating that the tumor is 3 cm or less in greatest dimension, surrounded by lung or visceral pleura without bronchoscopic evidence of invasion more proximal than the lobar bronchus (i.e., not in the main bronchus).
+ A pathologic primary tumor stage for lung according to AJCC 7th edition indicating that the tumor is 3 cm or less in greatest dimension, surrounded by lung or visceral pleura without bronchoscopic evidence of invasion more proximal than the lobar bronchus (i.e., not in the main bronchus).
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/lung/path_t/
NCI BBRB
@@ -885,7 +885,7 @@
- A pathologic primary tumor stage for lung according to AJCC 7th edition indicating that the tumor is 2 cm or less in greatest dimension.
+ A pathologic primary tumor stage for lung according to AJCC 7th edition indicating that the tumor is 2 cm or less in greatest dimension.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/lung/path_t/
NCI BBRB
@@ -898,7 +898,7 @@
- A pathologic primary tumor stage for lung according to AJCC 7th edition indicating that the tumor is more than 2 cm but not more than 3 cm in greatest dimension.
+ A pathologic primary tumor stage for lung according to AJCC 7th edition indicating that the tumor is more than 2 cm but not more than 3 cm in greatest dimension.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/lung/path_t/
NCI BBRB
@@ -911,7 +911,7 @@
- A pathologic primary tumor stage for lung according to AJCC 7th edition indicating that the tumor is more than 3 cm but not more than 7 cm or the tumor has any of the following features: involves main bronchus, 2 cm or more distal to the carina, invades visceral pleura, associated with atelectasis or obstructive pneumonitis that extends to the hilar region but does not involve the entire lung.
+ A pathologic primary tumor stage for lung according to AJCC 7th edition indicating that the tumor is more than 3 cm but not more than 7 cm or the tumor has any of the following features: involves main bronchus, 2 cm or more distal to the carina, invades visceral pleura, associated with atelectasis or obstructive pneumonitis that extends to the hilar region but does not involve the entire lung.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/lung/path_t/
NCI BBRB
@@ -924,7 +924,7 @@
- A pathologic primary tumor stage for lung according to AJCC 7th edition indicating that the tumor is more than 3 cm but not more than 5 cm in greatest dimension.
+ A pathologic primary tumor stage for lung according to AJCC 7th edition indicating that the tumor is more than 3 cm but not more than 5 cm in greatest dimension.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/lung/path_t/
NCI BBRB
@@ -937,7 +937,7 @@
- A pathologic primary tumor stage for lung according to AJCC 7th edition indicating that the tumor is more than 5 cm but not more than 7 cm in greatest dimension.
+ A pathologic primary tumor stage for lung according to AJCC 7th edition indicating that the tumor is more than 5 cm but not more than 7 cm in greatest dimension.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/lung/path_t/
NCI BBRB
@@ -950,7 +950,7 @@
- A pathologic primary tumor stage for lung according to AJCC 7th edition indicating that the tumor is more than 7 cm or one that directly invades any of: parietal pleura, chest wall (including superior sulcus tumors), diaphragm, phrenic nerve, mediastinal pleura, parietal pericardiu or the tumor is in the main bronchus less than 2 cm distal to the carina but without involvement of the carina or there is associated atelectasis or obstructive pneumonitis of the entire lung or there is separate tumor nodule(s) in the same lobe as the primary.
+ A pathologic primary tumor stage for lung according to AJCC 7th edition indicating that the tumor is more than 7 cm or one that directly invades any of: parietal pleura, chest wall (including superior sulcus tumors), diaphragm, phrenic nerve, mediastinal pleura, parietal pericardiu or the tumor is in the main bronchus less than 2 cm distal to the carina but without involvement of the carina or there is associated atelectasis or obstructive pneumonitis of the entire lung or there is separate tumor nodule(s) in the same lobe as the primary.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/lung/path_t/
NCI BBRB
@@ -963,7 +963,7 @@
- A pathologic primary tumor stage for lung according to AJCC 7th edition indicating that the tumor of any size that invades any of the following: mediastinum, heart, great vessels, trachea, recurrent laryngeal nerve, esophagus, vertebral body, carina or there is separate tumor nodule(s) in a different ipsilateral lobe to that of the primary.
+ A pathologic primary tumor stage for lung according to AJCC 7th edition indicating that the tumor of any size that invades any of the following: mediastinum, heart, great vessels, trachea, recurrent laryngeal nerve, esophagus, vertebral body, carina or there is separate tumor nodule(s) in a different ipsilateral lobe to that of the primary.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/lung/path_t/
NCI BBRB
@@ -976,7 +976,7 @@
- A pathologic primary tumor stage for kidney according to AJCC 7th edition indicating that there is no evidence of primary tumor.
+ A pathologic primary tumor stage for kidney according to AJCC 7th edition indicating that there is no evidence of primary tumor.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/kidney_parenchyma/path_t/
NCI BBRB
@@ -989,7 +989,7 @@
- A pathologic primary tumor stage for kidney according to AJCC 7th edition indicating that the tumor is 7 cm or less in greatest dimension and limited to the kidney.
+ A pathologic primary tumor stage for kidney according to AJCC 7th edition indicating that the tumor is 7 cm or less in greatest dimension and limited to the kidney.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/kidney_parenchyma/path_t/
NCI BBRB
@@ -1002,7 +1002,7 @@
- A pathologic primary tumor stage for kidney according to AJCC 7th edition indicating that the tumor is 4 cm or less.
+ A pathologic primary tumor stage for kidney according to AJCC 7th edition indicating that the tumor is 4 cm or less.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/kidney_parenchyma/path_t/
NCI BBRB
@@ -1015,7 +1015,7 @@
- A pathologic primary tumor stage for kidney according to AJCC 7th edition indicating that the tumor is more than 4 cm but not more than 7 cm.
+ A pathologic primary tumor stage for kidney according to AJCC 7th edition indicating that the tumor is more than 4 cm but not more than 7 cm.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/kidney_parenchyma/path_t/
NCI BBRB
@@ -1028,7 +1028,7 @@
- A pathologic primary tumor stage for kidney according to AJCC 7th edition indicating that the tumor is more than 7 cm in greatest dimension and limited to the kidney.
+ A pathologic primary tumor stage for kidney according to AJCC 7th edition indicating that the tumor is more than 7 cm in greatest dimension and limited to the kidney.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/kidney_parenchyma/path_t/
NCI BBRB
@@ -1041,7 +1041,7 @@
- A pathologic primary tumor stage for kidney according to AJCC 7th edition indicating that the tumor is more than 7 cm but not more than 10 cm.
+ A pathologic primary tumor stage for kidney according to AJCC 7th edition indicating that the tumor is more than 7 cm but not more than 10 cm.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/kidney_parenchyma/path_t/
NCI BBRB
@@ -1054,7 +1054,7 @@
- A pathologic primary tumor stage for kidney according to AJCC 7th edition indicating that the tumor is more than 10 cm and limited to the kidney.
+ A pathologic primary tumor stage for kidney according to AJCC 7th edition indicating that the tumor is more than 10 cm and limited to the kidney.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/kidney_parenchyma/path_t/
NCI BBRB
@@ -1067,7 +1067,7 @@
- A pathologic primary tumor stage for kidney according to AJCC 7th edition indicating that the tumor extends into major veins or perinephric tissues but not into the ipsilateral adrenal gland and not beyond the Gerota fascia.
+ A pathologic primary tumor stage for kidney according to AJCC 7th edition indicating that the tumor extends into major veins or perinephric tissues but not into the ipsilateral adrenal gland and not beyond the Gerota fascia.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/kidney_parenchyma/path_t/
NCI BBRB
@@ -1080,7 +1080,7 @@
- A pathologic primary tumor stage for kidney according to AJCC 7th edition indicating that the tumor grossly extends into the renal vein or its segmental (muscle containing) branches, or the tumor invades perirenal and/or renal sinus fat (peripelvic) fat but not beyond Gerota fascia.
+ A pathologic primary tumor stage for kidney according to AJCC 7th edition indicating that the tumor grossly extends into the renal vein or its segmental (muscle containing) branches, or the tumor invades perirenal and/or renal sinus fat (peripelvic) fat but not beyond Gerota fascia.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/kidney_parenchyma/path_t/
NCI BBRB
@@ -1093,7 +1093,7 @@
- A pathologic primary tumor stage for kidney according to AJCC 7th edition indicating that the tumor grossly extends into vena cava below diaphragm.
+ A pathologic primary tumor stage for kidney according to AJCC 7th edition indicating that the tumor grossly extends into vena cava below diaphragm.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/kidney_parenchyma/path_t/
NCI BBRB
@@ -1106,7 +1106,7 @@
- A pathologic primary tumor stage for kidney according to AJCC 7th edition indicating that the tumor grossly extends into vena cava above the diaphragm or Invades the wall of the vena cava.
+ A pathologic primary tumor stage for kidney according to AJCC 7th edition indicating that the tumor grossly extends into vena cava above the diaphragm or Invades the wall of the vena cava.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/kidney_parenchyma/path_t/
NCI BBRB
@@ -1119,7 +1119,7 @@
- A pathologic primary tumor stage for kidney according to AJCC 7th edition indicating that the tumor invades beyond Gerota fascia (including contiguous extension into the ipsilateral adrenal gland).
+ A pathologic primary tumor stage for kidney according to AJCC 7th edition indicating that the tumor invades beyond Gerota fascia (including contiguous extension into the ipsilateral adrenal gland).
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/kidney_parenchyma/path_t/
NCI BBRB
@@ -1132,7 +1132,7 @@
- A pathologic primary tumor stage for ovary according to AJCC 7th edition indicating that there is no evidence of primary tumor.
+ A pathologic primary tumor stage for ovary according to AJCC 7th edition indicating that there is no evidence of primary tumor.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/ovary/path_t/
NCI BBRB
@@ -1145,7 +1145,7 @@
- A pathologic primary tumor stage for ovary according to AJCC 7th edition indicating that the tumor is limited to the ovaries (one or both).
+ A pathologic primary tumor stage for ovary according to AJCC 7th edition indicating that the tumor is limited to the ovaries (one or both).
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/ovary/path_t/
NCI BBRB
@@ -1158,7 +1158,7 @@
- A pathologic primary tumor stage for ovary according to AJCC 7th edition indicating that the tumor is limited to one ovary; capsule intact, no tumor on ovarian surface and no malignant cells in ascites or peritoneal washings.
+ A pathologic primary tumor stage for ovary according to AJCC 7th edition indicating that the tumor is limited to one ovary; capsule intact, no tumor on ovarian surface and no malignant cells in ascites or peritoneal washings.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/ovary/path_t/
NCI BBRB
@@ -1171,7 +1171,7 @@
- A pathologic primary tumor stage for ovary according to AJCC 7th edition indicating that the tumor is limited to both ovaries; capsule intact, no tumor on ovarian surface and no malignant cells in ascites or peritoneal washings.
+ A pathologic primary tumor stage for ovary according to AJCC 7th edition indicating that the tumor is limited to both ovaries; capsule intact, no tumor on ovarian surface and no malignant cells in ascites or peritoneal washings.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/ovary/path_t/
NCI BBRB
@@ -1184,7 +1184,7 @@
- A pathologic primary tumor stage for ovary according to AJCC 7th edition indicating that the tumor is limited to one or both ovaries with capsule ruptured, tumor on ovarian surface, or malignant cells in ascites or peritoneal washings.
+ A pathologic primary tumor stage for ovary according to AJCC 7th edition indicating that the tumor is limited to one or both ovaries with capsule ruptured, tumor on ovarian surface, or malignant cells in ascites or peritoneal washings.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/ovary/path_t/
NCI BBRB
@@ -1197,7 +1197,7 @@
- A pathologic primary tumor stage for ovary according to AJCC 7th edition indicating that the tumor involves one or both ovaries with pelvic extension.
+ A pathologic primary tumor stage for ovary according to AJCC 7th edition indicating that the tumor involves one or both ovaries with pelvic extension.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/ovary/path_t/
NCI BBRB
@@ -1210,7 +1210,7 @@
- A pathologic primary tumor stage for ovary according to AJCC 7th edition indicating that the tumor has extension and/or implants on uterus and/or tube(s) and no malignant cells in ascites or peritoneal washings.
+ A pathologic primary tumor stage for ovary according to AJCC 7th edition indicating that the tumor has extension and/or implants on uterus and/or tube(s) and no malignant cells in ascites or peritoneal washings.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/ovary/path_t/
NCI BBRB
@@ -1223,7 +1223,7 @@
- A pathologic primary tumor stage for ovary according to AJCC 7th edition indicating that the tumor has extension to other pelvic tissues and no malignant cells in ascites or peritoneal washings.
+ A pathologic primary tumor stage for ovary according to AJCC 7th edition indicating that the tumor has extension to other pelvic tissues and no malignant cells in ascites or peritoneal washings.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/ovary/path_t/
NCI BBRB
@@ -1236,7 +1236,7 @@
- A pathologic primary tumor stage for ovary according to AJCC 7th edition indicating that the tumor has pelvic extension with malignant cells in ascites or peritoneal washings.
+ A pathologic primary tumor stage for ovary according to AJCC 7th edition indicating that the tumor has pelvic extension with malignant cells in ascites or peritoneal washings.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/ovary/path_t/
NCI BBRB
@@ -1249,7 +1249,7 @@
- A pathologic primary tumor stage for ovary according to AJCC 7th edition indicating that the tumor involves one or both ovaries with microscopically confirmed peritoneal metastasis outside the pelvis and/or regional lymph node metastasis.
+ A pathologic primary tumor stage for ovary according to AJCC 7th edition indicating that the tumor involves one or both ovaries with microscopically confirmed peritoneal metastasis outside the pelvis and/or regional lymph node metastasis.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/ovary/path_t/
NCI BBRB
@@ -1262,7 +1262,7 @@
- A pathologic primary tumor stage for ovary according to AJCC 7th edition indicating that the tumor has microscopic peritoneal metastasis beyond pelvis.
+ A pathologic primary tumor stage for ovary according to AJCC 7th edition indicating that the tumor has microscopic peritoneal metastasis beyond pelvis.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/ovary/path_t/
NCI BBRB
@@ -1275,7 +1275,7 @@
- A pathologic primary tumor stage for ovary according to AJCC 7th edition indicating that the tumor has macroscopic peritoneal, metastatasis beyond pelvis, 2 cm or less in greatest dimension.
+ A pathologic primary tumor stage for ovary according to AJCC 7th edition indicating that the tumor has macroscopic peritoneal, metastatasis beyond pelvis, 2 cm or less in greatest dimension.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/ovary/path_t/
NCI BBRB
@@ -1288,7 +1288,7 @@
- A pathologic primary tumor stage for ovary according to AJCC 7th edition indicating that the tumor has peritoneal metastasis beyond pelvis, more than 2 cm in greatest dimension and/or regional lymph node metastasis.
+ A pathologic primary tumor stage for ovary according to AJCC 7th edition indicating that the tumor has peritoneal metastasis beyond pelvis, more than 2 cm in greatest dimension and/or regional lymph node metastasis.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/ovary/path_t/
NCI BBRB
@@ -1301,7 +1301,7 @@
- A pathologic lymph node stage for colon and rectum according to AJCC 7th edition indicating no regional lymph node metastsis.
+ A pathologic lymph node stage for colon and rectum according to AJCC 7th edition indicating no regional lymph node metastsis.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/colon/path_n/
NCI BBRB
@@ -1314,7 +1314,7 @@
- A pathologic lymph node stage for colon and rectum according to AJCC 7th edition indicating metastasis in 1-3 regional lymph nodes.
+ A pathologic lymph node stage for colon and rectum according to AJCC 7th edition indicating metastasis in 1-3 regional lymph nodes.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/colon/path_n/
NCI BBRB
@@ -1327,7 +1327,7 @@
- A pathologic lymph node stage for colon and rectum according to AJCC 7th edition indicating metastasis in 1 regional lymph node.
+ A pathologic lymph node stage for colon and rectum according to AJCC 7th edition indicating metastasis in 1 regional lymph node.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/colon/path_n/
NCI BBRB
@@ -1340,7 +1340,7 @@
- A pathologic lymph node stage for colon and rectum according to AJCC 7th edition indicating metastasis in 2-3 regional lymph nodes.
+ A pathologic lymph node stage for colon and rectum according to AJCC 7th edition indicating metastasis in 2-3 regional lymph nodes.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/colon/path_n/
NCI BBRB
@@ -1353,7 +1353,7 @@
- A pathologic lymph node stage for colon and rectum according to AJCC 7th edition indicating tumor deposit(s), i.e., satellites in the subserosa, or in non-peritonealized pericolic or perirectal soft tissue without regional lymph node metastasis.
+ A pathologic lymph node stage for colon and rectum according to AJCC 7th edition indicating tumor deposit(s), i.e., satellites in the subserosa, or in non-peritonealized pericolic or perirectal soft tissue without regional lymph node metastasis.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/colon/path_n/
NCI BBRB
@@ -1366,7 +1366,7 @@
- A pathologic lymph node stage for colon and rectum according to AJCC 7th edition indicating metastasis in 4 or more regional lymph nodes.
+ A pathologic lymph node stage for colon and rectum according to AJCC 7th edition indicating metastasis in 4 or more regional lymph nodes.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/colon/path_n/
NCI BBRB
@@ -1379,7 +1379,7 @@
- A pathologic lymph node stage for colon and rectum according to AJCC 7th edition indicating metastasis in 4 to 6 regional lymph nodes.
+ A pathologic lymph node stage for colon and rectum according to AJCC 7th edition indicating metastasis in 4 to 6 regional lymph nodes.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/colon/path_n/
NCI BBRB
@@ -1392,7 +1392,7 @@
- A pathologic lymph node stage for colon and rectum according to AJCC 7th edition indicating metastasis in 7 or more regional lymph nodes.
+ A pathologic lymph node stage for colon and rectum according to AJCC 7th edition indicating metastasis in 7 or more regional lymph nodes.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/colon/path_n/
NCI BBRB
@@ -1405,7 +1405,7 @@
- A pathologic lymph node stage for lung according to AJCC 7th edition indicating no regional lymph node metastasis.
+ A pathologic lymph node stage for lung according to AJCC 7th edition indicating no regional lymph node metastasis.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/lung/path_n/
NCI BBRB
@@ -1418,7 +1418,7 @@
- A pathologic lymph node stage for lung according to AJCC 7th edition indicating metastasis in ipsilateral peribronchial and/or ipsilateral hilar lymph nodes and intrapulmonary nodes, including involvement by direct extension.
+ A pathologic lymph node stage for lung according to AJCC 7th edition indicating metastasis in ipsilateral peribronchial and/or ipsilateral hilar lymph nodes and intrapulmonary nodes, including involvement by direct extension.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/lung/path_n/
NCI BBRB
@@ -1431,7 +1431,7 @@
- A pathologic lymph node stage for lung according to AJCC 7th edition indicating metastasis in ipsilateral mediastinal and/or subcarinal lymph node(s).
+ A pathologic lymph node stage for lung according to AJCC 7th edition indicating metastasis in ipsilateral mediastinal and/or subcarinal lymph node(s).
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/lung/path_n/
NCI BBRB
@@ -1444,7 +1444,7 @@
- A pathologic lymph node stage for lung according to AJCC 7th edition indicating metastasis in contralateral mediastinal, contralateral hilar, ipsilateral or contralateral scalene, or supraclavicular lymph node(s).
+ A pathologic lymph node stage for lung according to AJCC 7th edition indicating metastasis in contralateral mediastinal, contralateral hilar, ipsilateral or contralateral scalene, or supraclavicular lymph node(s).
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/lung/path_n/
NCI BBRB
@@ -1457,7 +1457,7 @@
- A pathologic lymph node stage for kidney according to AJCC 7th edition indicating that there is no regional lymph node metastasis.
+ A pathologic lymph node stage for kidney according to AJCC 7th edition indicating that there is no regional lymph node metastasis.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/kidney_parenchyma/path_n/
NCI BBRB
@@ -1470,7 +1470,7 @@
- A pathologic lymph node stage for kidney according to AJCC 7th edition indicating that there is regional lymph node metastasis.
+ A pathologic lymph node stage for kidney according to AJCC 7th edition indicating that there is regional lymph node metastasis.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/kidney_parenchyma/path_n/
NCI BBRB
@@ -1483,7 +1483,7 @@
- A pathologic lymph node stage for ovary according to AJCC 7th edition indicating that there is no regional lymph node metastasis.
+ A pathologic lymph node stage for ovary according to AJCC 7th edition indicating that there is no regional lymph node metastasis.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/ovary/path_n/
NCI BBRB
@@ -1496,7 +1496,7 @@
- A pathologic lymph node stage for ovary according to AJCC 7th edition indicating that there is regional lymph node metastasis.
+ A pathologic lymph node stage for ovary according to AJCC 7th edition indicating that there is regional lymph node metastasis.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/ovary/path_n/
NCI BBRB
@@ -1509,7 +1509,7 @@
- A pathologic distant metastases stage for colon according to AJCC 7th edition indicating that there are no symptoms or signs of distant metastasis.
+ A pathologic distant metastases stage for colon according to AJCC 7th edition indicating that there are no symptoms or signs of distant metastasis.
Chris Stoeckert, Helena Ellis
https://en.wikipedia.org/wiki/Cancer_staging#Pathological_M_Categorization_.28cM_and_pM.29
NCI BBRB
@@ -1522,7 +1522,7 @@
- A pathologic distant metastases stage for colon according to AJCC 7th edition indicating that there is clinical evidence of distant metastases by history, physical examination, imaging studies, or invasive procedures, but without microscopic evidence of the presumed distant metastases.
+ A pathologic distant metastases stage for colon according to AJCC 7th edition indicating that there is clinical evidence of distant metastases by history, physical examination, imaging studies, or invasive procedures, but without microscopic evidence of the presumed distant metastases.
Chris Stoeckert, Helena Ellis
https://en.wikipedia.org/wiki/Cancer_staging#Pathological_M_Categorization_.28cM_and_pM.29
NCI BBRB
@@ -1535,7 +1535,7 @@
- A pathologic distant metastases stage for colon according to AJCC 7th edition indicating that metastasis is confined to one organ based on clinical assessment.
+ A pathologic distant metastases stage for colon according to AJCC 7th edition indicating that metastasis is confined to one organ based on clinical assessment.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/colon/path_m/
NCI BBRB
@@ -1548,7 +1548,7 @@
- A pathologic distant metastases stage for colon according to AJCC 7th edition indicating that metastasis is in more than one organ or the peritoneum based on clinical assessment.
+ A pathologic distant metastases stage for colon according to AJCC 7th edition indicating that metastasis is in more than one organ or the peritoneum based on clinical assessment.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/colon/path_m/
NCI BBRB
@@ -1561,7 +1561,7 @@
- A pathologic distant metastases stage for colon according to AJCC 7th edition indicating that there is microscopic evidence confirming distant metastatic disease.
+ A pathologic distant metastases stage for colon according to AJCC 7th edition indicating that there is microscopic evidence confirming distant metastatic disease.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/colon/path_m/
NCI BBRB
@@ -1574,7 +1574,7 @@
- A pathologic distant metastases stage for colon according to AJCC 7th edition indicating that metastasis is confined to one organ and histologically confirmed.
+ A pathologic distant metastases stage for colon according to AJCC 7th edition indicating that metastasis is confined to one organ and histologically confirmed.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/colon/path_m/
NCI BBRB
@@ -1587,7 +1587,7 @@
- A pathologic distant metastases stage for colon according to AJCC 7th edition indicating that metastasis is in more than one organ or the peritoneum and histologically confirmed.
+ A pathologic distant metastases stage for colon according to AJCC 7th edition indicating that metastasis is in more than one organ or the peritoneum and histologically confirmed.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/colon/path_m/
NCI BBRB
@@ -1600,7 +1600,7 @@
- A pathologic distant metastases stage for lung according to AJCC 7th edition indicating that there is no distant metastasis.
+ A pathologic distant metastases stage for lung according to AJCC 7th edition indicating that there is no distant metastasis.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/lung/path_m/
NCI BBRB
@@ -1613,7 +1613,7 @@
- A pathologic distant metastases stage for lung according to AJCC 7th edition indicating that there are distant metastases based on clinical assessment.
+ A pathologic distant metastases stage for lung according to AJCC 7th edition indicating that there are distant metastases based on clinical assessment.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/lung/path_m/
NCI BBRB
@@ -1626,7 +1626,7 @@
- A pathologic distant metastases stage for lung according to AJCC 7th edition indicating that metastasis is based on clinical assessment and a separate tumor nodule(s) in a contralateral lobe; tumor with pleural nodules OR malignant pleural or pericardial effusion.
+ A pathologic distant metastases stage for lung according to AJCC 7th edition indicating that metastasis is based on clinical assessment and a separate tumor nodule(s) in a contralateral lobe; tumor with pleural nodules OR malignant pleural or pericardial effusion.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/lung/path_m/
NCI BBRB
@@ -1639,7 +1639,7 @@
- A pathologic distant metastases stage for lung according to AJCC 7th edition indicating that there is a distant metastases based on clinical assessment.
+ A pathologic distant metastases stage for lung according to AJCC 7th edition indicating that there is a distant metastases based on clinical assessment.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/lung/path_m/
NCI BBRB
@@ -1652,7 +1652,7 @@
- A pathologic distant metastases stage for lung according to AJCC 7th edition indicating that there is a distant metastases that is histologically confirmed.
+ A pathologic distant metastases stage for lung according to AJCC 7th edition indicating that there is a distant metastases that is histologically confirmed.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/lung/path_m/
NCI BBRB
@@ -1665,7 +1665,7 @@
- A pathologic distant metastases stage for lung according to AJCC 7th edition indicating that metastasis is histologically confirmed and a separate tumor nodule(s) in a contralateral lobe; tumor with pleural nodules OR malignant pleural or pericardial effusion.
+ A pathologic distant metastases stage for lung according to AJCC 7th edition indicating that metastasis is histologically confirmed and a separate tumor nodule(s) in a contralateral lobe; tumor with pleural nodules OR malignant pleural or pericardial effusion.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/lung/path_m/
NCI BBRB
@@ -1678,7 +1678,7 @@
- A pathologic distant metastases stage for lung according to AJCC 7th edition indicating that there is a distant metastases that is histologically confirmed and associated with distant lymph nodes or carcinomatosis.
+ A pathologic distant metastases stage for lung according to AJCC 7th edition indicating that there is a distant metastases that is histologically confirmed and associated with distant lymph nodes or carcinomatosis.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/lung/path_m/
NCI BBRB
@@ -1691,7 +1691,7 @@
- A pathologic distant metastases stage for kidney according to AJCC 7th edition indicating that there is no distant metastasis.
+ A pathologic distant metastases stage for kidney according to AJCC 7th edition indicating that there is no distant metastasis.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/kidney_parenchyma/path_m/
NCI BBRB
@@ -1704,7 +1704,7 @@
- A pathologic distant metastases stage for kidney according to AJCC 7th edition indicating that there are distant metastases based on clinical assessment.
+ A pathologic distant metastases stage for kidney according to AJCC 7th edition indicating that there are distant metastases based on clinical assessment.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/kidney_parenchyma/path_m/
NCI BBRB
@@ -1717,7 +1717,7 @@
- A pathologic distant metastases stage for kidney according to AJCC 7th edition indicating that there is a distant metastases that is histologically confirmed.
+ A pathologic distant metastases stage for kidney according to AJCC 7th edition indicating that there is a distant metastases that is histologically confirmed.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/kidney_parenchyma/path_m/
NCI BBRB
@@ -1730,7 +1730,7 @@
- A pathologic distant metastases stage for ovary according to AJCC 7th edition indicating that there is no distant metastasis.
+ A pathologic distant metastases stage for ovary according to AJCC 7th edition indicating that there is no distant metastasis.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/ovary/path_m/
NCI BBRB
@@ -1743,7 +1743,7 @@
- A pathologic distant metastases stage for ovary according to AJCC 7th edition indicating that there is distant metastasis except peritoneal metastasis based on clinical assessment.
+ A pathologic distant metastases stage for ovary according to AJCC 7th edition indicating that there is distant metastasis except peritoneal metastasis based on clinical assessment.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/ovary/path_m/
NCI BBRB
@@ -1756,7 +1756,7 @@
- A pathologic distant metastases stage for ovary according to AJCC 7th edition indicating that there is distant metastasis except peritoneal metastasis that is histologically confirmed.
+ A pathologic distant metastases stage for ovary according to AJCC 7th edition indicating that there is distant metastasis except peritoneal metastasis that is histologically confirmed.
Chris Stoeckert, Helena Ellis
https://staging.seer.cancer.gov/tnm/input/1.0/ovary/path_m/
NCI BBRB
@@ -1769,7 +1769,7 @@
- A clinical tumor stage group according to AJCC 7th edition indicating a small carcinoma, either asymptomatic or giving rise to metastases without symptoms due to the primary carcinoma.
+ A clinical tumor stage group according to AJCC 7th edition indicating a small carcinoma, either asymptomatic or giving rise to metastases without symptoms due to the primary carcinoma.
Chris Stoeckert, Helena Ellis
Occult Carcinoma
http://www.medilexicon.com/dictionary/14371
@@ -1783,7 +1783,7 @@
- A clinical tumor stage group according to AJCC 7th edition indicating a carcinoma in situ (or melanoma in situ for melanoma of the skin or germ cell neoplasia in situ for testicular germ cell tumors) and generally is considered to have no metastatic potential.
+ A clinical tumor stage group according to AJCC 7th edition indicating a carcinoma in situ (or melanoma in situ for melanoma of the skin or germ cell neoplasia in situ for testicular germ cell tumors) and generally is considered to have no metastatic potential.
Chris Stoeckert, Helena Ellis
Stage 0
https://en.wikipedia.org/wiki/Cancer_staging
@@ -1797,7 +1797,7 @@
- A clinical tumor stage group according to AJCC 7th edition indicating cancers that are smaller or less deeply invasive without regional disease or nodes.
+ A clinical tumor stage group according to AJCC 7th edition indicating cancers that are smaller or less deeply invasive without regional disease or nodes.
Chris Stoeckert, Helena Ellis
Stage I
https://en.wikipedia.org/wiki/Cancer_staging
@@ -1811,7 +1811,7 @@
- A clinical tumor stage group according to AJCC 7th edition indicating cancers with increasing tumor or nodal extent but less than in Stage III and with differing characteristics from IIB and IIC.
+ A clinical tumor stage group according to AJCC 7th edition indicating cancers with increasing tumor or nodal extent but less than in Stage III and with differing characteristics from IIB and IIC.
Chris Stoeckert, Helena Ellis
Stage IIA
https://en.wikipedia.org/wiki/Cancer_staging
@@ -1825,7 +1825,7 @@
- A clinical tumor stage group according to AJCC 7th edition indicating cancers with increasing tumor or nodal extent but less than in Stage III and with differing characteristics from IIA and IIC.
+ A clinical tumor stage group according to AJCC 7th edition indicating cancers with increasing tumor or nodal extent but less than in Stage III and with differing characteristics from IIA and IIC.
Chris Stoeckert, Helena Ellis
Stage IIB
https://en.wikipedia.org/wiki/Cancer_staging
@@ -1839,7 +1839,7 @@
- A clinical tumor stage group according to AJCC 7th edition indicating cancers with increasing tumor or nodal extent but less than in Stage III and with differing characteristics from IIA and IIB.
+ A clinical tumor stage group according to AJCC 7th edition indicating cancers with increasing tumor or nodal extent but less than in Stage III and with differing characteristics from IIA and IIB.
Chris Stoeckert, Helena Ellis
Stage IIC
https://en.wikipedia.org/wiki/Cancer_staging
@@ -1853,7 +1853,7 @@
- A clinical tumor stage group according to AJCC 7th edition indicating cancers with increasing tumor or nodal extent greater than in Stage II and with differing characteristics from IIIB and IIIC.
+ A clinical tumor stage group according to AJCC 7th edition indicating cancers with increasing tumor or nodal extent greater than in Stage II and with differing characteristics from IIIB and IIIC.
Chris Stoeckert, Helena Ellis
Stage IIIA
https://en.wikipedia.org/wiki/Cancer_staging
@@ -1867,7 +1867,7 @@
- A clinical tumor stage group according to AJCC 7th edition indicating cancers with increasing tumor or nodal extent greater than in Stage II and with differing characteristics from IIIA and IIIC.
+ A clinical tumor stage group according to AJCC 7th edition indicating cancers with increasing tumor or nodal extent greater than in Stage II and with differing characteristics from IIIA and IIIC.
Chris Stoeckert, Helena Ellis
Stage IIIB
https://en.wikipedia.org/wiki/Cancer_staging
@@ -1881,7 +1881,7 @@
- A clinical tumor stage group according to AJCC 7th edition indicating cancers with increasing tumor or nodal extent greater than in Stage II and with differing characteristics from IIIA and IIIB.
+ A clinical tumor stage group according to AJCC 7th edition indicating cancers with increasing tumor or nodal extent greater than in Stage II and with differing characteristics from IIIA and IIIB.
Chris Stoeckert, Helena Ellis
Stage IIIC
https://en.wikipedia.org/wiki/Cancer_staging
@@ -1895,7 +1895,7 @@
- A clinical tumor stage group according to AJCC 7th edition indicating cancers in patients who present with distant metastases at diagnosis and with differing characteristics from IVB.
+ A clinical tumor stage group according to AJCC 7th edition indicating cancers in patients who present with distant metastases at diagnosis and with differing characteristics from IVB.
Chris Stoeckert, Helena Ellis
Stage IVA
https://en.wikipedia.org/wiki/Cancer_staging
@@ -1909,7 +1909,7 @@
- A clinical tumor stage group according to AJCC 7th edition indicating cancers in patients who present with distant metastases at diagnosis and with differing characteristics from IVA.
+ A clinical tumor stage group according to AJCC 7th edition indicating cancers in patients who present with distant metastases at diagnosis and with differing characteristics from IVA.
Chris Stoeckert, Helena Ellis
Stage IVB
https://en.wikipedia.org/wiki/Cancer_staging
@@ -1923,7 +1923,7 @@
- An International Federation of Gynecology and Obstetrics cervical cancer stage value specification indicating invasive carcinoma which can be diagnosed only by microscopy, with deepest invasion <5 mm and the largest extension <7 mm.
+ An International Federation of Gynecology and Obstetrics cervical cancer stage value specification indicating invasive carcinoma which can be diagnosed only by microscopy, with deepest invasion <5 mm and the largest extension <7 mm.
Chris Stoeckert, Helena Ellis
Stage IA
https://en.wikipedia.org/wiki/Cervical_cancer_staging
@@ -1937,7 +1937,7 @@
- An International Federation of Gynecology and Obstetrics cervical cancer stage value specification indicating measured stromal invasion of <3.0 mm in depth and extension of <7.0 mm.
+ An International Federation of Gynecology and Obstetrics cervical cancer stage value specification indicating measured stromal invasion of <3.0 mm in depth and extension of <7.0 mm.
Chris Stoeckert, Helena Ellis
Stage IA1
https://en.wikipedia.org/wiki/Cervical_cancer_staging
@@ -1951,7 +1951,7 @@
- An International Federation of Gynecology and Obstetrics cervical cancer stage value specification indicating measured stromal invasion of >3.0 mm and not >5.0 mm with an extension of not >7.0 mm.
+ An International Federation of Gynecology and Obstetrics cervical cancer stage value specification indicating measured stromal invasion of >3.0 mm and not >5.0 mm with an extension of not >7.0 mm.
Chris Stoeckert, Helena Ellis
Stage IA2
https://en.wikipedia.org/wiki/Cervical_cancer_staging
@@ -1965,7 +1965,7 @@
- An International Federation of Gynecology and Obstetrics cervical cancer stage value specification indicating clinically visible lesions limited to the cervix uteri or pre-clinical cancers greater than stage IA
+ An International Federation of Gynecology and Obstetrics cervical cancer stage value specification indicating clinically visible lesions limited to the cervix uteri or pre-clinical cancers greater than stage IA
Chris Stoeckert, Helena Ellis
Stage IB
https://en.wikipedia.org/wiki/Cervical_cancer_staging
@@ -1979,7 +1979,7 @@
- An International Federation of Gynecology and Obstetrics cervical cancer stage value specification indicating clinically visible lesion limited to the cervix uteri or pre-clinical cancers greater than stage IA <4.0 cm in greatest dimension.
+ An International Federation of Gynecology and Obstetrics cervical cancer stage value specification indicating clinically visible lesion limited to the cervix uteri or pre-clinical cancers greater than stage IA <4.0 cm in greatest dimension.
Chris Stoeckert, Helena Ellis
Stage IB1
https://en.wikipedia.org/wiki/Cervical_cancer_staging
@@ -1993,7 +1993,7 @@
- An International Federation of Gynecology and Obstetrics cervical cancer stage value specification indicating clinically visible lesion limited to the cervix uteri or pre-clinical cancers greater than stage IA >4.0 cm in greatest dimension.
+ An International Federation of Gynecology and Obstetrics cervical cancer stage value specification indicating clinically visible lesion limited to the cervix uteri or pre-clinical cancers greater than stage IA >4.0 cm in greatest dimension.
Chris Stoeckert, Helena Ellis
Stage IB2
https://en.wikipedia.org/wiki/Cervical_cancer_staging
@@ -2007,7 +2007,7 @@
- An International Federation of Gynecology and Obstetrics cervical cancer stage value specification indicating cervical carcinoma invades beyond the uterus, but not to the pelvic wall or to the lower third of the vagina without parametrial invasion.
+ An International Federation of Gynecology and Obstetrics cervical cancer stage value specification indicating cervical carcinoma invades beyond the uterus, but not to the pelvic wall or to the lower third of the vagina without parametrial invasion.
Chris Stoeckert, Helena Ellis
Stage IIA
https://en.wikipedia.org/wiki/Cervical_cancer_staging
@@ -2021,7 +2021,7 @@
- An International Federation of Gynecology and Obstetrics cervical cancer stage value specification indicating cervical carcinoma invades beyond the uterus, but not to the pelvic wall or to the lower third of the vagina without parametrial invasion and clinically visible lesion <4.0 cm in greatest dimension.
+ An International Federation of Gynecology and Obstetrics cervical cancer stage value specification indicating cervical carcinoma invades beyond the uterus, but not to the pelvic wall or to the lower third of the vagina without parametrial invasion and clinically visible lesion <4.0 cm in greatest dimension.
Chris Stoeckert, Helena Ellis
Stage IIA1
https://en.wikipedia.org/wiki/Cervical_cancer_staging
@@ -2035,7 +2035,7 @@
- An International Federation of Gynecology and Obstetrics cervical cancer stage value specification indicating cervical carcinoma invades beyond the uterus, but not to the pelvic wall or to the lower third of the vagina without parametrial invasion and clinically visible lesion >4.0 cm in greatest dimension.
+ An International Federation of Gynecology and Obstetrics cervical cancer stage value specification indicating cervical carcinoma invades beyond the uterus, but not to the pelvic wall or to the lower third of the vagina without parametrial invasion and clinically visible lesion >4.0 cm in greatest dimension.
Chris Stoeckert, Helena Ellis
Stage IIA2
https://en.wikipedia.org/wiki/Cervical_cancer_staging
@@ -2049,7 +2049,7 @@
- An International Federation of Gynecology and Obstetrics cervical cancer stage value specification indicating cervical carcinoma invades beyond the uterus, but not to the pelvic wall or to the lower third of the vagina with obvious parametrial invasion.
+ An International Federation of Gynecology and Obstetrics cervical cancer stage value specification indicating cervical carcinoma invades beyond the uterus, but not to the pelvic wall or to the lower third of the vagina with obvious parametrial invasion.
Chris Stoeckert, Helena Ellis
Stage IIB
https://en.wikipedia.org/wiki/Cervical_cancer_staging
@@ -2063,7 +2063,7 @@
- An International Federation of Gynecology and Obstetrics cervical cancer stage value specification indicating tumour involves lower third of the vagina, with no extension to the pelvic wall.
+ An International Federation of Gynecology and Obstetrics cervical cancer stage value specification indicating tumour involves lower third of the vagina, with no extension to the pelvic wall.
Chris Stoeckert, Helena Ellis
Stage IIIA
https://en.wikipedia.org/wiki/Cervical_cancer_staging
@@ -2077,7 +2077,7 @@
- An International Federation of Gynecology and Obstetrics cervical cancer stage value specification indicating extension to the pelvic wall and/or hydronephrosis or non-functioning kidney.
+ An International Federation of Gynecology and Obstetrics cervical cancer stage value specification indicating extension to the pelvic wall and/or hydronephrosis or non-functioning kidney.
Chris Stoeckert, Helena Ellis
Stage IIIB
https://en.wikipedia.org/wiki/Cervical_cancer_staging
@@ -2091,7 +2091,7 @@
- An International Federation of Gynecology and Obstetrics cervical cancer stage value specification indicating spread of the growth to adjacent organs.
+ An International Federation of Gynecology and Obstetrics cervical cancer stage value specification indicating spread of the growth to adjacent organs.
Chris Stoeckert, Helena Ellis
Stage IVA
https://en.wikipedia.org/wiki/Cervical_cancer_staging
@@ -2105,7 +2105,7 @@
- An International Federation of Gynecology and Obstetrics cervical cancer stage value specification indicating spread to distant organs.
+ An International Federation of Gynecology and Obstetrics cervical cancer stage value specification indicating spread to distant organs.
Chris Stoeckert, Helena Ellis
Stage IVB
https://en.wikipedia.org/wiki/Cervical_cancer_staging
@@ -2119,7 +2119,7 @@
- A International Federation of Gynecology and Obstetrics ovarian cancer stage value specification associated with TNM stage values of T1, N0, and M0.
+ A International Federation of Gynecology and Obstetrics ovarian cancer stage value specification associated with TNM stage values of T1, N0, and M0.
Chris Stoeckert, Helena Ellis
Stage 1
https://staging.seer.cancer.gov/tnm/input/1.0/ovary/path_stage_group_direct/
@@ -2133,7 +2133,7 @@
- A International Federation of Gynecology and Obstetrics ovarian cancer stage value specification associated with TNM stage values of T1a, N0, and M0.
+ A International Federation of Gynecology and Obstetrics ovarian cancer stage value specification associated with TNM stage values of T1a, N0, and M0.
Chris Stoeckert, Helena Ellis
Stage 1A
https://staging.seer.cancer.gov/tnm/input/1.0/ovary/path_stage_group_direct/
@@ -2147,7 +2147,7 @@
- A International Federation of Gynecology and Obstetrics ovarian cancer stage value specification associated with TNM stage values of T1b, N0, and M0.
+ A International Federation of Gynecology and Obstetrics ovarian cancer stage value specification associated with TNM stage values of T1b, N0, and M0.
Chris Stoeckert, Helena Ellis
Stage 1B
https://staging.seer.cancer.gov/tnm/input/1.0/ovary/path_stage_group_direct/
@@ -2161,7 +2161,7 @@
- A International Federation of Gynecology and Obstetrics ovarian cancer stage value specification associated with TNM stage values of T1c, N0, and M0.
+ A International Federation of Gynecology and Obstetrics ovarian cancer stage value specification associated with TNM stage values of T1c, N0, and M0.
Chris Stoeckert, Helena Ellis
Stage 1C
https://staging.seer.cancer.gov/tnm/input/1.0/ovary/path_stage_group_direct/
@@ -2175,7 +2175,7 @@
- A International Federation of Gynecology and Obstetrics ovarian cancer stage value specification associated with TNM stage values of T2, N0, and M0.
+ A International Federation of Gynecology and Obstetrics ovarian cancer stage value specification associated with TNM stage values of T2, N0, and M0.
Chris Stoeckert, Helena Ellis
Stage 2
https://staging.seer.cancer.gov/tnm/input/1.0/ovary/path_stage_group_direct/
@@ -2189,7 +2189,7 @@