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IVA is a de novo assembler designed to assemble virus genomes that have no repeat sequences, using Illumina read pairs sequenced from mixed populations at extremely high depth.
IVA's main algorithm works by iteratively extending contigs using aligned read pairs. Its input can be just read pairs, or additionally you can provide an existing set of contigs to be extended. Alternatively, it can take reads together with a reference sequence.
Please see the IVA homepage for installation instructions.
The installation of IVA can be tested by running an assembly on the test data set that is included with IVA.
Assembly is run with the script iva
. An explanation of all
options is here, or
you might want to look at the examples
first.
There are two scripts for QC:
-
iva_qc
- compares an assembly against a reference (or can choose the reference from a database). There is a page of options and also examples. The output files ofiva_qc
are explained here and the stats it makes are explained here. -
iva_qc_make_db
- makes a database for use as input toiva_qc
. See this page for more help.