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I have identified differentially methylated sites with methylKit, and I am interested in annotating the DML/DMR and potentially doing a Gene ontology analysis.
I first grabbed all the differentially methylated sites:
The refseq_anot is from a bed file with tracks of exons, introns, flanks tracks from the NCBI gff file.
It technically, worked well > refseq_anot <- readTranscriptFeatures("Bvos_refseq.bed", remove.unusual=FALSE) Reading the table...
Calculating intron coordinates...
Calculating exon coordinates...
Calculating TSS coordinates...
Calculating promoter coordinates...
Outputting the final GRangesList...
But then, when I try the annotation, I got this error message:
I used the same genome for annotation methylation calling. Can I trust the annotation results?
Is there a way to fix this error?
Lastly, after annotation, how can I retrieve/find the nearest gene to the DML/DMR?
I'd like to do, if possible, a gene set/functional enrichment analysis of the DML/DMR.
Thanks.
The text was updated successfully, but these errors were encountered:
Hi,
I have identified differentially methylated sites with methylKit, and I am interested in annotating the DML/DMR and potentially doing a Gene ontology analysis.
I first grabbed all the differentially methylated sites:
and then, I annotated them with annotateWithGeneParts
The refseq_anot is from a bed file with tracks of exons, introns, flanks tracks from the NCBI gff file.
It technically, worked well
> refseq_anot <- readTranscriptFeatures("Bvos_refseq.bed", remove.unusual=FALSE)
Reading the table...Calculating intron coordinates...
Calculating exon coordinates...
Calculating TSS coordinates...
Calculating promoter coordinates...
Outputting the final GRangesList...
But then, when I try the annotation, I got this error message:
Warning messages:
1: In .merge_two_Seqinfo_objects(x, y) :
Each of the 2 combined objects has sequence levels not in the other:
2: In .merge_two_Seqinfo_objects(x, y) :
Each of the 2 combined objects has sequence levels not in the other:
3: In .merge_two_Seqinfo_objects(x, y) :
Each of the 2 combined objects has sequence levels not in the other:
4: In .merge_two_Seqinfo_objects(x, y) :
Each of the 2 combined objects has sequence levels not in the other:
5: In .merge_two_Seqinfo_objects(x, y) :
Each of the 2 combined objects has sequence levels not in the other:
6: In .merge_two_Seqinfo_objects(x, y) :
Each of the 2 combined objects has sequence levels not in the other:
I used the same genome for annotation methylation calling. Can I trust the annotation results?
Is there a way to fix this error?
Lastly, after annotation, how can I retrieve/find the nearest gene to the DML/DMR?
I'd like to do, if possible, a gene set/functional enrichment analysis of the DML/DMR.
Thanks.
The text was updated successfully, but these errors were encountered: