Entering edit mode
9.5 years ago
Floris Brenk
★
1.0k
Hi all,
We have a bunch of gvcf files (400+) from exome data. What I would like to create coverage plots per exon, gene and/or genome wide. I know how to do this with bam files: like with depth of coverage of GATK and bedtools coverage hist, but cant find a way to do this with gvcf files. As far as I know the coverage information should be in the gvcf files.
I found this in GATK forum: http://gatkforums.broadinstitute.org/discussion/4315/depth-of-coverage-from-gvcf-files but I wouldnt know were to start scripting...
Does anyone has an idea or knows what the best way would be?
Thanks in advance...
Do you want the per sample depth or the average depth for each exon?
Both would be good to know in the end... But for now I'm interested in the average depth for each exon.