How to find the position of genes that their variants called by hs37d5?
Hi all,
I have used the PCAWG vcf files for my analysis. These variants have been called by the hs37d5 reference genome. Now I want to subset the list of my interest gene from these vcf files and don't know how to find the start and end positions.
Thanks for any help.
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The genome build is GRCH37: https://www.gencodegenes.org/human/release_19.html