Entering edit mode
2.8 years ago
Zahra
▴
110
Hi all,
I want to study mutations of some genes in cancer cases and I have patients’ VCF files (I want to know what type of mutation each gene has in cohort), but I don’t know how to start for my analysis? Should I separate my interest genes from the VCF file or not? Or maybe I should filter my VCF files panel-based?
Thanks for any help or suggestion, or maybe a related paper :)