Hi. I want to calculate variant allele frequency in regulatory regions in colon cancer versus genomad data.
I googled too much and likely
gVCF is individual-level vcf
pVCF is population-level vcf
but this is too confusion
Can I use pVCF files for my project or I must use WGS/WES gVCF files?
you might start by reading this: https://pubmed.ncbi.nlm.nih.gov/38057664/