Entering edit mode
17 months ago
Cèlia
•
0
Hey!
I have a vcf file from which I want to extract the samples (genotypes) that contain specific SNPs that I have in a list. That is since I ran a GWAS and came up with significant SNPs that might explain my phenotype. I want to see if the SNPs are correlated and for that, I only want to keep the genotypes that contain such SNPS.
Is it possible to use bcftools for that?
Thank you in advance!
explain/describe
Possibly you mean Use bcftools to find carriers of variants