One usage example is to refine genotypes based on the discovered allele frequency in an input VCF containing many samples
gatk --java-options "-Xmx4g" CalculateGenotypePosteriors \
-V multisample_input.vcf.gz \
-O output.vcf.gz
Now if I have a case-control cohort of autoimmune disease, I wonder if I should run the above step separately for case and control, or put them into one vcf file?
Thanks for any insight!