I have merged .bam files from the 1kGP (with samtools merge -r) and performed RetroSeq discovery phase on the merged .bam.
But now when I call the merged .bam I get only one .vcf output. How do I create .vcf's for each individual in the merged .bam?
This is similar to what Wildschutte did in a 2015 study. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4666360/
Thank you.
EDIT: (May 2017) I was mistaken, the merged (pooled) .bam is used during the calling phase NOT discovery.