It’s the latter. I’m okay with a bunch of no calls in the merged VCF with all the samples because these are somatic variant calls, and I don’t expect any variant to be common. If that was your concern.
Or is there another concern I’m not catching?
It’s the latter. I’m okay with a bunch of no calls in the merged VCF with all the samples because these are somatic variant calls, and I don’t expect any variant to be common. If that was your concern.
Or is there another concern I’m not catching?