Open zlskidmore opened 1 year ago
Looks like the tumor and normal sample names used didn't match the sample names in the tumor and normal input bams. When the detect variants subworkflow merged the VCF outputs from the multiple variant callers the results for the normal sample in the VCF file was split across two sample names and caused some variants to have no value the normal sample column that was being filtered.
Hey Guys,
I'm seeing the following error for a somatic_wgs run:
Execution appeared to stop at this variant
I see the Depth field does have a depth with an integer, so i'm a bit confused why execution would stop here, do you guys see something i'm not?
tagging @chrisamiller and @johnegarza