Closed kimin0402 closed 2 years ago
Each gets its own -t
flag. The idea of the multiple bams in one run is if they are related samples -- e.g. trios or multiple tumors from the same patient. I would not use this from unrelated tumors or patients. The results will be combined across all, and the genotype field will indicate which files have the variant supporting reads.
Hi, just a quick question
From the instruction of svaba, it says more than 1 bam file can be given as input for case bam.
I tried to call somatic SV in multiple bam files with one control bam, so the code was like the following
But svaba throws error. I tried spaced separated, comma separated list of bams, but it didn't work.
How can I fix this?