This takes two variant callers, calls variants on tumor and normal independently,
and outputs the variants in the tumor sample BUT NOT the normal sample.
This assumes that both read sets only contain a single sample, otherwise we should compare
on a sample identifier when joining the genotypes
Simple subtraction based somatic variant caller
This takes two variant callers, calls variants on tumor and normal independently, and outputs the variants in the tumor sample BUT NOT the normal sample.
This assumes that both read sets only contain a single sample, otherwise we should compare on a sample identifier when joining the genotypes