Is it possible to have Platypus call a variant at a position and output even if the ref is present?
I tried running with source and outputRefCalls, along with the args recommended for genotyping a list of known alleles:
--source=test.vcf.gz --minPosterior=0 --getVariantsFromBAMs=0 --outputRefCalls=1
But, I don't understand the results. I ended up with many more variant calls that I asked for in source, and the variant calls I wanted that do end up in the output file don't seem to be from the sample.
The test.vcf I'm using isn't a vcf generated from the sample. It's a vcf where I really only care about the chr and position. Is there another way to do this?
Thanks.