Open rfinkers opened 1 year ago
Hi @rfinkers. It's definitely possible, but I'll need to think about how to report the data in the VCF format. We could potentially report it in an (optional) FORMAT field and have a simple script to extract it from the VCF and write a plain text table.
Would it be possible to write a table, for each locus, in which the likelihood that a read belongs to an allele is reported?