Open rmcolq opened 3 years ago
Given that we already have a list of all the mutations in each sequence, could create a VCF-format file from these lists, rather than recalculating from the alignment with faToVcf - probably faster.
Given that we already have a list of all the mutations in each sequence, could create a VCF-format file from these lists, rather than recalculating from the alignment with faToVcf - probably faster.