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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.
The text was updated successfully, but these errors were encountered:
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.
The text was updated successfully, but these errors were encountered: