The workflow could be run on all amplicons only (and not specific target SNPs aswell). If we can reduce the number of inputs for some users that's a bonus.
Things like allele frequencies and coverage would have to be updated, to allow them to work with the all amplicons vcf
The workflow could be run on all amplicons only (and not specific target SNPs aswell). If we can reduce the number of inputs for some users that's a bonus.
Things like allele frequencies and coverage would have to be updated, to allow them to work with the all amplicons vcf