Hi,
I have SNP/indel calls in a VCF file, is there a script around that produces a consensus sequence using a reference and the calls in the VCF? I was checking the GATK pages but could not find any related stuff there.
Szilva
I have SNP/indel calls in a VCF file, is there a script around that produces a consensus sequence using a reference and the calls in the VCF? I was checking the GATK pages but could not find any related stuff there.
Szilva
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