G'day,
I have a vcf file from an amplicon sequencing run with a set of SNPs/INDELs identified and I want to construct fasta sequences containing every combination of SNPs/INDELs that I have identified without having to manual complete this task (as I am already doing at the moment).
Example: I have identified 12 variants that occur across a reference sequence (vcf file) and I want to produce a set of sequences that have the 12 variants in different combinations.
Does that make sense?
Thanks in advance
This is exactly what I wanted. I can't thank you enough!
cool , I want to be the 1st author. :-)