When running with an input fasta we would blast each fasta sequence.
In cases where the input is a pVACseq list of epitopes (+ VCF), we need to further discuss which sequence to blast. If blasting larger sequence for each epitopes we would almost certainly get false-positive hits to the reference proteome around the mutation position.
When running with an input fasta we would blast each fasta sequence.
In cases where the input is a pVACseq list of epitopes (+ VCF), we need to further discuss which sequence to blast. If blasting larger sequence for each epitopes we would almost certainly get false-positive hits to the reference proteome around the mutation position.