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From a combined VCF file with two genotypes {tumor, normal}, annotate the variants with SnpEff, and output a protein XML with those variations
Adapt Proteomics.VariantApplication in mzLib to handle generating separate protein entries for the different samples. It's built with multiple-sample VCF lines in mind...
The text was updated successfully, but these errors were encountered:
Proteomics.VariantApplication
in mzLib to handle generating separate protein entries for the different samples. It's built with multiple-sample VCF lines in mind...The text was updated successfully, but these errors were encountered: