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In many situations there is only junction_aa available in one file, and cdr3_aa in the other. Apart from how to specify the interface, would it be very complicated/give a lot of overhead to have some functionality that allows reading in junctions (with the leading and trailing amino acids) as cdr3s? That would mean: in the case of amino acid, remove the first and last. In the case of nucleotide, remove the first 3 and last 3 nucleotides. We can presume here that no additional checking needs to be done on if the removed aa’s are actually the conserved C and W/F residues (or maybe only check the first sequence). Need to determine user parameters (like how to specify this elegantly for a mix of cdr3/junction files).
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enhancementNew feature or requestNew feature or request