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For systems that target full gene but only interpret to the Exon level, it would be good to have a notion of validation/strictness defined only the 3rd field of nomenclature. For example if you have a sequence that is C_17:01:01 in the exons and you know its not C_17:01:01:01/C_17:01:01:02/C_17:01:01:03 then reporting it as an ambiguity across these three allele is not accurate.
The text was updated successfully, but these errors were encountered:
For systems that target full gene but only interpret to the Exon level, it would be good to have a notion of validation/strictness defined only the 3rd field of nomenclature. For example if you have a sequence that is C_17:01:01 in the exons and you know its not C_17:01:01:01/C_17:01:01:02/C_17:01:01:03 then reporting it as an ambiguity across these three allele is not accurate.
The text was updated successfully, but these errors were encountered: