Closed husensofteng closed 2 months ago
Also, would be good here to discuss, within the canonical pangenome and non-canonical what is the challenge to detect small AA variants, SAAVs. My point is that if the pangenome we have a lot of SAAVs would be more difficult for proteomics tools to detect specific peptides.
The purpose of this issue is to compare quantity and overlap between the protein biotypes and the sources (GRCh and GCA) in the non-canonical proteogenomics database