Problems in variation interpretation guidelines and in their implementation in computational tools.
Mauno VihinenPublished in: Molecular genetics & genomic medicine (2020)
Methods used for variation interpretation have to be carefully selected. It should be possible to use only one predictor, with proven good performance or a limited number of complementary predictors with state-of-the-art performance. Bear in mind that diseases and pathogenicity have a continuum and variants are not dichotomic i.e. either pathogenic or benign, either.