To better understand the health implications of personal genomes, we now face a largely unmet challenge to identify functional variants within disease-associated genes. Functional variants can be iden
Additional file 1: Table S1. Number of variants per class in complete, training, and testing datasets. Table S2. Description of features used for LoGoFunc’s development. Table S3. Fisher's exact test
Allele age estimated using GEVA on data from the 1000 Genomes Project (TGP), for variants annotated by PolyPhen-2 and SIFT (information available through Ensembl), across all autosomes.
