PredictSNP2: A Unified Platform for Accurately Evaluating SNP Effects by Exploiting the Different Characteristics of Variants in Distinct Genomic Regions
Fig 2
Workflow diagram describing the construction of the dataset of variants related to Mendelian diseases.
The dataset was prepared by combining deleterious variants from the ClinVar database with neutral variants from the VariSNP database. The resulting dataset was then divided into independent training and testing subsets for each individual category of variants.