Additional file 3 of Benchmarking splice variant prediction algorithms using massively parallel splicing assays

Additional file 3: Table S2. Tool specific thresholds at which 5%, 10%, and 20% of the 500,000 background variants are predicted to be splice disruptive. Transcriptomic normalized sensitivity values for each algorithm and benchmarked dataset overall, within exonic variants, within intronic variants, and within intronic variants after removing variants at essential splice sites. Tables of sensitivity values are provided at transcriptome normalized cut offs of 5%, 10%, and 20% as well as the area under the curve (AUC) values.