Identification of cancer-causing variants
-
Updated
Apr 19, 2024 - Python
Identification of cancer-causing variants
Snakemake workflow designed to annotate VCF files withe SnpEff / SniSift
Evidence-aware somatic variant pathogenicity classifier using topology (TDA), fractal (FCGR) features, and dynamic ensemble selection (KNORA). MCC=0.8702, AUROC=0.9666 on 207K variants from dbNSFP v5.3a.
Add a description, image, and links to the dbnsfp topic page so that developers can more easily learn about it.
To associate your repository with the dbnsfp topic, visit your repo's landing page and select "manage topics."