bioRxiv · 10.1101/270413
SMuRF: Portable and accurate ensemble-based somatic variant calling
Abstract
ABSTARCTO_ST_ABSSummaryC_ST_ABSSMuRF is an ensemble method for prediction of somatic point mutations (SNVs) and small insertions/deletions (indels) in cancer genomes. The method integrates predictions and auxiliary features from different somatic mutation callers using a Random Forest machine learning approach. SMuRF is trained on community-curated tumor whole genome sequencing data, is robust across cancer types, and achieves improved accuracy for both SNV and indel predictions of genome and exome-level data. The software is user-friendly and portable by design, operating as an add-on to the community-developed bcbio-nextgen somatic variant calling pipeline.\n\nContactskanderupamj@gis.a-star.edu.sg
Source connections
Explore related subjects
Keep this discovery
Huang, W., Guo, Y. A., Muthukumar, K., Baruah, P., Chang, M., Skanderup, A. J.. 2018-02-23. SMuRF: Portable and accurate ensemble-based somatic variant calling. https://doi.org/10.1101/270413
Cite the original work for its findings. Save a collection to share your selection of sources.