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Article

SMuRF: Portable and accurate ensemble-based somatic variant calling

2018-02-23

Abstract excerpt

<h4>ABSTARCT</h4> <h4>Summary</h4> SMuRF 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...

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Literature Corpus work
7666fbd6-8156-51c5-b636-a458902a9714
DOI
10.1101/270413
Open publication

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SMuRF: Portable and accurate ensemble-based somatic variant callingDOI 10.1101/270413
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