CScape: a tool for predicting oncogenic single-point mutations in the cancer genome

For somatic point mutations in coding and non-coding regions of the genome, we propose CScape , an integrative classifier for predicting the likelihood that mutations are cancer drivers. Tested on somatic mutations, CScape tends to outperform alternative methods, reaching 91% balanced accuracy in co...

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Vydané v:Scientific reports Ročník 7; číslo 1; s. 11597 - 10
Hlavní autori: Rogers, Mark F., Shihab, Hashem A., Gaunt, Tom R., Campbell, Colin
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: London Nature Publishing Group UK 14.09.2017
Nature Publishing Group
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ISSN:2045-2322, 2045-2322
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Shrnutí:For somatic point mutations in coding and non-coding regions of the genome, we propose CScape , an integrative classifier for predicting the likelihood that mutations are cancer drivers. Tested on somatic mutations, CScape tends to outperform alternative methods, reaching 91% balanced accuracy in coding regions and 70% in non-coding regions, while even higher accuracy may be achieved using thresholds to isolate high-confidence predictions. Positive predictions tend to cluster in genomic regions, so we apply a statistical approach to isolate coding and non-coding regions of the cancer genome that appear enriched for high-confidence predicted disease-drivers. Predictions and software are available at http://CScape.biocompute.org.uk/ .
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ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-017-11746-4