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CScape-somatic: distinguishing driver and passenger point mutations in the cancer genome
MOTIVATION: Next-generation sequencing technologies have accelerated the discovery of single nucleotide variants in the human genome, stimulating the development of predictors for classifying which of these variants are likely functional in disease, and which neutral. Recently, we proposed CScape, a...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Oxford University Press
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7320610/ https://www.ncbi.nlm.nih.gov/pubmed/32282885 http://dx.doi.org/10.1093/bioinformatics/btaa242 |
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