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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...
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| Publicado no: | Bioinformatics |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7320610/ https://ncbi.nlm.nih.gov/pubmed/32282885 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btaa242 |
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