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Predicting cancer drivers: are we there yet?
Genomic variants with a key role in causing cancer or affecting the response to cancer therapeutics need to be identified so that they can be targeted for therapy. The transFIC tool aims to identify somatic point mutations that drive cancer in sequencing projects. This package is available as a web...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3580422/ https://ncbi.nlm.nih.gov/pubmed/23181697 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/gm389 |
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