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Comprehensive benchmarking of SNV callers for highly admixed tumor data
Precision medicine attempts to individualize cancer therapy by matching tumor-specific genetic changes with effective targeted therapies. A crucial first step in this process is the reliable identification of cancer-relevant variants, which is considerably complicated by the impurity and heterogenei...
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| Publicado no: | PLoS One |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5636151/ https://ncbi.nlm.nih.gov/pubmed/29020110 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0186175 |
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