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Analysis on GENIE reveals novel recurrent variants that affect molecular diagnosis of sizable number of cancer patients
BACKGROUND: Significant numbers of variants detected in cancer patients are often left labeled only as variants of unknown significance (VUS). In order to expand precision medicine to a wider population, we need to extend our knowledge of pathogenicity and drug response in the context of VUS’s. METH...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2019
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6359859/ https://www.ncbi.nlm.nih.gov/pubmed/30709382 http://dx.doi.org/10.1186/s12885-019-5313-1 |