Učitavanje...
Personalized genomic analyses for cancer mutation discovery and interpretation
Massively parallel sequencing approaches are beginning to be used clinically to characterize individual patient tumors and to select therapies based on the identified mutations. A major question in these analyses is the extent to which these methods identify clinically actionable alterations and whe...
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| Izdano u: | Sci Transl Med |
|---|---|
| Glavni autori: | , , , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2015
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4442685/ https://ncbi.nlm.nih.gov/pubmed/25877891 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1126/scitranslmed.aaa7161 |
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