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Cancer Genomics and Inherited Risk
Next-generation sequencing (NGS) has enabled whole-exome and whole-genome sequencing of tumors for causative mutations, allowing for more accurate targeting of therapies. In the process of sequencing the tumor, comparisons to the germline genome may identify variants associated with susceptibility t...
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| Pubblicato in: | J Clin Oncol |
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| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
American Society of Clinical Oncology
2014
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5795694/ https://ncbi.nlm.nih.gov/pubmed/24449244 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1200/JCO.2013.49.7271 |
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