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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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| Publicado no: | J Clin Oncol |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society of Clinical Oncology
2014
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| Assuntos: | |
| Acesso em linha: | 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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