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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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Detalhes bibliográficos
Publicado no:J Clin Oncol
Main Authors: Stadler, Zsofia K., Schrader, Kasmintan A., Vijai, Joseph, Robson, Mark E., Offit, Kenneth
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Clinical Oncology 2014
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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