Integrating germline and somatic variation information using genomic data for the discovery of biomarkers in prostate cancer

BACKGROUND: Prostate cancer (PCa) is the most common diagnosed malignancy and the second leading cause of cancer-related deaths among men in the United States. High-throughput genotyping has enabled discovery of germline genetic susceptibility variants (herein referred to as germline mutations) asso...

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Detalles Bibliográficos
Autores principales: Mamidi, Tarun Karthik Kumar, Wu, Jiande, Hicks, Chindo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6417124/
https://www.ncbi.nlm.nih.gov/pubmed/30871495
http://dx.doi.org/10.1186/s12885-019-5440-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6417124/
https://www.ncbi.nlm.nih.gov/pubmed/30871495
http://dx.doi.org/10.1186/s12885-019-5440-8

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