Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic

Despite the potential of whole-genome sequencing (WGS) to improve patient diagnosis and care, the empirical value of WGS in the cancer genetics clinic is unknown. We performed WGS on members of two cohorts of cancer genetics patients: those with BRCA1/2 mutations (n = 176) and those without (n = 82)...

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Detalles Bibliográficos
Autores principales: Foley, Samantha B., Rios, Jonathan J., Mgbemena, Victoria E., Robinson, Linda S., Hampel, Heather L., Toland, Amanda E., Durham, Leslie, Ross, Theodora S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4444225/
https://www.ncbi.nlm.nih.gov/pubmed/26023681
http://dx.doi.org/10.1016/j.ebiom.2014.12.003

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4444225/
https://www.ncbi.nlm.nih.gov/pubmed/26023681
http://dx.doi.org/10.1016/j.ebiom.2014.12.003

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