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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Bibliografiske detaljer
Udgivet i:EBioMedicine
Main Authors: Foley, Samantha B., Rios, Jonathan J., Mgbemena, Victoria E., Robinson, Linda S., Hampel, Heather L., Toland, Amanda E., Durham, Leslie, Ross, Theodora S.
Format: Artigo
Sprog:Inglês
Udgivet: Elsevier 2014
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Original Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4444225/
https://ncbi.nlm.nih.gov/pubmed/26023681
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ebiom.2014.12.003
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