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

3 Dec 2014

Abstract excerpt

mutations and led to cancer risk diagnoses in 21% of non-BRCA cancer genetics patients after expanding our analysis to 3209 ClinVar genes. These data illustrate how WGS can be used to improve our ability to discover patients' cancer genetic risks.

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Identifiers

PMID: 26023681
DOI: 10.1016/j.ebiom.2014.12.003

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