A comprehensive BRCA1/2 NGS pipeline for an immediate Copy Number Variation (CNV) detection in breast and ovarian cancer molecular diagnosis

A comprehensive BRCA1/2 NGS pipeline for an immediate Copy Number Variation (CNV) detection in... BackgroundThe aim of this study was to assess the ability of a Next Generation Sequencing (NGS)-based approach in the detection of BRCA1/2 Large Genomic Rearrangements (LGRs). http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Clinica Chimica Acta Elsevier

A comprehensive BRCA1/2 NGS pipeline for an immediate Copy Number Variation (CNV) detection in breast and ovarian cancer molecular diagnosis

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Publisher
Elsevier
Copyright
Copyright © 2018 Elsevier B.V.
ISSN
0009-8981
eISSN
1873-3492
D.O.I.
10.1016/j.cca.2018.02.012
Publisher site
See Article on Publisher Site

Abstract

BackgroundThe aim of this study was to assess the ability of a Next Generation Sequencing (NGS)-based approach in the detection of BRCA1/2 Large Genomic Rearrangements (LGRs).

Journal

Clinica Chimica ActaElsevier

Published: May 1, 2018

References

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