An enhanced method for targeted next generation sequencing copy number variant detection using ExomeDepth [version 1; peer review: 1 approved, 1 approved with reservations]

Parrish, A, Caswell, R, Jones, G et al. (3 more authors) (2017) An enhanced method for targeted next generation sequencing copy number variant detection using ExomeDepth [version 1; peer review: 1 approved, 1 approved with reservations]. Wellcome Open Research, 2. 49. ISSN 2398-502X

Abstract

Metadata

Authors/Creators:
Copyright, Publisher and Additional Information: © 2017 Parrish A et al. This is an open access article under the terms of the Creative Commons Attribution 4.0 International (CC BY 4.0) (https://creativecommons.org/licenses/by/4.0/).
Keywords: CNV detection; NGS; Read depth; ExomeDepth
Dates:
  • Published: 14 July 2017
  • Accepted: 14 July 2017
  • Published (online): 14 July 2017
Institution: The University of Leeds
Academic Units: The University of Leeds > Faculty of Medicine and Health (Leeds) > Institute of Molecular Medicine (LIMM) (Leeds) > Section of Opthalmology and Neurosciences (Leeds)
Depositing User: Symplectic Publications
Date Deposited: 05 Jun 2019 12:39
Last Modified: 17 Jun 2019 14:41
Status: Published
Publisher: F1000Research
Identification Number: https://doi.org/10.12688/wellcomeopenres.11548.1

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