Using next-generation sequencing for high resolution multiplex analysis of copy number variation from nanogram quantities of DNA from formalin-fixed paraffin-embedded specimens

Wood, HM, Belvedere, O, Conway, C et al. (16 more authors) (2010) Using next-generation sequencing for high resolution multiplex analysis of copy number variation from nanogram quantities of DNA from formalin-fixed paraffin-embedded specimens. Nucleic Acids Research, 38 (14). e151. ISSN 0305-1048

Abstract

Metadata

Authors/Creators:
  • Wood, HM
  • Belvedere, O
  • Conway, C
  • Daly, C
  • Chalkley, R
  • Bickerdike, M
  • McKinley, C
  • Egan, P
  • Ross, L
  • Hayward, B
  • Morgan, J
  • Davidson, L
  • MacLennan, K
  • Ong, TK
  • Papagiannopoulos, K
  • Cook, I
  • Adams, DJ
  • Taylor, GR
  • Rabbitts, P
Copyright, Publisher and Additional Information: © The Author(s) 2010. Published by Oxford University Press. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Keywords: Squamous-cell carcinoma; Lung-cancer; Array CGH; Genome browser; Allelic loss; Variants; Identification; Lines; UCSC; MCC
Dates:
  • Published: August 2010
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 Experimental Therapeutics (Leeds)
Depositing User: Symplectic Publications
Date Deposited: 29 Sep 2015 14:15
Last Modified: 22 Oct 2019 15:14
Published Version: http://dx.doi.org/10.1093/nar/gkq510
Status: Published
Publisher: Oxford University Press
Identification Number: https://doi.org/10.1093/nar/gkq510

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