Using common variants to indicate cancer genes.

Stead, LF, Thygesen, H, Westhead, DR et al. (1 more author) (2015) Using common variants to indicate cancer genes. International Journal of Cancer, 136 (1). 241 - 245. ISSN 0020-7136

Abstract

Metadata

Authors/Creators:
  • Stead, LF
  • Thygesen, H
  • Westhead, DR
  • Rabbitts, P
Copyright, Publisher and Additional Information: (c) 2015, The Authors. Reproduced in accordance with the publisher's self-archiving policy. This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial No Derivates (CC BY-NC-ND 3.0) licence, which permits others to download this work and share it with others, provided the original work is unchanged, properly cited and the use is non-commercial.
Keywords: Cancer driver genes; Next-generation sequencing; Somatic mutation; DNA Mutational Analysis; Gene Frequency; Genes, Neoplasm; Genome-Wide Association Study; High-Throughput Nucleotide Sequencing; Humans; MicroRNAs; Models, Genetic; Mutation; Neoplasms; Polymorphism, Genetic; Software
Dates:
  • Published: 1 January 2015
Institution: The University of Leeds
Academic Units: The University of Leeds > Faculty of Biological Sciences (Leeds) > School of Molecular and Cellular Biology (Leeds)
Depositing User: Symplectic Publications
Date Deposited: 17 Mar 2015 10:51
Last Modified: 22 Aug 2015 11:53
Published Version: http://dx.doi.org/10.1002/ijc.28951
Status: Published
Publisher: Wiley
Identification Number: https://doi.org/10.1002/ijc.28951

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