Rare Variant, Gene-Based Association Study of Hereditary Melanoma Using Whole-Exome Sequencing

Artomov, M, Stratigos, AJ, Kim, I et al. (21 more authors) (2017) Rare Variant, Gene-Based Association Study of Hereditary Melanoma Using Whole-Exome Sequencing. JNCI: Journal of the National Cancer Institute, 109 (12). djx083. ISSN 0027-8874

Abstract

Metadata

Authors/Creators:
Copyright, Publisher and Additional Information: (c) The Author 2017. Published by Oxford University Press. This is a pre-copyedited, author-produced version of an article accepted for publication in JNCI: Journal of the National Cancer Institute following peer review. The version of record; Artomov, M, Stratigos, AJ, Kim, I et al. Rare Variant, Gene-Based Association Study of Hereditary Melanoma Using Whole-Exome Sequencing. JNCI: Journal of the National Cancer Institute, 109 (12). djx083. is available online at: https://doi.org/10.1093/jnci/djx083.
Keywords: cancer; cell lines; dna; genes; p16; genome; melanoma; protein; genetics, mice; neoplasms; tumor growth; mitf protein; bap1 gene; exome; hereditary melanoma; whole exome sequencing; eye melanomas
Dates:
  • Published: 1 December 2017
  • Accepted: 4 April 2017
  • Published (online): 3 June 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 Epidemiology and Biostatistics (Leeds)
Funding Information:
FunderGrant number
Cancer Research UKc588/A19167
Depositing User: Symplectic Publications
Date Deposited: 31 May 2018 09:55
Last Modified: 03 Jun 2018 00:38
Status: Published
Identification Number: https://doi.org/10.1093/jnci/djx083

Share / Export

Statistics