Rapid Visualisation of Microarray Copy Number Data for the Detection of Structural Variations Linked to a Disease Phenotype

Carr, IM orcid.org/0000-0001-9544-1068, Diggle, CP, Khan, K et al. (8 more authors) (2012) Rapid Visualisation of Microarray Copy Number Data for the Detection of Structural Variations Linked to a Disease Phenotype. PLoS One, 7 (8). ARTN e43466. ISSN 1552-4973

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Authors/Creators:
Copyright, Publisher and Additional Information: (c) 2012, Carr et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Keywords: Aniridia; Chromosome Aberrations; Chromosome Mapping; DNA Copy Number Variations; Family Health; Female; Genetic Association Studies; Genetic Predisposition to Disease; Genome, Human; Humans; Loss of Heterozygosity; Male; Oligonucleotide Array Sequence Analysis; Pedigree; Phenotype; Polymorphism, Single Nucleotide; Reproducibility of Results; Software
Dates:
  • Published: 17 August 2012
  • Accepted: 20 July 2012
Institution: The University of Leeds
Academic Units: The University of Leeds > Faculty of Medicine and Health (Leeds) > School of Medicine (Leeds) > Inst of Biomed & Clin Sciences (LIBACS) (Leeds) > Genetics (LIBACS) (Leeds)
The University of Leeds > Faculty of Medicine and Health (Leeds) > Institute of Molecular Medicine (LIMM) (Leeds) > Section of Opthalmology and Neurosciences (Leeds)
The University of Leeds > Faculty of Medicine and Health (Leeds) > Institute of Molecular Medicine (LIMM) (Leeds) > Section of Translational Medicine (Leeds)
Depositing User: Symplectic Publications
Date Deposited: 12 Aug 2016 10:59
Last Modified: 12 Aug 2016 10:59
Published Version: http://dx.doi.org/10.1371/journal.pone.0043466
Status: Published
Publisher: Wiley
Identification Number: https://doi.org/10.1371/journal.pone.0043466
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