Open Access Highly Accessed Research article

Identification and validation of copy number variants using SNP genotyping arrays from a large clinical cohort

Armand Valsesia123, Brian J Stevenson23, Dawn Waterworth4, Vincent Mooser45, Peter Vollenweider5, Gérard Waeber5, C Victor Jongeneel236, Jacques S Beckmann17, Zoltán Kutalik12 and Sven Bergmann12*

Author Affiliations

1 Department of Medical Genetics, University of Lausanne, Lausanne, Switzerland

2 Swiss Institute of Bioinformatics, Lausanne, Switzerland

3 Ludwig Institute for Cancer Research, Lausanne, Switzerland

4 Medical Genetics/Clinical Pharmacology and Discovery Medicine, GlaxoSmithKline, Philadelphia, Pennsylvania, USA

5 Department of Medicine, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland

6 Institute for Genomic Biology and National Center for Supercomputing Applications, University of Illinois, Illinois, USA

7 Service of Medical Genetics, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland

For all author emails, please log on.

BMC Genomics 2012, 13:241  doi:10.1186/1471-2164-13-241

Published: 15 June 2012

Additional files

Additional file 1:

Document containing supplementary methods, Figures S1-S18 and Tables S1-S5.

Format: DOC Size: 967KB Download file

This file can be viewed with: Microsoft Word Viewer

Open Data