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

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

<p>Abstract</p> <p>Background</p> <p>Genotypes obtained with commercial SNP arrays have been extensively used in many large case-control or population-based cohorts for SNP-based genome-wide association studies for a multitude of traits. Yet, these genotypes capture onl...

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Bibliographic Details
Main Authors: Valsesia Armand, Stevenson Brian J, Waterworth Dawn, Mooser Vincent, Vollenweider Peter, Waeber Gérard, Jongeneel C, Beckmann Jacques S, Kutalik Zoltán, Bergmann Sven
Format: Article
Language:English
Published: BMC 2012-06-01
Series:BMC Genomics
Online Access:http://www.biomedcentral.com/1471-2164/13/241

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http://www.biomedcentral.com/1471-2164/13/241

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