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