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

BACKGROUND: 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 only a small fraction of the variance of the studied trait...

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Detalles Bibliográficos
Autores principales:	Valsesia, Armand, Stevenson, Brian J, Waterworth, Dawn, Mooser, Vincent, Vollenweider, Peter, Waeber, Gérard, Jongeneel, C Victor, Beckmann, Jacques S, Kutalik, Zoltán, Bergmann, Sven
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2012
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3464625/ https://www.ncbi.nlm.nih.gov/pubmed/22702538 http://dx.doi.org/10.1186/1471-2164-13-241

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