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

Internet

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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