Assessment of Copy Number Variation Using the Illumina Infinium 1M SNP-Array: A Comparison of Methodological Approaches in the Spanish Bladder Cancer/EPICURO Study

High-throughput single nucleotide polymorphism (SNP)-array technologies allow to investigate copy number variants (CNVs) in genome-wide scans and specific calling algorithms have been developed to determine CNV location and copy number. We report the results of a reliability analysis comparing data...

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Detalhes bibliográficos
Main Authors: Marenne, Gaëlle, Rodríguez-Santiago, Benjamín, Closas, Montserrat García, Pérez-Jurado, Luis, Rothman, Nathaniel, Rico, Daniel, Pita, Guillermo, Pisano, David G., Kogevinas, Manolis, Silverman, Debra T., Valencia, Alfonso, Real, Francisco X., Chanock, Stephen J., Génin, Emmanuelle, Malats, Núria
Formato: Artigo
Idioma:Inglês
Publicado em: 2011
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3230937/
https://ncbi.nlm.nih.gov/pubmed/21089066
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/humu.21398
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