Genome-wide CNV analysis replicates the association between GSTM1 deletion and bladder cancer: a support for using continuous measurement from SNP-array data

BACKGROUND: Structural variations such as copy number variants (CNV) influence the expression of different phenotypic traits. Algorithms to identify CNVs through SNP-array platforms are available. The ability to evaluate well-characterized CNVs such as GSTM1 (1p13.3) deletion provides an important o...

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Detalles Bibliográficos
Autores principales: Marenne, Gaëlle, Real, Francisco X, Rothman, Nathaniel, Rodríguez-Santiago, Benjamin, Pérez-Jurado, Luis, Kogevinas, Manolis, García-Closas, Montse, Silverman, Debra T, Chanock, Stephen J, Génin, Emmanuelle, Malats, Núria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Methodology Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3425254/
https://www.ncbi.nlm.nih.gov/pubmed/22817656
http://dx.doi.org/10.1186/1471-2164-13-326

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3425254/
https://www.ncbi.nlm.nih.gov/pubmed/22817656
http://dx.doi.org/10.1186/1471-2164-13-326

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