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

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

<p>Abstract</p> <p>Background</p> <p>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...

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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: Artículo
Lenguaje:English
Publicado: BMC 2012-07-01
Colección:BMC Genomics
Materias:
Bladder cancer risk
Glutathione <it>S</it>-transferase mu 1 (<it>GSTM1</it>)
Copy number variation (CNV)
SNP-array
Acceso en línea:http://www.biomedcentral.com/1471-2164/13/326

Internet

http://www.biomedcentral.com/1471-2164/13/326

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