R-Gada: a fast and flexible pipeline for copy number analysis in association studies

BACKGROUND: Genome-wide association studies (GWAS) using Copy Number Variation (CNV) are becoming a central focus of genetic research. CNVs have successfully provided target genome regions for some disease conditions where simple genetic variation (i.e., SNPs) has previously failed to provide a clea...

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Detalles Bibliográficos
Autores principales: Pique-Regi, Roger, Cáceres, Alejandro, González, Juan R
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2915992/
https://www.ncbi.nlm.nih.gov/pubmed/20637081
http://dx.doi.org/10.1186/1471-2105-11-380

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2915992/
https://www.ncbi.nlm.nih.gov/pubmed/20637081
http://dx.doi.org/10.1186/1471-2105-11-380

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