Genome-wide algorithm for detecting CNV associations with diseases

BACKGROUND: SNP genotyping arrays have been developed to characterize single-nucleotide polymorphisms (SNPs) and DNA copy number variations (CNVs). Nonparametric and model-based statistical algorithms have been developed to detect CNVs from SNP data using the marker intensities. However, these algor...

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Detalles Bibliográficos
Autores principales: Xu, Yaji, Peng, Bo, Fu, Yunxin, Amos, Christopher I
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Methodology Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3173460/
https://www.ncbi.nlm.nih.gov/pubmed/21827692
http://dx.doi.org/10.1186/1471-2105-12-331

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3173460/
https://www.ncbi.nlm.nih.gov/pubmed/21827692
http://dx.doi.org/10.1186/1471-2105-12-331

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