Group sparse canonical correlation analysis for genomic data integration

BACKGROUND: The emergence of high-throughput genomic datasets from different sources and platforms (e.g., gene expression, single nucleotide polymorphisms (SNP), and copy number variation (CNV)) has greatly enhanced our understandings of the interplay of these genomic factors as well as their influe...

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Detalles Bibliográficos
Autores principales: Lin, Dongdong, Zhang, Jigang, Li, Jingyao, Calhoun, Vince D, Deng, Hong-Wen, Wang, Yu-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Methodology Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751310/
https://www.ncbi.nlm.nih.gov/pubmed/23937249
http://dx.doi.org/10.1186/1471-2105-14-245

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751310/
https://www.ncbi.nlm.nih.gov/pubmed/23937249
http://dx.doi.org/10.1186/1471-2105-14-245

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