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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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Lin, Dongdong, Zhang, Jigang, Li, Jingyao, Calhoun, Vince D, Deng, Hong-Wen, Wang, Yu-Ping
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: BioMed Central 2013
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC3751310/
https://ncbi.nlm.nih.gov/pubmed/23937249
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-14-245
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