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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Bibliografiske detaljer
Main Authors: Lin, Dongdong, Zhang, Jigang, Li, Jingyao, Calhoun, Vince D, Deng, Hong-Wen, Wang, Yu-Ping
Format: Artigo
Sprog:Inglês
Udgivet: BioMed Central 2013
Fag:
Methodology Article
Online adgang: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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