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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...

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Bibliografski detalji
Glavni autori: Lin, Dongdong, Zhang, Jigang, Li, Jingyao, Calhoun, Vince D, Deng, Hong-Wen, Wang, Yu-Ping
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2013
Teme:
Online pristup: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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