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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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Detalhes bibliográficos
Main Authors: Lin, Dongdong, Zhang, Jigang, Li, Jingyao, Calhoun, Vince D, Deng, Hong-Wen, Wang, Yu-Ping
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2013
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Acesso em linha: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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