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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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| Autores principales: | , , , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
BioMed Central
2013
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| Materias: | |
| Acceso en línea: | 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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