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SNP and gene networks construction and analysis from classification of copy number variations data

BACKGROUND: Detection of genomic DNA copy number variations (CNVs) can provide a complete and more comprehensive view of human disease. It is interesting to identify and represent relevant CNVs from a genome-wide data due to high data volume and the complexity of interactions. RESULTS: In this paper...

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Detalles Bibliográficos
Autores principales:	Liu, Yang, Lee, Yiu Fai, Ng, Michael K
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2011
Materias:	Proceedings
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3226254/ https://www.ncbi.nlm.nih.gov/pubmed/21989070 http://dx.doi.org/10.1186/1471-2105-12-S5-S4

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