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

Internet

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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