Computational tools for copy number variation (CNV) detection using next-generation sequencing data: features and perspectives

Copy number variation (CNV) is a prevalent form of critical genetic variation that leads to an abnormal number of copies of large genomic regions in a cell. Microarray-based comparative genome hybridization (arrayCGH) or genotyping arrays have been standard technologies to detect large regions subje...

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Detalles Bibliográficos
Autores principales: Zhao, Min, Wang, Qingguo, Wang, Quan, Jia, Peilin, Zhao, Zhongming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3846878/
https://www.ncbi.nlm.nih.gov/pubmed/24564169
http://dx.doi.org/10.1186/1471-2105-14-S11-S1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3846878/
https://www.ncbi.nlm.nih.gov/pubmed/24564169
http://dx.doi.org/10.1186/1471-2105-14-S11-S1

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