CNV-TV: A robust method to discover copy number variation from short sequencing reads

BACKGROUND: Copy number variation (CNV) is an important structural variation (SV) in human genome. Various studies have shown that CNVs are associated with complex diseases. Traditional CNV detection methods such as fluorescence in situ hybridization (FISH) and array comparative genomic hybridizatio...

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Detalles Bibliográficos
Autores principales: Duan, Junbo, Zhang, Ji-Gang, Deng, Hong-Wen, Wang, Yu-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Methodology Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3679874/
https://www.ncbi.nlm.nih.gov/pubmed/23634703
http://dx.doi.org/10.1186/1471-2105-14-150

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3679874/
https://www.ncbi.nlm.nih.gov/pubmed/23634703
http://dx.doi.org/10.1186/1471-2105-14-150

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