Copy number variation genotyping using family information

BACKGROUND: In recent years there has been a growing interest in the role of copy number variations (CNV) in genetic diseases. Though there has been rapid development of technologies and statistical methods devoted to detection in CNVs from array data, the inherent challenges in data quality associa...

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Detalles Bibliográficos
Autores principales: Chu, Jen-hwa, Rogers, Angela, Ionita-Laza, Iuliana, Darvishi, Katayoon, Mills, Ryan E, Lee, Charles, Raby, Benjamin A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Methodology Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3668900/
https://www.ncbi.nlm.nih.gov/pubmed/23656838
http://dx.doi.org/10.1186/1471-2105-14-157

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3668900/
https://www.ncbi.nlm.nih.gov/pubmed/23656838
http://dx.doi.org/10.1186/1471-2105-14-157

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