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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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Detalhes bibliográficos
Main Authors: Chu, Jen-hwa, Rogers, Angela, Ionita-Laza, Iuliana, Darvishi, Katayoon, Mills, Ryan E, Lee, Charles, Raby, Benjamin A
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3668900/
https://ncbi.nlm.nih.gov/pubmed/23656838
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-14-157
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