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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Bibliografske podrobnosti
Main Authors: Chu, Jen-hwa, Rogers, Angela, Ionita-Laza, Iuliana, Darvishi, Katayoon, Mills, Ryan E, Lee, Charles, Raby, Benjamin A
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2013
Teme:
Methodology Article
Online dostop: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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