Biological relevance of CNV calling methods using familial relatedness including monozygotic twins

BACKGROUND: Studies involving the analysis of structural variation including Copy Number Variation (CNV) have recently exploded in the literature. Furthermore, CNVs have been associated with a number of complex diseases and neurodevelopmental disorders. Common methods for CNV detection use SNP, CNV,...

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Detalhes bibliográficos
Main Authors: Castellani, Christina A, Melka, Melkaye G, Wishart, Andrea E, Locke, M Elizabeth O, Awamleh, Zain, O’Reilly, Richard L, Singh, Shiva M
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2014
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4021055/
https://ncbi.nlm.nih.gov/pubmed/24750645
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-15-114
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