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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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Detalles Bibliográficos
Autores principales: Castellani, Christina A, Melka, Melkaye G, Wishart, Andrea E, Locke, M Elizabeth O, Awamleh, Zain, O’Reilly, Richard L, Singh, Shiva M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4021055/
https://www.ncbi.nlm.nih.gov/pubmed/24750645
http://dx.doi.org/10.1186/1471-2105-15-114

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