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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,...
Autores principales: | Castellani, Christina A, Melka, Melkaye G, Wishart, Andrea E, Locke, M Elizabeth O, Awamleh, Zain, O’Reilly, Richard L, Singh, Shiva M |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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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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