Biological relevance of CNV calling methods using familial relatedness including monozygotic twins
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, or CGH arra...
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Veröffentlicht in: | BMC bioinformatics 2014-04, Vol.15 (1), p.114-114, Article 114 |
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