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Measuring DNA Copy Number Variation Using High-Density Methylation Microarrays.


ABSTRACT: Genetic and epigenetic changes drive carcinogenesis, and their integrated analysis provides insights into mechanisms of cancer development. Computational methods have been developed to measure copy number variation (CNV) from methylation array data, including ChAMP-CNV, CN450K, and, introduced here, Epicopy. Using paired single nucleotide polymorphism (SNP) and methylation array data from the public The Cancer Genome Atlas repository, we optimized CNV calling and benchmarked the performance of these methods. We optimized the thresholds of all three methods and showed comparable performance across methods. Using Epicopy as a representative analysis of Illumina450K array, we show that Illumina450K-derived CNV methods achieve a sensitivity of 0.7 and a positive predictive value of 0.75 in identifying CNVs, which is similar to results achieved when comparing competing SNP microarray platforms with each other.

SUBMITTER: Cho S 

PROVIDER: S-EPMC6479247 | biostudies-literature | 2019 Apr

REPOSITORIES: biostudies-literature

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Measuring DNA Copy Number Variation Using High-Density Methylation Microarrays.

Cho Soonweng S   Kim Hyun-Seok HS   Zeiger Martha A MA   Umbricht Christopher B CB   Cope Leslie M LM  

Journal of computational biology : a journal of computational molecular cell biology 20190221 4


Genetic and epigenetic changes drive carcinogenesis, and their integrated analysis provides insights into mechanisms of cancer development. Computational methods have been developed to measure copy number variation (CNV) from methylation array data, including ChAMP-CNV, CN450K, and, introduced here, Epicopy. Using paired single nucleotide polymorphism (SNP) and methylation array data from the public The Cancer Genome Atlas repository, we optimized CNV calling and benchmarked the performance of t  ...[more]

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