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• W2014010495 abstract "Recent advances in high-throughout sequencing technologies have made it possible to accurately assign copy number (CN) at CN variable loci. However, current analytic methods often perform poorly in regions in which complex CN variation is observed. Here we report the development of a read depth-based approach, CNVrd2, for investigation of CN variation using high-throughput sequencing data. This methodology was developed using data from the 1000 Genomes Project from the CCL3L1 locus, and tested using data from the DEFB103A locus. In both cases, samples were selected for which paralog ratio test data were also available for comparison. The CNVrd2 method first uses observed read-count ratios to refine segmentation results in one population. Then a linear regression model is applied to adjust the results across multiple populations, in combination with a Bayesian normal mixture model to cluster segmentation scores into groups for individual CN counts. The performance of CNVrd2 was compared to that of two other read depth-based methods (CNVnator, cn.mops) at the CCL3L1 and DEFB103A loci. The highest concordance with the paralog ratio test method was observed for CNVrd2 (77.8/90.4% for CNVrd2, 36.7/4.8% for cn.mops and 7.2/1% for CNVnator at CCL3L1 and DEF103A). CNVrd2 is available as an R package as part of the Bioconductor project: http://www.bioconductor.org/packages/release/bioc/html/CNVrd2.html." @default.
• W2014010495 created "2016-06-24" @default.
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• W2014010495 date "2014-08-01" @default.
• W2014010495 modified "2023-10-11" @default.
• W2014010495 title "The CNVrd2 package: measurement of copy number at complex loci using high-throughput sequencing data" @default.
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• W2014010495 doi "https://doi.org/10.3389/fgene.2014.00248" @default.
• W2014010495 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4117933" @default.
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