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17/03/2014 · Detection of DNA copy number aberrations by shallow whole-genome sequencing (WGS) faces many challenges, including lack of completion and errors in the human reference genome, repetitive sequences, polymorphisms, variable sample quality, and biases in the sequencing procedures.



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The revolutionary CNV File Analysis Tool™ scans, analyzes, and reports back every detail about your CNV file. Our patent-pending algorithm quickly analyzes your file, and within moments, presents this information to you in an elegant, easy-to-read format.†

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17/03/2014 · Detection of DNA copy number aberrations by shallow whole-genome sequencing (WGS) faces many challenges, including lack of completion and errors in the human reference genome, repetitive sequences, polymorphisms, variable sample quality, and biases in the sequencing procedures.

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17/03/2014 · Detection of DNA copy number aberrations by shallow whole-genome sequencing (WGS) faces many challenges, including lack of completion and errors in the human reference genome, repetitive sequences, polymorphisms, variable sample quality, and biases in the sequencing procedures.

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The OncoScan CNV Assay is a whole-genome copy number microarray-based assay that enables the detection of relevant copy number variations (CNVs) such as copy number gain and loss, loss of heterozygosity (LOH), copy neutral loss of heterozygosity (cnLOH), ploidy, allele specific changes, break point

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Copy Number Variation (CNV) detection in whole exome sequencing data for Mendelian disorders Peng Zhang, Hua Ling, Elizabeth Pugh, Kurt Hetrick, Dane …

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cn.mops Mixture of Poissons for CNV detection in NGS data

The Copy Number Variant (CNV) module of SFARI Gene is a comprehensive, up-to-date collection of all known CNVs that have been associated with ASD.

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An Overview of Illumina’s DNA Analysis Products – From Genotyping to CNV Jennifer Stone, PhD Associate Product Manager – DNA Analysis Products

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PDF Copy number variants (CNV) are a potentially important component of the genetic contribution to risk of common complex diseases. Analysis of the association between CNVs and disease requires

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RNA-Seq was conducted on skin tissue harvested in the basal state and from the wound site on days 1, 4, and 14 post-injury. RNA-Seq and gene ontology (GO) analyses were conducted using Hypergeometric Optimization of Motif EnRichment (HOMER) and Database for Annotation, Visualization and Integrated Discovery (DAVID).

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