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Article

Application of Nexus copy number software for CNV detection and analysis.

Current protocols in human genetics - 1 Apr 2010

Darvishi Katayoon

Abstract excerpt

Among human structural genomic variation, copy number variants (CNVs) are the most frequently known component, comprised of gains/losses of DNA segments that are generally 1 kb in length or longer. Array-based comparative genomic hybridization (aCGH) has emerged as a powerful tool for detecting genomic copy number variants (CNVs). With the rapid increase in the density of array technology and with the adaptation...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 20373515
DOI: 10.1002/0471142905.hg0414s65

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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