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Article

Computational tools for copy number variation (CNV) detection using next-generation sequencing data: features and perspectives.

BMC bioinformatics - 1 Jan 2013

Zhao Min, Wang Qingguo, Wang Quan, Jia Peilin, Zhao Zhongming

Abstract excerpt

Copy number variation (CNV) is a prevalent form of critical genetic variation that leads to an abnormal number of copies of large genomic regions in a cell. Microarray-based comparative genome hybridization (arrayCGH) or genotyping arrays have been standard technologies to detect large regions subject to copy number changes in genomes until most recently high-resolution sequence data can be analyzed by...

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PMID: 24564169
DOI: 10.1186/1471-2105-14-S11-S1
PMCID: PMC3846878

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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