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Article

Evaluation of copy number variation detection for a SNP array platform.

BMC bioinformatics - 21 Feb 2014

Zhang Xin, Du Renqian, Li Shilin, Zhang Feng, Jin Li, Wang Hongyan

Abstract excerpt

BACKGROUND: Copy Number Variations (CNVs) are usually inferred from Single Nucleotide Polymorphism (SNP) arrays by use of some software packages based on given algorithms. However, there is no clear understanding of the performance of these software packages; it is therefore difficult to select one or several software packages for CNV detection based on the SNP array platform.We selected four publicly available...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 24555668
DOI: 10.1186/1471-2105-15-50
PMCID: PMC4015297

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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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