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Article

CNVineta: a data mining tool for large case-control copy number variation datasets.

Bioinformatics (Oxford, England) - 1 Sept 2010

Wittig Michael, Helbig Ingo, Schreiber Stefan, Franke Andre

Abstract excerpt

MOTIVATION: Copy number variation (CNV), a major contributor to human genetic variation, comprises >/= 1 kb genomic deletions and insertions. Yet, the identification of CNVs from microarray data is still hampered by high false negative and positive prediction rates due to the noisy nature of the raw data. Here, we present CNVineta, an R package for rapid data mining and visualization of CNVs in large case-control...

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Identifiers

PMID: 20605930
DOI: 10.1093/bioinformatics/btq356
PMCID: PMC2922892

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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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