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Article

CONAN: copy number variation analysis software for genome-wide association studies.

BMC bioinformatics - 14 Jun 2010

Forer Lukas, Schönherr Sebastian, Weissensteiner Hansi, Haider Florian, Kluckner Thomas, Gieger Christian, Wichmann Heinz-Erich, Specht Günther, Kronenberg Florian, Kloss-Brandstätter Anita

Abstract excerpt

BACKGROUND: Genome-wide association studies (GWAS) based on single nucleotide polymorphisms (SNPs) revolutionized our perception of the genetic regulation of complex traits and diseases. Copy number variations (CNVs) promise to shed additional light on the genetic basis of monogenic as well as complex diseases and phenotypes. Indeed, the number of detected associations between CNVs and certain phenotypes are...

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Identifiers

PMID: 20546565
DOI: 10.1186/1471-2105-11-318
PMCID: PMC2894823

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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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