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Article

CNAnova: a new approach for finding recurrent copy number abnormalities in cancer SNP microarray data.

Bioinformatics (Oxford, England) - 1 Jun 2010

Ivakhno Sergii, Tavaré Simon

Abstract excerpt

MOTIVATION: The current generation of single nucleotide polymorphism (SNP) arrays allows measurement of copy number aberrations (CNAs) in cancer at more than one million locations in the genome in hundreds of tumour samples. Most research has focused on single-sample CNA discovery, the so-called segmentation problem. The availability of high-density, large sample-size SNP array datasets makes the identification...

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Identifiers

PMID: 20403815
DOI: 10.1093/bioinformatics/btq145

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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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CNAnova: a new approach for finding recurrent copy number abnormalities in cancer SNP microarray data.PMID 20403815Read ↗

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