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Article

Optimizing copy number variation analysis using genome-wide short sequence oligonucleotide arrays.

Nucleic acids research - 1 Jun 2010

Oldridge Derek A, Banerjee Samprit, Setlur Sunita R, Sboner Andrea, Demichelis Francesca

Abstract excerpt

The detection of copy number variants (CNV) by array-based platforms provides valuable insight into understanding human diversity. However, suboptimal study design and data processing negatively affect CNV assessment. We quantitatively evaluate their impact when short-sequence oligonucleotide arr...

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Identifiers

PMID: 20156996
DOI: 10.1093/nar/gkq073
PMCID: PMC2879534

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20156996-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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