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Article

CNV-seq, a new method to detect copy number variation using high-throughput sequencing.

BMC bioinformatics - 6 Mar 2009

Xie Chao, Tammi Martti T

Abstract excerpt

BACKGROUND: DNA copy number variation (CNV) has been recognized as an important source of genetic variation. Array comparative genomic hybridization (aCGH) is commonly used for CNV detection, but the microarray platform has a number of inherent limitations. RESULTS: Here, we describe a method to...

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Identifiers

PMID: 19267900
DOI: 10.1186/1471-2105-10-80
PMCID: PMC2667514

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-19267900-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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