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COKGEN: a software for the identification of rare copy number variation from SNP microarrays.

Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing - 1 Jan 2010

Yavaş Gökhan, Koyutürk Mehmet, Ozsoyoğlu Meral, Gould Meetha P, Laframboise Thomas

Abstract excerpt

Until fairly recently, it was believed that essentially all human cells harbor two copies of each locus in the autosomal genome. However, studies have now shown that there are segments of the genome that are polymorphic with regard to genomic copy number. These copy number variations (CNVs) have...

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PMID: 19908389

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19908389-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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