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Article

An accurate method for quantifying and analyzing copy number variation in porcine KIT by an oligonucleotide ligation assay.

BMC genetics - 23 Nov 2007

Seo Bo-Young, Park Eung-Woo, Ahn Sung-Jin, Lee Sang-Ho, Kim Jae-Hwan, Im Hyun-Tae, Lee Jun-Heon, Cho In-Cheol, Kong Il-Keun, Jeon Jin-Tae

Abstract excerpt

BACKGROUND: Aside from single nucleotide polymorphisms, copy number variations (CNVs) are the most important factors in susceptibility to genetic disorders because they affect expression levels of genes. In previous studies, pyrosequencing, mini-sequencing, real-time PCR, invader assays and other techniques have been used to detect CNVs. However, the higher the copy number in a genome, the more difficult it is to...

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PMID: 18036219
DOI: 10.1186/1471-2156-8-81
PMCID: PMC2228321

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KIT
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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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