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Article

A genome-wide detection of copy number variations using SNP genotyping arrays in swine.

BMC genomics - 22 Jun 2012

Wang Jiying, Jiang Jicai, Fu Weixuan, Jiang Li, Ding Xiangdong, Liu Jian-Feng, Zhang Qin

Abstract excerpt

BACKGROUND: Copy Number Variations (CNVs) have been shown important in both normal phenotypic variability and disease susceptibility, and are increasingly accepted as another important source of genetic variation complementary to single nucleotide polymorphism (SNP). Comprehensive identification...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 22726314
DOI: 10.1186/1471-2164-13-273
PMCID: PMC3464621

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-22726314-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

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

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