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Article

Genome-wide detection of copy number variations using high-density SNP genotyping platforms in Holsteins.

BMC genomics - 27 Feb 2013

Jiang Li, Jiang Jicai, Yang Jie, Liu Xuan, Wang Jiying, Wang Haifei, Ding Xiangdong, Liu Jianfeng, Zhang Qin

Abstract excerpt

BACKGROUND: Copy number variations (CNVs) are widespread in the human or animal genome and are a significant source of genetic variation, which has been demonstrated to play an important role in phenotypic diversity. Advances in technology have allowed for identification of a large number of CNVs in cattle. Comprehensive explore novel CNVs in the bovine genome would provide valuable information for functional...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 23442346
DOI: 10.1186/1471-2164-14-131
PMCID: PMC3639935

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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