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Article

Genome-wide copy number variant analysis reveals variants associated with 10 diverse production traits in Holstein cattle.

BMC genomics - 2 May 2018

Zhou Yang, Connor Erin E, Wiggans George R, Lu Yongfang, Tempelman Robert J, Schroeder Steven G, Chen Hong, Liu George E

Abstract excerpt

BACKGROUND: Copy number variation (CNV) is an important type of genetic variation contributing to phenotypic differences among mammals and may serve as an alternative molecular marker to single nucleotide polymorphism (SNP) for genome-wide association study (GWAS). Recently, GWAS analysis using CNV has been applied in livestock, although few studies have focused on Holstein cattle. RESULTS: We describe 191 CNV...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 29716533
DOI: 10.1186/s12864-018-4699-5
PMCID: PMC5930521

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RXFP4

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

Source receipt: pubmed, retrieved 7 Sept 2026.

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