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Article

Analysis of copy loss and gain variations in Holstein cattle autosomes using BeadChip SNPs.

BMC genomics - 29 Nov 2010

Seroussi Eyal, Glick Giora, Shirak Andrey, Yakobson Emanuel, Weller Joel I, Ezra Ephraim, Zeron Yoel

Abstract excerpt

BACKGROUND: Copy number variation (CNV) has been recently identified in human and other mammalian genomes, and there is a growing awareness of CNV's potential as a major source for heritable variation in complex traits. Genomic selection is a newly developed tool based on the estimation of breeding values for quantitative traits through the use of genome-wide genotyping of SNPs. Over 30,000 Holstein bulls have...

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Identifiers

PMID: 21114805
DOI: 10.1186/1471-2164-11-673
PMCID: PMC3091787

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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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