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Article

Genome-wide identification of copy number variation using high-density single-nucleotide polymorphism array in Japanese Black cattle.

BMC genetics - 25 Jan 2016

Sasaki Shinji, Watanabe Toshio, Nishimura Shota, Sugimoto Yoshikazu

Abstract excerpt

BACKGROUND: Copy number variation (CNV) is an important source of genetic variability associated with phenotypic variation and disease susceptibility. Comprehensive genome-wide CNV maps provide valuable information for genetic and functional studies. To identify CNV in Japanese Black cattle, we performed a genome-wide autosomal screen using genomic data from 1,481 animals analyzed with the Illumina Bovine...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 26809925
DOI: 10.1186/s12863-016-0335-z
PMCID: PMC4727303

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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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