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Article

Genome-wide copy number variant discovery in dogs using the CanineHD genotyping array.

BMC genomics - 19 Mar 2014

Molin Anna-Maja, Berglund Jonas, Webster Matthew T, Lindblad-Toh Kerstin

Abstract excerpt

BACKGROUND: Substantial contribution to phenotypic diversity is accounted for by copy number variants (CNV). In human, as well as other species, the effect of CNVs range from benign to directly disease-causing which motivates the continued investigations of CNVs. Previous canine genome-wide screenings for CNVs have been performed using high-resolution comparative genomic hybridisation arrays which have...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 24640994
DOI: 10.1186/1471-2164-15-210
PMCID: PMC4234435

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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