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Genome-wide copy number variant discovery in dogs using the CanineHD genotyping array
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 screenin...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2014
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4234435/ https://www.ncbi.nlm.nih.gov/pubmed/24640994 http://dx.doi.org/10.1186/1471-2164-15-210 |