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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...
Tallennettuna:
| Julkaisussa: | BMC Genomics |
|---|---|
| Päätekijät: | , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2014
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4234435/ https://ncbi.nlm.nih.gov/pubmed/24640994 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-15-210 |
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