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...

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Detalles Bibliográficos
Autores principales: Molin, Anna-Maja, Berglund, Jonas, Webster, Matthew T, Lindblad-Toh, Kerstin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research Article
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

Internet

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

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