Prediction of a deletion copy number variant by a dense SNP panel

BACKGROUND: A newly recognized type of genetic variation, Copy Number Variation (CNV), is detected in mammalian genomes, e.g. the cattle genome. This form of variation can potentially cause phenotypic variation. Our objective was to determine whether dense SNP (single nucleotide polymorphisms) panel...

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Detalles Bibliográficos
Autores principales: Kadri, Naveen K, Koks, Patrick D, Meuwissen, Theo H E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3366870/
https://www.ncbi.nlm.nih.gov/pubmed/22443295
http://dx.doi.org/10.1186/1297-9686-44-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3366870/
https://www.ncbi.nlm.nih.gov/pubmed/22443295
http://dx.doi.org/10.1186/1297-9686-44-7

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