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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...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2012
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| 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 |