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Inference of chromosome-specific copy numbers using population haplotypes
BACKGROUND: Using microarray and sequencing platforms, a large number of copy number variations (CNVs) have been identified in humans. In practice, because our human genome is a diploid, these platforms are limited to or more accurate for detecting total copy numbers rather than chromosome-specific...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2011
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3128032/ https://www.ncbi.nlm.nih.gov/pubmed/21605463 http://dx.doi.org/10.1186/1471-2105-12-194 |