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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...
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| Autors principals: | , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2011
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3128032/ https://ncbi.nlm.nih.gov/pubmed/21605463 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-12-194 |
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