Inference of chromosome-specific copy numbers using population haplotypes
<p>Abstract</p> <p>Background</p> <p>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...
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| Asıl Yazarlar: | , |
|---|---|
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BMC
2011-05-01
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| Seri Bilgileri: | BMC Bioinformatics |
| Online Erişim: | http://www.biomedcentral.com/1471-2105/12/194 |
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