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An Algorithm for Inferring Complex Haplotypes in a Region of Copy-Number Variation
Recent studies have extensively examined the large-scale genetic variants in the human genome known as copy-number variations (CNVs), and the universality of CNVs in normal individuals, along with their functional importance, has been increasingly recognized. However, the absence of a method to accu...
Gorde:
| Egile Nagusiak: | , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Elsevier
2008
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2495074/ https://ncbi.nlm.nih.gov/pubmed/18639202 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2008.06.021 |
| Etiketak: |
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