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Detecting structural variations in the human genome using next generation sequencing
Structural variations are widespread in the human genome and can serve as genetic markers in clinical and evolutionary studies. With the advances in the next-generation sequencing technology, recent methods allow for identification of structural variations with unprecedented resolution and accuracy....
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| Asıl Yazarlar: | , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Oxford University Press
2010
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3080742/ https://ncbi.nlm.nih.gov/pubmed/21216738 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bfgp/elq025 |
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