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High-throughput sequencing reveals extensive variation in human-specific L1 content in individual human genomes
Using high-throughput sequencing, we devised a technique to determine the insertion sites of virtually all members of the human-specific L1 retrotransposon family in any human genome. Using diagnostic nucleotides, we were able to locate the approximately 800 L1Hs copies corresponding specifically to...
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| Asıl Yazarlar: | , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Cold Spring Harbor Laboratory Press
2010
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2928504/ https://ncbi.nlm.nih.gov/pubmed/20488934 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.106419.110 |
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