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Short read alignment with populations of genomes
Summary: The increasing availability of high-throughput sequencing technologies has led to thousands of human genomes having been sequenced in the past years. Efforts such as the 1000 Genomes Project further add to the availability of human genome variation data. However, to date, there is no method...
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| Asıl Yazarlar: | , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Oxford University Press
2013
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3694645/ https://ncbi.nlm.nih.gov/pubmed/23813006 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btt215 |
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