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Mapping short DNA sequencing reads and calling variants using mapping quality scores
New sequencing technologies promise a new era in the use of DNA sequence. However, some of these technologies produce very short reads, typically of a few tens of base pairs, and to use these reads effectively requires new algorithms and software. In particular, there is a major issue in efficiently...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Cold Spring Harbor Laboratory Press
2008
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2577856/ https://ncbi.nlm.nih.gov/pubmed/18714091 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.078212.108 |
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