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SEQuel: improving the accuracy of genome assemblies
Motivation: Assemblies of next-generation sequencing (NGS) data, although accurate, still contain a substantial number of errors that need to be corrected after the assembly process. We develop SEQuel, a tool that corrects errors (i.e. insertions, deletions and substitution errors) in the assembled...
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| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2012
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3371851/ https://ncbi.nlm.nih.gov/pubmed/22689760 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/bts219 |
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