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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: Ronen, Roy, Boucher, Christina, Chitsaz, Hamidreza, Pevzner, Pavel
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 2012
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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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