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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Bibliographic Details
Main Authors: Ronen, Roy, Boucher, Christina, Chitsaz, Hamidreza, Pevzner, Pavel
Format: Online
Language:English
Published: Oxford University Press 2012
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3371851/