misFinder: identify mis-assemblies in an unbiased manner using reference and paired-end reads

BACKGROUND: Because of the short read length of high throughput sequencing data, assembly errors are introduced in genome assembly, which may have adverse impact to the downstream data analysis. Several tools have been developed to eliminate these errors by either 1) comparing the assembled sequence...

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Detalhes bibliográficos
Publicado no:BMC Bioinformatics
Main Authors: Zhu, Xiao, Leung, Henry C. M., Wang, Rongjie, Chin, Francis Y. L., Yiu, Siu Ming, Quan, Guangri, Li, Yajie, Zhang, Rui, Jiang, Qinghua, Liu, Bo, Dong, Yucui, Zhou, Guohui, Wang, Yadong
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2015
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4647709/
https://ncbi.nlm.nih.gov/pubmed/26573684
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-015-0818-3
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