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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Veröffentlicht in:BMC Bioinformatics
Hauptverfasser: 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
Format: Artigo
Sprache:Inglês
Veröffentlicht: BioMed Central 2015
Schlagworte:
Research Article
Online Zugang: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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