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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4647709/
https://www.ncbi.nlm.nih.gov/pubmed/26573684
http://dx.doi.org/10.1186/s12859-015-0818-3

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