Illumina error correction near highly repetitive DNA regions improves de novo genome assembly

BACKGROUND: Several standalone error correction tools have been proposed to correct sequencing errors in Illumina data in order to facilitate de novo genome assembly. However, in a recent survey, we showed that state-of-the-art assemblers often did not benefit from this pre-correction step. We found...

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Detalles Bibliográficos
Autores principales: Heydari, Mahdi, Miclotte, Giles, Van de Peer, Yves, Fostier, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6545690/
https://www.ncbi.nlm.nih.gov/pubmed/31159722
http://dx.doi.org/10.1186/s12859-019-2906-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6545690/
https://www.ncbi.nlm.nih.gov/pubmed/31159722
http://dx.doi.org/10.1186/s12859-019-2906-2

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