Evaluation of the impact of Illumina error correction tools on de novo genome assembly

BACKGROUND: Recently, many standalone applications have been proposed to correct sequencing errors in Illumina data. The key idea is that downstream analysis tools such as de novo genome assemblers benefit from a reduced error rate in the input data. Surprisingly, a systematic validation of this ass...

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Detaylı Bibliyografya
Yayımlandı:BMC Bioinformatics
Asıl Yazarlar: Heydari, Mahdi, Miclotte, Giles, Demeester, Piet, Van de Peer, Yves, Fostier, Jan
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2017
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5563063/
https://ncbi.nlm.nih.gov/pubmed/28821237
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-017-1784-8
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