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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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| Publicado no: | BMC Bioinformatics |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2017
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| Assuntos: | |
| Acesso em linha: | 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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