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EC: an efficient error correction algorithm for short reads
BACKGROUND: In highly parallel next-generation sequencing (NGS) techniques millions to billions of short reads are produced from a genomic sequence in a single run. Due to the limitation of the NGS technologies, there could be errors in the reads. The error rate of the reads can be reduced with trim...
Uloženo v:
| Vydáno v: | BMC Bioinformatics |
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| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2015
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4674864/ https://ncbi.nlm.nih.gov/pubmed/26678663 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-16-S17-S2 |
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