BFC: correcting Illumina sequencing errors
- PMID: 25953801
- PMCID: PMC4635656
- DOI: 10.1093/bioinformatics/btv290
BFC: correcting Illumina sequencing errors
Abstract
BFC is a free, fast and easy-to-use sequencing error corrector designed for Illumina short reads. It uses a non-greedy algorithm but still maintains a speed comparable to implementations based on greedy methods. In evaluations on real data, BFC appears to correct more errors with fewer overcorrections in comparison to existing tools. It particularly does well in suppressing systematic sequencing errors, which helps to improve the base accuracy of de novo assemblies.
Availability and implementation: https://github.com/lh3/bfc
Contact: hengli@broadinstitute.org
Supplementary information: Supplementary data are available at Bioinformatics online.
© The Author 2015. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.
References
-
- Chaisson M., et al. (2004) Fragment assembly with short reads. Bioinformatics, 20, 2067–2074. - PubMed
-
- Deorowicz S., et al. (2015) KMC 2: Fast and resource-frugal k-mer counting. Bioinformatics, 31, 1569–1576. - PubMed
-
- Garrison E., Marth G. (2012) Haplotype-based variant detection from short-read sequencing. arXiv:1207.3907.
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