BFC
BFC is a sequencing error corrector designed for Illumina short reads, which uses a non-greedy algorithm that maintains a speed comparable to implementations based on greedy methods. It outperforms existing tools in correcting errors and suppressing systematic sequencing errors, improving the accuracy of de novo assemblies.
Topic
DNA;Whole genome sequencing;Sequencing
Detail
Operation: Sequencing error detection
Software interface: Command-line user interface
Language: Javascript;C++;C
License: MIT License
Cost: Free
Version name: v1
Credit: NHGRI, NIH
Input: -
Output: -
Contact: Charlotte M Deane deane@stats.ox.ac.uk
Collection: -
Maturity: Emerging
Publications
- BFC: correcting Illumina sequencing errors.
- Li H. BFC: correcting Illumina sequencing errors. BFC: correcting Illumina sequencing errors. 2015; 31:2885-7. doi: 10.1093/bioinformatics/btv290
- https://doi.org/10.1093/bioinformatics/btv290
- PMID: 25953801
- PMC: PMC4635656
Download and documentation
Source: https://github.com/lh3/bfc/tags
Documentation: https://github.com/lh3/bfc/blob/master/README.md
Home page: https://github.com/lh3/bfc
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