The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Musket: a multistage k-mer spectrum-based error corrector for Illumina sequence data
Abstract
Motivation: The imperfect sequence data produced by next-generation sequencing technologies have motivated the development of a number of short-read error correctors in recent years. The majority of methods focus on the correction of substitution errors, which are the dominant error source in data produced by Illumina sequencing technology. Existing tools either score high in terms of recall or precision but not consistently high in terms of both measures. Results: In this article, we present Musket, an efficient multistage k-mer-based corrector for Illumina short-read data. We use the k-mer spectrum approach and introduce three correction techniques in a multistage workflow: two-sided conservative correction, one-sided aggressive correction and voting-based refinement. Our performance evaluation results, in terms of correction quality and de novo genome assembly measures, reveal that Musket is consistently one of the top performing correctors. In addition, Musket is multi-threaded using a master–slave model and demonstrates superior parallel scalability compared with all other evaluated correctors as well as a highly competitive overall execution time. Availability: Musket is available at http://musket.sourceforge.net. Contact: liuy@uni-mainz.de or bertil.schmidt@uni-mainz.de Supplementary information: Supplementary data are available at Bioinformatics online.
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Cites
Base-Calling of Automated Sequencer Traces Using Phred. II. Error Probabilities
Ewing, B., & Green, P. (1998) · Genome Research · doi:10.1101/gr.8.3.186 · Cited by 5,439
De novo assembly of human genomes with massively parallel short read sequencing
Li, R., Zhu, H., Ruan, J., Qian, W., Fang, X., Shi, Z., Li, Y., Li, S., Shan, G., Kristiansen, K., et al. (2010) · Genome Research · doi:10.1101/gr.097261.109 · Cited by 2,926
The sequence and de novo assembly of the giant panda genome
Li, R., Fan, W., Tian, G., Zhu, H., He, L., Cai, J., Huang, Q., Cai, Q., Li, B., Bai, Y., et al. (2010) · Nature · doi:10.1038/nature08696 · Cited by 1,180
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Domestication and Divergence of Saccharomyces cerevisiae Beer Yeasts
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Denoising DNA deep sequencing data—high-throughput sequencing errors and their correction
Laehnemann, D., Borkhardt, A., & McHardy, A. C. (2016) · Briefings in Bioinformatics · doi:10.1093/bib/bbv029 · Cited by 296
Lighter: fast and memory-efficient sequencing error correction without counting
Song, L., Florea, L., & Langmead, B. (2014) · Genome Biology · doi:10.1186/preaccept-9663167051308943 · Cited by 258
Analysis of plant microbe interactions in the era of next generation sequencing technologies
Knief, C. (2014) · Frontiers in Plant Science · doi:10.3389/fpls.2014.00216 · Cited by 253
A survey of k-mer methods and applications in bioinformatics
Moeckel, C., Mareboina, M., Konnaris, M. A., Chan, C. S. Y., Mouratidis, I., Montgomery, A., Chantzi, N., Pavlopoulos, G. A., & Georgakopoulos-Soares, I. (2024) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2024.05.025 · Cited by 131
“In terms of the first peak, k-mer spectrum-based algorithms have been developed to identify and remove sequencing read errors based on the infrequency of these k-mers [52 – 54].”
BackgroundMethod
Metadata
- Authors
- Liu, Y., Schröder, J., & Schmidt, B.
- Venue
- Bioinformatics
- Publisher
- Oxford University Press (OUP)
- Published
- 2012-11-29
- Volume
- 29
- Issue
- 3
- Pages
- 308-315
- ISSN
- 1367-4803 (ISSN-L)
- 1367-4811
- OpenAlex
- W2014099509
- Cited by
- 287
- References
- 3
- FWCI
- 6.39
- Type
- journal article
- Language
- en
- Open access
- closed
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