The DOI matches its Crossref record; 100 of the 100 references it cites were found in a registry or an index.
BioSeq-Analysis: a platform for DNA, RNA and protein sequence analysis based on machine learning approaches
Abstract
With the avalanche of biological sequences generated in the post-genomic age, one of the most challenging problems is how to computationally analyze their structures and functions. Machine learning techniques are playing key roles in this field. Typically, predictors based on machine learning techniques contain three main steps: feature extraction, predictor construction and performance evaluation. Although several Web servers and stand-alone tools have been developed to facilitate the biological sequence analysis, they only focus on individual step. In this regard, in this study a powerful Web server called BioSeq-Analysis (http://bioinformatics.hitsz.edu.cn/BioSeq-Analysis/) has been proposed to automatically complete the three main steps for constructing a predictor. The user only needs to upload the benchmark data set. BioSeq-Analysis can generate the optimized predictor based on the benchmark data set, and the performance measures can be reported as well. Furthermore, to maximize user’s convenience, its stand-alone program was also released, which can be downloaded from http://bioinformatics.hitsz.edu.cn/BioSeq-Analysis/download/, and can be directly run on Windows, Linux and UNIX. Applied to three sequence analysis tasks, experimental results showed that the predictors generated by BioSeq-Analysis even outperformed some state-of-the-art methods. It is anticipated that BioSeq-Analysis will become a useful tool for biological sequence analysis.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
1 retracted
Recombination spot identification Based on gapped k-mers
Wang, R., Xu, Y. D., & Liu, B. (2016) · Scientific Reports · doi:10.1038/srep23934 · Cited by 29
Self-citationRetractedLeCun, Y., Bengio, Y., & Hinton, G. (2015) · Nature · doi:10.1038/nature14539 · Cited by 84,126
Scikit-learn: Machine Learning in Python
Pedregosa, F., Varoquaux, G., Gramfort, A., Michel, V., Thirion, B., Grisel, O., Blondel, M., Müller, A., Nothman, J., Louppe, G., et al. (2012) · arXiv · doi:10.48550/arxiv.1201.0490 · Cited by 71,016
Cortes, C., & Vapnik, V. (1995) · Machine Learning · doi:10.1007/bf00994018 · Cited by 59,421
LIBSVM: A library for support vector machines
Chang, C.-C., & Lin, C.-J. (2011) · ACM Transactions on Intelligent Systems and Technology · doi:10.1145/1961189.1961199 · Cited by 40,918
An Introduction to the Bootstrap
Efron, B., & Tibshirani, R. J. (1994) · doi:10.1201/9780429246593 · Cited by 40,500
Berman, H. M. (2000) · Nucleic Acids Research · doi:10.1093/nar/28.1.235 · Cited by 40,196
An introduction to ROC analysis
Fawcett, T. (2006) · Pattern Recognition Letters · doi:10.1016/j.patrec.2005.10.010 · Cited by 21,879
The SWISS-PROT protein sequence data bank and its supplement TrEMBL
Bairoch, A., & Apweiler, R. (1997) · Nucleic Acids Research · doi:10.1093/nar/25.1.31 · Cited by 3,587
The SWISS-PROT protein sequence data bank and its supplement TrEMBL in 1998
Bairoch, A. (1998) · Nucleic Acids Research · doi:10.1093/nar/26.1.38 · Cited by 3,280
Research works printed but not linked: 5
- Zhang, 2003, Splice site prediction with quadratic discriminant analysis using diversity measure, Nucleic Acids Res, 31, 6214, 10.1093/nar/gkg805 · doi:10.1093/nar/gkg805
- Lu, 2008, Prediction for human transcription start site using diversity measure with quadratic discriminant, Bioinformation, 2, 316, 10.6026/97320630002316 · doi:10.6026/97320630002316
- Liu, 2016, iRSpot-DACC: a computational predictor for recombination hot/cold spots identification based on dinucleotide-based auto-cross covariance, Sci Rep, 6, 33483, 10.1038/srep33483 · doi:10.1038/srep33483
- Liu, 2012, Using amino acid physicochemical distance transformation for fast protein remote homology detection, PLoS One, 7, e46633, 10.1371/journal.pone.0046633 · doi:10.1371/journal.pone.0046633
- Webb-Robertson, 2010, Physicochemical property distributions for accurate and rapid pairwise protein homology detection, BMC Bioinformatics, 11, 145, 10.1186/1471-2105-11-145 · doi:10.1186/1471-2105-11-145
Cited by
Wei, L., Chen, H., & Su, R. (2018) · Molecular Therapy Nucleic Acids · doi:10.1016/j.omtn.2018.07.004 · Cited by 179
Amino acid encoding methods for protein sequences: a comprehensive review and assessment
Jing, X., Dong, Q., Hong, D., & Lu, R. (2020) · IEEE/ACM Transactions on Computational Biology and Bioinformatics · doi:10.1109/tcbb.2019.2911677 · Cited by 97
SeqSVM: A Sequence-Based Support Vector Machine Method for Identifying Antioxidant Proteins
Xu, L., Liang, G., Shi, S., & Liao, C. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19061773 · Cited by 95
Yuan, H., Yu, K., Xie, F., Liu, M., & Sun, S. (2024) · Medicine Advances · doi:10.1002/med4.75 · Cited by 61
Metadata
- Authors
- Liu, B.
- Venue
- Briefings in Bioinformatics
- Publisher
- Oxford University Press (OUP)
- Published
- 2017-12-19
- Volume
- 20
- Issue
- 4
- Pages
- 1280-1294
- ISSN
- 1467-5463 (ISSN-L)
- 1477-4054
- OpenAlex
- W2780936345
- Cited by
- 322
- References
- 100
- FWCI
- 16.01
- Type
- journal article
- Language
- en
- Open access
- closed
- Funders
- National Natural Science Foundation of China (61672184 and 61732012)
- Natural Science Foundation of Guangdong Province (2014A030313695)
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: BioSeq-Analysis: a platform for DNA, RNA and protein sequence analysis based on machine learning approaches. https://app.cochat.ai/papers/10.1093/bib/bbx165
- The paper
- Liu, B. (2019). BioSeq-Analysis: a platform for DNA, RNA and protein sequence analysis based on machine learning approaches. Briefings in Bioinformatics. https://doi.org/10.1093/bib/bbx165
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.