SpliceFinder : ab initio prediction of splice sites using convolutional neural network
Research output: Journal Publications and Reviews › RGC 21 - Publication in refereed journal › peer-review
Author(s)
Related Research Unit(s)
Detail(s)
Original language | English |
---|---|
Article number | 652 |
Journal / Publication | BMC Bioinformatics |
Volume | 20 |
Issue number | Supp. 23 |
Online published | 27 Dec 2019 |
Publication status | Published - 2019 |
Conference
Title | 30th International Conference on Genome Informatics (GIW 2019) |
---|---|
Location | University of Sydney |
Place | Australia |
City | Sydney |
Period | 9 - 12 December 2019 |
Link(s)
DOI | DOI |
---|---|
Attachment(s) | Documents
Publisher's Copyright Statement
|
Link to Scopus | https://www.scopus.com/record/display.uri?eid=2-s2.0-85077275196&origin=recordpage |
Permanent Link | https://scholars.cityu.edu.hk/en/publications/publication(986865cc-e57b-4ee9-b2c0-ba2fa04ca999).html |
Abstract
Background: Identifying splice sites is a necessary step to analyze the location and structure of genes. Two dinucleotides, GT and AG, are highly frequent on splice sites, and many other patterns are also on splice sites with important biological functions. Meanwhile, the dinucleotides occur frequently at the sequences without splice sites, which makes the prediction prone to generate false positives. Most existing tools select all the sequences with the two dimers and then focus on distinguishing the true splice sites from those pseudo ones. Such an approach will lead to a decrease in false positives; however, it will result in non-canonical splice sites missing. Result: We have designed SpliceFinder based on convolutional neural network (CNN) to predict splice sites. To achieve the ab initio prediction, we used human genomic data to train our neural network. An iterative approach is adopted to reconstruct the dataset, which tackles the data unbalance problem and forces the model to learn more features of splice sites. The proposed CNN obtains the classification accuracy of 90.25%, which is 10% higher than the existing algorithms. The method outperforms other existing methods in terms of area under receiver operating characteristics (AUC), recall, precision, and F1 score. Furthermore, SpliceFinder can find the exact position of splice sites on long genomic sequences with a sliding window. Compared with other state-of-the-art splice site prediction tools, SpliceFinder generates results in about half lower false positive while keeping recall higher than 0.8. Also, SpliceFinder captures the non-canonical splice sites. In addition, SpliceFinder performs well on the genomic sequences of Drosophila melanogaster, Mus musculus, Rattus, and Danio rerio without retraining. Conclusion: Based on CNN, we have proposed a new ab initio splice site prediction tool, SpliceFinder, which generates less false positives and can detect non-canonical splice sites. Additionally, SpliceFinder is transferable to other species without retraining. The source code and additional materials are available at https://gitlab.deepomics.org/wangruohan/SpliceFinder.
Research Area(s)
- Canonical and non-canonical splice sites, Convolutional neural network, Splice site prediction
Citation Format(s)
SpliceFinder: ab initio prediction of splice sites using convolutional neural network. / Wang, Ruohan; Wang, Zishuai; Wang, Jianping et al.
In: BMC Bioinformatics, Vol. 20, No. Supp. 23, 652, 2019.
In: BMC Bioinformatics, Vol. 20, No. Supp. 23, 652, 2019.
Research output: Journal Publications and Reviews › RGC 21 - Publication in refereed journal › peer-review
Download Statistics
No data available