Zhou, Jiyun and Lu, Qin and Gui, Lin and Xu, Ruifeng and Long, Yunfei and Wang, Hongpeng (2019) MTTFsite: cross-cell type TF binding site prediction by using multi-task learning. Bioinformatics, 35 (24). pp. 5067-5077. DOI https://doi.org/10.1093/bioinformatics/btz451
Zhou, Jiyun and Lu, Qin and Gui, Lin and Xu, Ruifeng and Long, Yunfei and Wang, Hongpeng (2019) MTTFsite: cross-cell type TF binding site prediction by using multi-task learning. Bioinformatics, 35 (24). pp. 5067-5077. DOI https://doi.org/10.1093/bioinformatics/btz451
Zhou, Jiyun and Lu, Qin and Gui, Lin and Xu, Ruifeng and Long, Yunfei and Wang, Hongpeng (2019) MTTFsite: cross-cell type TF binding site prediction by using multi-task learning. Bioinformatics, 35 (24). pp. 5067-5077. DOI https://doi.org/10.1093/bioinformatics/btz451
Abstract
MOTIVATION:The prediction of transcription factor binding sites (TFBSs) is crucial for gene expression analysis. Supervised learning approaches for TFBS predictions require large amounts of labeled data. However, many TFs of certain cell types either do not have sufficient labeled data or do not have any labeled data. RESULTS:In this paper, a multi-task learning framework (called MTTFsite) is proposed to address the lack of labeled data problem by leveraging on labeled data available in cross-cell types. The proposed MTTFsite contains a shared CNN to learn common features for all cell types and a private CNN for each cell type to learn private features. The common features are aimed to help predicting TFBSs for all cell types especially those cell types that lack labeled data. MTTFsite is evaluated on 241 cell type TF pairs and compared with a baseline method without using any multi-task learning model and a fully shared multi-task model that uses only a shared CNN and do not use private CNNs. For cell types with insufficient labeled data, results show that MTTFsite performs better than the baseline method and the fully shared model on more than 89% pairs. For cell types without any labeled data, MTTFsite outperforms the baseline method and the fully shared model by more than 80 and 93% pairs, respectively. A novel gene expression prediction method (called TFChrome) using both MTTFsite and histone modification features is also presented. Results show that TFBSs predicted by MTTFsite alone can achieve good performance. When MTTFsite is combined with histone modification features, a significant 5.7% performance improvement is obtained. AVAILABILITY AND IMPLEMENTATION:The resource and executable code are freely available at http://hlt.hitsz.edu.cn/MTTFsite/ and http://www.hitsz-hlt.com:8080/MTTFsite/. SUPPLEMENTARY INFORMATION:Supplementary data are available at Bioinformatics online.
Item Type: | Article |
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Uncontrolled Keywords: | Transcription Factors; Gene Expression; Binding Sites; Protein Binding |
Divisions: | Faculty of Science and Health Faculty of Science and Health > Computer Science and Electronic Engineering, School of |
SWORD Depositor: | Unnamed user with email elements@essex.ac.uk |
Depositing User: | Unnamed user with email elements@essex.ac.uk |
Date Deposited: | 15 Dec 2020 08:49 |
Last Modified: | 30 Oct 2024 20:33 |
URI: | http://repository.essex.ac.uk/id/eprint/29362 |
Available files
Filename: MTTFsite cross-cell type TF binding site prediction by using multi-task learning.pdf
Licence: Creative Commons: Attribution-Noncommercial 3.0