DTi2Vec: Drug–target interaction prediction using network embedding and ensemble learning
Open accessAbstract
Drug–target interaction (DTI) prediction is a crucial step in drug discovery and repositioning as it reduces experimental validation costs if done right. Thus, developing in-silico methods to predict potential DTI has become a competitive research niche, with one of its main focuses being improving the prediction accuracy. Using machine learning (ML) models for this task, specifically network-based approaches, is effective and has shown great advantages over the other computational methods. However, ML model development involves upstream hand-crafted feature extraction and other processes that impact prediction accuracy. Thus, network-based representation learning techniques that provide automated feature extraction combined with traditional ML classifiers dealing with downstream link prediction tasks may be better-suited paradigms. Here, we present such a method, DTi2Vec, which identifies DTIs using network representation learning and ensemble learning techniques. DTi2Vec constructs the heterogeneous network, and then it automatically generates features for each drug and target using the nodes embedding technique. DTi2Vec demonstrated its ability in drug–target link prediction compared to several state-of-the-art network-based methods, using four benchmark datasets and large-scale data compiled from DrugBank. DTi2Vec showed a statistically significant increase in the prediction performances in terms of AUPR. We verified the "novel" predicted DTIs using several databases and scientific literature. DTi2Vec is a simple yet effective method that provides high DTI prediction performance while being scalable and efficient in computation, translating into a powerful drug repositioning tool.
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Graph representation learning applied to gene or cell similarity networks can impute single-cell RNA sequencing data and predict cell clusters.
“Applied to such networks, graph representation learning can impute scRNA-seq data [156, 157], predict cell clusters [157, 158], etc.”
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References 75 · Cited by 70
- Authors
- Thafar, M. A., Olayan, R. S., Albaradei, S., Bajic, V. B., Gojobori, T., Essack, M., & Gao, X.
- Affiliations
- Taif University (SA)
- The Jackson Laboratory for Genomic Medicine (US)
- King Abdulaziz University (SA)
- King Abdullah University of Science and Technology (SA)
- Corresponding author
- Essack, Magbubah
- Gao, Xin
- Venue
- Journal of Cheminformatics
- Published
- 2021-09-22
- Volume
- 13
- Issue
- 1
- Pages
- 71-71
- ISSN
- 1758-2946 (ISSN-L)
- PMC
- PMC8459562
- OpenAlex
- W3201477029
- Cited by
- 70
- References
- 75
- Citations by year
- 2026: 8 · 2025: 13 · 2024: 23 · 2023: 14 · 2022: 12
- FWCI
- 6.46
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Journal of Cheminformatics (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, other-oa)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- King Abdullah University of Science and Technology Repository (King Abdullah University of Science and Technology) (submittedVersion, other-oa)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- The Mouseion at the JAXlibrary (Jackson Laboratory) (submittedVersion, cc-by)
- Funders
- King Abdullah University of Science and Technology (FCC/1/1976-26-01, BAS/1/1606-01-01, BAS/1/1059-01-01, BAS/1/1624-01-01, FCC/1/1976-17-01)
- Topics
- Physical Sciences › Computer Science › Computational Theory and Mathematics › Computational Drug Discovery Methods
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bioinformatics and Genomic Networks
- Physical Sciences › Computer Science › Artificial Intelligence › Advanced Graph Neural Networks
- Keywords
- drug-target interaction prediction, graph embedding, ensemble learning, heterogeneous networks, link prediction, drug repurposing, network representation learning, automatic feature extraction, DrugBank
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