Evidence map›Paper›PMID 42584520›Full record

ArticleMolecular diversity2026

Multimodal deep learning with a joint uncertainty quantification scheme for drug-target interaction prediction.

Xingyu Xu, Huilin Xie, Yun Chen

Abstract read
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In one paragraph

Article in Molecular diversity, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Xingyu XuSchool of Mathematics and Computational Science, Xiangtan University, Xiangtan, 411105, Hunan, China.
Huilin XieSchool of Mathematics and Computational Science, Xiangtan University, Xiangtan, 411105, Hunan, China.
Yun ChenSchool of Mathematics and Computational Science, Xiangtan University, Xiangtan, 411105, Hunan, China. cheny@xtu.edu.cn.

Funding

National Natural Science Foundation of China 62388101; 62371476Natural Science Foundation of Hunan Province 2022JJ40419Youth Project of Hunan Provincial Department of Education 24B0176
6 · The paper itself

Abstract

AI-driven prediction of drug-target interaction (DTI) has emerged as a critical component in modern drug discovery and development. However, this approach is constrained by model and data uncertainties, which substantially affect its reliability and accuracy in DTI prediction. To overcome these limitations, we introduce EUQTri-DTI, a novel evidence-guided uncertainty quantification-based multimodal deep learning framework for DTI prediction. Specifically, EUQTri-DTI is designed to integrate three modality-specific networks to encode 1D protein sequences, 2D molecular images, and 3D drug structures. Here, a bidirectional cross-attention mechanism is employed to facilitate information exchange between different modalities. Additionally, we develop a joint uncertainty quantification scheme by calculating the weight summation of evidential uncertainty and prediction entropy from the aforementioned output, enabling a more comprehensive and nuanced assessment of uncertainties. Experiments are presented to demonstrate that EUQTri-DTI achieves stable and competitive performance through multiple evaluation metrics on three benchmark datasets, compared to baseline and state-of-the-art methods. Specifically, EUQTri-DTI achieves ROC-AUC and PR-AUC values of 85.28% and 84.53% on DrugBank, 93.45% and 83.02% on KIBA, and 92.41% and 85.32% on Davis, respectively. Moreover, the uncertainty analyses indicate that misclassified samples generally exhibit higher uncertainty, supporting sample-level confidence assessment and reliability-aware decision making. Overall, EUQTri-DTI combines competitive predictive performance with sample-level reliability assessment and shows potential for uncertainty-aware virtual screening.

Indexed as

Drug-target interactionEntropyEvidenceMultiple modalitiesNeural networkUncertainty quantification

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.