Evidence map›Paper›PMID 41985062›Full record

ArticleBriefings in bioinformatics2026

MELGene: knowledge-enhanced multimodel ensemble learning for disease-gene association prediction.

Haoyu Tian, Kuo Yang, Zeyu Liu, Hong Gao, Jian Yu, Lei Zhang, Xuezhong Zhou

Abstract read
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Haoyu TianBeijing Key Lab of Traffic Data Analysis and Mining, School of Computer Science & Technology, Beijing Jiaotong University, No. 3 Shangyuancun, Haidian District, Beijing, 100044, China.
Kuo YangBeijing Key Lab of Traffic Data Analysis and Mining, School of Computer Science & Technology, Beijing Jiaotong University, No. 3 Shangyuancun, Haidian District, Beijing, 100044, China.
Zeyu LiuBeijing Key Lab of Traffic Data Analysis and Mining, School of Computer Science & Technology, Beijing Jiaotong University, No. 3 Shangyuancun, Haidian District, Beijing, 100044, China.
Hong GaoBeijing Key Lab of Traffic Data Analysis and Mining, School of Computer Science & Technology, Beijing Jiaotong University, No. 3 Shangyuancun, Haidian District, Beijing, 100044, China.
Jian YuBeijing Key Lab of Traffic Data Analysis and Mining, School of Computer Science & Technology, Beijing Jiaotong University, No. 3 Shangyuancun, Haidian District, Beijing, 100044, China.
Lei ZhangNational Data Center of Traditional Chinese Medicine, China Academy of Chinese Medical Sciences, No. 16, Nanxiao street, Dongzhimen, Dongcheng District, Beijing, 100700, China.
Xuezhong ZhouBeijing Key Lab of Traffic Data Analysis and Mining, School of Computer Science & Technology, Beijing Jiaotong University, No. 3 Shangyuancun, Haidian District, Beijing, 100044, China.

Funding

Fundamental Research Funds for the Central Universities 2025JBMC002Fundamental Research Funds for the Central Universities 2025JBZX064National Natural Science Foundation of China 82374302National Natural Science Foundation of China 82374624National Natural Science Foundation of China U23B2062Natural Science Foundation of Beijing L232033Prevention and Control of Emerging and Major Infectious Diseases-National Science and Technology Major Project 2025ZD01903102Prevention and Control of Emerging and Major Infectious Diseases-National Science and Technology Major Project 2026ZD0555105Prevention and Control of Emerging and Major Infectious Diseases-National Science and Technology Major Project 2026ZD0555106
6 · The paper itself

Abstract

Disease-gene prediction (DGP) plays a pivotal role in understanding the genetic underpinnings of various diseases, offering insights for disease diagnosis, treatment, and prevention. Accurate identification of disease-related genes can enhance personalized medicine and the development of targeted therapies. While numerous methods for DGP have been proposed in the field, a significant challenge remains in effectively capturing and modeling the complex relationships among biological entities, such as diseases, symptoms, genes, and pathways. These intricate interactions are essential for learning robust representations of phenotypes and genotypes, which are critical for accurate DGP. In this study, we introduce MELGene, a knowledge-enhanced multimodel ensemble learning framework for DGP. MELGene leverages an adaptive integration of multiple pretrained knowledge inference models based on knowledge graph, effectively integrating the collective intelligence of diverse models to achieve more accurate gene predictions. The framework incorporates Model-aware Importance Learning, which dynamically adjusts the contributions of individual models, and introduces a dynamic ensemble mechanism to obtain robust consensus predictions. Finally, we conducted comprehensive experiments, including performance comparisons, which demonstrated the excellent performance of MELGene. Ablation experiments highlighted the positive impact of each module, while case studies showcased the reliability of the biological relevance of gastric, lung, and liver cancers, as supported by the analysis of network medicine, functional enrichment, and literature mining. MELGene offers a flexible framework for DGP through knowledge enhancement and adaptive ensemble learning, with broad potential for decoding disease mechanisms.

Indexed as

Computational BiologyGenetic Association StudiesGenetic Predisposition to DiseaseMachine LearningAlgorithmsEnsemble LearningHumansDisease–gene predictionensemble learningknowledge graph completion

Identifiers

PMID41985062
PMCPMC13082380

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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.