Evidence map›Paper›PMID 42123713›Full record

ArticleInternational journal of molecular sciences2026

TGBWDriver: A Cancer Driver Gene Identification Method Based on GraphSAGE and Bidirectional Weighted Feature Aggregation.

Jiaxin Chen, Yingzan Ren, Haihui Wang, Cong Zhan, Yusen Zhang

Abstract read
In one paragraph

Article in International journal of molecular sciences, 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Jiaxin ChenSchool of Mathematics and Statistics, Shandong University, Weihai 264209, China.
Yingzan RenSchool of Mathematics and Statistics, Shandong University, Weihai 264209, China.
Haihui WangSchool of Mathematics and Statistics, Shandong University, Weihai 264209, China.
Cong ZhanSchool of Mathematics and Statistics, Shandong University, Weihai 264209, China.
Yusen ZhangSchool of Mathematics and Statistics, Shandong University, Weihai 264209, China.ORCID 0000-0003-3842-1153

Funding

National Natural Science Foundation of China 61877064
6 · The paper itself

Abstract

Identifying cancer driver genes is fundamental for understanding tumor initiation and guiding therapeutic strategies. However, most existing methods assess gene importance from a global or static perspective, overlooking sample-specific functional differences in the same gene. To address this, we propose TGBWDriver, which integrates a two-layer GraphSAGE with bidirectional weighted feature aggregation to capture structural characteristics while distinguishing context-dependent gene functions. An exponential pairwise voting strategy prioritizes candidate driver genes, improving ranking stability and accuracy. Systematic experiments on BRCA, LUAD, and PRAD datasets show that TGBWDriver outperforms five existing methods in precision, recall, and F1-score. Ablation studies confirm the critical role of each component. Moreover, TGBWDriver demonstrates strong capability in identifying potential novel cancer driver genes, with predictions showing significant biological relevance in GO enrichment and KEGG pathway analyses. The method provides an effective computational framework for cancer driver gene identification. The source code and datasets are freely available at https://github.com/SCSMDyeah/TGBW [Accessed on 4 May 2026].

Indexed as

Computational BiologyGenes, NeoplasmNeoplasmsSoftwareAlgorithmsDatabases, GeneticGene Regulatory NetworksHumanscancer driver genesGraphSAGEmulti-omics dataPPI network

Identifiers

PMID42123713
PMCPMC13163706

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Registered trials

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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.