Evidence map›Paper›PMID 42168843›Full record

ArticleBMC bioinformatics2026

Transcriptome graph transformer: a graph transformer-based unsupervised model for transcriptome data analysis.

Teng Long, Sachit Satyal, Jean Gao

Abstract read
In one paragraph

Article in BMC bioinformatics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

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

3 authors.

Teng LongComputer Science and Engineering, The University of Texas at Arlington, 500 UTA Blvd, Arlington, TX, 76010, USA.
Sachit SatyalComputer Science and Engineering, The University of Texas at Arlington, 500 UTA Blvd, Arlington, TX, 76010, USA.
Jean GaoComputer Science and Engineering, The University of Texas at Arlington, 500 UTA Blvd, Arlington, TX, 76010, USA. gao@uta.edu.

Funding

National Science Foundation 2400785
6 · The paper itself

Abstract

backgroundRapidly growing transcriptomic datasets pose challenges for traditional analytical methods, which struggle with high dimensionality, heterogeneity, and nonlinear gene relationships. Existing deep learning models often require fixed-length inputs and fail to integrate biological network information.

methodsWe introduce Transcriptome Graph Transformer (TGT), an unsupervised graph Transformer framework that constructs a heterogeneous gene-pathway graph using expression data, STRING interactions, and GO/KEGG/Reactome pathway annotations. TGT is pretrained with a masked-node prediction task and fine-tuned for disease classification, biomarker discovery, and zero-shot clustering of single-cell and spatial transcriptomics.

resultsTGT achieves superior performance across Alzheimer's disease, cancer, acute kidney injury, and COVID-19 datasets, outperforming state-of-the-art baselines. The model generalizes well across platforms and yields biologically meaningful gene and pathway importance scores consistent with known disease mechanisms.

conclusionsTGT provides an effective and generalizable approach for transcriptomic representation learning by integrating biological network knowledge with graph Transformer architectures. Its strong performance highlights its utility for broad transcriptomic applications and precision medicine.

Indexed as

Computational BiologyGene Expression ProfilingTranscriptomeUnsupervised Machine LearningGraph Neural NetworksHumansSpatial TranscriptomicsBiomarker discoveryDisease classificationGene expression analysisGraph transformerUnsupervised learning

Identifiers

PMID42168843
PMCPMC13463954

What OpenQuestion holds

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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.