Evidence map›Paper›PMID 41883144›Full record

ArticleBioinformatics (Oxford, England)2026

GRNFormer: accurate gene regulatory network inference using graph transformer.

Akshata Hegde, Jianlin Cheng

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 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

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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

2 authors.

Akshata HegdeDepartment of Electrical Engineering and Computer Science, University of Missouri, Columbia, Missouri, 65211, United States.ORCID 0009-0009-7077-9420
Jianlin ChengDepartment of Electrical Engineering and Computer Science, University of Missouri, Columbia, Missouri, 65211, United States.ORCID 0000-0003-0305-2853

Funding

Department of Energy DE-SC0026121National Sscience Foundation (NSF) CCF2343612National Sscience Foundation (NSF) IOS2525780
6 · The paper itself

Abstract

motivationDeciphering gene regulatory networks (GRNs) from single-cell transcriptomics data remains a fundamental challenge in computational biology. It is hindered by data sparsity, high dimensionality, and the lack of scalable, generalizable inference models. To address this, we present GRNFormer, a generalizable graph transformer framework for accurate GRN inference from transcriptomics data across species, cell types, and platforms without requiring cell-type annotations or prior regulatory information.

resultsGRNFormer integrates a transformer-based gene expression encoder (Gene-Transcoder) with a variational graph autoencoder (GraViTAE) employing pairwise attention to jointly learn the representations of genes (nodes) and their co-expression relationships (edges). Leveraging TF-Walker, a transcription factor-anchored subgraph sampling strategy, it effectively captures gene regulatory interactions from either single-cell or bulk RNA-seq datasets. Benchmarking on standard datasets demonstrates that GRNFormer outperforms existing traditional and deep learning state-of-the-art methods in blind evaluations, achieving average sampled area under the receiver operating characteristic curve (Sampled_AUROC) and sampled area under the precision-recall curve (Sampled_AUPRC) values between 0.90 and 0.98 as well as 0.87-0.98 average sampled F1 score. The model robustly recovers both known and novel regulatory networks, including pluripotency circuits in human embryonic stem cells (hESCs) and immune cell modules in peripheral blood mononuclear cells (PBMCs). The architecture enables scalable, biologically interpretable GRN inference across various datasets, cell types, and species, establishing GRNFormer as a robust and transferable tool for network biology. AVAILABILITY AND IMPLEMENTATION: GRNFormer is available on GitHub (https://github.com/BioinfoMachineLearning/GRNformer); the version used in this work is archived on Zenodo (https://doi.org/10.5281/zenodo.18868395), with evaluation resources for reproducibility.

Indexed as

Computational BiologyGene Regulatory NetworksSoftwareAlgorithmsAnimalsAutoencoderGene Expression ProfilingHumansSingle-Cell Gene Expression Analysis

Identifiers

PMID41883144
PMCPMC13069479

What Socratic holds

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LicenceCC BY
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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 Socratic graph.