Evidence map›Paper›PMID 41288963›Full record

ArticleBioinformatics (Oxford, England)2025

scRegulate: single-cell regulatory-embedded variational inference of transcription factor activity from gene expression.

Mehrdad Zandigohar, Jalees Rehman, Yang Dai

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2025. 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

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Mehrdad ZandigoharDepartment of Biomedical Engineering, University of Illinois Chicago, Chicago, IL 60607, United States.ORCID 0000-0003-3772-2683
Jalees RehmanDepartment of Biomedical Engineering, University of Illinois Chicago, Chicago, IL 60607, United States.
Yang DaiDepartment of Biomedical Engineering, University of Illinois Chicago, Chicago, IL 60607, United States.ORCID 0000-0002-7638-849X

Funding

Coordinating and Bioinformatics Unit for the MMPC/DiaCompU24DK076169 · NIDDK · AUGUSTA UNIVERSITY · PI MCINDOE, RICHARD A. · 2006 to 2018
$42.4M
Coordinating Unit for DiaCompU24DK115255 · NIDDK · AUGUSTA UNIVERSITY · PI MCINDOE, RICHARD A. · 2017 to 2020
$11.6M
Diabetic Complications Consortium DK076169Diabetic Complications Consortium DK115255NIDDK NIH HHS U24 DK076169NIDDK NIH HHS U24 DK115255
6 · The paper itself

Abstract

motivationAccurately inferring transcription factor (TF) activity from single-cell RNA sequencing (scRNA-seq) data remains a fundamental challenge in computational biology. While existing methods rely on statistical models, motif enrichment, or prior-based inference, they often depend on deterministic assumptions about regulatory relationships and rely on static regulatory databases. Few approaches effectively integrate prior biological knowledge with data-driven inference to capture novel, dynamic, and context-specific regulatory interactions.

resultsTo address these limitations, we develop scRegulate, a generative deep-learning framework leveraging variational inference to estimate TF activities guided by experimental TF-target gene relationships and progressively adapted based on the input scRNA-seq data. By integrating structured biological constraints with a probabilistic latent space model, scRegulate offers a scalable and biologically grounded estimation of TF activity and gene regulatory network (GRN). Comprehensively benchmarking on public experimental and synthetic datasets demonstrates scRegulate's superior ability. Further, scRegulate accurately recapitulates experimentally validated TF knockdown effects on a Perturb-seq dataset for key TFs. Applied to experimental human PBMC scRNA-seq data, scRegulate infers cell-type-specific GRNs and identifies differentially active TFs aligned with known regulatory pathways. scRegulate's TF activity representations capture transcriptional heterogeneity, enabling accurate clustering of cell types. scRegulate is highly efficient, frequently an order of magnitude faster than common baselines. Collectively, our results establish scRegulate as a powerful, interpretable, and scalable framework for inferring TF activities and GRNs from single-cell transcriptomics. AVAILABILITY AND IMPLEMENTATION: Results and scripts available at github.com/YDaiLab/scRegulate.

Indexed as

Computational BiologyGene Regulatory NetworksSingle-Cell AnalysisSoftwareTranscription FactorsAlgorithmsDeep LearningGene Expression RegulationHumansSequence Analysis, RNATranscription Factors

Identifiers

PMID41288963
PMCPMC12701802

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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.