ArticleBioinformatics (Oxford, England)2025
scRegulate: single-cell regulatory-embedded variational inference of transcription factor activity from gene expression.
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.
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1 citing paper in PubMed.
- Benchmarking methods for inferring single-cell transcription factor activity using large-scale perturbation sequencing data.Briefings in bioinformatics · 2026Article
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3 authors.
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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.
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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.