ArticleBioinformatics (Oxford, England)2026
CeSpGRN: inferring cell-specific gene regulatory networks from single-cell multi-omics and spatial data.
Article in Bioinformatics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed.
- Decoding Spatial Heterogeneity and Multi-Omics Regulation with Hierarchical Graph Learning.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026Article
- Scalable cell-specific coexpression networks for granular regulatory pattern discovery with NeighbourNet.Genome research · 2026Article
- Spatially varying gene regulation network inference from spatial transcriptomics.Bioinformatics advances · 2026Article
- MAGNET: Multi-view graph autoencoder with cell-gene attention for cell interaction network reconstruction from spatial transcriptomics.PLoS computational biology · 2025Article
- ScReNI: Single-cell Regulatory Network Inference Through Integrating scRNA-seq and scATAC-seq Data.Genomics, proteomics & bioinformatics · 2025Article
- Model Architecture Analysis and Implementation of TENET for Cell-Cell Interaction Network Reconstruction Using Spatial Transcriptomics Data.Bio-protocol · 2025Article
- A single-cell multimodal view on gene regulatory network inference from transcriptomics and chromatin accessibility data.Briefings in bioinformatics · 2024Review
- GRouNdGAN: GRN-guided simulation of single-cell RNA-seq data using causal generative adversarial networks.Nature communications · 2024Article
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Authors and funding
4 authors.
Funding
Abstract
motivationSingle-cell sequencing technologies allow researchers to study cell-cell variation within a cell population. Variations between cells are driven by the underlying biological network, particularly gene regulatory networks (GRNs). GRNs rewire as cells evolve, and different cells can have different GRNs. However, while single-cell RNA-sequencing (scRNA-seq) and single-cell multi-omics data have been used to reconstruct GRNs, the output GRNs are rarely cell-specific, but rather, most existing methods infer population-level or cell-type-level GRNs.
resultsWe propose CeSpGRN (Cell-Specific Gene Regulatory Network inference), a method that infers cell-specific GRNs from scRNA-seq, paired scRNA-seq and scATAC-seq, or spatial transcriptomic data. In particular, existing methods that use matching scRNA-seq and scATAC-seq data incorporate population-level region information in GRN inference, whereas CeSpGRN utilizes single-cell resolution region information. CeSpGRN infers cell-specific GRNs using a kernel-weighted Gaussian Copula Graphical Model, and incorporates multi-omic or spatial location information when constructing the objective function. We tested CeSpGRN on both simulated and real datasets, and the results show that CeSpGRN has a superior performance compared to baseline methods in reconstructing GRNs and detecting regulatory interactions that differ between cells. CeSpGRN uncovered regulatory interactions that rewire during biological processes on real datasets. AVAILABILITY AND IMPLEMENTATION: CeSpGRN is a Python package available at https://github.com/PeterZZQ/CeSpGRN.
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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.