Evidence map›Paper›PMID 42225598›Full record

ArticleBioinformatics (Oxford, England)2026

CeSpGRN: inferring cell-specific gene regulatory networks from single-cell multi-omics and spatial data.

Ziqi Zhang, Jongseok Han, Le Song, Xiuwei Zhang

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. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Decoding Spatial Heterogeneity and Multi-Omics Regulation with Hierarchical Graph Learning.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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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

4 authors.

Ziqi ZhangSchool of Computational Science and Engineering, Georgia Institute of Technology, Atlanta, GA 30332, United States.ORCID 0000-0002-8198-0260
Jongseok HanSchool of Computational Science and Engineering, Georgia Institute of Technology, Atlanta, GA 30332, United States.
Le SongMohamed bin Zayed University of Artificial Intelligence, Abu Dhabi, United Arab Emirates.
Xiuwei ZhangSchool of Computational Science and Engineering, Georgia Institute of Technology, Atlanta, GA 30332, United States.ORCID 0000-0002-1713-772X

Funding

Studying temporal dynamics and regulatory mechanisms of single cells with a unified framework and multi-omics dataR35GM143070 · NIGMS · GEORGIA INSTITUTE OF TECHNOLOGY · PI ZHANG, XIUWEI · 2021 to 2025
$1.8M
NIGMS NIH HHS R35 GM143070NIH HHS R35GM143070US National Science Foundation DBI-2019771
6 · The paper itself

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.

Indexed as

Gene Regulatory NetworksMultiomicsSingle-Cell Gene Expression AnalysisSoftwareSpatial TranscriptomicsAlgorithmsSequence Analysis, RNA

Identifiers

PMID42225598
PMCPMC13242928

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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.