Cited by 116Gene Regulatory Network AnalysisSingle-cell and spatial transcriptomicsGenomics and Chromatin Dynamics

Gene regulation inference from single-cell RNA-seq data with linear differential equations and velocity inference

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Aubin-Frankowski, Pierre-Cyril, Vert, Jean-Philippe·2020·Bioinformatics

Published version of a preprint

Abstract

Motivation: Single-cell RNA sequencing (scRNA-seq) offers new possibilities to infer gene regulatory network (GRNs) for biological processes involving a notion of time, such as cell differentiation or cell cycles. It also raises many challenges due to the destructive measurements inherent to the technology. Results: In this work, we propose a new method named GRISLI for de novo GRN inference from scRNA-seq data. GRISLI infers a velocity vector field in the space of scRNA-seq data from profiles of individual cells, and models the dynamics of cell trajectories with a linear ordinary differential equation to reconstruct the underlying GRN with a sparse regression procedure. We show on real data that GRISLI outperforms a recently proposed state-of-the-art method for GRN reconstruction from scRNA-seq data. Availability and implementation: The MATLAB code of GRISLI is available at: https://github.com/PCAubin/GRISLI. Supplementary information: Supplementary data are available at Bioinformatics online.

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Crossref · 10.1093/bioinformatics/btaa576

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  • Single-cell RNA sequencing data enables cell type-specific trans-regulation inference through co-expression analysis.

    “Single-cell RNA sequencing (scRNA-seq) data enables cell type-specific trans-regulation inference through co-expression analysis such as PIDC and SCENIC21–30.”

    From Inferring gene regulatory networks from single-cell multiome data using atlas-scale external data (2025) · cites this paper as [27]

    The Abstract says scRNA-seq offers possibilities for inferring gene regulatory networks, supporting the general inference claim. It describes the paper’s approach as velocity inference and differential-equation modeling, but does not support the more specific claim of cell type-specific inference through co-expression analysis such as PIDC or SCENIC. (LLM, conf=0.85)

    Experimental — accuracy not yet measured

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Authors
Aubin-Frankowski, P.-C., & Vert, J.-P.
Affiliations
  • Université Paris Sciences et Lettres (FR)
  • Google (United States) (US)
Corresponding author
  • Aubin-Frankowski, Pierre-Cyril
  • Vert, Jean-Philippe
Venue
Bioinformatics
Published
2020-06-17
Volume
36
Issue
18
Pages
4774-4780
ISSN
  • 1367-4803 (ISSN-L)
  • 1367-4811
OpenAlex
W3036077871
Cited by
116
References
38
Citations by year
2026: 9 · 2025: 18 · 2024: 20 · 2023: 23 · 2022: 23 · 2021: 17 · 2020: 4 · 2019: 2
FWCI
5.44
Type
journal article
Language
en
Open access
Locations
  • Bioinformatics (publishedVersion)
  • bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by)
  • PubMed (publishedVersion)
  • HAL (submittedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gene Regulatory Network Analysis
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Single-cell and spatial transcriptomics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
Keywords
gene regulatory network inference, single-cell RNA sequencing, linear differential equations, sparse regression, cell differentiation, cell cycle
MeSH terms
RNA-Seq, Sequence Analysis, RNA, Gene Expression Profiling, Gene Regulatory Networks, Single-Cell Analysis

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