Gene regulation inference from single-cell RNA-seq data with linear differential equations and velocity inference
Pierre-Cyril Aubin-Frankowski1, Jean-Philippe Vert1,2
1MINES ParisTech, PSL Research University, CBIO - Centre for Computational Biology, F-75006 Paris, France.
Bioinformatics (Oxford, England)
|October 7, 2020
Summary
We developed GRISLI, a new method for inferring gene regulatory networks (GRNs) from single-cell RNA sequencing (scRNA-seq) data. GRISLI reconstructs GRNs by modeling cell trajectory dynamics, outperforming existing methods.
Area of Science:
- Computational biology
- Genomics
- Systems biology
Background:
- Single-cell RNA sequencing (scRNA-seq) enables the study of gene regulatory networks (GRNs) in dynamic biological processes like cell differentiation.
- scRNA-seq presents challenges for GRN inference due to inherent measurement limitations.
Purpose of the Study:
- To introduce GRISLI, a novel computational method for de novo GRN inference from scRNA-seq data.
- To reconstruct GRNs by modeling cell trajectory dynamics.
Main Methods:
- GRISLI infers a velocity vector field from scRNA-seq data.
- Cell trajectory dynamics are modeled using linear ordinary differential equations.
- GRNs are reconstructed via a sparse regression procedure.
Main Results:
- GRISLI successfully reconstructs GRNs from scRNA-seq data.
- The proposed method demonstrates superior performance compared to a state-of-the-art GRN inference technique on real-world data.
Conclusions:
- GRISLI offers a robust approach for GRN inference from scRNA-seq data.
- The method effectively captures the dynamics of biological processes at the single-cell level.
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