Optimal transport reveals dynamic gene regulatory networks via gene velocity estimation

Inferring gene regulatory networks from gene expression data is an important and challenging problem in the biology community. We propose OTVelo, a methodology that takes time-stamped single-cell gene expression data as input and predicts gene regulation across two time points. It is known that the rate of change of gene expression, which we will refer to as gene velocity, provides crucial information that enhances such inference; however, this information is not always available due to the limitations in sequencing depth. Our algorithm overcomes this limitation by estimating gene velocities using optimal transport. We then infer gene regulation using time-lagged correlation and Granger causality via regularized linear regression. Instead of providing an aggregated network across all time points, our method uncovers the underlying dynamical mechanism across time points. We validate our algorithm on 13 simulated datasets with both synthetic and curated networks and demonstrate its efficacy on 9 experimental data sets.

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Publication Details

Journal
PLoS Computational Biology
Published
2025-05-08
DOI
https://doi.org/10.1371/journal.pcbi.1012476
Citations
6
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
4.84

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article

Optimal transport reveals dynamic gene regulatory networks via gene velocity estimation

Björn Sandstede, Ritambhara Singh, Erica Larschan, Wenjun Zhao
6 citations
PLoS Computational Biology
Single-cell and spatial transcriptomics
4.84
article

Optimal transport reveals dynamic gene regulatory networks via gene velocity estimation

Björn Sandstede, Ritambhara Singh, Erica Larschan, Wenjun Zhao
article en
6 citations

Abstract

Inferring gene regulatory networks from gene expression data is an important and challenging problem in the biology community. We propose OTVelo, a methodology that takes time-stamped single-cell gene expression data as input and predicts gene regulation across two time points. It is known that the rate of change of gene expression, which we will refer to as gene velocity, provides crucial information that enhances such inference; however, this information is not always available due to the limitations in sequencing depth. Our algorithm overcomes this limitation by estimating gene velocities using optimal transport. We then infer gene regulation using time-lagged correlation and Granger causality via regularized linear regression. Instead of providing an aggregated network across all time points, our method uncovers the underlying dynamical mechanism across time points. We validate our algorithm on 13 simulated datasets with both synthetic and curated networks and demonstrate its efficacy on 9 experimental data sets.

PLoS Computational BiologyVol. 21(5)
University of British Columbia (CA), Brown University (US)
National Science Foundation
Openalex Percentile: Top 5%
Single-cell and spatial transcriptomics
4.84
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