Back

CardamomOT: a mechanistic optimal transport-based framework for gene regulatory network inference, trajectory reconstruction and generative modeling

Mauge, Y.; Ventre, E.

2026-04-02 bioinformatics
10.64898/2026.03.31.715390 bioRxiv
Show abstract

A key challenge in inferring gene regulatory networks (GRNs) governing cellular processes such as differentiation and reprogramming from experimental data lies in the impossibility of directly measuring protein dynamics at the single-cell level, which prevents establishing causal relationships between regulator activity and target responses. In earlier work, we introduced CARDAMOM, an algorithm that uses temporal snapshots of scRNA-seq data to calibrate a GRN-driven mechanistic model of gene expression. However, this method had several limitations: it could only rely on the relative ordering of time points rather than their exact labels, imposed restrictive quasi-stationary assumptions on protein dynamics, and depended on multiple hyperparameters. Here, we present CardamomOT, a new method based on the same mechanistic model that jointly reconstructs the GRN and unobserved protein trajectories from the data within a mechanistic optimal transport framework. By incorporating exact time labels and priors on protein kinetic rates from the literature, and substantially reducing the number of required hyperparameters, our approach addresses these limitations and substantially improves the accuracy and robustness of GRN calibration. We validate our framework on both in silico and experimental datasets, demonstrating computational scalability and consistently improved performance over state-of-the-art methods in both GRN and trajectory reconstruction. In particular, CardamomOT accurately recovers velocity fields driving cellular trajectories and unobserved protein levels, alongside reliable GRN structures. We also show that these improvements make the calibrated mechanistic model suitable to be used as a generative model to predict cellular responses to unseen perturbations. To our knowledge, this is among the first methods to explicitly integrate mechanistic GRN inference, trajectory reconstruction, and simulation of realistic datasets into a unified framework for scRNA-seq time series analysis.

Matching journals

The top 4 journals account for 50% of the predicted probability mass.

1
Bioinformatics
1061 papers in training set
Top 1%
18.7%
2
Genome Biology
555 papers in training set
Top 0.2%
12.4%
3
Cell Systems
167 papers in training set
Top 0.9%
10.5%
4
Nature Communications
4913 papers in training set
Top 17%
10.1%
50% of probability mass above
5
Nature Methods
336 papers in training set
Top 2%
4.9%
6
Genome Research
409 papers in training set
Top 0.7%
4.3%
7
PLOS Computational Biology
1633 papers in training set
Top 9%
3.9%
8
Nature Biotechnology
147 papers in training set
Top 2%
3.7%
9
Proceedings of the National Academy of Sciences
2130 papers in training set
Top 24%
2.7%
10
Nucleic Acids Research
1128 papers in training set
Top 8%
2.4%
11
Briefings in Bioinformatics
326 papers in training set
Top 3%
1.9%
12
Nature Computational Science
50 papers in training set
Top 0.6%
1.7%
13
BMC Bioinformatics
383 papers in training set
Top 6%
1.0%
14
Nature Machine Intelligence
61 papers in training set
Top 3%
1.0%
15
NAR Genomics and Bioinformatics
214 papers in training set
Top 3%
0.9%
16
Communications Biology
886 papers in training set
Top 19%
0.9%
17
Scientific Reports
3102 papers in training set
Top 73%
0.8%
18
Cell Reports Methods
141 papers in training set
Top 5%
0.8%
19
The American Journal of Human Genetics
206 papers in training set
Top 3%
0.8%
20
PLOS ONE
4510 papers in training set
Top 66%
0.8%
21
Computational and Structural Biotechnology Journal
216 papers in training set
Top 9%
0.7%
22
Cell Reports
1338 papers in training set
Top 33%
0.7%
23
Genome Medicine
154 papers in training set
Top 8%
0.7%
24
PLOS Genetics
756 papers in training set
Top 15%
0.7%
25
Bioinformatics Advances
184 papers in training set
Top 5%
0.7%
26
iScience
1063 papers in training set
Top 34%
0.7%
27
Development
440 papers in training set
Top 4%
0.6%
28
Frontiers in Molecular Biosciences
100 papers in training set
Top 6%
0.6%