Plate IV.95 · Publications
CellFlow enables generative single-cell phenotype modeling with flow matching
Preprint in bioRxiv, 17 April 2025.
Abstract
High-content phenotypic screens provide a powerful strategy for studying biological systems, but the scale of possible perturbations and cell states makes exhaustive experiments unfeasible. Computational models that are trained on existing data and extrapolate to correctly predict outcomes in unseen contexts have the potential to accelerate biological discovery. Here, we present CellFlow, a flexible framework based on flow matching that can model single cell phenotypes induced by complex perturbations. We apply CellFlow to various phenotypic screens, accurately predicting expression responses to a wide range of perturbations, including cytokine stimulation, drug treatments and gene knockouts. CellFlow successfully modeled developmental perturbations at the whole-embryo scale and guided cell fate and organoid engineering by predicting heterogeneous cell populations arising from combinatorial morphogen treatments and by performing a virtual organoid protocol screen. Taken together, CellFlow has the potential to accelerate discovery from phenotypic screens by learning from existing data and generating phenotypes induced by unseen conditions.
Cite
@misc{klein2025cellflow,
title = {{CellFlow enables generative single-cell phenotype modeling with flow matching}},
author = {Klein, Dominik and Fleck, Jonas Simon and Bobrovskiy, Daniil and Zimmermann, Lea and Becker, Sören and Palma, Alessandro and Dony, Leander and Tejada-Lapuerta, Alejandro and Huguet, Guillaume and Lin, Hsiu-Chuan and Azbukina, Nadezhda and Sanchís-Calleja, Fátima and Uscidda, Theo and Szalata, Artur and Gander, Manuel and Regev, Aviv and Treutlein, Barbara and Camp, J. Gray and Theis, Fabian J.},
howpublished = {bioRxiv},
publisher = {openRxiv},
year = {2025},
month = apr,
doi = {10.1101/2025.04.11.648220},
url = {https://doi.org/10.1101/2025.04.11.648220},
note = {Preprint}
}