PRiMeFlow: Capturing Complex Expression Heterogeneity in Perturbation Response Modelling
- URL: http://arxiv.org/abs/2604.13986v1
- Date: Wed, 15 Apr 2026 15:33:07 GMT
- Title: PRiMeFlow: Capturing Complex Expression Heterogeneity in Perturbation Response Modelling
- Abstract summary: PRiMeFlow is an end-to-end flow matching based approach to directly model the effects of genetic and small molecule perturbations in the gene expression space.<n>The distribution-fitting approach taken by PRiMeFlow enables it to accurately approximate the empirical distribution of single-cell gene expression.
- Score: 2.0981373472250033
- License: http://arxiv.org/licenses/nonexclusive-distrib/1.0/
- Abstract: Predicting the effects of perturbations in-silico on cell state can identify drivers of cell behavior at scale and accelerate drug discovery. However, modeling challenges remain due to the inherent heterogeneity of single cell gene expression and the complex, latent gene dependencies. Here, we present PRiMeFlow, an end-to-end flow matching based approach to directly model the effects of genetic and small molecule perturbations in the gene expression space. The distribution-fitting approach taken by PRiMeFlow enables it to accurately approximate the empirical distribution of single-cell gene expression, which we demonstrate through extensive benchmarking inside PerturBench. Through ablation studies, we also validate important model design choices such as operating in gene expression space and parameterizing the velocity field with a U-Net architecture. The PRiMeFlow architecture was used as the basis for the model that won the Generalist Prize in the first ARC Virtual Cell Challenge.
Related papers
- Influence-Guided Symbolic Regression: Scientific Discovery via LLM-Driven Equation Search with Granular Feedback [56.69850045068714]
We introduce textitInfluence-Guided Regression (IGSR), a method that frames equation discovery as an iterative two-step process.<n>We demonstrate IGSRs effectiveness on a diverse suite of benchmarks, including LLM-SRBench, pharmacological PKPD models, an epidemiological simulation, and real-world genomic data.
arXiv Detail & Related papers (2026-05-27T23:48:01Z) - Modeling Temporal scRNA-seq Data with Latent Gaussian Process and Optimal Transport [8.719471378063078]
We propose a generative framework that models population trends using a latent heteroscedastic Gaussian process (GP) approximated by Hilbert space methods.<n>Our method explicitly captures biological extrapolation by incorporating cell-specific latent time and cell type conditioning to disentangle temporal asynchrony trajectories to different cell types.
arXiv Detail & Related papers (2026-05-20T10:24:51Z) - SAVE: A Generalizable Framework for Multi-Condition Single-Cell Generation with Gene Block Attention [10.404186274295222]
SAVE is a unified generative framework based on conditional Transformers for single-cell modeling.<n>We evaluate SAVE on a range of benchmarks including conditional generation, batch effect correction, and perturbation prediction.<n>Save offers a scalable and generalizable solution for modeling complex single-cell data.
arXiv Detail & Related papers (2026-04-18T01:45:16Z) - Lingshu-Cell: A generative cellular world model for transcriptome modeling toward virtual cells [48.885716676667776]
Lingshu-Cell is a discrete diffusion model that learns transcriptomic state distributions and supports conditional simulation under perturbations.<n>It captures complex transcriptome-wide expression dependencies across approximately 18,000 genes without relying on prior gene selection.<n>It achieves leading performance on the Virtual Cell Challenge H1 genetic perturbation benchmark and in predicting cytokine-induced responses in human PBMCs.
arXiv Detail & Related papers (2026-03-26T09:46:27Z) - Parameter-free representations outperform single-cell foundation models on downstream benchmarks [0.0]
Single-cell RNA sequencing (scRNA-seq) data exhibit strong and reproducible statistical structure.<n>Large-scale foundation models, such as TranscriptFormer, learn a generative model for gene expression by embedding genes into a latent vector space.<n>We ask whether similar performance can be achieved without utilizing computationally intensive deep learning-based representations.
arXiv Detail & Related papers (2026-02-18T18:42:29Z) - Latent Causal Diffusions for Single-Cell Perturbation Modeling [83.47931153555321]
We present a generative model that frames single-cell gene expression as a stationary diffusion process observed under measurement noise.<n> LCD outperforms established approaches in predicting the distributional shifts of unseen perturbation combinations in single-cell RNA-sequencing screens.<n>We develop an approach we call causal linearization via perturbation responses (CLIPR), which yields an approximation of the direct causal effects between all genes.
arXiv Detail & Related papers (2026-01-20T16:15:38Z) - Departures: Distributional Transport for Single-Cell Perturbation Prediction with Neural Schrödinger Bridges [51.83259180910313]
A major bottleneck in gene function analysis is the unpaired nature of single-cell data.<n>We approximate Schrdinger Bridge (SB) to tackle unpaired single-cell perturbation data.<n>Our model effectively captures heterogeneous single-cell responses and achieves state-of-the-art performance.
arXiv Detail & Related papers (2025-11-17T08:27:13Z) - Scalable Single-Cell Gene Expression Generation with Latent Diffusion Models [11.343106383645441]
We introduce a scalable latent diffusion model for single-cell gene expression data, which we refer to as scLDM.<n>We show its superior performance in a variety of experiments for both observational and perturbational single-cell data, as well as downstream tasks like cell-level classification.
arXiv Detail & Related papers (2025-11-04T20:44:12Z) - Unlasting: Unpaired Single-Cell Multi-Perturbation Estimation by Dual Conditional Diffusion Implicit Bridges [68.98973318553983]
We propose a framework based on Dual Diffusion Implicit Bridges (DDIB) to learn the mapping between different data distributions.<n>We integrate gene regulatory network (GRN) information to propagate perturbation signals in a biologically meaningful way.<n>We also incorporate a masking mechanism to predict silent genes, improving the quality of generated profiles.
arXiv Detail & Related papers (2025-06-26T09:05:38Z) - A scalable gene network model of regulatory dynamics in single cells [88.48246132084441]
We introduce a Functional Learnable model of Cell dynamicS, FLeCS, that incorporates gene network structure into coupled differential equations to model gene regulatory functions.<n>Given (pseudo)time-series single-cell data, FLeCS accurately infers cell dynamics at scale.
arXiv Detail & Related papers (2025-03-25T19:19:21Z) - Stochastic gradient descent estimation of generalized matrix factorization models with application to single-cell RNA sequencing data [39.146761527401424]
Single-cell RNA sequencing allows the quantification of gene expression at the individual cell level.<n> Dimensionality reduction is a common preprocessing step critical for the visualization, clustering, and phenotypic characterization of samples.<n>We present a generalized matrix factorization model assuming a general exponential dispersion family distribution.<n>We show that our method scales seamlessly to millions of cells, enabling dimensionality reduction in large single-cell datasets.
arXiv Detail & Related papers (2024-12-29T16:02:15Z) - Multi-Modal and Multi-Attribute Generation of Single Cells with CFGen [76.02070962797794]
This work introduces CellFlow for Generation (CFGen), a flow-based conditional generative model that preserves the inherent discreteness of single-cell data.<n>CFGen generates whole-genome multi-modal single-cell data reliably, improving the recovery of crucial biological data characteristics.
arXiv Detail & Related papers (2024-07-16T14:05:03Z)
This list is automatically generated from the titles and abstracts of the papers in this site.
This site does not guarantee the quality of this site (including all information) and is not responsible for any consequences.