arXiv:2606. 27752v1 Announce Type: new Abstract: Single-cell perturbation models can reduce costly wet-lab screening by predicting how cells respond transcriptionally to interventions.
The paper introduces scEGFlow, an energy‑guided flow matching framework that predicts how single cells respond to perturbations by modeling continuous transitions from control to perturbed states. It uses conditional flow matching and condition‑specific energy gradients to dynamically adjust predictions without retraining, achieving superior performance on imaging and transcriptomic benchmarks, even for unseen perturbations or limited data. The method preserves cellular manifold geometry, heterogeneity, and accurately recapitulates gene‑expression regulatory patterns.
arXiv:2608. 16419v1 Announce Type: cross Abstract: Large language models can describe mechanisms, yet scalable post-training still depends on costly, manually curated biological reasoning traces.
CellRFT is a reinforcement fine‑tuning framework designed to improve single‑cell perturbation modeling by directly optimizing biological evaluation metrics. It employs policy‑gradient methods to learn from non‑differentiable biological rewards and aggregates multiple rewards hierarchically. Experiments show that CellRFT enhances perturbation prediction across various pretrained models and reveals interactions between different biological criteria, suggesting new ways to shape model behavior and evaluation design.
arXiv:2606. 13713v1 Announce Type: cross Abstract: Predicting cellular transcriptional responses to genetic perturbations is a central problem in single-cell biology, especially in the zero-shot setting where the perturbed gene or gene combination is unseen during training.
The paper introduces PT‑RAG, a retrieval‑augmented generation framework that enhances cellular perturbation response prediction by incorporating context from related perturbations. PT‑RAG uses a two‑stage retrieval process—semantic retrieval to shortlist candidate perturbations followed by a differentiable Gumbel‑Softmax selector that adapts the selection based on cell state and query perturbation. Experiments on two backbones, a frozen STATE‑style generator and a fully trained scGPT, show that PT‑RAG improves distributional similarity and predictive quality, achieving a 5.9% reduction in 2‑Wasserstein distance on cross‑cell‑type tasks.
The paper introduces PT‑RAG, a retrieval‑augmented generation framework that enhances deep learning models for predicting cellular transcriptional responses to gene perturbations. PT‑RAG adds a two‑stage retrieval module—semantic retrieval followed by a Gumbel‑Softmax selector—to supply contextually relevant perturbation information, improving predictive accuracy across cell types and perturbations. Experiments on STATE‑style and scGPT backbones show consistent gains, such as a 5.9% reduction in 2‑Wasserstein distance for cross‑cell‑type predictions.
arXiv:2610.13966v1 Announce Type: cross Abstract: Predicting cellular responses to chemical and genetic perturbations is a central test for AI virtual cells, yet many single-cell models reduce each c...
arXiv:2608. 15288v1 Announce Type: new Abstract: Predicting single-cell transcriptomic responses to genetic perturbations is central to functional genomics and virtual-cell modeling.
PopPert is a framework that models population-level joint gene expression distributions to predict transcriptional responses to perturbations in single-cell RNA sequencing data. By using a low‑rank Gaussian Copula, it captures gene co‑expression patterns and eliminates the need for cell‑to‑cell correspondence, thereby reducing sensitivity to single‑cell noise. Across multiple benchmarks, PopPert outperforms existing methods in differential expression recovery, perturbation effect estimation, and distribution matching, demonstrating the effectiveness of population‑level joint distribution learning for unpaired single‑cell data.
arXiv:2606. 11286v1 Announce Type: cross Abstract: High-content imaging assays quantify cellular responses to chemical and genetic perturbations, yet continuous trajectories of individual cells are unobservable because cells are chemically fixed at acquisition.
arXiv:2608.23114v1 Announce Type: cross Abstract: Predicting transcriptome-wide responses to unseen genetic perturbations remains a major computational challenge because accurate prediction requires...