bioRxivBioinformaticsPreprint
CellOS: Learning a World Model of Cellular State through Joint Embedding Prediction
Q ZhouiD, Yuan Le, Xiaoning QiiD, Hanshuo LuiD, Shaole Chang, Yujia WuiD, H Z WangiD, Ruoyao Ran, X F LiiD
- Citations
- 1
Abstract
Foundation models learned from single-cell transcriptomes are central to the prospect of AI virtual cell that can represent, query and predict cellular state. However, most current single-cell foundation models learn from a single view of gene expression and are optimized primarily through reconstruction or next-token prediction. As a result, they capture expression abundance but cannot explicitly reconcile complementary views of cellular state. Here we present CellOS, a multi-view foundation model that learns cellular representations from paired expression and perception views. CellOS integrates complementary views through a scalable three-stage training strategy that combines causal cell-sentence language modelling, function-preserving dense-to-mixture-of-experts expansion and latent-space alignment via an LLM-JEPA objective. Using this framework, we trained a 12-billion-parameter model on 390.5 million single-cell transcriptomes. Across diverse benchmarks spanning cell-state annotation, batch integration and perturbation-response prediction, CellOS consistently outperformed state-of-the-art single-cell foundation models. Together, these results suggest that predictive alignment between complementary cellular views provides a scalable path toward representation-centric cellular world models and transferable AI virtual cells.
- organism: human
- assay: scRNA-seq
- research focus: cell type annotation
- research focus: batch correction / integration
- research focus: perturbation response prediction
- approach: deep learning
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