Semantic occupancy has emerged as a powerful representation in world models for its ability to capture rich spatial semantics. However, most existing occupancy world models rely on static and fixed embeddings or grids, which inherently limit the flexibility of perception. Moreover, their ``in-place classification" over grids exhibits a potential misalignment with the dynamic and continuous nature of real scenarios. In this paper, we propose SparseWorld, a novel 4D occupancy world model that is flexible, adaptive, and efficient, powered by sparse and dynamic queries. We propose a Range-Adaptive Perception module, in which learnable queries are modulated by the ego vehicle states and enriched with temporal-spatial associations to enable extended-range perception. To effectively capture the dynamics of the scene, we design a State-Conditioned Forecasting module, which replaces classification-based forecasting with regression-guided formulation, precisely aligning the dynamic queries with the continuity of the 4D environment. In addition, We specifically devise a Temporal-Aware Self-Scheduling training strategy to enable smooth and efficient training. Extensive experiments demonstrate that SparseWorld achieves state-of-the-art performance across perception, forecasting, and planning tasks. Comprehensive visualizations and ablation studies further validate the advantages of SparseWorld in terms of flexibility, adaptability, and efficiency.

Precise prediction of perturbation responses is essential in systems biology research, as it plays a pivotal role in characterizing cellular identities and elucidating the regulatory mechanisms of biological pathways. Existing perturbation-responses prediction approaches are predominantly confined to single-modality transcriptomic data, limiting their capacity to capture cross-layer molecular effects. Here, we present MultiPert, a deep learning framework specifically designed for predicting perturbation responses in single-cell multi-omics data. MultiPert employs modality-specific encoders with dedicated pretraining, integrates perturbation through a dual-attention mechanism, and achieves cross-modal alignment via adversarial training. Benchmarking on human THP-1 and kidney multi-omics datasets demonstrates that MultiPert reliably predicts both perturbed gene expression and protein abundance profiles, achieving superior accuracy and stability compared to state-of-the-art strategies. MultiPert generalizes to unseen perturbations and uncovers regulatory mechanisms of immune checkpoint molecules based on perturbed proteomic predictions. In addition, enrichment analyses of perturbed transcriptomic predictions reveal immune-related pathways. By providing an integrated and interpretable framework, MultiPert expands the scope of perturbation modeling at the multi-omics level, thereby offering a robust methodological foundation for comprehensive research into pathogenesis and drug discovery.