Haruka Resolves Perturbation Response Heterogeneity in Spatial Cell Niches
Cui, Y.; Blandin, J.; Weiskopf, K.; Sun, N.
Show abstract
Understanding how tissues remodel in response to perturbations requires computational tools that can untangle condition-specific changes from the conserved tissue architecture. We present Haruka, a spatially aware contrastive learning framework that identifies salient (condition-specific) and background (shared) spatial domains across tissue slices and experimental conditions. Haruka integrates contrastive variational inference with an auxiliary microenvironment reconstruction task, enabling the model to learn spatial-context-informed embeddings that capture both perturbation effects and local neighborhood context. Through benchmarking on simulated and real datasets, Haruka outperforms state-of-the-art methods in detecting spatially heterogeneous responses. Applied to diverse spatial omics platforms, Haruka distinguished immunotherapy responders in melanoma, traced fibrosis progression in human lung tissue, and mapped treatment-resistant microenvironments in KRASG12D-mutated lung cancer. Thus, Haruka provides a generalizable framework for spatial contrastive analysis, enabling systematic dissection of tissue organization, cellular plasticity, and microenvironmental remodeling across disease, development, and therapeutic response.
Matching journals
The top 3 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- A new transcriptional metastatic signature predicts survival in clear cell renal cell carcinoma 98%
- GraphVelo allows for accurate inference of multimodal velocities and molecular mechanisms for single cells 98%
- Ascertaining cells' synaptic connections and RNA expression simultaneously with massively barcoded rabies virus libraries 98%
Similar papers in this journal
Similar papers in this journal
- Integrative, high-resolution analysis of single cell gene expression across experimental conditions with PARAFAC2-RISE 95%
- Simple visualization of submicroscopic protein clusters with a phase-separation-based fluorescent reporter. 94%
- Emergence of synchronized multicellular mechanosensing from spatiotemporal integration of heterogeneous single-cell information transfer 94%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.