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Paper · 2605.00925 · 2026

Linking spatial biology and clinical histology via Haiku

Zhi Huang, Wenhui Lei, Yan Cui, Zhenqin Wu, Jacob Leiby, Dokyoon Kim, Yanxiang Deng, Aaron Mayer, Alexandro Trevino

arXiv · PDF · Open in the Atlas

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RepositoryRoleRan
zhihuanglab/Haiku — 1 of 2
FunctionStatusWhere it lives
MarkerEmbedding Ran zhihuanglab/Haiku/src/models/haiku_model.py
pointer only (licence: NONE) · get_code("343fd38f6d583e4d")
Haiku Not yet run zhihuanglab/Haiku/src/models/haiku_model.py
pointer only (licence: NONE) · get_code("56fa1d9902797933")

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Abstract

Integrating molecular, morphological, and clinical data is essential for basic and translational biomedical research, yet systematic frameworks for jointly modeling these modalities remain limited. Here we present Haiku, a tri-modal contrastive learning model trained on multiplexed immunofluorescence (mIF). It comprises 26.7 million spatial proteomics patches from 3,218 tissue sections across 1,606 patients spanning 11 organ type, with matched hematoxylin and eosin (H&E) histology and clinical metadata aligned in a shared embedding space. Haiku enables three-way cross-modal retrieval, improves a variety of downstream classification and clinical prediction tasks over unimodal baselines, and supports zero-shot biomarker inference through fusion retrieval conditioned on clinical metadata-only text descriptions. Across tasks, Haiku outperforms competing approaches, achieving cross-modal retrieval (Recall@50 up to 0.611 versus near-zero baseline), survival prediction (C-index 0.737, +7.91% relative improvement), and zero-shot biomarker inference (mean Pearson correlation 0.718 across 52 biomarkers). Furthermore, we introduce a counterfactual prediction framework in which modifying only clinical metadata while fixing tissue morphology surfaces niche-specific molecular shifts associated with breast cancer stage progression and lung cancer survival outcomes. In a lung adenocarcinoma case study, the counterfactual analysis recovers niche-specific shifts characterized by increased CD8 and granzyme B, reduced PD-L1, and decreased Ki67, broadly consistent with patterns reported in the literature for favorable outcomes. We present these counterfactual results as exploratory, hypothesis-generating signals rather than mechanistic claims. These capabilities demonstrate that tri-modal alignment via Haiku enables integrative analysis of spatial biology, bridging molecular measurements with clinical context to support biological exploration and downstream investigation.

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