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Linking spatial biology and clinical histology via Haiku

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Haiku is a tri-modal contrastive learning model that integrates multiplexed immunofluorescence, H&E histology, and clinical metadata, enabling cross-modal retrieval, improved clinical predictions, zero-shot biomarker inference, and counterfactual analysis revealing niche-specific molecular shifts in cancer progression.

SourcearXiv Machine LearningAuthor: Yan Cui, Jacob S. Leiby, Wenhui Lei, Dokyoon Kim, Yanxiang Deng, Aaron T. Mayer, Zhenqin Wu, Alexandro E. Trevino, Zhi Huang
Linking spatial biology and clinical histology via Haiku
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[2605.00925] Linking spatial biology and clinical histology via Haiku

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Computer Science > Machine Learning

arXiv:2605.00925 (cs)

[Submitted on 30 Apr 2026]

Title:Linking spatial biology and clinical histology via Haiku

Authors:Yan Cui, Jacob S. Leiby, Wenhui Lei, Dokyoon Kim, Yanxiang Deng, Aaron T. Mayer, Zhenqin Wu, Alexandro E. Trevino, Zhi Huang

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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 types, 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 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 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 for biological exploration.

Subjects:

Machine Learning (cs.LG); Computer Vision and Pattern Recognition (cs.CV); Quantitative Methods (q-bio.QM)

Cite as: arXiv:2605.00925 [cs.LG]

(or arXiv:2605.00925v1 [cs.LG] for this version)

https://doi.org/10.48550/arXiv.2605.00925

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arXiv-issued DOI via DataCite (pending registration)

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From: Yan Cui [view email] [v1] Thu, 30 Apr 2026 18:53:32 UTC (4,927 KB)

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Key points

  • Trained on 26.7 million spatial proteomics patches from 3,218 tissue sections across 1,606 patients and 11 organ types.
  • Outperforms baselines in cross-modal retrieval, survival prediction (C-index 0.737), and zero-shot biomarker inference (Pearson correlation 0.718).
  • Introduces a counterfactual prediction framework that modifies clinical metadata while fixing tissue morphology to uncover molecular shifts.
  • Lung adenocarcinoma case study recovers increased CD8 and granzyme B, reduced PD-L1 and Ki67, consistent with favorable outcomes.

Highlights and analysis are generated automatically and may contain errors. Check the original source.