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Author

Jichao Chen

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Open access Aug 2026

A Conversational Multi-Agent AI System for Integrated Multi-Omics Analysis and Biomedical Discovery

Single-cell and spatial omics offer unprecedented opportunities to decipher the mechanisms of disease, however, this process requires teams of experts, iterative trial-and-error and reasoning across modalities. Here we present LungChat (https://chat.lungmap.net), a conversational system for integrated multi-omics analysis and biomedical discovery, deployed as a hierarchical multi-agent architecture in which a supervisor decomposes natural-language questions into parallel, tool-grounded tasks spanning single-cell and spatial analyses, literature and clinical-trial synthesis, and drug repurposing. To predict new therapeutics, LungChat implements Direction-Aware Repurposing and Targeting (DART) to distinguish perturbations that reverse disease transcriptional programs from those that reinforce them, at the cell-type level, for safety prediction. Controlled architecture ablations showed that hierarchical orchestration improved grounded abstention and token efficiency and preserved strong performance on complex multi-step tasks. In pulmonary disease case studies, LungChat independently prioritized saracatinib for IPF through drug-connectivity screening, followed by DART-based cell-type analysis; the same compound has been evaluated in the STOP-IPF clinical trial (NCT04598919). The system also recovered fluticasone propionate, an established COPD therapy, through a single orchestrated analysis. This tissue-agnostic system provides a blueprint for verifiable agentic AI systems that support reproducible scientific discovery.

Pankaj Rajdeo, Shunya Asanuma, Michal Kouril et al. · 0 citations
Open access Aug 2026

Multi-modal Graph Integration for Biologically Interpretable Domain Identification Using Spatial Transcriptomics

Functional domain identification in spatial transciptomics transforms spatial molecular measurements into mechanistic insights into tissue physiology and pathology. However, the inherent noise and sparsity of gene expression data, along with the locality-biased design of conventional graph-based approaches, fundamentally limit the accurate identification of complex tissue domains. In this study, we propose a novel Biologically Interpretable multi-modal Graph using Spatial Transcriptomics, called BIGraph-ST, that integrates pathway activity scores and histological image features for robust spatial domain identification. BIGraph-ST represents modality-specific similarity through affinity graphs and propagates spatial topology to capture higher-order connectivity within the tissue microenvironment. Experimental results demonstrated robust performance and notable improvements across multiple gold-standard benchmark datasets, particularly in cancer tissues. Moreover, BIGraph-ST provides biologically interpretable pathway-level representations of domains, which ultimately offers a valuable tool to gain biological in-sights into complex tissue architectures. The source code will be publicly available upon acceptance.

Seungeun Lee, Guolon Wang, Kyungtae Kang et al. · 0 citations

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