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April 5, 2026Cancer Research0 citations

Abstract 21: AI analysis agent to accelerate end-to-end spatial biology analysis for MERSCOPE.

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HMHarihara Subrahmaniam MuralidharanCCCheng-Yi ChenFPFriedrich Preusser

Key Points

  • The research aims to streamline spatial biology analysis using AI to handle large datasets from MERSCOPE.
  • Developed an AI-driven agent to process MERSCOPE outputs efficiently.
  • Utilized large language models for interactive user queries on data.
  • Integrated bioinformatics pipelines for advanced data analysis.
  • Validated performance on breast and colorectal cancer samples.
  • AI agent completed full analyses in approximately 6 hours, significantly faster than the traditional 72 hours.
  • Reduction in manual scripting and dependency management efforts by about 60%.
  • Improved pipeline reliability with decreased downstream errors.
  • Provided interactive notebooks for rapid review of analysis results.

Abstract

Abstract Background: Spatial biology assays on the MERSCOPE platform enable subcellular mapping of RNA transcripts and proteins within the tumor architecture. However, these assays generate terabyte-scale datasets that require complex computational workflows. Post-acquisition analysis including cell segmentation, cell typing, and spatial domain detection remains computationally intensive and requires specialized bioinformatics expertise. This can limit accessibility for many cancer biology laboratories. To overcome these barriers, Vizgen and LatchBio have developed an AI-driven workflow powered by large language model (LLM) agents, designed to streamline and simplify end-to-end spatial biology analysis for MERSCOPE in oncology research. Methods: We implemented an LLM-driven agent tailored to the Vizgen data ecosystem. The agent (1) parses MERSCOPE outputs (multi-channel z-stack images, transcript coordinate files, metadata) and launches optimized GPU-accelerated workflows for image segmentation and transcript assignment; (2) presents an interactive notebook interface (Markdown, plots, widgets) so users can specify downstream questions in natural language (e.g., “Identify Cytotoxic T-Cells within tumor border regions”); (3) triggers bioinformatics pipelines for clustering, cell-type annotation, spatial domain detection, and differential expression/regulation; and (4) integrates with LatchBio’s scalable compute/storage infrastructure for large-scale runs (1 TB per dataset). We validated performance on breast cancer and colorectal cancer samples processed on MERSCOPE. Results: The agent successfully handled large-scale, multi-sample MERFISH spatial transcriptomics datasets. It performed end-to-end analysis (cell re-segmentation, unsupervised clustering, spatial domain detection, and differential expression in selected cell populations) within a single run. Outputs were delivered as interactive, reproducible notebooks for a rapid review of cell-type-annotated clusters, spatial domain maps, and differential expression summaries. Compared with a conventional manually scripted workflow, the agent completed full analyses in ∼6 hours (vs ∼72 h traditionally). In end-user testing, it reduced manual scripting and dependency management efforts by ∼60 % and decreased downstream errors, improving pipeline reliability. Conclusions: The Vizgen-LatchBio AI-agentic workflow provides a scalable, user-friendly solution for advanced MERSCOPE data analysis, enabling spatial biology labs to self-serve complex computational tasks. By abstracting computational complexity and embedding domain-specific logic, this system empowers biologists to focus on biological insights rather than technical tool-chaining. Consequently, it shortens time-to-insight and facilitates high-throughput workflows across drug discovery, disease research, and academic studies. Citation Format: Harihara Muralidharan, Cheng-Yi Chen, Friedrich Preusser, Ruben Cardenes, Kenny Workman, Hannah Le, Alfredo Andere, Lorenz Rognoni. AI analysis agent to accelerate end-to-end spatial biology analysis for MERSCOPE abstract. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 21.

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Muralidharan et al. (2026) studied this question.

synapsesocial.com/papers/69d1fd4ea79560c99a0a33f5https://doi.org/10.1158/1538-7445.am2026-21
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