Interpretable spatially aware dimension reduction of spatial transcriptomics with STAMP.

Nat Methods

Bioinformatics Institute (BII), Agency for Science, Technology and Research (A*STAR), Singapore, Singapore.

Published: November 2024

AI Article Synopsis

  • STOMP is a new method for analyzing spatial transcriptomics data that simplifies complex information into meaningful, low-dimensional representations.
  • It utilizes a deep generative model to identify spatial patterns and gene modules that are biologically relevant, enhancing the interpretation of data like lung cancer samples and mouse embryonic development.
  • The method is highly scalable, capable of analyzing datasets with over 500,000 cells, making it versatile for various biological studies.

Article Abstract

Spatial transcriptomics produces high-dimensional gene expression measurements with spatial context. Obtaining a biologically meaningful low-dimensional representation of such data is crucial for effective interpretation and downstream analysis. Here, we present Spatial Transcriptomics Analysis with topic Modeling to uncover spatial Patterns (STAMP), an interpretable spatially aware dimension reduction method built on a deep generative model that returns biologically relevant, low-dimensional spatial topics and associated gene modules. STAMP can analyze data ranging from a single section to multiple sections and from different technologies to time-series data, returning topics matching known biological domains and associated gene modules containing established markers highly ranked within. In a lung cancer sample, STAMP delineated cell states with supporting markers at a higher resolution than the original annotation and uncovered cancer-associated fibroblasts concentrated on the tumor edge's exterior. In time-series data of mouse embryonic development, STAMP disentangled the erythro-myeloid hematopoiesis and hepatocytes developmental trajectories within the liver. STAMP is highly scalable and can handle more than 500,000 cells.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11541207PMC
http://dx.doi.org/10.1038/s41592-024-02463-8DOI Listing

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