Staff and Researcher Publications

Language

English

Publication Date

8-19-2024

Journal

Cell Reports Methods

DOI

10.1016/j.crmeth.2024.100838

PMID

39127044

PMCID

PMC11384092

PubMedCentral® Posted Date

8-9-2024

PubMedCentral® Full Text Version

Post-print

Abstract

Tissues are organized into anatomical and functional units at different scales. New technologies for high-dimensional molecular profiling in situ have enabled the characterization of structure-function relationships in increasing molecular detail. However, it remains a challenge to consistently identify key functional units across experiments, tissues, and disease contexts, a task that demands extensive manual annotation. Here, we present spatial cellular graph partitioning (SCGP), a flexible method for the unsupervised annotation of tissue structures. We further present a reference-query extension pipeline, SCGP-Extension, that generalizes reference tissue structure labels to previously unseen samples, performing data integration and tissue structure discovery. Our experiments demonstrate reliable, robust partitioning of spatial data in a wide variety of contexts and best-in-class accuracy in identifying expertly annotated structures. Downstream analysis on SCGP-identified tissue structures reveals disease-relevant insights regarding diabetic kidney disease, skin disorder, and neoplastic diseases, underscoring its potential to drive biological insight and discovery from spatial datasets.

Keywords

Humans, Animals, Computational Biology, Diabetic Nephropathies, Mice, Skin Diseases, spatial omics, artificial intelligence, unsupervised annotation

Published Open-Access

yes

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