Quantitative characterization of tissue states using multiomics and ecological spatial analysis

The spatial organization of cells in tissues underlies biological function, and recent advances in spatial profiling technologies have enhanced our ability to analyze such arrangements to study biological processes and disease progression. We propose MESA (multiomics and ecological spatial analysis), a framework drawing inspiration from ecological concepts to delineate functional and spatial shifts across tissue states. MESA introduces metrics to systematically quantify spatial diversity and identify hot spots, linking spatial patterns to phenotypic outcomes, including disease progression. Furthermore, MESA integrates spatial and single-cell multiomics data to facilitate an in-depth, molecular understanding of cellular neighborhoods and their spatial interactions within tissue microenvironments. Applying MESA to diverse datasets demonstrates additional insights it brings over prior methods, including newly identified spatial structures and key cell populations linked to disease states. Available as a Python package, MESA offers a versatile framework for quantitative decoding of tissue architectures in spatial omics across health and disease.

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Publication Details

Journal
Nature Genetics
Published
2025-04-01
DOI
https://doi.org/10.1038/s41588-025-02119-z
Citations
17
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
13.70
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article

Quantitative characterization of tissue states using multiomics and ecological spatial analysis

Daisy Yi Ding, Hongyu Ren, Bokai Zhu, Robert John Tibshirani et al.
17 citations
Nature Genetics
Single-cell and spatial transcriptomics
13.70
article

Quantitative characterization of tissue states using multiomics and ecological spatial analysis

Daisy Yi Ding, Hongyu Ren, Bokai Zhu, Robert John Tibshirani, Garry P. Nolan, Zeyu Tang, Alex K. Shalek
article en
17 citations

Abstract

The spatial organization of cells in tissues underlies biological function, and recent advances in spatial profiling technologies have enhanced our ability to analyze such arrangements to study biological processes and disease progression. We propose MESA (multiomics and ecological spatial analysis), a framework drawing inspiration from ecological concepts to delineate functional and spatial shifts across tissue states. MESA introduces metrics to systematically quantify spatial diversity and identify hot spots, linking spatial patterns to phenotypic outcomes, including disease progression. Furthermore, MESA integrates spatial and single-cell multiomics data to facilitate an in-depth, molecular understanding of cellular neighborhoods and their spatial interactions within tissue microenvironments. Applying MESA to diverse datasets demonstrates additional insights it brings over prior methods, including newly identified spatial structures and key cell populations linked to disease states. Available as a Python package, MESA offers a versatile framework for quantitative decoding of tissue architectures in spatial omics across health and disease.

Nature GeneticsVol. 57(4)
Broad Institute (US), Cornell University (US), Ragon Institute of MGH, MIT and Harvard (US), IIT@MIT (US), Stanford Medicine (US), Allen Institute (US), Weill Cornell Medicine (US), Koch Institute for Integrative Cancer Research At MIT (US), Stanford University (US)
Openalex Percentile: Top 1%
Single-cell and spatial transcriptomics
13.70
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Quantitative characterization of tissue states using multiomics and ecological spatial analysis — Daisy Yi Ding, Hongyu Ren, et al. · Nature Genetics (2025) | TGRS Research Map | TGRS