Evidence map›Paper›PMID 39753600›Full record

ArticleNature communications2025

Characterizing cell-type spatial relationships across length scales in spatially resolved omics data.

Rafael Dos Santos Peixoto, Brendan F Miller, Maigan A Brusko, Gohta Aihara, Lyla Atta, Manjari Anant, Mark A Atkinson, Todd M Brusko, Clive H Wasserfall, Jean Fan

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Rafael Dos Santos PeixotoCenter for Computational Biology, Whiting School of Engineering, Johns Hopkins University, Baltimore, MD, USA.ORCID 0000-0002-7184-2868
Brendan F MillerCenter for Computational Biology, Whiting School of Engineering, Johns Hopkins University, Baltimore, MD, USA.
Maigan A BruskoDepartment of Pathology, Immunology, and Laboratory Medicine, University of Florida, Gainesville, FL, USA.
Gohta AiharaCenter for Computational Biology, Whiting School of Engineering, Johns Hopkins University, Baltimore, MD, USA.
Lyla AttaCenter for Computational Biology, Whiting School of Engineering, Johns Hopkins University, Baltimore, MD, USA.ORCID 0000-0002-6113-0082
Manjari AnantCenter for Computational Biology, Whiting School of Engineering, Johns Hopkins University, Baltimore, MD, USA.
Mark A AtkinsonDepartment of Pathology, Immunology, and Laboratory Medicine, University of Florida, Gainesville, FL, USA.
Todd M BruskoDepartment of Pathology, Immunology, and Laboratory Medicine, University of Florida, Gainesville, FL, USA.ORCID 0000-0003-2878-9296
Clive H WasserfallDepartment of Pathology, Immunology, and Laboratory Medicine, University of Florida, Gainesville, FL, USA.
Jean FanCenter for Computational Biology, Whiting School of Engineering, Johns Hopkins University, Baltimore, MD, USA. jeanfan@jhu.edu.ORCID 0000-0002-0212-5451

Funding

Project 3P01AI042288 · NIAID · UNIVERSITY OF FLORIDA · PI Todd Michael Brusko · 1997 to 2026
$32.9M
Project 3 - Lymph NodesU54AI142766 · NIAID · UNIVERSITY OF FLORIDA · PI BODENMILLER, BERND · 2018 to 2021
$6.9M
Comprehensive reference atlas construction, geolocation and data integration for HuBMAP HIVE [5 of 5]OT2OD033760 · OD · NEW YORK GENOME CENTER · PI SATIJA, RAHUL · 2022 to 2025
$6.1M
Comprehensive reference map construction, geolocation and data integration for HuBMAP HIVEOT2OD026673 · OD · NEW YORK GENOME CENTER · PI MARIONI, JOHN CARLO, SATIJA, RAHUL · 2018 to 2021
$2.9M
Computational methods for delineating subcellular and cellular spatial transcriptional heterogeneity along developmental trajectoriesR35GM142889 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI FAN, JEAN · 2021 to 2025
$2.0M
NIAID NIH HHS P01 AI042288NIAID NIH HHS U54 AI142766NIGMS NIH HHS R35 GM142889NIH HHS OT2 OD026673NIH HHS OT2 OD033760U.S. Department of Health & Human Services | National Institutes of Health (NIH) OT2-OD033760U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R35-GM142889U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) U54AI-142766
6 · The paper itself

Abstract

Spatially resolved omics (SRO) technologies enable the identification of cell types while preserving their organization within tissues. Application of such technologies offers the opportunity to delineate cell-type spatial relationships, particularly across different length scales, and enhance our understanding of tissue organization and function. To quantify such multi-scale cell-type spatial relationships, we present CRAWDAD, Cell-type Relationship Analysis Workflow Done Across Distances, as an open-source R package. To demonstrate the utility of such multi-scale characterization, recapitulate expected cell-type spatial relationships, and evaluate against other cell-type spatial analyses, we apply CRAWDAD to various simulated and real SRO datasets of diverse tissues assayed by diverse SRO technologies. We further demonstrate how such multi-scale characterization enabled by CRAWDAD can be used to compare cell-type spatial relationships across multiple samples. Finally, we apply CRAWDAD to SRO datasets of the human spleen to identify consistent as well as patient and sample-specific cell-type spatial relationships. In general, we anticipate such multi-scale analysis of SRO data enabled by CRAWDAD will provide useful quantitative metrics to facilitate the identification, characterization, and comparison of cell-type spatial relationships across axes of interest.

Indexed as

SpleenAnimalsComputational BiologyGenomicsHumansSoftware

Identifiers

PMID39753600
PMCPMC11699133

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.