Evidence map›Paper›PMID 39314450›Full record

ArticlebioRxiv : the preprint server for biology2024

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 readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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 21211.ORCID 0000-0002-7184-2868
Brendan F MillerCenter for Computational Biology, Whiting School of Engineering, Johns Hopkins University, Baltimore, MD 21211.ORCID 0000-0002-9559-4045
Maigan A BruskoDepartment of Pathology, Immunology, and Laboratory Medicine, University of Florida, Gainesville, FL 32610.
Gohta AiharaCenter for Computational Biology, Whiting School of Engineering, Johns Hopkins University, Baltimore, MD 21211.ORCID 0000-0002-2492-9610
Lyla AttaCenter for Computational Biology, Whiting School of Engineering, Johns Hopkins University, Baltimore, MD 21211.ORCID 0000-0002-6113-0082
Manjari AnantCenter for Computational Biology, Whiting School of Engineering, Johns Hopkins University, Baltimore, MD 21211.ORCID 0000-0002-6600-3410
Mark A AtkinsonDepartment of Pathology, Immunology, and Laboratory Medicine, University of Florida, Gainesville, FL 32610.ORCID 0000-0001-8489-4782
Todd M BruskoDepartment of Pathology, Immunology, and Laboratory Medicine, University of Florida, Gainesville, FL 32610.ORCID 0000-0003-2878-9296
Clive H WasserfallDepartment of Pathology, Immunology, and Laboratory Medicine, University of Florida, Gainesville, FL 32610.ORCID 0000-0002-3522-8932
Jean FanCenter for Computational Biology, Whiting School of Engineering, Johns Hopkins University, Baltimore, MD 21211.ORCID 0000-0002-0212-5451

Funding

Project 3 - Lymph NodesU54AI142766 · NIAID · UNIVERSITY OF FLORIDA · PI BRUSKO, TODD MICHAEL · 2018 to 2021
$6.9M
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 U54 AI142766NIGMS NIH HHS R35 GM142889NIH HHS OT2 OD026673
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 developed CRAWDAD, Cell-type Relationship Analysis Workflow Done Across Distances, as an open-source R package with source code and additional documentation at https://jef.works/CRAWDAD/. To demonstrate the utility of such multi-scale characterization, recapitulate expected cell-type spatial relationships, and evaluate against other cell-type spatial analyses, we applied 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 applied 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

colocalizationsingle cellspatial omicsspatial relationshipsspatial subsetting

Identifiers

PMID39314450
PMCPMC11418938

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.