Evidence map›Paper›PMID 38417823›Full record

ArticleJournal of proteome research2024

SpaceANOVA: Spatial Co-occurrence Analysis of Cell Types in Multiplex Imaging Data Using Point Process and Functional ANOVA.

Souvik Seal, Brian Neelon, Peggi M Angel, Elizabeth C O'Quinn, Elizabeth Hill, Thao Vu, Debashis Ghosh, Anand S Mehta, Kristin Wallace, Alexander V Alekseyenko

Abstract read
In one paragraph

Article in Journal of proteome research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Differences in T-cell Densities and Neighborhood Patterns in Human Colorectal Adenomas and Sessile Serrated Lesions.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Observational
  7. Article
  8. A Spatial Omnibus Test (SPOT) for Spatial Proteomic Data.Bioinformatics (Oxford, England) · 2024
    Article
  9. A Spatial Omnibus Test (SPOT) for Spatial Proteomic Data.bioRxiv : the preprint server for biology · 2024
    Article
  10. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Souvik SealDepartment of Public Health Sciences, Medical University of South Carolina Charleston, South Carolina 29425, United States.ORCID 0000-0003-3268-610X
Brian NeelonDepartment of Public Health Sciences, Medical University of South Carolina Charleston, South Carolina 29425, United States.
Peggi M AngelDepartment of Cell and Molecular Pharmacology and Experimental Therapeutics, Medical University of South Carolina Charleston, South Carolina 29425, United States.ORCID 0000-0002-4436-555X
Elizabeth C O'QuinnTranslational Science Laboratory, Hollings Cancer Center, Medical University of South Carolina Charleston, South Carolina 29425, United States.
Elizabeth HillDepartment of Public Health Sciences, Medical University of South Carolina Charleston, South Carolina 29425, United States.
Thao VuDepartment of Biostatistics and Informatics, University of Colorado CU Anschutz Medical Campus Aurora, Colorado 80045, United States.
Debashis GhoshDepartment of Biostatistics and Informatics, University of Colorado CU Anschutz Medical Campus Aurora, Colorado 80045, United States.
Anand S MehtaDepartment of Cell and Molecular Pharmacology and Experimental Therapeutics, Medical University of South Carolina Charleston, South Carolina 29425, United States.ORCID 0000-0002-9846-9389
Kristin WallaceDepartment of Public Health Sciences, Medical University of South Carolina Charleston, South Carolina 29425, United States.
Alexander V AlekseyenkoDepartment of Public Health Sciences, Medical University of South Carolina Charleston, South Carolina 29425, United States.

Funding

Translational Science Laboratory Shared ResourceP30CA138313 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI John J Lemasters · 2009 to 2026
$42.7M
South Carolina Cancer Disparities Research Center (SC CADRE)U54CA210962 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI FORD, MARVELLA ELIZABETH, SALLEY, JUDITH · 2017 to 2023
$6.7M
The immune contexture of colorectal adenomas and serrated polypsR01CA226086 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI WALLACE, KRISTIN · 2019 to 2023
$3.1M
Distance-based Panomic Analytics for Microbiome DataR01LM012517 · NLM · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI ALEKSEYENKO, ALEXANDER V · 2018 to 2021
$1.3M
Multivariate spatiotemporal models to quantify disparities in COVID-19 health outcomesR21MD016947 · NIMHD · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI NEELON, BRIAN · 2022 to 2023
$428k
NCI NIH HHS P30 CA138313NCI NIH HHS R01 CA226086NCI NIH HHS U54 CA210962NIMHD NIH HHS R21 MD016947NLM NIH HHS R01 LM012517
6 · The paper itself

Abstract

Multiplex imaging platforms have enabled the identification of the spatial organization of different types of cells in complex tissue or the tumor microenvironment. Exploring the potential variations in the spatial co-occurrence or colocalization of different cell types across distinct tissue or disease classes can provide significant pathological insights, paving the way for intervention strategies. However, the existing methods in this context either rely on stringent statistical assumptions or suffer from a lack of generalizability. We present a highly powerful method to study differential spatial co-occurrence of cell types across multiple tissue or disease groups, based on the theories of the Poisson point process and functional analysis of variance. Notably, the method accommodates multiple images per subject and addresses the problem of missing tissue regions, commonly encountered due to data-collection complexities. We demonstrate the superior statistical power and robustness of the method in comparison with existing approaches through realistic simulation studies. Furthermore, we apply the method to three real data sets on different diseases collected using different imaging platforms. In particular, one of these data sets reveals novel insights into the spatial characteristics of various types of colorectal adenoma.

Indexed as

Computer SimulationAnalysis of Varianceco-localizationcolorectal adenomadifferential studyIMCMIBImultiplex immunofluorescenceR package

Identifiers

PMID38417823
PMCPMC11002919

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.