Evidence map›Paper›PMID 37461579›Full record

ArticlebioRxiv : the preprint server for biology2023

SpaceANOVA: Spatial co-occurrence analysis of cell types in multiplex imaging data using point process and functional ANOVA.

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

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. 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.

Souvik SealDepartment of Public Health Sciences, Medical University of South Carolina, Charleston, South Carolina.
Brian NeelonDepartment of Public Health Sciences, Medical University of South Carolina, Charleston, South Carolina.
Peggi AngelDepartment of Cell and Molecular Pharmacology and Experimental Therapeutics, Medical University of South Carolina, Charleston, South Carolina.
Elizabeth C O'QuinnTranslational Science Laboratory, Hollings Cancer Center, Medical University of South Carolina, Charleston, South Carolina.
Elizabeth HillDepartment of Public Health Sciences, Medical University of South Carolina, Charleston, South Carolina.
Thao VuDepartment of Biostatistics and Informatics, University of Colorado CU Anschutz Medical Campus, Aurora, Colorado.
Debashis GhoshDepartment of Biostatistics and Informatics, University of Colorado CU Anschutz Medical Campus, Aurora, Colorado.
Anand MehtaDepartment of Cell and Molecular Pharmacology and Experimental Therapeutics, Medical University of South Carolina, Charleston, South Carolina.
Kristin WallaceDepartment of Public Health Sciences, Medical University of South Carolina, Charleston, South Carolina.
Alexander V AlekseyenkoDepartment of Public Health Sciences, Medical University of South Carolina, Charleston, South Carolina.

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 TURNER, DAVID PAUL · 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
NCI NIH HHS P30 CA138313NCI NIH HHS R01 CA226086NCI NIH HHS U54 CA210962NLM NIH HHS R01 LM012517
6 · The paper itself

Abstract

Motivation: Multiplex imaging platforms have enabled the identification of the spatial organization of different types of cells in complex tissue or tumor microenvironment (TME). Exploring the potential variations in the spatial co-occurrence or co-localization 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. Results: 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 (PPP) and functional analysis of variance (FANOVA). Notably, the method accommodates multiple images per subject and addresses the problem of missing tissue regions, commonly encountered in such a context due to the complex nature of the data-collection procedure. We demonstrate the superior statistical power and robustness of the method in comparison to existing approaches through realistic simulation studies. Furthermore, we apply the method to three real datasets on different diseases collected using different imaging platforms. In particular, one of these datasets reveals novel insights into the spatial characteristics of various types of precursor lesions associated with colorectal cancer. Availability: The associated

Identifiers

PMID37461579
PMCPMC10350074

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.