Evidence map›Paper›PMID 30032263›Full record

ArticleBioinformatics (Oxford, England)2019

CIRCOAST: a statistical hypothesis test for cellular colocalization with network structures.

Bruce A Corliss, H Clifton Ray, James T Patrie, Jennifer Mansour, Sam Kesting, Janice H Park, Gustavo Rohde, Paul A Yates, Kevin A Janes, Shayn M Peirce

Erratum issuedAbstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Bruce A CorlissDepartment of Biomedical Engineering, University of Virginia, Charlottesville, VA, USA.
H Clifton RayDepartment of Biomedical Engineering, University of Virginia, Charlottesville, VA, USA.
James T PatrieDepartment of Public Health Sciences, University of Virginia, Charlottesville, VA, USA.
Jennifer MansourDepartment of Biology, University of Virginia, Charlottesville, VA, USA.
Sam KestingDepartment of Biomedical Engineering, University of Virginia, Charlottesville, VA, USA.
Janice H ParkDepartment of Biology, University of Virginia, Charlottesville, VA, USA.
Gustavo RohdeDepartment of Biomedical Engineering, University of Virginia, Charlottesville, VA, USA.
Paul A YatesDepartment of Ophthalmology, University of Virginia, Charlottesville, VA, USA.
Kevin A JanesDepartment of Biomedical Engineering, University of Virginia, Charlottesville, VA, USA.
Shayn M PeirceDepartment of Biomedical Engineering, University of Virginia, Charlottesville, VA, USA.

Funding

Image-derived Spatiotemporal Models of Cellular Organization and PerturbationR01GM090033 · NIGMS · CARNEGIE-MELLON UNIVERSITY · PI MURPHY, ROBERT F, ROHDE, GUSTAVO KUNDE · 2010 to 2018
$2.4M
An Integrated Systems Approach for Incompletely Penetrant Onco-phenotypes.U01CA215794 · NCI · UNIVERSITY OF VIRGINIA · PI JANES, KEVIN A · 2017 to 2021
$2.4M
Adipose Stem Cells for Diabetic RetinopathyR01EY022063 · NEI · UNIVERSITY OF VIRGINIA · PI HERMAN, IRA M, PEIRCE-COTTLER, SHAYN · 2012 to 2015
$2.0M
Heterogeneous Loss of GDF11 Tumor Suppression in Triple-negative Breast CancerR01CA214718 · NCI · UNIVERSITY OF VIRGINIA · PI JANES, KEVIN A · 2018 to 2022
$1.8M
NCI NIH HHS R01 CA214718NCI NIH HHS U01 CA215794NEI NIH HHS R01 EY022063NIGMS NIH HHS R01 GM090033
6 · The paper itself

Abstract

Motivation: Colocalization of structures in biomedical images can lead to insights into biological behaviors. One class of colocalization problems is examining an annular structure (disk-shaped such as a cell, vesicle or molecule) interacting with a network structure (vascular, neuronal, cytoskeletal, organellar). Examining colocalization events across conditions is often complicated by changes in density of both structure types, confounding traditional statistical approaches since colocalization cannot be normalized to the density of both structure types simultaneously. We have developed a technique to measure colocalization independent of structure density and applied it to characterizing intercellular colocation with blood vessel networks. This technique could be used to analyze colocalization of any annular structure with an arbitrarily shaped network structure. Results: We present the circular colocalization affinity with network structures test (CIRCOAST), a novel statistical hypothesis test to probe for enriched network colocalization in 2D z-projected multichannel images by using agent-based Monte Carlo modeling and image processing to generate the pseudo-null distribution of random cell placement unique to each image. This hypothesis test was validated by confirming that adipose-derived stem cells (ASCs) exhibit enriched colocalization with endothelial cells forming arborized networks in culture and then applied to show that locally delivered ASCs have enriched colocalization with murine retinal microvasculature in a model of diabetic retinopathy. We demonstrate that the CIRCOAST test provides superior power and type I error rates in characterizing intercellular colocalization compared to generic approaches that are confounded by changes in cell or vessel density. Availability and implementation: CIRCOAST source code available at: https://github.com/uva-peirce-cottler-lab/ARCAS. Supplementary information: Supplementary data are available at Bioinformatics online.

Indexed as

SoftwareAdipose TissueAnimalsCells, CulturedDiabetic RetinopathyEndothelial CellsImage Processing, Computer-AssistedMiceMonte Carlo MethodNeuronsStem Cells

Identifiers

PMID30032263
PMCPMC6361237

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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.