Evidence map›Paper›PMID 37152666›Full record

ArticleMethodsX2023

Semi-automated micro-computed tomography lung segmentation and analysis in mouse models.

Jonathan D Luisi, Jonathan L Lin, Lorenzo F Ochoa, Ryan J McAuley, Madison G Tanner, Obada Alfarawati, Casey W Wright, Gracie Vargas, Massoud Motamedi, Bill T Ameredes

Open access · goldAbstract read
In one paragraph

Article in MethodsX, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 24% of its field
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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Jonathan D LuisiUniversity of Texas Medical Branch, 301 University Blvd., Galveston, TX 77555, United States.
Jonathan L LinUniversity of Texas Medical Branch, 301 University Blvd., Galveston, TX 77555, United States.
Lorenzo F OchoaUniversity of Texas Medical Branch, 301 University Blvd., Galveston, TX 77555, United States.
Ryan J McAuleyUniversity of Texas Medical Branch, 301 University Blvd., Galveston, TX 77555, United States.
Madison G TannerUniversity of Texas Medical Branch, 301 University Blvd., Galveston, TX 77555, United States.
Obada AlfarawatiUniversity of Texas Medical Branch, 301 University Blvd., Galveston, TX 77555, United States.
Casey W WrightUniversity of Texas Medical Branch, 301 University Blvd., Galveston, TX 77555, United States.
Gracie VargasUniversity of Texas Medical Branch, 301 University Blvd., Galveston, TX 77555, United States.
Massoud MotamediUniversity of Texas Medical Branch, 301 University Blvd., Galveston, TX 77555, United States.
Bill T AmeredesUniversity of Texas Medical Branch, 301 University Blvd., Galveston, TX 77555, United States.
The University of Texas Medical Branch at Galveston · US

Funding

Translational Research Support CoreP30ES030285 · NIEHS · BAYLOR COLLEGE OF MEDICINE · PI Cheryl L. Walker · 2019 to 2026
$14.7M
Molecular Mechanisms of Environmental InjuryT32ES007254 · NIEHS · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI AMEREDES, BILL T · 1990 to 2022
$6.6M
Novel ARNT-mediated Regulatory Paradigm of AHR SignalingR01ES025809 · NIEHS · UNIVERSITY OF TEXAS MED BR GALVESTON · PI WRIGHT, CASEY W · 2016 to 2021
$1.9M
NIEHS NIH HHS R01 ES025809NIEHS NIH HHS T32 ES007254
6 · The paper itself

Abstract

Computed Tomography (CT) is a standard clinical tool utilized to diagnose known lung pathologies based on established grading methods. However, for preclinical trials and toxicity investigations in animal models, more comprehensive datasets are typically needed to determine discriminative features between experimental treatments, which oftentimes require analysis of multiple images and their associated differential quantification using manual segmentation methods. Furthermore, for manual segmentation of image data, three or more readers is the gold standard of analysis, but this requirement can be time-consuming and inefficient, depending on variability due to reader bias. In previous papers, microCT image manual segmentation was a valuable tool for assessment of lung pathology in several animal models; however, the manual segmentation approach and the commercial software used was typically a major rate-limiting step. To improve the efficiency, the semi-manual segmentation method was streamlined, and a semi-automated segmentation process was developed to produce:•Quantifiable segmentations: using manual and semi-automated analysis methods for assessing experimental injury and toxicity models,•Deterministic results and efficiency through automation in an unbiased and parameter free process, thereby reducing reader variance, user time, and increases throughput in data analysis,•Cost-Effectiveness: portable with low computational resource demand, based on a cross-platform open-source ImageJ program.

Indexed as

Automated Image SegmentationBleomycinImage analysisLung tissue densityManual image segmentationPulmonary toxicologySemiautomated Micro-CT Lung Segmentation and Analysis in Mouse Models

Identifiers

PMID37152666
PMCPMC10154963
OpenAlexW4366526295

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.