Evidence map›Paper›PMID 40272653›Full record

ArticleNeuroinformatics2025

Semi-automated Analysis of Beading in Degenerating Axons.

Pretheesh Kumar V C, Pramod Pullarkat

Abstract read
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In one paragraph

Article in Neuroinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

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

2 authors.

Pretheesh Kumar V CRaman Research Institute, Bangalore, India. pretheesh@rrimail.rri.res.in.
Pramod PullarkatRaman Research Institute, Bangalore, India.

Funding

Wellcome Trust DBT India Alliance IA/TSG/20/1/ 600137
6 · The paper itself

Abstract

Axonal beading is a key morphological indicator of axonal degeneration, which plays a significant role in various neurodegenerative diseases and drug-induced neuropathies. Quantification of axonal susceptibility to beading using neuronal cell culture can be used as a facile assay to evaluate induced degenerative conditions, and thus aid in understanding mechanisms of beading and in drug development. Manual analysis of axonal beading for large datasets is labor-intensive and prone to subjectivity, limiting the reproducibility of results. To address these challenges, we developed a semi-automated Python-based tool to track axonal beading in time-lapse microscopy images. The software significantly reduces human effort by detecting the onset of axonal swelling. Our method is based on classical image processing techniques rather than an AI approach. This provides interpretable results while allowing the extraction of additional quantitative data, such as bead density, coarsening dynamics, and morphological changes over time. Comparison of results obtained through human analysis and the software shows strong agreement. The code can be easily extended to analyze diameter information of ridge-like structures in branched networks of rivers, road networks, blood vessels, etc.

Indexed as

AxonsImage Processing, Computer-AssistedNerve DegenerationAnimalsCells, CulturedHumansSoftwareTime-Lapse ImagingAxonal beadingAxonal degenerationDiameter fluctuations of axonsImage processingMorphological analysis of axonsNeurodegenerative diseasesTime-lapse microscopy

Identifiers

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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.