Evidence map›Paper›PMID 41821868›Full record

ArticleBio-protocol2026

Machine Learning-Assisted Quantification of Organelle Abundance.

Alexander James Long, Diogo Candeias, Nicki Frederick Coveña, Luc Reymond, Milena Schuhmacher, Stephan Kemp, Noémie Hamilton, Triana Amen

Abstract read
In one paragraph

Article in Bio-protocol, 2026. 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
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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

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

8 authors.

Alexander James LongSchool of Biological Sciences, University of Southampton, Southampton, UK.
Diogo CandeiasDepartment of Biology, University of York, York, UK.
Nicki Frederick CoveñaDepartment of Complex Trait Genetics, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Luc ReymondBiomolecular Screening Facility, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.
Milena SchuhmacherGlobal Health Institute, Faculty of Life Sciences, Ecole Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.
Stephan KempLaboratory Genetic Metabolic Diseases, Department of Laboratory Medicine, Amsterdam UMC, Amsterdam Gastroenterology Endocrinology Metabolism, University of Amsterdam, Amsterdam, The Netherlands.
Noémie HamiltonDepartment of Biology, University of York, York, UK.
Triana AmenSchool of Biological Sciences, University of Southampton, Southampton, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Organelle abundance is a key microscopic readout of organelle formation and, in many cases, function. Quantification of organelle abundance using confocal microscopy requires estimating their area based on the fluorescence intensity of compartment-specific markers. This analysis usually depends on a user-defined intensity threshold to distinguish organelle regions from the surrounding cytoplasm, which introduces potential bias and variability. To address this issue, we present a machine learning-assisted algorithm that allows for the quantification of organelle density using the open-source Fiji platform and WEKA segmentation. Our method enables the automated quantification of organelle number, area, and density by learning from training data. This standardizes threshold selection and minimizes user intervention. We demonstrate the utility of this approach for both membrane and non-membrane organelles, such as peroxisomes, lipid droplets, and stress granules, in human cells and whole fish samples. Key features • The organelle abundance algorithm is an automated, open-source, Fiji-based tool that extracts organelle number and area and calculates abundance based on a single marker. • The macro measures the average intensity of all the segmented areas and quantifies their area. • The algorithm is applicable to cellular compartments, including membrane-bound and membrane-less organelles. • The training is performed on a sample dataset, enabling the algorithm to be applied to all images obtained with the same imaging parameters.

Indexed as

AbundanceDensityFijiMachine learningOrganellePeroxisomePeroxiSPYQuantificationStress granuleWEKA segmentation

Identifiers

PMID41821868
PMCPMC12976879

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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.