Evidence map›Paper›PMID 42516583›Full record

ArticleBio-protocol2026

Actin Quantification Using the Filamentous Actin Segmentation Tool (FAST).

Vineeth Aljapur, Adam Gardner, Jason Carayanniotis, Andrew R Harris

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
–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

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

4 authors.

Vineeth AljapurMAAE, Carleton University, Ottawa, ON, Canada.
Adam GardnerArtinus Consulting Inc, Ottawa, ON, Canada.
Jason CarayanniotisArtinus Consulting Inc, Ottawa, ON, Canada.
Andrew R HarrisMAAE, Carleton University, Ottawa, ON, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Studying actin-filament assembly into distinct subcellular structures can provide insights into both physiological cellular processes and the mechanisms of disease. However, there are a limited number of tools that can quantify the organization and abundance of different actin structures from confocal microscopy images of cells expressing Lifeact or fixed and stained with phalloidin. Filamentous actin segmentation tool (FAST) is a deep learning model trained with a unique approach of antibody-assisted annotation, resulting in accurate and efficient quantification of distinct classes of actin structures. Here, we detail the protocol for using antibody-assisted annotation to generate datasets that could be applied to train machine learning models. Additionally, we provide step-by-step instructions for applying FAST on phalloidin-stained or live-cell confocal imaging data using our pretrained model. FAST is open source and freely available, with user-friendly notebooks that enable quantification of different classes of actin structure, without the need for structure-specific antibodies. As such, FAST can be a practical tool for researchers investigating the role of cytoskeletal organization in a range of processes. Key features • This antibody-assisted labeling approach can be used for identifying different classes of actin structure and generating labeled datasets for training machine learning algorithms. • The trained FAST model then enables the detection of distinct classes of actin structure without the need for multiple structure-specific antibodies. • FAST generates segmentation masks that can be used to quantify the abundance and organization of detected classes. • This protocol provides a graphical user interface for fine-tuning custom phalloidin-stained images and provides instructions on using trained model on Ilastik interface.

Indexed as

ActinCell segmentationConfocal microscopyCytoskeletonDeep learningFluorescence microscopy

Identifiers

PMID42516583
PMCPMC13403133

What OpenQuestion holds

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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.