Evidence map›Paper›PMID 41105693›Full record

ArticlePloS one2025

High throughput machine learning pipeline to characterize larval zebrafish motor behavior.

John Hageter, John Efromson, Brooke Alban, Audrey DelGaudio, Veton Saliu, Monica Wassef, Mark Harfouche, Eric J Horstick

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

John HageterWest Virginia University, Department of Biology, Morgantown, West Virginia, United States of America.
John EfromsonRamona Optics Inc., Durham, North Carolina, United States of America.
Brooke AlbanWest Virginia University, Department of Biology, Morgantown, West Virginia, United States of America.
Audrey DelGaudioWest Virginia University, Department of Biology, Morgantown, West Virginia, United States of America.
Veton SaliuRamona Optics Inc., Durham, North Carolina, United States of America.
Monica WassefRamona Optics Inc., Durham, North Carolina, United States of America.
Mark HarfoucheRamona Optics Inc., Durham, North Carolina, United States of America.
Eric J HorstickWest Virginia University, Department of Biology, Morgantown, West Virginia, United States of America.ORCID https://orcid.org/0000-0003-3846-7450

Funding

VS-CoBRE Administrative CoreP20GM144230 · NIGMS · WEST VIRGINIA UNIVERSITY · PI Visvanathan Ramamurthy · 2022 to 2026
$13.9M
A parallelized computational microscope platform for high-throughput live imaging of patient-derived organoidsR44CA285197 · NCI · RAMONA OPTICS, INC. · PI Mark Harfouche · 2024 to 2026
$2.4M
High-content behavioral phenotyping of model organisms in three dimensions with a gigapixel microscopeR44OD036187 · OD · RAMONA OPTICS, INC. · PI HARFOUCHE, MARK · 2024 to 2025
$2.0M
A parallelized imaging platform for accurate and efficient long-term assessment of brain organoid developmentR43MH133521 · NIMH · RAMONA OPTICS, INC. · PI HARFOUCHE, MARK · 2024 to 2025
$950k
Examining how visual experience modulates the thalamus and visuomotor responses.R15EY036226 · NEI · WEST VIRGINIA UNIVERSITY · PI HORSTICK, ERIC JAMES · 2024 to 2024
$444k
Integrating developmental neurotoxicity screening using automated neuro-behavioral, morphological and neuro-developmental tests in the larval zebrafishR43ES036389 · NIEHS · RAMONA OPTICS, INC. · PI HARFOUCHE, MARK · 2024 to 2024
$295k
NCI NIH HHS R44 CA285197NEI NIH HHS R15 EY036226NIEHS NIH HHS R43 ES036389NIGMS NIH HHS P20 GM144230NIH HHS R44 OD036187NIMH NIH HHS R43 MH133521
6 · The paper itself

Abstract

Using machine learning, we developed models that rigorously detect and classify larval zebrafish spontaneous and stimulus-evoked behaviors in various well plate formats. Zebrafish are an ideal model system for investigating the neural substrates underlying behavior due to their simple nervous system and well-documented responses to environmental stimuli. To track movement, we utilized an 8 key point pose estimation model, allowing precise capture of zebrafish kinematics. Using this kinematic data, we trained two random forest classifiers in a semi-supervised learning framework to classify various discreet behavioral outputs including stationary, scoot, turn, acoustic-startle like behavior, and visual-startle like behavior. The classifiers were trained on a manually labeled dataset, and their accuracy was validated showing high precision. To validate our machine learning models, we analyzed behavioral outputs during various stimulus evoked responses and during spontaneous behavior. For additional validation, and to show the utility of our recording and analysis pipeline, we investigated the locomotor effects of several established drugs with well-defined impacts on neurophysiology. Here we show that machine learning model development, enabled by semi-supervised learning developed classification models, provide detailed insights into the behavioral phenotypes of zebrafish, offering a powerful, high throughput method for studying neural control of behavior.

Indexed as

Behavior, AnimalMachine LearningMotor ActivityZebrafishAnimalsBiomechanical PhenomenaLarvaLocomotion

Identifiers

PMID41105693
PMCPMC12533844

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.