Scientific Reports· 2026Q1
Design and implementation of an automated Drosophila locomotor assay using computer vision tracking
- 2citations
- Q1SCImago
- 2026year
Short summary
A new automated platform using computer vision and deep learning tracks Drosophila locomotor behavior in 12 vials simultaneously, achieving 2.8x faster processing and 800x higher data density than manual scoring.
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Key points
- Developed an integrated hardware-software platform for automated, high-throughput Drosophila locomotor analysis in 12 vials.
- Utilizes deep learning for vial segmentation (IoU > 0.95) and computer vision for 60 fps tracking of climbing trajectories and velocity.
- Achieves 2.8x faster processing and 800x higher data density compared to manual scoring.
- Uncovered reproducible, sex-specific age-related locomotor phenotypes in Clockᴼᵘᵗ and PolG mutant models.
AI-generated from the title and abstract; the full text is not read.
Abstract
Abstract Drosophila has long served as a powerful model for investigating locomotor behavior, using geotaxis assays to generate valuable insights into genetics, aging, and neurobiology. Nonetheless, mostly their use can be constrained by subjective scoring, modest thought, and challenges in reproducibility. We developed and validated an integrated hardware–software platform that enables automated, high-resolution locomotor analysis across 12 vials in parallel. The system integrates 3D-printed mechanical components, Raspberry Pi–based video acquisition, and programmable environmental controls to ensure standardized conditions. A deep learning pipeline segments vials with near-perfect accuracy (IoU > 0.95), while computer vision algorithms quantify climbing trajectories, velocity, and positional zone occupancy at 60 frames per second. The end-to-end workflow converts raw video into time-resolved metrics, supports sex-specific aggregation, and incorporates advanced statistical analyses, including Linear Mixed Effects regression, harmonic mean p-values, and Mann–Whitney U tests. Relative to manual scoring, this automated pipeline yields 2.8-fold faster processing and about 800-fold higher data density. Application of the platform uncovered reproducible phenotypes of multiple genotypes. For example, in circadian Clockᴼᵘᵗ mutation, males displayed progressive climbing deficits with age, whereas females-maintained age-resilient trajectories. Moreover, male Clockᴼᵘᵗ exhibited a reduced locomotor performance compared to age-matched control ( w 1118 ) males, however, female Clockᴼᵘᵗ showed subtle reduction in locomotor performance. Additionally, glial-specific knockdown of PolG , encoding the DNA polymerase gamma catalytic subunit, revealed striking sex-dimorphic aging patterns: females outperformed controls at older age in Glaz driven and at younger age in Elav driven, while males exhibited some marked decline. To promote broad adoption, a user-friendly Python interface (Tkinter GUI) enables accessibility independent of computational expertise. Collectively, this standardized, high-throughput framework advances the resolution of genotype-, age-, and sex-dependent locomotor dynamics, offering new opportunities in aging, circadian biology, and neurodegeneration research.
The authors' abstract, as published at the source. Scientific Reports, 2026 · DOI ↗
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Field: Cellular and Molecular Neuroscience
Cellular and Molecular NeuroscienceNeuroscience