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Unsupervised Annotation Transfer in Phase-Contrast Microscopy Using a CycleGAN
Mokhaled N A Al-Hamadani1,2,3, Stathis Hadjidemetriou4, Gabor Szeman-Nagy5
1Department of Data Science and Visualization, Faculty of Informatics, University of Debrecen, H-4032 Debrecen, Hungary.
Sensors (Basel, Switzerland)
|August 13, 2026
Summary
This study introduces a Cycle-Consistent Generative Adversarial Network (CycleGAN) framework to transfer cell annotations between microscopy domains, significantly reducing manual labeling efforts for deep learning models.
Area of Science:
- Microscopy imaging
- Deep learning
- Computational biology
Background:
- Domain shift in microscopy imaging hinders deep learning model deployment.
- Manual annotation of new datasets is costly and time-consuming.
Purpose of the Study:
- To develop a Cycle-Consistent Generative Adversarial Network (CycleGAN)-based framework for annotation transfer.
- To adapt a labeled B16BL6 cell microscopy domain to a HeLa target domain without extensive manual annotation.
Main Methods:
- Utilized a detection-oriented CycleGAN for image translation from B16BL6 to HeLa domains.
- Retained bounding-box annotations during image translation.
- Trained YOLOv8x object detectors on source-only and translated datasets.
- Evaluated performance using standard object detection metrics and unsupervised proxy metrics.
Main Results:
- The CycleGAN-translated configuration achieved superior performance (mAP@0.50: 0.186) compared to baselines (mAP@0.50: 0.027 and 0.009).
- Achieved highest precision (0.244), recall (0.353), and F1-score (0.288) on the target domain.
- Demonstrated improved detector generalization and reduced need for manual annotation.
Conclusions:
- Source-to-target image translation effectively addresses domain shift challenges in microscopy.
- The proposed CycleGAN framework significantly enhances deep learning model adaptability across different experimental setups.
- Reduces the burden of manual annotation for new microscopy datasets.

