Semi supervised GAN for smart microscopy, fast and data efficient cell cycle classification
Rajeev Manick, Youssef El Habouz, Maëlle Guillout, Celia Martin, Julia Bonnet + 6 more
TLDR
This paper introduces SGAN for robust, data-efficient cell cycle classification in smart microscopy, achieving high accuracy with minimal labeled data.
Key contributions
- Introduces SGAN for robust cell-cycle stage classification in smart microscopy.
- Combines unlabelled images with synthetic samples to mitigate limited data annotation.
- Achieved 93% accuracy on Mitocheck dataset using only 80 labeled images per class.
- Generic and adaptable to new labeling schemes, cell lines, or microscopy modalities.
Why it matters
This paper addresses the critical need for data-efficient and adaptable classification in smart microscopy. By reducing reliance on large annotated datasets, it enables real-time, automated analysis across diverse biological applications. This advances the development of truly smart, autonomous microscope systems.
Original Abstract
Modern optical microscopes are fully motorised; however, transforming them into truly smart systems requires real-time adjustment of acquisition settings in response to detected objects and dynamic biological events. At the core are classification algorithms that commonly depend on customised softwares and are generally designed for narrowly-defined biological applications. In addition, they often require substantial annotated datasets for effective training. We introduce a semi-supervised generative adversarial network (SGAN) for robust cell-cycle stage classification under low-resource conditions, adaptable to diverse cellular structures. The framework combines unlabelled microscopy images with synthetically generated samples to mitigate limited annotation, while preserving stable performance even when the unlabelled subset is class-imbalanced. Tested on the Mitocheck dataset, which features five mitosis classes, the model achieved $93 \pm 2\%$ accuracy using only 80 labelled per class and 600 unlabelled images. The proposed algorithm is generic and can be readily adapted to new labeling schemes, classification targets, cell lines, or microscopy modalities through transfer learning. SGAN is well suited for integration into automated microscopes, enabling efficient and adaptable image analysis across diverse biological and microscopy applications.
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