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3C-GAN: class-consistent CycleGAN for malaria domain adaptation model
Aimon Rahman1, M Sohel Rahman2, M R C Mahdy1
1Department of Electrical and Computer Engineering, North South University, Dhaka-1229, Bangladesh.
CycleGAN models can alter medical image classes by hallucinating features. This study introduces a modified loss to prevent feature hallucination in malaria image translation, preserving original class labels for safer clinical use.
Area of Science:
- Medical Imaging
- Artificial Intelligence
- Computer Vision
Background:
- Unpaired domain translation models like CycleGAN are used for medical image synthesis.
- CycleGAN can hallucinate features, potentially altering the original image class and leading to misdiagnosis.
- This is particularly problematic in datasets like malaria images, where features (e.g., parasites) can be unintentionally added or removed.
Purpose of the Study:
- To modify CycleGAN's distribution matching loss to eliminate feature hallucination.
- To ensure domain translation in medical images preserves the original class labels.
- To enhance the safety and reliability of unsupervised generative adversarial networks (GANs) for clinical applications.
Main Methods:
- Introduction of a modified distribution matching loss function for CycleGAN.
- Application of the modified CycleGAN to a malaria image dataset for domain translation.
- Experimental evaluation comparing the modified approach against the classic CycleGAN.
Main Results:
- The modified loss function significantly reduced feature hallucination in synthesized malaria images.
- Original class labels were preserved during domain translation, preventing misclassification.
- Experimental results demonstrated superior performance compared to the baseline CycleGAN.
Conclusions:
- The proposed modified loss effectively eliminates feature hallucination in unpaired domain translation of medical images.
- This approach ensures the integrity of class labels, making GANs safer for clinical use.
- The method holds promise for advancing unsupervised, clinically safe GAN development.
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