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Improving unsupervised stain-to-stain translation using self-supervision and meta-learning
Nassim Bouteldja1,2, Barbara M Klinkhammer2, Tarek Schlaich1
1Institute of Imaging and Computer Vision, RWTH Aachen University, Aachen, Germany.
Journal of Pathology Informatics
|October 21, 2022
Summary
Unsupervised stain-to-stain translation using CycleGANs shows promise for digital pathology, but current methods struggle to create universally applicable simulated histological stains for deep learning models.
Area of Science:
- Digital pathology
- Computational pathology
- Medical image analysis
Background:
- Digital pathology image analysis requires extensive manual annotation due to image variability.
- Unsupervised domain adaptation, particularly image-to-image translation, offers a solution to reduce manual annotation overhead.
- Histological stain variations present a significant challenge for deep learning models in digital pathology.
Purpose of the Study:
- To enable stain-independent applicability of deep learning segmentation models.
- To address variability in histological stains using unsupervised stain-to-stain translation.
- To improve the effectiveness of unsupervised stain-to-stain translation in kidney histopathology.
Main Methods:
- Utilized CycleGANs for stain-to-stain translation in kidney histopathology images.
- Proposed integrating a prior segmentation network for self-supervised, semantic guidance during translation.
- Incorporated extra channels into the translation output to handle meta-information and underdetermined reconstructions.
Main Results:
- The proposed method with semantic guidance achieved the best performance, with instance-level Dice scores between 78% and 92% for most kidney structures.
- CycleGANs showed limited performance for translating structures like arteries.
- Translation performance was generally lower compared to segmentation performed on the original stain.
Conclusions:
- Current unsupervised stain-to-stain translation technologies are unlikely to produce "generally" applicable simulated stains.
- Further advancements are needed to overcome limitations in translating diverse histological structures and achieve stain-independent applicability.
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