Unsupervised learning has been a long-standing goal of machine learning and is especially important for medical image analysis, where the learning can compensate for the scarcity of labeled datasets. A promising subclass of unsupervised learning is self-supervised learning, which aims to learn salient features using the raw input as the learning signal. In this paper, we use a contrastive self-supervised learning method Chen et al. ( 2020a) that achieved state-of-the-art results on natural-scene images, and apply this method to digital histopathology by collecting and training on 60 histopathology datasets without any labels. We find that combining multiple multi-organ datasets with different types of staining and resolution properties improves the quality of the learned features. Furthermore, we find drastically subsampling a dataset (e.g.,
using1% of the available image patches) does not negatively impact the learned representations, unlike training on natural-scene images. Linear classifiers trained on top of the learned features show that networks pretrained on digital histopathology datasets perform better than ImageNet pretrained networks, boosting task performances up to 7.5% in accuracy and 8.9% in F 1 . These findings may also be useful when applying newer contrastive techniques to histopathology data. Pretrained PyTorch models are made publicly available at https://github.com/ozanciga/self-supervised-histopathology.
Despite their success in many computer vision tasks, convolutional networks tend to require large amounts of labeled data to achieve generalization. Furthermore, the performance is not guaranteed on a sample from an unseen domain at test time, if the network was not exposed to similar samples from that domain at training time. This hinders the adoption of these techniques in clinical setting where the imaging data is scarce, and where the intra-and inter-domain variance of the data can be substantial. We propose a domain adaptation technique that is especially suitable for deep networks to alleviate this requirement of labeled data. Our method utilizes gradient reversal layers [4] and Squeezeand-Excite modules [6] to stabilize the training in deep networks. The proposed method was applied to publicly available histopathology and chest X-ray databases and achieved superior performance to existing state-of-the-art networks with and without domain adaptation. Depending on the application, our method can improve multi-class classification accuracy by 5-20% compared to DANN introduced in [4].
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