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Multi-centred Strong Augmentation via Contrastive Learning for Unsupervised Lesion Detection and Segmentation

2021-09-03 04:25:57
Yu Tian, Fengbei Liu, Guansong Pang, Yuanhong Chen, Yuyuan Liu, Johan W. Verjans, Rajvinder Singh, Gustavo Carneiro

Abstract

The scarcity of high quality medical image annotations hinders the implementation of accurate clinical applications for detecting and segmenting abnormal lesions. To mitigate this issue, the scientific community is working on the development of unsupervised anomaly detection (UAD) systems that learn from a training set containing only normal (i.e., healthy) images, where abnormal samples (i.e., unhealthy) are detected and segmented based on how much they deviate from the learned distribution of normal samples. One significant challenge faced by UAD methods is how to learn effective low-dimensional image representations that are sensitive enough to detect and segment abnormal lesions of varying size, appearance and shape. To address this challenge, we propose a novel self-supervised UAD pre-training algorithm, named Multi-centred Strong Augmentation via Contrastive Learning (MSACL). MSACL learns representations by separating several types of strong and weak augmentations of normal image samples, where the weak augmentations represent normal images and strong augmentations denote synthetic abnormal images. To produce such strong augmentations, we introduce MedMix, a novel data augmentation strategy that creates new training images with realistic looking lesions (i.e., anomalies) in normal images. The pre-trained representations from MSACL are generic and can be used to improve the efficacy of different types of off-the-shelf state-of-the-art (SOTA) UAD models. Comprehensive experimental results show that the use of MSACL largely improves these SOTA UAD models on four medical imaging datasets from diverse organs, namely colonoscopy, fundus screening and covid-19 chest-ray datasets.

Abstract (translated)

URL

https://arxiv.org/abs/2109.01303

PDF

https://arxiv.org/pdf/2109.01303.pdf


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