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arXiv 2206.03461cs.CVeess.IVq-bio.QM

Fast Unsupervised Brain Anomaly Detection and Segmentation with Diffusion Models

King’s College London(伦敦国王学院);University College London(伦敦大学学院);Birkbeck College(伯克贝克学院);King’s College Hospital NHS Foundation Trust(国王学院医院国民保健服务基金会信托);St George’s University Hospitals NHS Foundation Trust(圣乔治大学医院国民保健服务基金会信托);Atkinson Morley Regional Neuroscience Centre(阿特金森·莫利地区神经科学中心);UCL Queen Square Institute of Neurology(伦敦大学学院皇后广场神经病学研究所)
Walter H. L. Pinaya, Mark S. Graham, Robert Gray, Pedro F Da Costa, Petru-Daniel Tudosiu, Paul Wright, Yee H. Mah, Andrew D. MacKinnon, James T. Teo, Rolf Jager… 展开作者

Walter H. L. Pinaya, Mark S. Graham, Robert Gray, Pedro F Da Costa, Petru-Daniel Tudosiu, Paul Wright, Yee H. Mah, Andrew D. MacKinnon, James T. Teo, Rolf Jager, David Werring, Geraint Rees, Parashkev Nachev, Sebastien Ourselin, M. Jorge Cardoso

英文摘要:

Deep generative models have emerged as promising tools for detecting arbitrary anomalies in data, dispensing with the necessity for manual labelling. Recently, autoregressive transformers have achieved state-of-the-art performance for anomaly detection in medical imaging. Nonetheless, these models still have some intrinsic weaknesses, such as requiring images to be modelled as 1D sequences, the accumulation of errors during the sampling process, and the significant inference times associated with transformers. Denoising diffusion probabilistic models are a class of non-autoregressive generative models recently shown to produce excellent samples in computer vision (surpassing Generative Adversarial Networks), and to achieve log-likelihoods that are competitive with transformers while having fast inference times. Diffusion models can be applied to the latent representations learnt by autoencoders, making them easily scalable and great candidates for application to high dimensional data, such as medical images. Here, we propose a method based on diffusion models to detect and segment anomalies in brain imaging. By training the models on healthy data and then exploring its diffusion and reverse steps across its Markov chain, we can identify anomalous areas in the latent space and hence identify anomalies in the pixel space. Our diffusion models achieve competitive performance compared with autoregressive approaches across a series of experiments with 2D CT and MRI data involving synthetic and real pathological lesions with much reduced inference times, making their usage clinically viable.

机构、总结、中文摘要均由AI分析而来,可能存在错误,请以论文正文为准。

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