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Reducing annotation effort in digital pathology: A Co-Representation learning framework for classification tasks
Institution:1. IBM Zurich Research Lab, Zurich, Switzerland;2. Computer-Assisted Applications in Medicine, ETH Zurich, Zurich, Switzerland;1. Department of Computer Science, Stony Brook University, Stony Brook, NY, USA;2. Montreal Institute for Learning Algorithms, University of Montreal, Montreal, Canada;3. Department of Biomedical Informatics, Stony Brook University, Stony Brook, NY, USA;4. Oak Ridge National Laboratory, Oak Ridge, TN, USA;5. Department of Pathology, Stony Brook University Medical Center, Stony Brook, NY, USA;6. School of Biomedical Engineering, Health Science Center, Shenzhen University, China;7. Center for Biomedical Imaging & Informatics, Rutgers, the State University of New Jersey, New Brunswick, NJ, USA;8. Rutgers Cancer Institute of New Jersey, Rutgers, the State University of New Jersey, NJ, USA;9. Division of Medical Informatics, Rutgers-Robert Wood Johnson Medical School, Piscataway Township, NJ, USA;10. Cancer Center, Stony Brook University Hospital, Stony Brook, NY, USA;1. Department of Biomedical Engineering, Case Western Reserve University, Cleveland, OH, United States;2. Louis Stokes Cleveland Veterans Administration Medical Center, Cleveland, OH, United States;3. City, University of London, London, United Kingdom;1. College of Information Sciences and Technology, The Pennsylvania State University, University Park, PA 16802, USA;2. Lister Hill National Center for Biomedical Communications, National Library of Medicine, Bethesda, MD 20892, USA;3. Department of Pathology, Penn State Health Milton S. Hershey Medical Center and Penn State College Of Medicine, Hershey, PA 17033, USA;1. Department of Electrical and Computer Engineering, Duke University, Durham, NC 27708, USA;2. Department of Mathematics, Duke University, Durham, NC 27708, USA;3. Department of Surgery, Duke University Medical Center, Durham, NC 27710, USA;4. Department of Pathology, Duke University Medical Center, Durham, NC 27710, USA;1. College of Computer Science, Sichuan University, Chengdu 610065, China;2. Department of Electronic Engineering, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong;3. College of Biomedical Engineering, Sichuan University, Chengdu 610065, China;4. Department of Biomedical Engineering, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong;5. Tencent AI Lab, Shenzhen 518057, China;1. School of Computer Science and Engineering, University of Electronic Science and Technology of China, Xiyuan Ave, Chengdu 611731, Sichuan, China;2. Institute of Clinical Pathology, West China Hospital, Sichuan University, Guo Xue Xiang, Chengdu 610041, Sichuan, China
Abstract:Classification of digital pathology images is imperative in cancer diagnosis and prognosis. Recent advancements in deep learning and computer vision have greatly benefited the pathology workflow by developing automated solutions for classification tasks. However, the cost and time for acquiring high quality task-specific large annotated training data are subject to intra- and inter-observer variability, thus challenging the adoption of such tools. To address these challenges, we propose a classification framework via co-representation learning to maximize the learning capability of deep neural networks while using a reduced amount of training data. The framework captures the class-label information and the local spatial distribution information by jointly optimizing a categorical cross-entropy objective and a deep metric learning objective respectively. A deep metric learning objective is incorporated to enhance the classification, especially in the low training data regime. Further, a neighborhood-aware multiple similarity sampling strategy, and a soft-multi-pair objective that optimizes interactions between multiple informative sample pairs, is proposed to accelerate deep metric learning. We evaluate the proposed framework on five benchmark datasets from three digital pathology tasks, i.e., nuclei classification, mitosis detection, and tissue type classification. For all the datasets, our framework achieves state-of-the-art performance when using approximately only 50% of the training data. On using complete training data, the proposed framework outperforms the state-of-the-art on all the five datasets.
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