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Integration of Deep Learning and Graph Theory for Analyzing Histopathology Whole-slide Images

机译:深度学习与图理论分析组织病理学全幻灯片图像的整合

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Characterization of collagen deposition in immunostained images is relevant to various pathological conditions, particularly in human immunodeficiency virus (HIV) infection. Accurate segmentation of these collagens and extracting representative features of underlying diseases are important steps to achieve quantitative diagnosis. While a first order statistic derived from the segmented collagens can be useful in representing pathological evolutions at different timepoints, it fails to capture morphological changes and spatial arrangements. In this work, we demonstrate a complete pipeline for extracting key histopathology features representing underlying disease progression from histopathology whole-slide images (WSIs) via integration of deep learning and graph theory. A convolutional neural network is trained and utilized for histopathological WSI segmentation. Parallel processing is applied to convert 100K ~ 150K segmented collagen fibrils into a single collective attributed relational graph, and graph theory is applied to extract topological and relational information from the collagenous framework. Results are in good agreement with the expected pathogenicity induced by collagen deposition, highlighting potentials in clinical applications for analyzing various meshwork-structures in whole-slide histology images.
机译:免疫图像中胶原沉积的表征与各种病理病症相关,特别是在人免疫缺陷病毒(HIV)感染中有关。这些胶原的准确细分和提取潜在疾病的代表特征是实现定量诊断的重要步骤。虽然衍生自分段胶原蛋白的第一阶统计可以是有用的,但在不同时间点的病理演进中可以是有用的,但是它不能捕获形态变化和空间布置。在这项工作中,我们证明了一种完整的管道,用于通过集成深度学习和图形理论来提取代表从组织病理学全幻灯片(WSIS)的潜在疾病进展的关键组织病理学特征。训练卷积神经网络并用于组织病理学WSI分段。将平行处理应用于将100k〜150k分段的胶原纤维转换成单个集体归属关系图,并且绘图理论用于从胶原框架中提取拓扑和关系信息。结果与胶原沉积诱导的预期致病性吻合,突出显示临床应用中的潜力,以分析全载组织学图像中的各种网状结构的潜力。

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