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Robust hierarchical density estimation and regression for re-stained histological whole slide image co-registration

机译:鲁棒的层次密度估计和回归,用于重新染色的组织学整体幻灯片图像共配准

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摘要

For many disease conditions, tissue samples are colored with multiple dyes and stains to add contrast and location information for specific proteins to accurately identify and diagnose disease. This presents a computational challenge for digital pathology, as whole-slide images (WSIs) need to be properly overlaid (i.e. registered) to identify co-localized features. Traditional image registration methods sometimes fail due to the high variation of cell density and insufficient texture information in WSIs–particularly at high magnifications. In this paper, we proposed a robust image registration strategy to align re-stained WSIs precisely and efficiently. This method is applied to 30 pairs of immunohistochemical (IHC) stains and their hematoxylin and eosin (H&E) counterparts. Our approach advances the existing methods in three key ways. First, we introduce refinements to existing image registration methods. Second, we present an effective weighting strategy using kernel density estimation to mitigate registration errors. Third, we account for the linear relationship across WSI levels to improve accuracy. Our experiments show significant decreases in registration errors when matching IHC and H&E pairs, enabling subcellular-level analysis on stained and re-stained histological images. We also provide a tool to allow users to develop their own registration benchmarking experiments.
机译:对于许多疾病状况,组织样本都用多种染料和染色剂上色,以添加特定蛋白质的对比度和位置信息,以准确地识别和诊断疾病。由于整个幻灯片图像(WSI)需要正确叠加(即对齐)以识别共定位的特征,因此这给数字病理学带来了计算上的挑战。传统的图像配准方法有时会由于细胞密度的高变化和WSI中纹理信息不足而失败,尤其是在高倍率下。在本文中,我们提出了一种鲁棒的图像配准策略,可以精确高效地对齐重新着色的WSI。此方法适用于30对免疫组织化学(IHC)染色剂及其苏木精和曙红(H&E)对应物。我们的方法在三个关键方面改进了现有方法。首先,我们对现有的图像配准方法进行改进。其次,我们提出一种有效的加权策略,使用核密度估计来减轻配准误差。第三,我们考虑了WSI级别之间的线性关系,以提高准确性。我们的实验显示,当匹配IHC和H&E对时,配准错误显着减少,从而可以对染色和重新染色的组织学图像进行亚细胞水平分析。我们还提供了一种工具,允许用户开发自己的注册基准测试。

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