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Cell detection in pathology and microscopy images with multi-scale fully convolutional neural networks

机译:多尺度全卷积神经网络在病理学和显微镜图像中的细胞检测

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Automated nucleus/cell detection is usually considered as the basis and a critical prerequisite step of computer assisted pathology and microscopy image analysis. However, due to the enormous variability (cell types, stains and different microscopes) and data complexity (cell overlapping, inhomogeneous intensities, background clutters and image artifacts), robust and accurate nucleus/cell detection is usually a difficult problem. To address this issue, we propose a novel multi-scale fully convolutional neural networks approach for regression of a density map to robustly detect the nuclei of pathology and microscopy images. The procedure can be divided into three main stages. Initially, instead of working on the simple dot label space, regression on the proposed structured proximity space for patches is performed so that centers of image patches are explicitly forced to produce larger values than their adjacent areas. Then, several multi-scale fully convolutional regression networks are developed for this task; this will enlarge the receptive field and not only can detect the single, small size cells, but also benefit to detecting cells with big size and overlapping states. In this stage, we copy the full feature maps from the contracting path and merge with the feature maps of the expansive path. This operation will make full use of shallow and deep semantic information of the networks. The networks do not have any fully connected layers; this strategy allows the seamless probability map prediction of arbitrarily large images. At the same time, data augmentations (e.g., small range shift, zoom and randomly flip) are carefully used to enhance the robustness of detection. Finally, morphological operations and suitable filters are employed and some prior information is introduced to find the centers of the cells more robustly. Our method achieves about 99.25% detection precision and the F1-measure is 0.9924 on fluorescence microscopy cell images; about 85.90% detection precision and the F1-measure is 0.9020 on Lymphocyte cell images and about 78.41% detection precision and the F1-measure is 0.8440 on breast histopathological images. This result leads to a promising detection performance that equates and sometimes exceeds the recently published leading detection approaches with the same benchmark datasets.
机译:自动核/细胞检测通常被认为是计算机辅助病理学和显微镜图像分析的基础和关键的前提步骤。然而,由于巨大的可变性(细胞类型,染色剂和不同的显微镜)和数据复杂性(细胞重叠,强度不均匀,背景杂乱和图像伪影)​​,稳健而准确的核/细胞检测通常是一个难题。为了解决这个问题,我们提出了一种新颖的多尺度全卷积神经网络方法,用于密度图的回归,以可靠地检测病理和显微图像的核。该过程可分为三个主要阶段。最初,不是在简单的点标签空间上工作,而是对建议的补丁结构邻近空间进行回归,以便显着强制图像补丁的中心产生比其相邻区域更大的值。然后,为此任务开发了几个多尺度的全卷积回归网络。这将扩大接收范围,不仅可以检测单个的,小尺寸的细胞,而且有利于检测大尺寸和重叠状态的细胞。在此阶段,我们从收缩路径复制完整的特征图,然后与扩展路径的特征图合并。该操作将充分利用网络的浅层和深层语义信息。网络没有任何完全连接的层。这种策略允许任意大图像的无缝概率图预测。同时,小心地使用数据增强(例如,小范围移位,缩放和随机翻转)以增强检测的鲁棒性。最后,采用形态学运算和合适的过滤器,并引入一些先验信息以更可靠地找到细胞中心。我们的方法达到了约99.25%的检测精度,在荧光显微镜细胞图像上的F1测度为0.9924。在淋巴细胞图像上,检测精度约为85.90%,F1测度为0.9020;在乳腺组织病理学图像上,F1测量为约78.41%,F1测度为0.8440。该结果导致了有希望的检测性能,该性能等同于有时甚至超过了使用相同基准数据集的最新发布的领先检测方法。

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