The field of computational pathology has witnessed great advancements since deep neural networks have been widely applied. These networks usually require large numbers of annotated data to train vast parameters. However, it takes significant effort to annotate a large histopathology dataset. We introduce a light-weight and interpretable model for nuclei detection and weakly-supervised segmentation. It only requires annotations on isolated nucleus, rather than on all nuclei in the dataset. Besides, it is a generative compositional model that first locates parts of nucleus, then learns the spatial correlation of the parts to further locate the nucleus. This process brings interpretability in its prediction. Empirical results on an in-house dataset show that in detection, the proposed method achieved comparable or better performance than its deep network counterparts, especially when the annotated data is limited. It also outperforms popular weakly-supervised segmentation methods. The proposed method could be an alternative solution for the data-hungry problem of deep learning methods.
翻译:自深神经网络被广泛应用以来,计算病理学领域取得了巨大进步。这些网络通常需要大量附加说明的数据来训练庞大的参数。然而,它需要大量的努力来说明一个庞大的病理学数据集。我们引入了一个轻量和可解释的核探测和微弱监视分化模型。它只要求对孤立核进行说明,而不是数据集中的所有核分化方法。此外,它是一种基因化的构成模型,它首先定位核的部位,然后学习各部分的空间相关性以进一步定位核。这一过程在预测中带来了解释性。内部数据集的经验显示,在探测中,拟议的方法比其深层网络对口单位取得了可比较或更好的性能,特别是在附加说明的数据有限的情况下。它也优于流行的弱监视分化方法。提议的方法是解决深层学习方法的数据-饥饿问题的替代方法。