强大的组织病理学图像分析:贴标签还是合成?

Le Hou, Ayush Agarwal, Dimitris Samaras, Tahsin M Kurc, Rajarsi R Gupta, Joel H Saltz
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引用次数: 0

摘要

细胞核的检测、分割和分类是数字病理学的基本分析操作。现有的先进方法需要病理学家提供大量有监督的训练数据,但在处理未见组织类型的图像时仍可能表现不佳。我们提出了一种用于组织病理学图像分割的无监督方法,它能合成各种组织类型的异质训练图像补丁集。虽然我们合成的样本质量并不总是很高,但我们通过一种普遍适用的重要度抽样方法,对生成的样本进行了综合利用。这种方法首次对合成数据的训练损失进行了重新权衡,从而使真实数据分布的理想(无偏)泛化损失最小化。这使我们能够使用随机多边形生成器合成近似的细胞结构(即核掩膜),而在许多组织类型中,并没有给出这种结构的真实示例,因此基于 GAN 的方法并不适用。此外,我们还提出了一种混合合成管道,利用真实组织病理学斑块中的纹理和 GAN 模型来解决组织纹理的异质性问题。与现有的最先进的监督模型相比,我们的方法在没有训练数据的癌症类型中的泛化效果明显更好。即使在有训练数据的癌症类型中,我们的方法也能实现相同的性能,而无需监督成本。我们在癌症基因组图谱(TCGA)资源库中的 5000 多张全切片图像(WSI)上发布了代码和分割结果,这个数据集比目前可用的数据集要大得多。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Robust Histopathology Image Analysis: to Label or to Synthesize?

Detection, segmentation and classification of nuclei are fundamental analysis operations in digital pathology. Existing state-of-the-art approaches demand extensive amount of supervised training data from pathologists and may still perform poorly in images from unseen tissue types. We propose an unsupervised approach for histopathology image segmentation that synthesizes heterogeneous sets of training image patches, of every tissue type. Although our synthetic patches are not always of high quality, we harness the motley crew of generated samples through a generally applicable importance sampling method. This proposed approach, for the first time, re-weighs the training loss over synthetic data so that the ideal (unbiased) generalization loss over the true data distribution is minimized. This enables us to use a random polygon generator to synthesize approximate cellular structures (i.e., nuclear masks) for which no real examples are given in many tissue types, and hence, GAN-based methods are not suited. In addition, we propose a hybrid synthesis pipeline that utilizes textures in real histopathology patches and GAN models, to tackle heterogeneity in tissue textures. Compared with existing state-of-the-art supervised models, our approach generalizes significantly better on cancer types without training data. Even in cancer types with training data, our approach achieves the same performance without supervision cost. We release code and segmentation results on over 5000 Whole Slide Images (WSI) in The Cancer Genome Atlas (TCGA) repository, a dataset that would be orders of magnitude larger than what is available today.

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MAPSeg: Unified Unsupervised Domain Adaptation for Heterogeneous Medical Image Segmentation Based on 3D Masked Autoencoding and Pseudo-Labeling. Learned representation-guided diffusion models for large-image generation. SI-MIL: Taming Deep MIL for Self-Interpretability in Gigapixel Histopathology. Calibrating Multi-modal Representations: A Pursuit of Group Robustness without Annotations. Representing Part-Whole Hierarchies in Foundation Models by Learning Localizability, Composability, and Decomposability from Anatomy via Self-Supervision.
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