无需标注数据,通过局部到全局自监督方法实现细胞实例分割
LG-NuSegHop: A Local-to-Global Self-Supervised Pipeline For Nuclei Instance Segmentation
- 基于局部操作生成伪标签,全局后处理提升分割精度
- 在三个公开数据集上超越多数自监督与弱监督方法
- 模块透明可解释,适合医学影像研究者使用
细胞分割是组织学图像分析的核心任务,有助于揭示分子模式并辅助疾病或癌症诊断。然而,该任务依赖专业医生,且不同器官组织和成像条件导致细胞形态差异大,难以自动化。此外,人工标注成本高,深度学习模型难以跨域泛化。本文提出局部到全局自监督框架 LG-NuSegHop,包含三个模块:(1) 局部处理生成伪标签,(2) 新型数据驱动特征提取模型 NuSegHop,(3) 全局后处理优化预测结果。尽管不依赖任何人工标注数据或领域适应,该方法在多个未见数据集上仍保持良好泛化能力。在三个公开数据集上的实验表明,其性能优于其他自监督与弱监督方法,并达到全监督方法的竞争力水平。所有模块均对医生可解释、透明。
原文摘要 · Abstract (English)
Nuclei segmentation is the cornerstone task in histology image reading, shedding light on the underlying molecular patterns and leading to disease or cancer diagnosis. Yet, it is a laborious task that requires expertise from trained physicians. The large nuclei variability across different organ tissues and acquisition processes challenges the automation of this task. On the other hand, data annotations are expensive to obtain, and thus, Deep Learning (DL) models are challenged to generalize to unseen organs or different domains. This work proposes Local-to-Global NuSegHop (LG-NuSegHop), a self-supervised pipeline developed on prior knowledge of the problem and molecular biology. There are three distinct modules: (1) a set of local processing operations to generate a pseudolabel, (2) NuSegHop a novel data-driven feature extraction model and (3) a set of global operations to post-process the predictions of NuSegHop. Notably, even though the proposed pipeline uses { no manually annotated training data} or domain adaptation, it maintains a good generalization performance on other datasets. Experiments in three publicly available datasets show that our method outperforms other self-supervised and weakly supervised methods while having a competitive standing among fully supervised methods. Remarkably, every module within LG-NuSegHop is transparent and explainable to physicians.
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