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CellSeg3D,用于荧光显微镜的自监督三维细胞分割

CellSeg3D, Self-supervised 3D cell segmentation for fluorescence microscopy.

作者信息

Achard Cyril, Kousi Timokleia, Frey Markus, Vidal Maxime, Paychere Yves, Hofmann Colin, Iqbal Asim, Hausmann Sebastien B, Pagès Stéphane, Mathis Mackenzie Weygandt

机构信息

Brain Mind Institute and Neuro X, École Polytechnique Fédérale de Lausanne (EPFL), Geneva, Switzerland.

Wyss Center for Bio and Neuroengineering, Geneva, Switzerland.

出版信息

Elife. 2025 Jun 24;13:RP99848. doi: 10.7554/eLife.99848.

DOI:10.7554/eLife.99848
PMID:40551545
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12187128/
Abstract

Understanding the complex three-dimensional structure of cells is crucial across many disciplines in biology and especially in neuroscience. Here, we introduce a set of models including a 3D transformer (SwinUNetR) and a novel 3D self-supervised learning method (WNet3D) designed to address the inherent complexity of generating 3D ground truth data and quantifying nuclei in 3D volumes. We developed a Python package called CellSeg3D that provides access to these models in Jupyter Notebooks and in a napari GUI plugin. Recognizing the scarcity of high-quality 3D ground truth data, we created a fully human-annotated mesoSPIM dataset to advance evaluation and benchmarking in the field. To assess model performance, we benchmarked our approach across four diverse datasets: the newly developed mesoSPIM dataset, a 3D platynereis-ISH-Nuclei confocal dataset, a separate 3D Platynereis-Nuclei light-sheet dataset, and a challenging and densely packed Mouse-Skull-Nuclei confocal dataset. We demonstrate that our self-supervised model, WNet3D - trained without any ground truth labels - achieves performance on par with state-of-the-art supervised methods, paving the way for broader applications in label-scarce biological contexts.

摘要

了解细胞复杂的三维结构在生物学的许多学科中都至关重要,尤其是在神经科学领域。在此,我们介绍了一组模型,包括一个3D变压器(SwinUNetR)和一种新颖的3D自监督学习方法(WNet3D),旨在解决生成3D真实数据和量化3D体积中的细胞核所固有的复杂性。我们开发了一个名为CellSeg3D的Python包,可在Jupyter Notebook和napari GUI插件中访问这些模型。鉴于高质量3D真实数据的稀缺性,我们创建了一个完全由人工注释的mesoSPIM数据集,以推动该领域的评估和基准测试。为了评估模型性能,我们在四个不同的数据集上对我们的方法进行了基准测试:新开发的mesoSPIM数据集、一个3D多毛类动物原位杂交细胞核共聚焦数据集、一个单独的3D多毛类动物细胞核光片数据集,以及一个具有挑战性且密集排列的小鼠颅骨细胞核共聚焦数据集。我们证明,我们的自监督模型WNet3D——在没有任何真实标签的情况下进行训练——实现了与最先进的监督方法相当的性能,为在标签稀缺的生物学背景下的更广泛应用铺平了道路。

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本文引用的文献

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Deep 3D histology powered by tissue clearing, omics and AI.由组织透明化、组学和人工智能驱动的深度三维组织学。
Nat Methods. 2024 Jul;21(7):1153-1165. doi: 10.1038/s41592-024-02327-1. Epub 2024 Jul 12.
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The multimodality cell segmentation challenge: toward universal solutions.多模态细胞分割挑战赛:迈向通用解决方案。
Nat Methods. 2024 Jun;21(6):1103-1113. doi: 10.1038/s41592-024-02233-6. Epub 2024 Mar 26.
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CellViT: Vision Transformers for precise cell segmentation and classification.CellViT:用于精确细胞分割和分类的视觉Transformer
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Multi-layered maps of neuropil with segmentation-guided contrastive learning.基于分割引导对比学习的神经突多层图谱。
Nat Methods. 2023 Dec;20(12):2011-2020. doi: 10.1038/s41592-023-02059-8. Epub 2023 Nov 20.
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Segmentation metric misinterpretations in bioimage analysis.生物影像分析中的分割度量误读。
Nat Methods. 2024 Feb;21(2):213-216. doi: 10.1038/s41592-023-01942-8. Epub 2023 Jul 27.
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Cellpose 2.0: how to train your own model.Cellpose 2.0:如何训练自己的模型。
Nat Methods. 2022 Dec;19(12):1634-1641. doi: 10.1038/s41592-022-01663-4. Epub 2022 Nov 7.
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EmbedSeg: Embedding-based Instance Segmentation for Biomedical Microscopy Data.EmbedSeg:基于嵌入的生物医学显微镜数据实例分割。
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Analyzing Cell-Scaffold Interaction through Unsupervised 3D Nuclei Segmentation.通过无监督3D细胞核分割分析细胞-支架相互作用
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Accurate determination of marker location within whole-brain microscopy images.准确确定全脑显微镜图像中的标记位置。
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