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UNSEG:复杂组织样本中细胞及其细胞核的无监督分割。

UNSEG: unsupervised segmentation of cells and their nuclei in complex tissue samples.

机构信息

Department of Computational and Systems Biology, University of Pittsburgh, Pittsburgh, PA, USA.

UPMC Hillman Cancer Center, Pittsburgh, PA, USA.

出版信息

Commun Biol. 2024 Aug 30;7(1):1062. doi: 10.1038/s42003-024-06714-4.

DOI:10.1038/s42003-024-06714-4
PMID:39215205
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11364851/
Abstract

Multiplexed imaging technologies have made it possible to interrogate complex tissue microenvironments at sub-cellular resolution within their native spatial context. However, proper quantification of this complexity requires the ability to easily and accurately segment cells into their sub-cellular compartments. Within the supervised learning paradigm, deep learning-based segmentation methods demonstrating human level performance have emerged. However, limited work has been done in developing such generalist methods within the unsupervised context. Here we present an easy-to-use unsupervised segmentation (UNSEG) method that achieves deep learning level performance without requiring any training data via leveraging a Bayesian-like framework, and nucleus and cell membrane markers. We show that UNSEG is internally consistent and better at generalizing to the complexity of tissue morphology than current deep learning methods, allowing it to unambiguously identify the cytoplasmic compartment of a cell, and localize molecules to their correct sub-cellular compartment. We also introduce a perturbed watershed algorithm for stably and automatically segmenting a cluster of cell nuclei into individual nuclei that increases the accuracy of classical watershed. Finally, we demonstrate the efficacy of UNSEG on a high-quality annotated gastrointestinal tissue dataset we have generated, on publicly available datasets, and in a range of practical scenarios.

摘要

多重成像技术使得在其天然空间背景下以亚细胞分辨率研究复杂的组织微环境成为可能。然而,要正确量化这种复杂性,就需要能够轻松、准确地将细胞分割成亚细胞区室。在监督学习范例中,基于深度学习的分割方法已经展现出了接近人类水平的性能。然而,在无监督背景下,开发这种通用方法的工作还很有限。在这里,我们提出了一种易于使用的无监督分割(UNSEG)方法,该方法通过利用类似于贝叶斯的框架以及核和细胞膜标记物,无需任何训练数据即可实现深度学习水平的性能。我们表明,UNSEG 在内部是一致的,并且比当前的深度学习方法更善于泛化组织形态的复杂性,从而能够明确识别细胞的细胞质区室,并将分子定位到其正确的亚细胞区室。我们还引入了一种经过扰动的分水岭算法,用于将细胞核簇稳定、自动地分割成单个核,从而提高经典分水岭算法的准确性。最后,我们在我们生成的高质量注释胃肠道组织数据集、公开可用的数据集以及一系列实际场景中展示了 UNSEG 的有效性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d231/11364851/9283223b0232/42003_2024_6714_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d231/11364851/69645759c5fc/42003_2024_6714_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d231/11364851/c1599d890e62/42003_2024_6714_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d231/11364851/76f2d1f865c6/42003_2024_6714_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d231/11364851/f71946fdb6e2/42003_2024_6714_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d231/11364851/ed22421999eb/42003_2024_6714_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d231/11364851/9283223b0232/42003_2024_6714_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d231/11364851/69645759c5fc/42003_2024_6714_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d231/11364851/c1599d890e62/42003_2024_6714_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d231/11364851/76f2d1f865c6/42003_2024_6714_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d231/11364851/f71946fdb6e2/42003_2024_6714_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d231/11364851/ed22421999eb/42003_2024_6714_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d231/11364851/9283223b0232/42003_2024_6714_Fig6_HTML.jpg

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