Pagano Lucas, Thibault Guillaume, Bousselham Walid, Riesterer Jessica L, Song Xubo, Gray Joe W
Department of Biomedical Engineering, Oregon Health and Science University, Portland, OR, USA.
Knight Cancer Institute, Oregon Health and Science University, Portland, OR, USA.
bioRxiv. 2023 Nov 1:2023.10.30.563998. doi: 10.1101/2023.10.30.563998.
Electron microscopy (EM) enables imaging at nanometer resolution and can shed light on how cancer evolves to develop resistance to therapy. Acquiring these images has become a routine task; however, analyzing them is now the bottleneck, as manual structure identification is very time-consuming and can take up to several months for a single sample. Deep learning approaches offer a suitable solution to speed up the analysis. In this work, we present a study of several state-of-the-art deep learning models for the task of segmenting nuclei and nucleoli in volumes from tumor biopsies. We compared previous results obtained with the ResUNet architecture to the more recent UNet++, FracTALResNet, SenFormer, and CEECNet models. In addition, we explored the utilization of unlabeled images through semi-supervised learning with Cross Pseudo Supervision. We have trained and evaluated all of the models on sparse manual labels from three fully annotated in-house datasets that we have made available on demand, demonstrating improvements in terms of 3D Dice score. From the analysis of these results, we drew conclusions on the relative gains of using more complex models, semi-supervised learning as well as next steps for the mitigation of the manual segmentation bottleneck.
电子显微镜(EM)能够实现纳米级分辨率成像,并有助于揭示癌症如何演变以产生治疗抗性。获取这些图像已成为一项常规任务;然而,分析这些图像现在却成了瓶颈,因为手动进行结构识别非常耗时,对单个样本而言可能需要长达数月时间。深度学习方法为加快分析提供了合适的解决方案。在这项工作中,我们针对从肿瘤活检样本的体积中分割细胞核和核仁的任务,对几种最先进的深度学习模型展开了研究。我们将之前使用ResUNet架构获得的结果与更新的UNet++、FracTALResNet、SenFormer和CEECNet模型进行了比较。此外,我们还通过交叉伪监督的半监督学习探索了未标记图像的利用。我们在三个按需提供的完全注释的内部数据集的稀疏手动标签上对所有模型进行了训练和评估,结果表明在三维骰子系数方面有了改进。通过对这些结果的分析,我们得出了关于使用更复杂模型、半监督学习的相对优势以及缓解手动分割瓶颈的后续步骤的结论。