Xiong Juming, Deng Ruining, Yue Jialin, Lu Siqi, Guo Junlin, Lionts Marilyn, Yao Tianyuan, Cui Can, Zhu Junchao, Qu Chongyu, Yang Yuechen, Yin Mengmeng, Yang Haichun, Huo Yuankai
Vanderbilt University, Department of Electrical and Computer Engineering, Nashville, Tennessee, United States.
Vanderbilt University, Department of Computer Science, Nashville, Tennessee, United States.
J Med Imaging (Bellingham). 2025 Jul;12(4):044002. doi: 10.1117/1.JMI.12.4.044002. Epub 2025 Aug 5.
Histological analysis plays a crucial role in understanding tissue structure and pathology. Although recent advancements in registration methods have improved 2D histological analysis, they often struggle to preserve critical 3D spatial relationships, limiting their utility in both clinical and research applications. Specifically, constructing accurate 3D models from 2D slices remains challenging due to tissue deformation, sectioning artifacts, variability in imaging techniques, and inconsistent illumination. Deep learning-based registration methods have demonstrated improved performance but suffer from limited generalizability and require large-scale training data. In contrast, non-deep-learning approaches offer better generalizability but often compromise on accuracy.
We introduce ZeroReg3D, a zero-shot registration pipeline that integrates zero-shot deep learning-based keypoint matching and non-deep-learning registration techniques to effectively mitigate deformation and sectioning artifacts without requiring extensive training data.
Comprehensive evaluations demonstrate that our pairwise 2D image registration method improves registration accuracy by over baseline methods, outperforming existing strategies in both accuracy and robustness. High-fidelity 3D reconstructions further validate the effectiveness of our approach, establishing ZeroReg3D as a reliable framework for precise 3D reconstruction from consecutive 2D histological images.
We introduced ZeroReg3D, a zero-shot registration pipeline tailored for accurate 3D reconstruction from serial histological sections. By combining zero-shot deep learning-based keypoint matching with optimization-based affine and non-rigid registration techniques, ZeroReg3D effectively addresses critical challenges such as tissue deformation, sectioning artifacts, staining variability, and inconsistent illumination without requiring retraining or fine-tuning.
组织学分析在理解组织结构和病理学方面起着至关重要的作用。尽管配准方法的最新进展改进了二维组织学分析,但它们往往难以保留关键的三维空间关系,限制了其在临床和研究应用中的效用。具体而言,由于组织变形、切片伪影、成像技术的差异以及照明不一致,从二维切片构建准确的三维模型仍然具有挑战性。基于深度学习的配准方法已显示出更好的性能,但存在泛化性有限且需要大规模训练数据的问题。相比之下,非深度学习方法具有更好的泛化性,但往往在准确性上有所妥协。
我们引入了ZeroReg3D,这是一种零样本配准管道,它集成了基于零样本深度学习的关键点匹配和非深度学习配准技术,以有效减轻变形和切片伪影,而无需大量训练数据。
综合评估表明,我们的成对二维图像配准方法比基线方法提高了配准精度,在准确性和鲁棒性方面均优于现有策略。高保真三维重建进一步验证了我们方法的有效性,将ZeroReg3D确立为从连续二维组织学图像进行精确三维重建的可靠框架。
我们引入了ZeroReg3D,这是一种专为从连续组织学切片进行准确三维重建量身定制的零样本配准管道。通过将基于零样本深度学习的关键点匹配与基于优化的仿射和非刚性配准技术相结合,ZeroReg3D有效地解决了诸如组织变形、切片伪影、染色变异性和照明不一致等关键挑战,而无需重新训练或微调。