Bayesian Transformers and Higher-Order Graph Matching for Cell Tracking in Serial Tissue Sections.

Mostafa Karami, Sahand Hamzehei, David Arce, Gianna Raimondi, Linnaea Ostroff, Sheida Nabavi
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Abstract

Reliable 3D reconstruction of tissue architecture from sequential 2D multiplex images is challenging due to the noise and distortions introduced by ultrathin (50 nm) slicing and complex alignment procedures. Conventional cell tracking methods often fail under such conditions, resulting in inaccurate linkage of cells across sections. To bridge this gap, we propose a Bayesian Transformer framework that incorporates uncertainty-aware feature embeddings and higher-order graph matching with belief propagation. By tracking cells across consecutive sections, our method facilitates the 3D reconstruction of volumetric tissue organization, even in highly noise-prone scenarios. The methodology begins with a standard segmentation step, followed by feature extraction that computes morphological, shape, and texture descriptors, as well as deep CNN embeddings. These rich, uncertainty-sensitive representations reduce errors caused by both registration artifacts and morphological variability. We validate the effectiveness of the proposed approach on a private multiplex dataset of fixed tissue sections and further demonstrate its generalizability on public time-lapse microscopy videos, showcasing adaptability to diverse datasets. Experimental comparisons reveal that our method outperforms baseline tracking techniques, achieving higher accuracy and more consistent cell linkages across multiple serial sections. The code used in this research with sample dataset are publicly available at https://github.com/NabaviLab/bayesian-transformer-cell-tracking.

连续组织切片中细胞跟踪的贝叶斯变换和高阶图匹配。
由于超薄(50纳米)切片和复杂的对准过程带来的噪声和畸变,从连续的二维多路图像中可靠的组织结构三维重建具有挑战性。在这种情况下,传统的细胞跟踪方法往往失败,导致细胞横断面的不准确连接。为了弥补这一差距,我们提出了一个贝叶斯转换框架,该框架结合了不确定性感知特征嵌入和高阶图匹配与信念传播。通过在连续切片上跟踪细胞,我们的方法可以促进体积组织的3D重建,即使在高度容易产生噪声的情况下也是如此。该方法从标准分割步骤开始,然后是计算形态、形状和纹理描述符的特征提取,以及深度CNN嵌入。这些丰富的、对不确定性敏感的表示减少了由配准伪影和形态变化引起的错误。我们在固定组织切片的私人多重数据集上验证了所提出方法的有效性,并进一步证明了其在公共延时显微镜视频上的通用性,展示了对不同数据集的适应性。实验比较表明,我们的方法优于基线跟踪技术,在多个序列切片中实现更高的准确性和更一致的细胞连接。本研究中使用的带有样本数据集的代码可在https://github.com/NabaviLab/bayesian-transformer-cell-tracking上公开获得。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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