Stouffer Kaitlin, Chen Xiaoyin, Zeng Hongkui, Charlier Benjamin, Younes Laurent, Trouve Alain, Miller Michael I
bioRxiv. 2025 Jun 14:2024.11.04.621983. doi: 10.1101/2024.11.04.621983.
Advancements in imaging and molecular techniques enable the collection of subcellular-scale data. Diversity in measured features, resolution, and physical scope of capture across technologies and experimental protocols pose numerous challenges to integrating data with reference coordinate systems and across scales. This paper describes a collection of technologies that we have developed for mapping data across scales and modalities, such as genes to tissues, specifically in a 3D setting. Our collection of technologies include (i) an explicit censored data representation for the partial matching problem mapping whole brains to subsampled subvolumes, (ii) a multi, scale-space optimization technology for generating resampling grids optimized to represent spatial geometry at fixed complexities, and (iii) mutual-information based functional feature selection. We integrate these technologies with our cross-modality mapping algorithm through the use of image-varifold measure norms to represent universally data across scales and imaging modalities. Collectively, these methods afford efficient representations of peta-scale imagery providing the algorithms for mapping from the nano to millimeter scales, which we term cross-modality image-varifold LDDMM (xIV-LDDMM).
成像技术和分子技术的进步使得亚细胞尺度数据的收集成为可能。不同技术和实验方案在测量特征、分辨率以及捕获的物理范围方面存在差异,这给将数据与参考坐标系进行整合以及跨尺度整合带来了诸多挑战。本文介绍了我们开发的一系列用于跨尺度和模态映射数据的技术,例如从基因到组织的映射,特别是在三维环境中。我们的技术包括:(i) 一种用于将全脑映射到下采样子体积的部分匹配问题的显式删失数据表示;(ii) 一种多尺度空间优化技术,用于生成在固定复杂度下优化以表示空间几何的重采样网格;(iii) 基于互信息的功能特征选择。我们通过使用图像变分曲面测度范数将这些技术与我们的跨模态映射算法相结合,以跨尺度和成像模态统一表示数据。总体而言,这些方法能够高效表示千万亿字节规模的图像,提供从纳米尺度到毫米尺度的映射算法,我们将其称为跨模态图像变分曲面大变形微分同胚度量映射(xIV-LDDMM)。