Zhen Xingjian, Chakraborty Rudrasis, Vogt Nicholas, Bendlin Barbara B, Singh Vikas
University of Wisconsin Madison.
University of California, Berkeley.
Proc IEEE Int Conf Comput Vis. 2019 Oct-Nov;2019:10620-10630. doi: 10.1109/iccv.2019.01072. Epub 2020 Feb 27.
Efforts are underway to study ways via which the power of deep neural networks can be extended to non-standard data types such as structured data (e.g., graphs) or manifold-valued data (e.g., unit vectors or special matrices). Often, sizable empirical improvements are possible when the geometry of such data spaces are incorporated into the design of the model, architecture, and the algorithms. Motivated by neuroimaging applications, we study formulations where the data are sequential manifold-valued measurements. This case is common in brain imaging, where the samples correspond to symmetric positive definite matrices or orientation distribution functions. Instead of a recurrent model which poses computational/technical issues, and inspired by recent results showing the viability of dilated convolutional models for sequence prediction, we develop a dilated convolutional neural network architecture for this task. On the technical side, we show how the modules needed in our network can be derived while explicitly taking the Riemannian manifold structure into account. We show how the operations needed can leverage known results for calculating the weighted Fréchet Mean (wFM). Finally, we present scientific results for group difference analysis in Alzheimer's disease (AD) where the groups are derived using AD pathology load: here the model finds several brain fiber bundles that are related to AD even when the subjects are all still cognitively healthy.
目前正在努力研究各种方法,以便将深度神经网络的能力扩展到非标准数据类型,如结构化数据(如图)或多值数据(如单位向量或特殊矩阵)。通常,当将此类数据空间的几何结构纳入模型、架构和算法的设计中时,可能会在经验上取得显著改进。受神经成像应用的启发,我们研究数据为序列多值测量的公式。这种情况在脑成像中很常见,其中样本对应于对称正定矩阵或方向分布函数。我们没有采用存在计算/技术问题的循环模型,而是受最近显示扩张卷积模型用于序列预测可行性的结果启发,为该任务开发了一种扩张卷积神经网络架构。在技术方面,我们展示了如何在明确考虑黎曼流形结构的同时推导出我们网络中所需的模块。我们展示了所需的操作如何利用计算加权弗雷歇均值(wFM)的已知结果。最后,我们展示了在阿尔茨海默病(AD)中进行组间差异分析的科学结果,其中组是根据AD病理负荷得出的:在这里,即使受试者在认知上仍然健康,该模型也发现了几个与AD相关的脑纤维束。