There is increasing interest in identifying changes in the underlying states of brain networks. The availability of large scale neuroimaging data creates a strong need to develop fast, scalable methods for detecting and localizing in time such changes and also identify their drivers, thus enabling neuroscientists to hypothesize about potential mechanisms. This paper presents a fast method for detecting break points in exceedingly long time series neuroimaging data, based on vector autoregressive (Granger causal) models. It uses a multi-step strategy based on a regularized objective function that leads to fast identification of candidate break points, followed by clustering steps to select the final set of break points and subsequent estimation with false positives control of the underlying Granger causal networks. The latter provides insights into key changes in network connectivity that led to the presence of break points. The proposed methodology is illustrated on synthetic data varying in their length, dimensionality, number of break points, strength of the signal, and also applied to EEG data related to visual tasks.
翻译:大规模神经成像数据的提供使得非常需要制定快速、可扩缩的方法,以便及时发现和定位这些变化,并查明其驱动因素,从而使神经科学家能够对潜在机制进行假设。本文件根据矢量自动递减(因果)模型,为探测超长时间序列神经成像数据中的断点提供了一个快速方法。它使用基于常规目标功能的多步骤战略,导致快速识别候选断点,随后采取集群步骤,选择最后一组断点并随后进行估算,对根基Granger因果关系网络进行错误的正面控制。后者揭示了导致断点存在的网络连接的关键变化。拟议方法以不同长度、维度、断点数目、信号强度等合成数据为例,还用于与视觉任务有关的 EEG数据。