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DCM for complex-valued data: Cross-spectra coherence and phase-delays

机译:DCM用于复数值数据:互谱相干和相位延迟

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摘要

This note describes an extension of Bayesian model inversion procedures for the Dynamic Causal Modeling (DCM) of complex-valued data. Modeling complex data can be particularly useful in the analysis of multivariate ergodic (stationary) time-series. We illustrate this with a generalization of DCM for steady-state responses that models both the real and imaginary parts of sample cross-spectra. DCM allows one to infer underlying biophysical parameters generating data (like synaptic time constants, connection strengths and conduction delays). Because transfer functions and complex cross-spectra can be generated from these parameters, one can also describe the implicit system architecture in terms of conventional (linear systems) measures; like coherence, phase-delay or cross-correlation functions. Crucially, these measures can be derived in both sensor and source-space. In other words, one can examine the cross-correlation or phase-delay functions between hidden neuronal sources using non-invasive data and relate these functions to synaptic parameters and neuronal conduction delays. We illustrate these points using local field potential recordings from the subthalamic nucleus and globus pallidus, with a special focus on the relationship between conduction delays and the ensuing phase relationships and cross-correlation time lags between population activities.
机译:本说明描述了贝叶斯模型反演程序的扩展,用于复杂值数据的动态因果建模(DCM)。对复杂数据进行建模在多维遍历(固定)时间序列的分析中尤其有用。我们通过对DCM的稳态响应进行概括来说明这一点,该模型对样品互谱的实部和虚部进行建模。 DCM允许人们推断潜在的生物物理参数以生成数据(如突触时间常数,连接强度和传导延迟)。因为可以从这些参数生成传递函数和复杂的互谱,所以还可以用常规(线性系统)度量来描述隐式系统架构。例如相干,相位延迟或互相关函数。至关重要的是,这些度量可以在传感器和源空间中导出。换句话说,可以使用非侵入性数据检查隐藏的神经元源之间的互相关或相位延迟功能,并将这些功能与突触参数和神经元传导延迟相关联。我们使用来自丘脑底核和苍白球的局部场电势记录来说明这些点,并特别着重于传导延迟与随后的相位关系之间的关系以及种群活动之间的互相关时间滞后。

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