To capture the slowly time-varying spectral content of real-world time-series, a common paradigm is to partition the data into approximately stationary intervals and perform inference in the time-frequency domain. However, this approach lacks a corresponding nonstationary time-domain generative model for the entire data and thus, time-domain inference occurs in each interval separately. This results in distortion/discontinuity around interval boundaries and, consequently, can lead to erroneous inferences based on any quantities derived from the posterior, such as the phase. To address these shortcomings, we propose the Piecewise Locally Stationary Oscillation (PLSO) generative model for decomposing time-series data with slowly time-varying spectra into several oscillatory, piecewise-stationary processes. PLSO, being a nonstationary time-domain generative model, enables inference on the entire time-series, without boundary effects, and, at the same time, provides a characterization of its time-varying spectral properties. For inference, we propose a novel two-stage algorithm that combines Kalman theory and an accelerated proximal gradient algorithm for the nonconvex objective. We demonstrate these points through experiments on simulated data and real neural data from the rat and the human brain.
翻译:为了捕捉现实世界时间序列中缓慢时间变化的光谱内容,一个共同的范式是将数据分成大约固定间隔,并在时间频域中进行推断。然而,这一方法缺乏一个相应的非静止时间光谱变异模型,因此,每个间隔中都分别出现时间变化的推断。这导致在间隔界限周围扭曲/断裂,从而可能导致根据从后台(例如阶段)得到的任何数量错误推断。为了解决这些缺点,我们建议使用微小的局部静止观察(PLSO)基因化模型,用于将时间序列数据分解,缓慢时间变化的光谱变光谱形成若干动、片动的静止过程。PLSO是一个非静止时间变异模型,因此,每个间隔间隔间隔间隔中会发生时间变异/断异,从而可能导致根据从后台(例如阶段)得到的任何数量错误推断。为了纠正这些缺点,我们建议用微小的局部静止观察(PLSO)基因模型模型模型模型模型模型模型模型,从两个阶段级的模型数据模型中将Kalx模型和模型模型模型模型模型数据结合起来。