bioRxiv · 10.1101/2020.07.09.195784
A data-driven method to identify frequency boundaries in multichannel electrophysiology data
Abstract
BackgroundElectrophysiological recordings of the brain often exhibit neural oscillations, defined as narrowband bumps that deviate from the background power spectrum. These narrowband dynamics are grouped into frequency ranges, and the study of how activities in these ranges are related to cognition and disease is a major part of the neuroscience corpus. Frequency ranges are nearly always defined according to integer boundaries, such as 4-8 Hz for the theta band and 8-12 Hz for the alpha band. New methodA data-driven multivariate method is presented to identify empirical frequency boundaries based on clustering of spatiotemporal similarities across a range of frequencies. The method, termed gedBounds, identifies patterns in covariance matrices that maximally separate narrowband from broadband activity, and then identifies clusters in the correlation matrix of those spatial patterns over all frequencies, using the dbscan algorithm. Those clusters are empirically derived frequency bands, from which boundaries can be extracted. ResultsgedBounds recovers ground truth results in simulated data with high accuracy. The method was tested on EEG resting-state data from Parkinsons patients and control, and several features of the frequency components differed between patients and controls. Comparison with existing methodsThe proposed method offers higher precision in defining subject-specific frequency boundaries compared to the current standard approach. ConclusionsgedBounds can increase the precision and feature extraction of spectral dynamics in electrophysiology data.
Source connections
Explore related subjects
Keep this discovery
Explore connections, maps & timelines
Michael Cohen. 2020-07-10. A data-driven method to identify frequency boundaries in multichannel electrophysiology data. https://doi.org/10.1101/2020.07.09.195784
Cite the original work for its findings. Save a collection to share your selection of sources.