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Sinusoidal Signal Assisted Multivariate Empirical Mode Decomposition for Brain–Computer Interfaces | IEEE Journals & Magazine | IEEE Xplore

Sinusoidal Signal Assisted Multivariate Empirical Mode Decomposition for Brain–Computer Interfaces


Abstract:

A brain-computer interface (BCI) is a communication approach that permits cerebral activity to control computers or external devices. Brain electrical activity recorded w...Show More

Abstract:

A brain-computer interface (BCI) is a communication approach that permits cerebral activity to control computers or external devices. Brain electrical activity recorded with electroencephalography (EEG) is most commonly used for BCI. Noise-assisted multivariate empirical mode decomposition (NA-MEMD) is a data-driven time-frequency analysis method that can be applied to nonlinear and nonstationary EEG signals for BCI data processing. However, because white Gaussian noise occupies a broad range of frequencies, some redundant components are introduced. To solve this leakage problem, in this study, we propose using a sinusoidal assisted signal that occupies the same frequency ranges as the original signals to improve MEMD performance. To verify the effectiveness of the proposed sinusoidal signal assisted MEMD (SA-MEMD) method, we compared the decomposition performances of MEMD, NA-MEMD, and the proposed SA-MEMD using synthetic signals and a real-world BCI dataset. The spectral decomposition results indicate that the proposed SA-MEMD can avoid the generation of redundant components and over decomposition, thus, substantially reduce the mode mixing and misalignment that occurs in MEMD and NA-MEMD. Moreover, using SA-MEMD as a signal preprocessing method instead of MEMD or NA-MEMD can significantly improve BCI classification accuracy and reduce calculation time, which indicates that SA-MEMD is a powerful spectral decomposition method for BCI.
Published in: IEEE Journal of Biomedical and Health Informatics ( Volume: 22, Issue: 5, September 2018)
Page(s): 1373 - 1384
Date of Publication: 20 November 2017

ISSN Information:

PubMed ID: 29990114

Funding Agency:


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