Literature DB >> 9013362

Spatial filtering of multichannel electroencephalographic recordings through principal component analysis by singular value decomposition.

T D Lagerlund1, F W Sharbrough, N E Busacker.   

Abstract

Principal component analysis (PCA) by singular value decomposition (SVD) may be used to analyze an epoch of a multichannel electroencephalogram (EEG) into multiple linearly independent (temporally and spatially noncorrelated) components, or features; the original epoch of the EEG may be reconstructed as a linear combination of the components. The result of SVD includes the components, expressible as time series waveforms, and the factors that determine how much each component waveform contributes to each EEG channel. By omission of some component waveforms from the linear combination, a new EEG can be reconstructed, differing from the original in useful ways. For example, artifacts can be removed and features such as ictal or interictal discharges can be enhanced by suppressing the remainder of the EEG. We developed a variation of this technique in which the factors that reconstruct the modified EEG from the original are stored as a matrix. This matrix is applied to multichannel EEG at successive times to create a new EEG continuously in real time, without redoing the time-consuming SVD. This matrix acts as a spatial filter with useful properties. We successfully applied this method to remove artifacts, including ocular movement and electrocardiographic artifacts. Removal of myogenic artifacts was much less complete, but there was significant improvement in the ability to visualize underlying activity in the presence of myogenic artifacts. The major limitations of the method are its inability to completely separate some artifacts from cerebral activity, especially when both have similar amplitudes, and the possibility that a spatial filter may distort the distribution of activities that overlap with the artifacts being removed.

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Year:  1997        PMID: 9013362     DOI: 10.1097/00004691-199701000-00007

Source DB:  PubMed          Journal:  J Clin Neurophysiol        ISSN: 0736-0258            Impact factor:   2.177


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