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Comparative Analysis of Wavelet-based Feature Extraction for Intramuscular EMG Signal Decomposition

BACKGROUND: Electromyographic (EMG) signal decomposition is the process by which an EMG signal is decomposed into its constituent motor unit potential trains (MUPTs). A major step in EMG decomposition is feature extraction in which each detected motor unit potential (MUP) is represented by a feature...

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Autores principales: Ghofrani Jahromi, M., Parsaei, H., Zamani, A., Dehbozorgi, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Journal of Biomedical Physics and Engineering 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5758715/
https://www.ncbi.nlm.nih.gov/pubmed/29392120
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author Ghofrani Jahromi, M.
Parsaei, H.
Zamani, A.
Dehbozorgi, M.
author_facet Ghofrani Jahromi, M.
Parsaei, H.
Zamani, A.
Dehbozorgi, M.
author_sort Ghofrani Jahromi, M.
collection PubMed
description BACKGROUND: Electromyographic (EMG) signal decomposition is the process by which an EMG signal is decomposed into its constituent motor unit potential trains (MUPTs). A major step in EMG decomposition is feature extraction in which each detected motor unit potential (MUP) is represented by a feature vector. As with any other pattern recognition system, feature extraction has a significant impact on the performance of a decomposition system. EMG decomposition has been studied well and several systems were proposed, but feature extraction step has not been investigated in detail. OBJECTIVE: Several EMG signals were generated using a physiologically-based EMG signal simulation algorithm. For each signal, the firing patterns of motor units (MUs) provided by the simulator were used to extract MUPs of each MU. For feature extraction, different wavelet families including Daubechies (db), Symlets, Coiflets, bi-orthogonal, reverse bi-orthogonal and discrete Meyer were investigated. Moreover, the possibility of reducing the dimensionality of MUP feature vector is explored in this work. The MUPs represented using wavelet-domain features are transformed into a new coordinate system using Principal Component Analysis (PCA). The features were evaluated regarding their capability in discriminating MUPs of individual MUs. RESULTS: Extensive studies on different mother wavelet functions revealed that db2, coif1, sym5, bior2.2, bior4.4, and rbior2.2 are the best ones in differentiating MUPs of different MUs. The best results were achieved at the 4th detail coefficient. Overall, rbior2.2 outperformed all wavelet functions studied; nevertheless for EMG signals composed of more than 12 MUPTs, syms5 wavelet function is the best function. Applying PCA slightly enhanced the results.
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spelling pubmed-57587152018-02-01 Comparative Analysis of Wavelet-based Feature Extraction for Intramuscular EMG Signal Decomposition Ghofrani Jahromi, M. Parsaei, H. Zamani, A. Dehbozorgi, M. J Biomed Phys Eng Original Article BACKGROUND: Electromyographic (EMG) signal decomposition is the process by which an EMG signal is decomposed into its constituent motor unit potential trains (MUPTs). A major step in EMG decomposition is feature extraction in which each detected motor unit potential (MUP) is represented by a feature vector. As with any other pattern recognition system, feature extraction has a significant impact on the performance of a decomposition system. EMG decomposition has been studied well and several systems were proposed, but feature extraction step has not been investigated in detail. OBJECTIVE: Several EMG signals were generated using a physiologically-based EMG signal simulation algorithm. For each signal, the firing patterns of motor units (MUs) provided by the simulator were used to extract MUPs of each MU. For feature extraction, different wavelet families including Daubechies (db), Symlets, Coiflets, bi-orthogonal, reverse bi-orthogonal and discrete Meyer were investigated. Moreover, the possibility of reducing the dimensionality of MUP feature vector is explored in this work. The MUPs represented using wavelet-domain features are transformed into a new coordinate system using Principal Component Analysis (PCA). The features were evaluated regarding their capability in discriminating MUPs of individual MUs. RESULTS: Extensive studies on different mother wavelet functions revealed that db2, coif1, sym5, bior2.2, bior4.4, and rbior2.2 are the best ones in differentiating MUPs of different MUs. The best results were achieved at the 4th detail coefficient. Overall, rbior2.2 outperformed all wavelet functions studied; nevertheless for EMG signals composed of more than 12 MUPTs, syms5 wavelet function is the best function. Applying PCA slightly enhanced the results. Journal of Biomedical Physics and Engineering 2017-12-01 /pmc/articles/PMC5758715/ /pubmed/29392120 Text en Copyright: © Journal of Biomedical Physics and Engineering http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Ghofrani Jahromi, M.
Parsaei, H.
Zamani, A.
Dehbozorgi, M.
Comparative Analysis of Wavelet-based Feature Extraction for Intramuscular EMG Signal Decomposition
title Comparative Analysis of Wavelet-based Feature Extraction for Intramuscular EMG Signal Decomposition
title_full Comparative Analysis of Wavelet-based Feature Extraction for Intramuscular EMG Signal Decomposition
title_fullStr Comparative Analysis of Wavelet-based Feature Extraction for Intramuscular EMG Signal Decomposition
title_full_unstemmed Comparative Analysis of Wavelet-based Feature Extraction for Intramuscular EMG Signal Decomposition
title_short Comparative Analysis of Wavelet-based Feature Extraction for Intramuscular EMG Signal Decomposition
title_sort comparative analysis of wavelet-based feature extraction for intramuscular emg signal decomposition
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5758715/
https://www.ncbi.nlm.nih.gov/pubmed/29392120
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