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Refined multiscale fuzzy entropy based on standard deviation for biomedical signal analysis
Multiscale entropy (MSE) has been a prevalent algorithm to quantify the complexity of biomedical time series. Recent developments in the field have tried to alleviate the problem of undefined MSE values for short signals. Moreover, there has been a recent interest in using other statistical moments...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5644759/ https://www.ncbi.nlm.nih.gov/pubmed/28462498 http://dx.doi.org/10.1007/s11517-017-1647-5 |
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author | Azami, Hamed Fernández, Alberto Escudero, Javier |
author_facet | Azami, Hamed Fernández, Alberto Escudero, Javier |
author_sort | Azami, Hamed |
collection | PubMed |
description | Multiscale entropy (MSE) has been a prevalent algorithm to quantify the complexity of biomedical time series. Recent developments in the field have tried to alleviate the problem of undefined MSE values for short signals. Moreover, there has been a recent interest in using other statistical moments than the mean, i.e., variance, in the coarse-graining step of the MSE. Building on these trends, here we introduce the so-called refined composite multiscale fuzzy entropy based on the standard deviation (RCMFE(σ)) and mean (RCMFE(μ)) to quantify the dynamical properties of spread and mean, respectively, over multiple time scales. We demonstrate the dependency of the RCMFE(σ) and RCMFE(μ), in comparison with other multiscale approaches, on several straightforward signal processing concepts using a set of synthetic signals. The results evidenced that the RCMFE(σ) and RCMFE(μ) values are more stable and reliable than the classical multiscale entropy ones. We also inspect the ability of using the standard deviation as well as the mean in the coarse-graining process using magnetoencephalograms in Alzheimer’s disease and publicly available electroencephalograms recorded from focal and non-focal areas in epilepsy. Our results indicated that when the RCMFE(μ) cannot distinguish different types of dynamics of a particular time series at some scale factors, the RCMFE(σ) may do so, and vice versa. The results showed that RCMFE(σ)-based features lead to higher classification accuracies in comparison with the RCMFE(μ)-based ones. We also made freely available all the Matlab codes used in this study at 10.7488/ds/1477. |
format | Online Article Text |
id | pubmed-5644759 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-56447592017-10-27 Refined multiscale fuzzy entropy based on standard deviation for biomedical signal analysis Azami, Hamed Fernández, Alberto Escudero, Javier Med Biol Eng Comput Original Article Multiscale entropy (MSE) has been a prevalent algorithm to quantify the complexity of biomedical time series. Recent developments in the field have tried to alleviate the problem of undefined MSE values for short signals. Moreover, there has been a recent interest in using other statistical moments than the mean, i.e., variance, in the coarse-graining step of the MSE. Building on these trends, here we introduce the so-called refined composite multiscale fuzzy entropy based on the standard deviation (RCMFE(σ)) and mean (RCMFE(μ)) to quantify the dynamical properties of spread and mean, respectively, over multiple time scales. We demonstrate the dependency of the RCMFE(σ) and RCMFE(μ), in comparison with other multiscale approaches, on several straightforward signal processing concepts using a set of synthetic signals. The results evidenced that the RCMFE(σ) and RCMFE(μ) values are more stable and reliable than the classical multiscale entropy ones. We also inspect the ability of using the standard deviation as well as the mean in the coarse-graining process using magnetoencephalograms in Alzheimer’s disease and publicly available electroencephalograms recorded from focal and non-focal areas in epilepsy. Our results indicated that when the RCMFE(μ) cannot distinguish different types of dynamics of a particular time series at some scale factors, the RCMFE(σ) may do so, and vice versa. The results showed that RCMFE(σ)-based features lead to higher classification accuracies in comparison with the RCMFE(μ)-based ones. We also made freely available all the Matlab codes used in this study at 10.7488/ds/1477. Springer Berlin Heidelberg 2017-05-02 2017 /pmc/articles/PMC5644759/ /pubmed/28462498 http://dx.doi.org/10.1007/s11517-017-1647-5 Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Azami, Hamed Fernández, Alberto Escudero, Javier Refined multiscale fuzzy entropy based on standard deviation for biomedical signal analysis |
title | Refined multiscale fuzzy entropy based on standard deviation for biomedical signal analysis |
title_full | Refined multiscale fuzzy entropy based on standard deviation for biomedical signal analysis |
title_fullStr | Refined multiscale fuzzy entropy based on standard deviation for biomedical signal analysis |
title_full_unstemmed | Refined multiscale fuzzy entropy based on standard deviation for biomedical signal analysis |
title_short | Refined multiscale fuzzy entropy based on standard deviation for biomedical signal analysis |
title_sort | refined multiscale fuzzy entropy based on standard deviation for biomedical signal analysis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5644759/ https://www.ncbi.nlm.nih.gov/pubmed/28462498 http://dx.doi.org/10.1007/s11517-017-1647-5 |
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