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Automatic bad channel detection in intracranial electroencephalographic recordings using ensemble machine learning

OBJECTIVE: Intracranial electroencephalographic (iEEG) recordings contain “bad channels”, which show non-neuronal signals. Here, we developed a new method that automatically detects iEEG bad channels using machine learning of seven signal features. METHODS: The features quantified signals’ variance,...

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Autores principales: Tuyisenge, Viateur, Trebaul, Lena, Bhattacharjee, Manik, Chanteloup-Forêt, Blandine, Saubat-Guigui, Carole, Mîndruţă, Ioana, Rheims, Sylvain, Maillard, Louis, Kahane, Philippe, Taussig, Delphine, David, Olivier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5819872/
https://www.ncbi.nlm.nih.gov/pubmed/29353183
http://dx.doi.org/10.1016/j.clinph.2017.12.013
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author Tuyisenge, Viateur
Trebaul, Lena
Bhattacharjee, Manik
Chanteloup-Forêt, Blandine
Saubat-Guigui, Carole
Mîndruţă, Ioana
Rheims, Sylvain
Maillard, Louis
Kahane, Philippe
Taussig, Delphine
David, Olivier
author_facet Tuyisenge, Viateur
Trebaul, Lena
Bhattacharjee, Manik
Chanteloup-Forêt, Blandine
Saubat-Guigui, Carole
Mîndruţă, Ioana
Rheims, Sylvain
Maillard, Louis
Kahane, Philippe
Taussig, Delphine
David, Olivier
author_sort Tuyisenge, Viateur
collection PubMed
description OBJECTIVE: Intracranial electroencephalographic (iEEG) recordings contain “bad channels”, which show non-neuronal signals. Here, we developed a new method that automatically detects iEEG bad channels using machine learning of seven signal features. METHODS: The features quantified signals’ variance, spatial–temporal correlation and nonlinear properties. Because the number of bad channels is usually much lower than the number of good channels, we implemented an ensemble bagging classifier known to be optimal in terms of stability and predictive accuracy for datasets with imbalanced class distributions. This method was applied on stereo-electroencephalographic (SEEG) signals recording during low frequency stimulations performed in 206 patients from 5 clinical centers. RESULTS: We found that the classification accuracy was extremely good: It increased with the number of subjects used to train the classifier and reached a plateau at 99.77% for 110 subjects. The classification performance was thus not impacted by the multicentric nature of data. CONCLUSIONS: The proposed method to automatically detect bad channels demonstrated convincing results and can be envisaged to be used on larger datasets for automatic quality control of iEEG data. SIGNIFICANCE: This is the first method proposed to classify bad channels in iEEG and should allow to improve the data selection when reviewing iEEG signals.
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spelling pubmed-58198722018-03-01 Automatic bad channel detection in intracranial electroencephalographic recordings using ensemble machine learning Tuyisenge, Viateur Trebaul, Lena Bhattacharjee, Manik Chanteloup-Forêt, Blandine Saubat-Guigui, Carole Mîndruţă, Ioana Rheims, Sylvain Maillard, Louis Kahane, Philippe Taussig, Delphine David, Olivier Clin Neurophysiol Article OBJECTIVE: Intracranial electroencephalographic (iEEG) recordings contain “bad channels”, which show non-neuronal signals. Here, we developed a new method that automatically detects iEEG bad channels using machine learning of seven signal features. METHODS: The features quantified signals’ variance, spatial–temporal correlation and nonlinear properties. Because the number of bad channels is usually much lower than the number of good channels, we implemented an ensemble bagging classifier known to be optimal in terms of stability and predictive accuracy for datasets with imbalanced class distributions. This method was applied on stereo-electroencephalographic (SEEG) signals recording during low frequency stimulations performed in 206 patients from 5 clinical centers. RESULTS: We found that the classification accuracy was extremely good: It increased with the number of subjects used to train the classifier and reached a plateau at 99.77% for 110 subjects. The classification performance was thus not impacted by the multicentric nature of data. CONCLUSIONS: The proposed method to automatically detect bad channels demonstrated convincing results and can be envisaged to be used on larger datasets for automatic quality control of iEEG data. SIGNIFICANCE: This is the first method proposed to classify bad channels in iEEG and should allow to improve the data selection when reviewing iEEG signals. Elsevier 2018-03 /pmc/articles/PMC5819872/ /pubmed/29353183 http://dx.doi.org/10.1016/j.clinph.2017.12.013 Text en © 2017 International Federation of Clinical Neurophysiology. Elsevier Ireland Ltd. All rights reserved. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Tuyisenge, Viateur
Trebaul, Lena
Bhattacharjee, Manik
Chanteloup-Forêt, Blandine
Saubat-Guigui, Carole
Mîndruţă, Ioana
Rheims, Sylvain
Maillard, Louis
Kahane, Philippe
Taussig, Delphine
David, Olivier
Automatic bad channel detection in intracranial electroencephalographic recordings using ensemble machine learning
title Automatic bad channel detection in intracranial electroencephalographic recordings using ensemble machine learning
title_full Automatic bad channel detection in intracranial electroencephalographic recordings using ensemble machine learning
title_fullStr Automatic bad channel detection in intracranial electroencephalographic recordings using ensemble machine learning
title_full_unstemmed Automatic bad channel detection in intracranial electroencephalographic recordings using ensemble machine learning
title_short Automatic bad channel detection in intracranial electroencephalographic recordings using ensemble machine learning
title_sort automatic bad channel detection in intracranial electroencephalographic recordings using ensemble machine learning
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5819872/
https://www.ncbi.nlm.nih.gov/pubmed/29353183
http://dx.doi.org/10.1016/j.clinph.2017.12.013
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