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Signature methods for brain-computer interfaces

Brain-computer interfaces (BCIs) allow direct communication between one’s central nervous system and a computer without any muscle movement hence by-passing the peripheral nervous system. They can restore disabled people’s ability to interact with their environment, e.g. communication and wheelchair...

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Autores principales: Xu, Xiaoqi, Lee, Darrick, Drougard, Nicolas, Roy, Raphaëlle N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10696092/
https://www.ncbi.nlm.nih.gov/pubmed/38049438
http://dx.doi.org/10.1038/s41598-023-41326-8
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author Xu, Xiaoqi
Lee, Darrick
Drougard, Nicolas
Roy, Raphaëlle N.
author_facet Xu, Xiaoqi
Lee, Darrick
Drougard, Nicolas
Roy, Raphaëlle N.
author_sort Xu, Xiaoqi
collection PubMed
description Brain-computer interfaces (BCIs) allow direct communication between one’s central nervous system and a computer without any muscle movement hence by-passing the peripheral nervous system. They can restore disabled people’s ability to interact with their environment, e.g. communication and wheelchair control. However, to this day their performance is still hindered by the non-stationarity of electroencephalography (EEG) signals, as well as their susceptibility to noise from the users’ environment and from their own physiological activity. Moreover, a non-negligible amount of users struggle to use BCI systems based on motor imagery. In this paper, a new method based on the path signature is introduced to tackle this problem by using features which are different from the usual power-based ones. The path signature is a series of iterated integrals computed from a multidimensional path. It is invariant under translation and time reparametrization, which makes it a robust feature for multichannel EEG time series. The performance can be further boosted by combining the path signature with the gold standard Riemannian classifier in the BCI field exploiting the geometric structure of symmetric positive definite (SPD) matrices. The results obtained on publicly available datasets show that the signature method is more robust to inter-user variability than classical ones, especially on noisy and low-quality data. Hence, this study paves the way towards the use of mathematical tools that until now have been neglected, in order to tackle the EEG-based BCI variability issue. It also sheds light on the lead-lag relationship captured by path signature which seems relevant to assess the underlying neural mechanisms.
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spelling pubmed-106960922023-12-06 Signature methods for brain-computer interfaces Xu, Xiaoqi Lee, Darrick Drougard, Nicolas Roy, Raphaëlle N. Sci Rep Article Brain-computer interfaces (BCIs) allow direct communication between one’s central nervous system and a computer without any muscle movement hence by-passing the peripheral nervous system. They can restore disabled people’s ability to interact with their environment, e.g. communication and wheelchair control. However, to this day their performance is still hindered by the non-stationarity of electroencephalography (EEG) signals, as well as their susceptibility to noise from the users’ environment and from their own physiological activity. Moreover, a non-negligible amount of users struggle to use BCI systems based on motor imagery. In this paper, a new method based on the path signature is introduced to tackle this problem by using features which are different from the usual power-based ones. The path signature is a series of iterated integrals computed from a multidimensional path. It is invariant under translation and time reparametrization, which makes it a robust feature for multichannel EEG time series. The performance can be further boosted by combining the path signature with the gold standard Riemannian classifier in the BCI field exploiting the geometric structure of symmetric positive definite (SPD) matrices. The results obtained on publicly available datasets show that the signature method is more robust to inter-user variability than classical ones, especially on noisy and low-quality data. Hence, this study paves the way towards the use of mathematical tools that until now have been neglected, in order to tackle the EEG-based BCI variability issue. It also sheds light on the lead-lag relationship captured by path signature which seems relevant to assess the underlying neural mechanisms. Nature Publishing Group UK 2023-12-04 /pmc/articles/PMC10696092/ /pubmed/38049438 http://dx.doi.org/10.1038/s41598-023-41326-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Xu, Xiaoqi
Lee, Darrick
Drougard, Nicolas
Roy, Raphaëlle N.
Signature methods for brain-computer interfaces
title Signature methods for brain-computer interfaces
title_full Signature methods for brain-computer interfaces
title_fullStr Signature methods for brain-computer interfaces
title_full_unstemmed Signature methods for brain-computer interfaces
title_short Signature methods for brain-computer interfaces
title_sort signature methods for brain-computer interfaces
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10696092/
https://www.ncbi.nlm.nih.gov/pubmed/38049438
http://dx.doi.org/10.1038/s41598-023-41326-8
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