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Novel fNIRS study on homogeneous symmetric feature-based transfer learning for brain–computer interface

The brain–computer interface (BCI) provides an alternate means of communication between the brain and external devices by recognizing the brain activities and translating them into external commands. The functional Near-Infrared Spectroscopy (fNIRS) is becoming popular as a non-invasive modality for...

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Autores principales: Khalil, Khurram, Asgher, Umer, Ayaz, Yasar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8873341/
https://www.ncbi.nlm.nih.gov/pubmed/35210460
http://dx.doi.org/10.1038/s41598-022-06805-4
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author Khalil, Khurram
Asgher, Umer
Ayaz, Yasar
author_facet Khalil, Khurram
Asgher, Umer
Ayaz, Yasar
author_sort Khalil, Khurram
collection PubMed
description The brain–computer interface (BCI) provides an alternate means of communication between the brain and external devices by recognizing the brain activities and translating them into external commands. The functional Near-Infrared Spectroscopy (fNIRS) is becoming popular as a non-invasive modality for brain activity detection. The recent trends show that deep learning has significantly enhanced the performance of the BCI systems. But the inherent bottleneck for deep learning (in the domain of BCI) is the requirement of the vast amount of training data, lengthy recalibrating time, and expensive computational resources for training deep networks. Building a high-quality, large-scale annotated dataset for deep learning-based BCI systems is exceptionally tedious, complex, and expensive. This study investigates the novel application of transfer learning for fNIRS-based BCI to solve three objective functions (concerns), i.e., the problem of insufficient training data, reduced training time, and increased accuracy. We applied symmetric homogeneous feature-based transfer learning on convolutional neural network (CNN) designed explicitly for fNIRS data collected from twenty-six (26) participants performing the n-back task. The results suggested that the proposed method achieves the maximum saturated accuracy sooner and outperformed the traditional CNN model on averaged accuracy by 25.58% in the exact duration of training time, reducing the training time, recalibrating time, and computational resources.
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spelling pubmed-88733412022-02-25 Novel fNIRS study on homogeneous symmetric feature-based transfer learning for brain–computer interface Khalil, Khurram Asgher, Umer Ayaz, Yasar Sci Rep Article The brain–computer interface (BCI) provides an alternate means of communication between the brain and external devices by recognizing the brain activities and translating them into external commands. The functional Near-Infrared Spectroscopy (fNIRS) is becoming popular as a non-invasive modality for brain activity detection. The recent trends show that deep learning has significantly enhanced the performance of the BCI systems. But the inherent bottleneck for deep learning (in the domain of BCI) is the requirement of the vast amount of training data, lengthy recalibrating time, and expensive computational resources for training deep networks. Building a high-quality, large-scale annotated dataset for deep learning-based BCI systems is exceptionally tedious, complex, and expensive. This study investigates the novel application of transfer learning for fNIRS-based BCI to solve three objective functions (concerns), i.e., the problem of insufficient training data, reduced training time, and increased accuracy. We applied symmetric homogeneous feature-based transfer learning on convolutional neural network (CNN) designed explicitly for fNIRS data collected from twenty-six (26) participants performing the n-back task. The results suggested that the proposed method achieves the maximum saturated accuracy sooner and outperformed the traditional CNN model on averaged accuracy by 25.58% in the exact duration of training time, reducing the training time, recalibrating time, and computational resources. Nature Publishing Group UK 2022-02-24 /pmc/articles/PMC8873341/ /pubmed/35210460 http://dx.doi.org/10.1038/s41598-022-06805-4 Text en © The Author(s) 2022 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
Khalil, Khurram
Asgher, Umer
Ayaz, Yasar
Novel fNIRS study on homogeneous symmetric feature-based transfer learning for brain–computer interface
title Novel fNIRS study on homogeneous symmetric feature-based transfer learning for brain–computer interface
title_full Novel fNIRS study on homogeneous symmetric feature-based transfer learning for brain–computer interface
title_fullStr Novel fNIRS study on homogeneous symmetric feature-based transfer learning for brain–computer interface
title_full_unstemmed Novel fNIRS study on homogeneous symmetric feature-based transfer learning for brain–computer interface
title_short Novel fNIRS study on homogeneous symmetric feature-based transfer learning for brain–computer interface
title_sort novel fnirs study on homogeneous symmetric feature-based transfer learning for brain–computer interface
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8873341/
https://www.ncbi.nlm.nih.gov/pubmed/35210460
http://dx.doi.org/10.1038/s41598-022-06805-4
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