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Retinotopic and topographic analyses with gaze restriction for steady-state visual evoked potentials
Although the mechanisms of steady-state visual evoked potentials (SSVEPs) have been well studied, none of them have been implemented with strictly experimental conditions. Our objective was to create an ideal observer condition to exploit the features of SSVEPs. We present here an electroencephalogr...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6418283/ https://www.ncbi.nlm.nih.gov/pubmed/30872723 http://dx.doi.org/10.1038/s41598-019-41158-5 |
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author | Zhang, Nannan Liu, Yadong Yin, Erwei Deng, Baosong Cao, Lu Jiang, Jun Zhou, Zongtan Hu, Dewen |
author_facet | Zhang, Nannan Liu, Yadong Yin, Erwei Deng, Baosong Cao, Lu Jiang, Jun Zhou, Zongtan Hu, Dewen |
author_sort | Zhang, Nannan |
collection | PubMed |
description | Although the mechanisms of steady-state visual evoked potentials (SSVEPs) have been well studied, none of them have been implemented with strictly experimental conditions. Our objective was to create an ideal observer condition to exploit the features of SSVEPs. We present here an electroencephalographic (EEG) eye tracking experimental paradigm that provides biofeedback for gaze restriction during the visual stimulation. Specifically, we designed an EEG eye tracking synchronous data recording system for successful trial selection. Forty-six periodic flickers within a visual field of 11.5° were successively presented to evoke SSVEP responses, and online biofeedback based on an eye tracker was provided for gaze restriction. For eight participants, SSVEP responses in the visual field and topographic maps from full-brain EEG were plotted and analyzed. The experimental results indicated that the optimal visual flicking arrangement to boost SSVEPs should include the features of circular stimuli within a 4–6° spatial distance and increased stimulus area below the fixation point. These findings provide a basis for determining stimulus parameters for neural engineering studies, e.g. SSVEP-based brain-computer interface (BCI) designs. The proposed experimental paradigm could also provide a precise framework for future SSVEP-related studies. |
format | Online Article Text |
id | pubmed-6418283 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64182832019-03-18 Retinotopic and topographic analyses with gaze restriction for steady-state visual evoked potentials Zhang, Nannan Liu, Yadong Yin, Erwei Deng, Baosong Cao, Lu Jiang, Jun Zhou, Zongtan Hu, Dewen Sci Rep Article Although the mechanisms of steady-state visual evoked potentials (SSVEPs) have been well studied, none of them have been implemented with strictly experimental conditions. Our objective was to create an ideal observer condition to exploit the features of SSVEPs. We present here an electroencephalographic (EEG) eye tracking experimental paradigm that provides biofeedback for gaze restriction during the visual stimulation. Specifically, we designed an EEG eye tracking synchronous data recording system for successful trial selection. Forty-six periodic flickers within a visual field of 11.5° were successively presented to evoke SSVEP responses, and online biofeedback based on an eye tracker was provided for gaze restriction. For eight participants, SSVEP responses in the visual field and topographic maps from full-brain EEG were plotted and analyzed. The experimental results indicated that the optimal visual flicking arrangement to boost SSVEPs should include the features of circular stimuli within a 4–6° spatial distance and increased stimulus area below the fixation point. These findings provide a basis for determining stimulus parameters for neural engineering studies, e.g. SSVEP-based brain-computer interface (BCI) designs. The proposed experimental paradigm could also provide a precise framework for future SSVEP-related studies. Nature Publishing Group UK 2019-03-14 /pmc/articles/PMC6418283/ /pubmed/30872723 http://dx.doi.org/10.1038/s41598-019-41158-5 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Zhang, Nannan Liu, Yadong Yin, Erwei Deng, Baosong Cao, Lu Jiang, Jun Zhou, Zongtan Hu, Dewen Retinotopic and topographic analyses with gaze restriction for steady-state visual evoked potentials |
title | Retinotopic and topographic analyses with gaze restriction for steady-state visual evoked potentials |
title_full | Retinotopic and topographic analyses with gaze restriction for steady-state visual evoked potentials |
title_fullStr | Retinotopic and topographic analyses with gaze restriction for steady-state visual evoked potentials |
title_full_unstemmed | Retinotopic and topographic analyses with gaze restriction for steady-state visual evoked potentials |
title_short | Retinotopic and topographic analyses with gaze restriction for steady-state visual evoked potentials |
title_sort | retinotopic and topographic analyses with gaze restriction for steady-state visual evoked potentials |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6418283/ https://www.ncbi.nlm.nih.gov/pubmed/30872723 http://dx.doi.org/10.1038/s41598-019-41158-5 |
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