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MEA Viewer: A high-performance interactive application for visualizing electrophysiological data

Action potentials can be recorded extracellularly from hundreds of neurons simultaneously with multi-electrode arrays. These can typically have as many as 120 or more electrodes. The brief duration of action potentials requires a high sampling frequency to reliably capture each waveform. The resulti...

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Detalles Bibliográficos
Autores principales: Bridges, Daniel C., Tovar, Kenneth R., Wu, Bian, Hansma, Paul K., Kosik, Kenneth S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5806868/
https://www.ncbi.nlm.nih.gov/pubmed/29425223
http://dx.doi.org/10.1371/journal.pone.0192477
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author Bridges, Daniel C.
Tovar, Kenneth R.
Wu, Bian
Hansma, Paul K.
Kosik, Kenneth S.
author_facet Bridges, Daniel C.
Tovar, Kenneth R.
Wu, Bian
Hansma, Paul K.
Kosik, Kenneth S.
author_sort Bridges, Daniel C.
collection PubMed
description Action potentials can be recorded extracellularly from hundreds of neurons simultaneously with multi-electrode arrays. These can typically have as many as 120 or more electrodes. The brief duration of action potentials requires a high sampling frequency to reliably capture each waveform. The resulting raw data files are therefore large and difficult to visualize with traditional plotting tools. Common approaches to deal with the difficulties of data display, such as extracting spike times and performing spike train analysis, are useful in many contexts but they also significantly reduce data dimensionality. The use of tools which minimize data processing enable the development of heuristic perspective of experimental results. Here we introduce MEA Viewer, a high-performance open source application for the direct visualization of multi-channel electrophysiological data. MEA Viewer includes several high-performance visualizations, including an easily navigable overview of recorded extracellular action potentials from all data channels overlaid with spike timestamp data and an interactive raster plot. MEA Viewer can also display the two dimensional extent of action potential propagation in single neurons by signal averaging extracellular action potentials (eAPs) from single neurons detected on multiple electrodes. This view extracts and displays eAP timing information and eAP waveforms that are otherwise below the spike detection threshold. This entirely new method of using MEAs opens up novel research applications for medium density arrays. MEA Viewer is licensed under the General Public License version 3, GPLv3, and is available at http://github.com/dbridges/mea-tools.
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spelling pubmed-58068682018-02-23 MEA Viewer: A high-performance interactive application for visualizing electrophysiological data Bridges, Daniel C. Tovar, Kenneth R. Wu, Bian Hansma, Paul K. Kosik, Kenneth S. PLoS One Research Article Action potentials can be recorded extracellularly from hundreds of neurons simultaneously with multi-electrode arrays. These can typically have as many as 120 or more electrodes. The brief duration of action potentials requires a high sampling frequency to reliably capture each waveform. The resulting raw data files are therefore large and difficult to visualize with traditional plotting tools. Common approaches to deal with the difficulties of data display, such as extracting spike times and performing spike train analysis, are useful in many contexts but they also significantly reduce data dimensionality. The use of tools which minimize data processing enable the development of heuristic perspective of experimental results. Here we introduce MEA Viewer, a high-performance open source application for the direct visualization of multi-channel electrophysiological data. MEA Viewer includes several high-performance visualizations, including an easily navigable overview of recorded extracellular action potentials from all data channels overlaid with spike timestamp data and an interactive raster plot. MEA Viewer can also display the two dimensional extent of action potential propagation in single neurons by signal averaging extracellular action potentials (eAPs) from single neurons detected on multiple electrodes. This view extracts and displays eAP timing information and eAP waveforms that are otherwise below the spike detection threshold. This entirely new method of using MEAs opens up novel research applications for medium density arrays. MEA Viewer is licensed under the General Public License version 3, GPLv3, and is available at http://github.com/dbridges/mea-tools. Public Library of Science 2018-02-09 /pmc/articles/PMC5806868/ /pubmed/29425223 http://dx.doi.org/10.1371/journal.pone.0192477 Text en © 2018 Bridges et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Bridges, Daniel C.
Tovar, Kenneth R.
Wu, Bian
Hansma, Paul K.
Kosik, Kenneth S.
MEA Viewer: A high-performance interactive application for visualizing electrophysiological data
title MEA Viewer: A high-performance interactive application for visualizing electrophysiological data
title_full MEA Viewer: A high-performance interactive application for visualizing electrophysiological data
title_fullStr MEA Viewer: A high-performance interactive application for visualizing electrophysiological data
title_full_unstemmed MEA Viewer: A high-performance interactive application for visualizing electrophysiological data
title_short MEA Viewer: A high-performance interactive application for visualizing electrophysiological data
title_sort mea viewer: a high-performance interactive application for visualizing electrophysiological data
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5806868/
https://www.ncbi.nlm.nih.gov/pubmed/29425223
http://dx.doi.org/10.1371/journal.pone.0192477
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