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A normalized template matching method for improving spike detection in extracellular voltage recordings
Spike sorting is the process of detecting and clustering action potential waveforms of putative single neurons from extracellular voltage recordings. Typically, spike detection uses a fixed voltage threshold and shadow period, but this approach often misses spikes during high firing rate epochs or n...
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/PMC6700190/ https://www.ncbi.nlm.nih.gov/pubmed/31427615 http://dx.doi.org/10.1038/s41598-019-48456-y |
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author | Laboy-Juárez, Keven J. Ahn, Seoiyoung Feldman, Daniel E. |
author_facet | Laboy-Juárez, Keven J. Ahn, Seoiyoung Feldman, Daniel E. |
author_sort | Laboy-Juárez, Keven J. |
collection | PubMed |
description | Spike sorting is the process of detecting and clustering action potential waveforms of putative single neurons from extracellular voltage recordings. Typically, spike detection uses a fixed voltage threshold and shadow period, but this approach often misses spikes during high firing rate epochs or noisy conditions. We developed a simple, data-driven spike detection method using a scaled form of template matching, based on the sliding cosine similarity between the extracellular voltage signal and mean spike waveforms of candidate single units. Performance was tested in whisker somatosensory cortex (S1) of anesthetized mice in vivo. The method consistently detected whisker-evoked spikes that were missed by the standard fixed threshold. Detection was improved most for spikes evoked by strong stimuli (40–70% increase), improved less for weaker stimuli, and unchanged for spontaneous spiking. This represents improved detection during spatiotemporally dense spiking, and yielded sharper sensory tuning estimates. We also benchmarked performance using computationally generated voltage data. Template matching detected ~85–90% of spikes compared to ~70% for the standard fixed threshold method, and was more tolerant to high firing rates and simulated recording noise. Thus, a simple template matching approach substantially improves detection of single-unit spiking for cortical physiology. |
format | Online Article Text |
id | pubmed-6700190 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67001902019-08-21 A normalized template matching method for improving spike detection in extracellular voltage recordings Laboy-Juárez, Keven J. Ahn, Seoiyoung Feldman, Daniel E. Sci Rep Article Spike sorting is the process of detecting and clustering action potential waveforms of putative single neurons from extracellular voltage recordings. Typically, spike detection uses a fixed voltage threshold and shadow period, but this approach often misses spikes during high firing rate epochs or noisy conditions. We developed a simple, data-driven spike detection method using a scaled form of template matching, based on the sliding cosine similarity between the extracellular voltage signal and mean spike waveforms of candidate single units. Performance was tested in whisker somatosensory cortex (S1) of anesthetized mice in vivo. The method consistently detected whisker-evoked spikes that were missed by the standard fixed threshold. Detection was improved most for spikes evoked by strong stimuli (40–70% increase), improved less for weaker stimuli, and unchanged for spontaneous spiking. This represents improved detection during spatiotemporally dense spiking, and yielded sharper sensory tuning estimates. We also benchmarked performance using computationally generated voltage data. Template matching detected ~85–90% of spikes compared to ~70% for the standard fixed threshold method, and was more tolerant to high firing rates and simulated recording noise. Thus, a simple template matching approach substantially improves detection of single-unit spiking for cortical physiology. Nature Publishing Group UK 2019-08-19 /pmc/articles/PMC6700190/ /pubmed/31427615 http://dx.doi.org/10.1038/s41598-019-48456-y 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 Laboy-Juárez, Keven J. Ahn, Seoiyoung Feldman, Daniel E. A normalized template matching method for improving spike detection in extracellular voltage recordings |
title | A normalized template matching method for improving spike detection in extracellular voltage recordings |
title_full | A normalized template matching method for improving spike detection in extracellular voltage recordings |
title_fullStr | A normalized template matching method for improving spike detection in extracellular voltage recordings |
title_full_unstemmed | A normalized template matching method for improving spike detection in extracellular voltage recordings |
title_short | A normalized template matching method for improving spike detection in extracellular voltage recordings |
title_sort | normalized template matching method for improving spike detection in extracellular voltage recordings |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6700190/ https://www.ncbi.nlm.nih.gov/pubmed/31427615 http://dx.doi.org/10.1038/s41598-019-48456-y |
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