Accurate detection of low signal-to-noise ratio neuronal calcium transient waves using a matched filter
•We develop a matched filter for multi-unit calcium event detection in neurons.•We tested the detector on simulated and experimentally recorded calcium imaging data.•The detector had near perfect performance on simulated data with SNR as low as 0.2.•The detector also performed well on experimentally...
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creator | Szymanska, Agnieszka F. Kobayashi, Chiaki Norimoto, Hiroaki Ishikawa, Tomoe Ikegaya, Yuji Nenadic, Zoran |
description | •We develop a matched filter for multi-unit calcium event detection in neurons.•We tested the detector on simulated and experimentally recorded calcium imaging data.•The detector had near perfect performance on simulated data with SNR as low as 0.2.•The detector also performed well on experimentally recorded data.•The detector is written in MATLAB and freely available.
Calcium imaging has become a fundamental modality for studying neuronal circuit dynamics both in vitro and in vivo. However, identifying calcium events (CEs) from spectral data remains laborious and difficult, especially since the signal-to-noise ratio (SNR) often falls below 2. Existing automated signal detection methods are generally applied at high SNRs, leaving a large need for an automated algorithm that can accurately extract CEs from fluorescence intensity data of SNR 2 and below.
In this work we develop a Matched filter for Multi-unit Calcium Event (MMiCE) detection to extract CEs from fluorescence intensity traces of simulated and experimentally recorded neuronal calcium imaging data.
MMiCE reached perfect performance on simulated data with SNR ≥ 2 and a true positive (TP) rate of 98.27% (± 1.38% with a 95% confidence interval), and a false positive(FP) rate of 6.59% (± 2.56%) on simulated data with SNR 0.2. On real data, verified by patch-clamp recording, MMiCE performed with a TP rate of 100.00% (± 0.00) and a FP rate of 2.04% (± 4.10).
This high level of performance exceeds existing methods at SNRs as low as 0.2, which are well below those used in previous studies (SNR ≃ 5–10).
Overall, the MMiCE detector performed exceptionally well on both simulated data, and experimentally recorded neuronal calcium imaging data. The MMiCE detector is accurate, reliable, well suited for wide-spread use, and freely available at sites.uci.edu/aggies or from the corresponding author. |
doi_str_mv | 10.1016/j.jneumeth.2015.10.014 |
format | Article |
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Calcium imaging has become a fundamental modality for studying neuronal circuit dynamics both in vitro and in vivo. However, identifying calcium events (CEs) from spectral data remains laborious and difficult, especially since the signal-to-noise ratio (SNR) often falls below 2. Existing automated signal detection methods are generally applied at high SNRs, leaving a large need for an automated algorithm that can accurately extract CEs from fluorescence intensity data of SNR 2 and below.
In this work we develop a Matched filter for Multi-unit Calcium Event (MMiCE) detection to extract CEs from fluorescence intensity traces of simulated and experimentally recorded neuronal calcium imaging data.
MMiCE reached perfect performance on simulated data with SNR ≥ 2 and a true positive (TP) rate of 98.27% (± 1.38% with a 95% confidence interval), and a false positive(FP) rate of 6.59% (± 2.56%) on simulated data with SNR 0.2. On real data, verified by patch-clamp recording, MMiCE performed with a TP rate of 100.00% (± 0.00) and a FP rate of 2.04% (± 4.10).
This high level of performance exceeds existing methods at SNRs as low as 0.2, which are well below those used in previous studies (SNR ≃ 5–10).
Overall, the MMiCE detector performed exceptionally well on both simulated data, and experimentally recorded neuronal calcium imaging data. The MMiCE detector is accurate, reliable, well suited for wide-spread use, and freely available at sites.uci.edu/aggies or from the corresponding author.</description><identifier>ISSN: 0165-0270</identifier><identifier>EISSN: 1872-678X</identifier><identifier>DOI: 10.1016/j.jneumeth.2015.10.014</identifier><identifier>PMID: 26561771</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Calcium - metabolism ; Calcium transients ; Dendritic spines ; Detection ; Hippocampus - cytology ; Low SNR ; Matched filter ; Mice ; Mice, Inbred C57BL ; Multineuron calcium imaging ; Neurons - cytology ; Optical Imaging - methods ; Patch-Clamp Techniques ; Rats ; Rats, Wistar ; Signal-To-Noise Ratio ; Somatic calcium fluctuations</subject><ispartof>Journal of neuroscience methods, 2016-02, Vol.259, p.1-12</ispartof><rights>2015 Elsevier B.V.</rights><rights>Copyright © 2015 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c515t-eab211023a3c11752c398f399c8f72d511579eeca524d595b51b95015235d5313</citedby><cites>FETCH-LOGICAL-c515t-eab211023a3c11752c398f399c8f72d511579eeca524d595b51b95015235d5313</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jneumeth.2015.10.014$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26561771$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Szymanska, Agnieszka F.</creatorcontrib><creatorcontrib>Kobayashi, Chiaki</creatorcontrib><creatorcontrib>Norimoto, Hiroaki</creatorcontrib><creatorcontrib>Ishikawa, Tomoe</creatorcontrib><creatorcontrib>Ikegaya, Yuji</creatorcontrib><creatorcontrib>Nenadic, Zoran</creatorcontrib><title>Accurate detection of low signal-to-noise ratio neuronal calcium transient waves using a matched filter</title><title>Journal of neuroscience methods</title><addtitle>J Neurosci Methods</addtitle><description>•We develop a matched filter for multi-unit calcium event detection in neurons.•We tested the detector on simulated and experimentally recorded calcium imaging data.•The detector had near perfect performance on simulated data with SNR as low as 0.2.•The detector also performed well on experimentally recorded data.•The detector is written in MATLAB and freely available.
Calcium imaging has become a fundamental modality for studying neuronal circuit dynamics both in vitro and in vivo. However, identifying calcium events (CEs) from spectral data remains laborious and difficult, especially since the signal-to-noise ratio (SNR) often falls below 2. Existing automated signal detection methods are generally applied at high SNRs, leaving a large need for an automated algorithm that can accurately extract CEs from fluorescence intensity data of SNR 2 and below.
In this work we develop a Matched filter for Multi-unit Calcium Event (MMiCE) detection to extract CEs from fluorescence intensity traces of simulated and experimentally recorded neuronal calcium imaging data.
MMiCE reached perfect performance on simulated data with SNR ≥ 2 and a true positive (TP) rate of 98.27% (± 1.38% with a 95% confidence interval), and a false positive(FP) rate of 6.59% (± 2.56%) on simulated data with SNR 0.2. On real data, verified by patch-clamp recording, MMiCE performed with a TP rate of 100.00% (± 0.00) and a FP rate of 2.04% (± 4.10).
This high level of performance exceeds existing methods at SNRs as low as 0.2, which are well below those used in previous studies (SNR ≃ 5–10).
Overall, the MMiCE detector performed exceptionally well on both simulated data, and experimentally recorded neuronal calcium imaging data. The MMiCE detector is accurate, reliable, well suited for wide-spread use, and freely available at sites.uci.edu/aggies or from the corresponding author.</description><subject>Animals</subject><subject>Calcium - metabolism</subject><subject>Calcium transients</subject><subject>Dendritic spines</subject><subject>Detection</subject><subject>Hippocampus - cytology</subject><subject>Low SNR</subject><subject>Matched filter</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Multineuron calcium imaging</subject><subject>Neurons - cytology</subject><subject>Optical Imaging - methods</subject><subject>Patch-Clamp Techniques</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Signal-To-Noise Ratio</subject><subject>Somatic calcium fluctuations</subject><issn>0165-0270</issn><issn>1872-678X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkUtr3DAUhUVJSSaPvxC07MYTXXmuJe8SQl4Q6KaF7IRGvp5osK1UkhPy76thkmzbleDwXR04H2PnIJYgoLnYLrcTzSPl56UUgCVcClh9YwvQSlaN0k8HbFFArIRU4ogdp7QVQqxa0RyyI9lgA0rBgm2unJujzcQ7yuSyDxMPPR_CG09-M9mhyqGagk_EC-UDL60xlJw7Ozg_jzxHOyVPU-Zv9pUSn5OfNtzy0Wb3TB3v_ZApnrLvvR0SnX28J-z37c2v6_vq8efdw_XVY-UQMFdk1xJAyNrWDkChdHWr-7ptne6V7BAAVUvkLMpVhy2uEdYtlgFkjR3WUJ-wH_t_X2L4M1PKZvTJ0TDYicKcDKhGo5ai1f-DCo0roeuCNnvUxZBSpN68RD_a-G5AmJ0PszWfPszOxy4vPsrh-UfHvB6p-zr7FFCAyz1AZZRXT9EkV8Z01PlYdJgu-H91_AU2zJ9z</recordid><startdate>20160201</startdate><enddate>20160201</enddate><creator>Szymanska, Agnieszka F.</creator><creator>Kobayashi, Chiaki</creator><creator>Norimoto, Hiroaki</creator><creator>Ishikawa, Tomoe</creator><creator>Ikegaya, Yuji</creator><creator>Nenadic, Zoran</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7TK</scope></search><sort><creationdate>20160201</creationdate><title>Accurate detection of low signal-to-noise ratio neuronal calcium transient waves using a matched filter</title><author>Szymanska, Agnieszka F. ; Kobayashi, Chiaki ; Norimoto, Hiroaki ; Ishikawa, Tomoe ; Ikegaya, Yuji ; Nenadic, Zoran</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c515t-eab211023a3c11752c398f399c8f72d511579eeca524d595b51b95015235d5313</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Calcium - metabolism</topic><topic>Calcium transients</topic><topic>Dendritic spines</topic><topic>Detection</topic><topic>Hippocampus - cytology</topic><topic>Low SNR</topic><topic>Matched filter</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Multineuron calcium imaging</topic><topic>Neurons - cytology</topic><topic>Optical Imaging - methods</topic><topic>Patch-Clamp Techniques</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Signal-To-Noise Ratio</topic><topic>Somatic calcium fluctuations</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Szymanska, Agnieszka F.</creatorcontrib><creatorcontrib>Kobayashi, Chiaki</creatorcontrib><creatorcontrib>Norimoto, Hiroaki</creatorcontrib><creatorcontrib>Ishikawa, Tomoe</creatorcontrib><creatorcontrib>Ikegaya, Yuji</creatorcontrib><creatorcontrib>Nenadic, Zoran</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Neurosciences Abstracts</collection><jtitle>Journal of neuroscience methods</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Szymanska, Agnieszka F.</au><au>Kobayashi, Chiaki</au><au>Norimoto, Hiroaki</au><au>Ishikawa, Tomoe</au><au>Ikegaya, Yuji</au><au>Nenadic, Zoran</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Accurate detection of low signal-to-noise ratio neuronal calcium transient waves using a matched filter</atitle><jtitle>Journal of neuroscience methods</jtitle><addtitle>J Neurosci Methods</addtitle><date>2016-02-01</date><risdate>2016</risdate><volume>259</volume><spage>1</spage><epage>12</epage><pages>1-12</pages><issn>0165-0270</issn><eissn>1872-678X</eissn><abstract>•We develop a matched filter for multi-unit calcium event detection in neurons.•We tested the detector on simulated and experimentally recorded calcium imaging data.•The detector had near perfect performance on simulated data with SNR as low as 0.2.•The detector also performed well on experimentally recorded data.•The detector is written in MATLAB and freely available.
Calcium imaging has become a fundamental modality for studying neuronal circuit dynamics both in vitro and in vivo. However, identifying calcium events (CEs) from spectral data remains laborious and difficult, especially since the signal-to-noise ratio (SNR) often falls below 2. Existing automated signal detection methods are generally applied at high SNRs, leaving a large need for an automated algorithm that can accurately extract CEs from fluorescence intensity data of SNR 2 and below.
In this work we develop a Matched filter for Multi-unit Calcium Event (MMiCE) detection to extract CEs from fluorescence intensity traces of simulated and experimentally recorded neuronal calcium imaging data.
MMiCE reached perfect performance on simulated data with SNR ≥ 2 and a true positive (TP) rate of 98.27% (± 1.38% with a 95% confidence interval), and a false positive(FP) rate of 6.59% (± 2.56%) on simulated data with SNR 0.2. On real data, verified by patch-clamp recording, MMiCE performed with a TP rate of 100.00% (± 0.00) and a FP rate of 2.04% (± 4.10).
This high level of performance exceeds existing methods at SNRs as low as 0.2, which are well below those used in previous studies (SNR ≃ 5–10).
Overall, the MMiCE detector performed exceptionally well on both simulated data, and experimentally recorded neuronal calcium imaging data. The MMiCE detector is accurate, reliable, well suited for wide-spread use, and freely available at sites.uci.edu/aggies or from the corresponding author.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>26561771</pmid><doi>10.1016/j.jneumeth.2015.10.014</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Calcium - metabolism Calcium transients Dendritic spines Detection Hippocampus - cytology Low SNR Matched filter Mice Mice, Inbred C57BL Multineuron calcium imaging Neurons - cytology Optical Imaging - methods Patch-Clamp Techniques Rats Rats, Wistar Signal-To-Noise Ratio Somatic calcium fluctuations |
title | Accurate detection of low signal-to-noise ratio neuronal calcium transient waves using a matched filter |
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