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Quantifying Neural Coding of Event Timing

Single-neuron firing is often analyzed relative to an external event, such as successful task performance or the delivery of a stimulus. The perievent time histogram (PETH) examines how, on average, neural firing modulates before and after the alignment event. However, the PETH contains no informati...

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Detalles Bibliográficos
Autores principales: Soteropoulos, Demetris S., Baker, Stuart N.
Formato: Texto
Lenguaje:English
Publicado: American Physiological Society 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2637006/
https://www.ncbi.nlm.nih.gov/pubmed/19019976
http://dx.doi.org/10.1152/jn.90767.2008
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author Soteropoulos, Demetris S.
Baker, Stuart N.
author_facet Soteropoulos, Demetris S.
Baker, Stuart N.
author_sort Soteropoulos, Demetris S.
collection PubMed
description Single-neuron firing is often analyzed relative to an external event, such as successful task performance or the delivery of a stimulus. The perievent time histogram (PETH) examines how, on average, neural firing modulates before and after the alignment event. However, the PETH contains no information about the single-trial reliability of the neural response, which is important from the perspective of a target neuron. In this study, we propose the concept of using the neural activity to predict the timing of the occurrence of an event, as opposed to using the event to predict the neural response. We first estimate the likelihood of an observed spike train, under the assumption that it was generated by an inhomogeneous gamma process with rate profile similar to the PETH shifted by a small time. This is used to generate a probability distribution of the event occurrence, using Bayes’ rule. By an information theoretic approach, this method yields a single value (in bits) that quantifies the reduction in uncertainty regarding the time of an external event following observation of the spike train. We show that the approach is sensitive to the amplitude of a response, to the level of baseline firing, and to the consistency of a response between trials, all of which are factors that will influence a neuron's ability to code for the time of the event. The technique can provide a useful means not only of determining which of several behavioral events a cell encodes best, but also of permitting objective comparison of different cell populations.
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spelling pubmed-26370062009-02-09 Quantifying Neural Coding of Event Timing Soteropoulos, Demetris S. Baker, Stuart N. J Neurophysiol Articles Single-neuron firing is often analyzed relative to an external event, such as successful task performance or the delivery of a stimulus. The perievent time histogram (PETH) examines how, on average, neural firing modulates before and after the alignment event. However, the PETH contains no information about the single-trial reliability of the neural response, which is important from the perspective of a target neuron. In this study, we propose the concept of using the neural activity to predict the timing of the occurrence of an event, as opposed to using the event to predict the neural response. We first estimate the likelihood of an observed spike train, under the assumption that it was generated by an inhomogeneous gamma process with rate profile similar to the PETH shifted by a small time. This is used to generate a probability distribution of the event occurrence, using Bayes’ rule. By an information theoretic approach, this method yields a single value (in bits) that quantifies the reduction in uncertainty regarding the time of an external event following observation of the spike train. We show that the approach is sensitive to the amplitude of a response, to the level of baseline firing, and to the consistency of a response between trials, all of which are factors that will influence a neuron's ability to code for the time of the event. The technique can provide a useful means not only of determining which of several behavioral events a cell encodes best, but also of permitting objective comparison of different cell populations. American Physiological Society 2009-01 2008-11-19 /pmc/articles/PMC2637006/ /pubmed/19019976 http://dx.doi.org/10.1152/jn.90767.2008 Text en Copyright © 2009, American Physiological Society This document may be redistributed and reused, subject to www.the-aps.org/publications/journals/funding_addendum_policy.htm (http://www.the-aps.org/publications/journals/funding_addendum_policy.htm) .
spellingShingle Articles
Soteropoulos, Demetris S.
Baker, Stuart N.
Quantifying Neural Coding of Event Timing
title Quantifying Neural Coding of Event Timing
title_full Quantifying Neural Coding of Event Timing
title_fullStr Quantifying Neural Coding of Event Timing
title_full_unstemmed Quantifying Neural Coding of Event Timing
title_short Quantifying Neural Coding of Event Timing
title_sort quantifying neural coding of event timing
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2637006/
https://www.ncbi.nlm.nih.gov/pubmed/19019976
http://dx.doi.org/10.1152/jn.90767.2008
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