ANALYSIS METHODOLOGY OF SYNCHRONY IN SIMULTANEOUSLY RECORDED SINGLE UNIT ACTIVITY IN THE VISUAL CORTEX
Our brains process and interpret sensory information in order to generate perceptions of the environment or motivate behavior. However, the underlying mechanisms by which salient stimulus qualities are represented by neuronal response patterns remain a mystery. Precise coordination of spike ev...
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ndltd-VANDERBILT-oai-VANDERBILTETD-etd-04032006-1302162013-01-08T17:16:10Z ANALYSIS METHODOLOGY OF SYNCHRONY IN SIMULTANEOUSLY RECORDED SINGLE UNIT ACTIVITY IN THE VISUAL CORTEX Bernard, Melanie Rebecca Biomedical Engineering Our brains process and interpret sensory information in order to generate perceptions of the environment or motivate behavior. However, the underlying mechanisms by which salient stimulus qualities are represented by neuronal response patterns remain a mystery. Precise coordination of spike events, or synchrony, is an attractive candidate to play a role in (visual) coding since it exists among (visual) cortical neurons, but its functional significance is largely unknown. Proving synchrony's importance in signaling is difficult since adequate methods to measure synchrony have not been developed. Current approaches quantify synchrony as a relationship between two neurons. However, synchrony allows for the formation of transient functional groups which could include tens, hundreds, thousands, or even larger numbers of neurons. Furthermore, very few studies have investigated how to measure the quality of synchrony in an assembly as well as develop some means to display these quantities. <br> The work presented here derives a measure for synchrony within assemblies of arbitrary size by modeling the biological process of postsynaptic potential integration. We derive measures for the magnitude and quality of synchrony as well as show how our results are consistent with the Joint Peri-Stimulus Time Histogram approach for assemblies of two neurons. We also evaluate synchrony's role as a possible neural substrate for contour integration by investigating dynamic grouping and characteristics of group membership. Finally, we propose future investigation of synchrony as a biological sparse code employed by the visual cortex to represent high-order stimulus features in natural scenes. A. B. Bonds, III Richard Shiavi VANDERBILT 2006-04-18 text application/pdf http://etd.library.vanderbilt.edu/available/etd-04032006-130216/ http://etd.library.vanderbilt.edu/available/etd-04032006-130216/ en unrestricted I hereby certify that, if appropriate, I have obtained and attached hereto a written permission statement from the owner(s) of each third party copyrighted matter to be included in my thesis, dissertation, or project report, allowing distribution as specified below. I certify that the version I submitted is the same as that approved by my advisory committee. I hereby grant to Vanderbilt University or its agents the non-exclusive license to archive and make accessible, under the conditions specified below, my thesis, dissertation, or project report in whole or in part in all forms of media, now or hereafter known. I retain all other ownership rights to the copyright of the thesis, dissertation or project report. I also retain the right to use in future works (such as articles or books) all or part of this thesis, dissertation, or project report. |
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Biomedical Engineering Bernard, Melanie Rebecca ANALYSIS METHODOLOGY OF SYNCHRONY IN SIMULTANEOUSLY RECORDED SINGLE UNIT ACTIVITY IN THE VISUAL CORTEX |
description |
Our brains process and interpret sensory information in order to generate perceptions of the environment or motivate behavior. However, the underlying mechanisms by which salient stimulus qualities are represented by neuronal response patterns remain a mystery. Precise coordination of spike events, or synchrony, is an attractive candidate to play a role in (visual) coding since it exists among (visual) cortical neurons, but its functional significance is largely unknown. Proving synchrony's importance in signaling is difficult since adequate methods to measure synchrony have not been developed. Current approaches quantify synchrony as a relationship between two neurons. However, synchrony allows for the formation of transient functional groups which could include tens, hundreds, thousands, or even larger numbers of neurons. Furthermore, very few studies have investigated how to measure the quality of synchrony in an assembly as well as develop some means to display these quantities.
<br> The work presented here derives a measure for synchrony within assemblies of arbitrary size by modeling the biological process of postsynaptic potential integration. We derive measures for the magnitude and quality of synchrony as well as show how our results are consistent with the Joint Peri-Stimulus Time Histogram approach for assemblies of two neurons. We also evaluate synchrony's role as a possible neural substrate for contour integration by investigating dynamic grouping and characteristics of group membership. Finally, we propose future investigation of synchrony as a biological sparse code employed by the visual cortex to represent high-order stimulus features in natural scenes. |
author2 |
A. B. Bonds, III |
author_facet |
A. B. Bonds, III Bernard, Melanie Rebecca |
author |
Bernard, Melanie Rebecca |
author_sort |
Bernard, Melanie Rebecca |
title |
ANALYSIS METHODOLOGY OF SYNCHRONY IN SIMULTANEOUSLY RECORDED SINGLE UNIT ACTIVITY IN THE VISUAL CORTEX |
title_short |
ANALYSIS METHODOLOGY OF SYNCHRONY IN SIMULTANEOUSLY RECORDED SINGLE UNIT ACTIVITY IN THE VISUAL CORTEX |
title_full |
ANALYSIS METHODOLOGY OF SYNCHRONY IN SIMULTANEOUSLY RECORDED SINGLE UNIT ACTIVITY IN THE VISUAL CORTEX |
title_fullStr |
ANALYSIS METHODOLOGY OF SYNCHRONY IN SIMULTANEOUSLY RECORDED SINGLE UNIT ACTIVITY IN THE VISUAL CORTEX |
title_full_unstemmed |
ANALYSIS METHODOLOGY OF SYNCHRONY IN SIMULTANEOUSLY RECORDED SINGLE UNIT ACTIVITY IN THE VISUAL CORTEX |
title_sort |
analysis methodology of synchrony in simultaneously recorded single unit activity in the visual cortex |
publisher |
VANDERBILT |
publishDate |
2006 |
url |
http://etd.library.vanderbilt.edu/available/etd-04032006-130216/ |
work_keys_str_mv |
AT bernardmelanierebecca analysismethodologyofsynchronyinsimultaneouslyrecordedsingleunitactivityinthevisualcortex |
_version_ |
1716533069994786816 |