Cargando…
Extracting single-trial neural interaction using latent dynamical systems model
In systems neuroscience, advances in simultaneous recording technology have helped reveal the population dynamics that underlie the complex neural correlates of animal behavior and cognitive processes. To investigate these correlates, neural interactions are typically abstracted from spike trains of...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7885376/ https://www.ncbi.nlm.nih.gov/pubmed/33588875 http://dx.doi.org/10.1186/s13041-021-00740-7 |
_version_ | 1783651591355629568 |
---|---|
author | Huh, Namjung Kim, Sung-Phil Lee, Joonyeol Sohn, Jeong-woo |
author_facet | Huh, Namjung Kim, Sung-Phil Lee, Joonyeol Sohn, Jeong-woo |
author_sort | Huh, Namjung |
collection | PubMed |
description | In systems neuroscience, advances in simultaneous recording technology have helped reveal the population dynamics that underlie the complex neural correlates of animal behavior and cognitive processes. To investigate these correlates, neural interactions are typically abstracted from spike trains of pairs of neurons accumulated over the course of many trials. However, the resultant averaged values do not lead to understanding of neural computation in which the responses of populations are highly variable even under identical external conditions. Accordingly, neural interactions within the population also show strong fluctuations. In the present study, we introduce an analysis method reflecting the temporal variation of neural interactions, in which cross-correlograms on rate estimates are applied via a latent dynamical systems model. Using this method, we were able to predict time-varying neural interactions within a single trial. In addition, the pairwise connections estimated in our analysis increased along behavioral epochs among neurons categorized within similar functional groups. Thus, our analysis method revealed that neurons in the same groups communicate more as the population gets involved in the assigned task. We also showed that the characteristics of neural interaction from our model differ from the results of a typical model employing cross-correlation coefficients. This suggests that our model can extract nonoverlapping information about network topology, unlike the typical model. |
format | Online Article Text |
id | pubmed-7885376 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-78853762021-02-17 Extracting single-trial neural interaction using latent dynamical systems model Huh, Namjung Kim, Sung-Phil Lee, Joonyeol Sohn, Jeong-woo Mol Brain Methodology In systems neuroscience, advances in simultaneous recording technology have helped reveal the population dynamics that underlie the complex neural correlates of animal behavior and cognitive processes. To investigate these correlates, neural interactions are typically abstracted from spike trains of pairs of neurons accumulated over the course of many trials. However, the resultant averaged values do not lead to understanding of neural computation in which the responses of populations are highly variable even under identical external conditions. Accordingly, neural interactions within the population also show strong fluctuations. In the present study, we introduce an analysis method reflecting the temporal variation of neural interactions, in which cross-correlograms on rate estimates are applied via a latent dynamical systems model. Using this method, we were able to predict time-varying neural interactions within a single trial. In addition, the pairwise connections estimated in our analysis increased along behavioral epochs among neurons categorized within similar functional groups. Thus, our analysis method revealed that neurons in the same groups communicate more as the population gets involved in the assigned task. We also showed that the characteristics of neural interaction from our model differ from the results of a typical model employing cross-correlation coefficients. This suggests that our model can extract nonoverlapping information about network topology, unlike the typical model. BioMed Central 2021-02-15 /pmc/articles/PMC7885376/ /pubmed/33588875 http://dx.doi.org/10.1186/s13041-021-00740-7 Text en © The Author(s) 2021 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Methodology Huh, Namjung Kim, Sung-Phil Lee, Joonyeol Sohn, Jeong-woo Extracting single-trial neural interaction using latent dynamical systems model |
title | Extracting single-trial neural interaction using latent dynamical systems model |
title_full | Extracting single-trial neural interaction using latent dynamical systems model |
title_fullStr | Extracting single-trial neural interaction using latent dynamical systems model |
title_full_unstemmed | Extracting single-trial neural interaction using latent dynamical systems model |
title_short | Extracting single-trial neural interaction using latent dynamical systems model |
title_sort | extracting single-trial neural interaction using latent dynamical systems model |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7885376/ https://www.ncbi.nlm.nih.gov/pubmed/33588875 http://dx.doi.org/10.1186/s13041-021-00740-7 |
work_keys_str_mv | AT huhnamjung extractingsingletrialneuralinteractionusinglatentdynamicalsystemsmodel AT kimsungphil extractingsingletrialneuralinteractionusinglatentdynamicalsystemsmodel AT leejoonyeol extractingsingletrialneuralinteractionusinglatentdynamicalsystemsmodel AT sohnjeongwoo extractingsingletrialneuralinteractionusinglatentdynamicalsystemsmodel |