Extracting single-trial neural interaction using latent dynamical systems model

Abstract 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...

Full description

Bibliographic Details
Main Authors: Namjung Huh, Sung-Phil Kim, Joonyeol Lee, Jeong-woo Sohn
Format: Article
Language:English
Published: BMC 2021-02-01
Series:Molecular Brain
Subjects:
Online Access:https://doi.org/10.1186/s13041-021-00740-7
_version_ 1819170496826048512
author Namjung Huh
Sung-Phil Kim
Joonyeol Lee
Jeong-woo Sohn
author_facet Namjung Huh
Sung-Phil Kim
Joonyeol Lee
Jeong-woo Sohn
author_sort Namjung Huh
collection DOAJ
description Abstract 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.
first_indexed 2024-12-22T19:36:19Z
format Article
id doaj.art-a33ee84de04a46eca6a8a1de8501f29d
institution Directory Open Access Journal
issn 1756-6606
language English
last_indexed 2024-12-22T19:36:19Z
publishDate 2021-02-01
publisher BMC
record_format Article
series Molecular Brain
spelling doaj.art-a33ee84de04a46eca6a8a1de8501f29d2022-12-21T18:14:58ZengBMCMolecular Brain1756-66062021-02-0114111210.1186/s13041-021-00740-7Extracting single-trial neural interaction using latent dynamical systems modelNamjung Huh0Sung-Phil Kim1Joonyeol Lee2Jeong-woo Sohn3Department of Medical Science, College of Medicine, Catholic Kwandong UniversityDepartment of Biomedical Engineering, Ulsan National Institute of Science and TechnologyCenter for Neuroscience Imaging Research, Institute for Basic Science (IBS)Department of Medical Science, College of Medicine, Catholic Kwandong UniversityAbstract 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.https://doi.org/10.1186/s13041-021-00740-7Neural interactionLatent dynamical systems modelCross-correlogramOptimized neural activity
spellingShingle Namjung Huh
Sung-Phil Kim
Joonyeol Lee
Jeong-woo Sohn
Extracting single-trial neural interaction using latent dynamical systems model
Molecular Brain
Neural interaction
Latent dynamical systems model
Cross-correlogram
Optimized neural activity
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 Neural interaction
Latent dynamical systems model
Cross-correlogram
Optimized neural activity
url https://doi.org/10.1186/s13041-021-00740-7
work_keys_str_mv AT namjunghuh extractingsingletrialneuralinteractionusinglatentdynamicalsystemsmodel
AT sungphilkim extractingsingletrialneuralinteractionusinglatentdynamicalsystemsmodel
AT joonyeollee extractingsingletrialneuralinteractionusinglatentdynamicalsystemsmodel
AT jeongwoosohn extractingsingletrialneuralinteractionusinglatentdynamicalsystemsmodel