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Modeling inter-trial variability of pointing movements during visuomotor adaptation

Trial-to-trial variability during visuomotor adaptation is usually explained as the result of two different sources, planning noise and execution noise. The estimation of the underlying variance parameters from observations involving varying feedback conditions cannot be achieved by standard techniq...

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Autores principales: Eggert, Thomas, Henriques, Denise Y. P., ’t Hart, Bernard M., Straube, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7925509/
https://www.ncbi.nlm.nih.gov/pubmed/33575896
http://dx.doi.org/10.1007/s00422-021-00858-w
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author Eggert, Thomas
Henriques, Denise Y. P.
’t Hart, Bernard M.
Straube, Andreas
author_facet Eggert, Thomas
Henriques, Denise Y. P.
’t Hart, Bernard M.
Straube, Andreas
author_sort Eggert, Thomas
collection PubMed
description Trial-to-trial variability during visuomotor adaptation is usually explained as the result of two different sources, planning noise and execution noise. The estimation of the underlying variance parameters from observations involving varying feedback conditions cannot be achieved by standard techniques (Kalman filter) because they do not account for recursive noise propagation in a closed-loop system. We therefore developed a method to compute the exact likelihood of the output of a time-discrete and linear adaptation system as has been used to model visuomotor adaptation (Smith et al. in PLoS Biol 4(6):e179, 2006), observed under closed-loop and error-clamp conditions. We identified the variance parameters by maximizing this likelihood and compared the model prediction of the time course of variance and autocovariance with empiric data. The observed increase in variability during the early training phase could not be explained by planning noise and execution noise with constant variances. Extending the model by signal-dependent components of either execution noise or planning noise showed that the observed temporal changes of the trial-to-trial variability can be modeled by signal-dependent planning noise rather than signal-dependent execution noise. Comparing the variance time course between different training schedules showed that the signal-dependent increase of planning variance was specific for the fast adapting mechanism, whereas the assumption of constant planning variance was sufficient for the slow adapting mechanisms.
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spelling pubmed-79255092021-03-19 Modeling inter-trial variability of pointing movements during visuomotor adaptation Eggert, Thomas Henriques, Denise Y. P. ’t Hart, Bernard M. Straube, Andreas Biol Cybern Original Article Trial-to-trial variability during visuomotor adaptation is usually explained as the result of two different sources, planning noise and execution noise. The estimation of the underlying variance parameters from observations involving varying feedback conditions cannot be achieved by standard techniques (Kalman filter) because they do not account for recursive noise propagation in a closed-loop system. We therefore developed a method to compute the exact likelihood of the output of a time-discrete and linear adaptation system as has been used to model visuomotor adaptation (Smith et al. in PLoS Biol 4(6):e179, 2006), observed under closed-loop and error-clamp conditions. We identified the variance parameters by maximizing this likelihood and compared the model prediction of the time course of variance and autocovariance with empiric data. The observed increase in variability during the early training phase could not be explained by planning noise and execution noise with constant variances. Extending the model by signal-dependent components of either execution noise or planning noise showed that the observed temporal changes of the trial-to-trial variability can be modeled by signal-dependent planning noise rather than signal-dependent execution noise. Comparing the variance time course between different training schedules showed that the signal-dependent increase of planning variance was specific for the fast adapting mechanism, whereas the assumption of constant planning variance was sufficient for the slow adapting mechanisms. Springer Berlin Heidelberg 2021-02-11 2021 /pmc/articles/PMC7925509/ /pubmed/33575896 http://dx.doi.org/10.1007/s00422-021-00858-w 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/.
spellingShingle Original Article
Eggert, Thomas
Henriques, Denise Y. P.
’t Hart, Bernard M.
Straube, Andreas
Modeling inter-trial variability of pointing movements during visuomotor adaptation
title Modeling inter-trial variability of pointing movements during visuomotor adaptation
title_full Modeling inter-trial variability of pointing movements during visuomotor adaptation
title_fullStr Modeling inter-trial variability of pointing movements during visuomotor adaptation
title_full_unstemmed Modeling inter-trial variability of pointing movements during visuomotor adaptation
title_short Modeling inter-trial variability of pointing movements during visuomotor adaptation
title_sort modeling inter-trial variability of pointing movements during visuomotor adaptation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7925509/
https://www.ncbi.nlm.nih.gov/pubmed/33575896
http://dx.doi.org/10.1007/s00422-021-00858-w
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