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Unsupervised Learning Facilitates Neural Coordination Across the Functional Clusters of the C. elegans Connectome
Modeling of complex adaptive systems has revealed a still poorly understood benefit of unsupervised learning: when neural networks are enabled to form an associative memory of a large set of their own attractor configurations, they begin to reorganize their connectivity in a direction that minimizes...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7805867/ https://www.ncbi.nlm.nih.gov/pubmed/33501208 http://dx.doi.org/10.3389/frobt.2020.00040 |
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author | Morales, Alejandro Froese, Tom |
author_facet | Morales, Alejandro Froese, Tom |
author_sort | Morales, Alejandro |
collection | PubMed |
description | Modeling of complex adaptive systems has revealed a still poorly understood benefit of unsupervised learning: when neural networks are enabled to form an associative memory of a large set of their own attractor configurations, they begin to reorganize their connectivity in a direction that minimizes the coordination constraints posed by the initial network architecture. This self-optimization process has been replicated in various neural network formalisms, but it is still unclear whether it can be applied to biologically more realistic network topologies and scaled up to larger networks. Here we continue our efforts to respond to these challenges by demonstrating the process on the connectome of the widely studied nematode worm C. elegans. We extend our previous work by considering the contributions made by hierarchical partitions of the connectome that form functional clusters, and we explore possible beneficial effects of inter-cluster inhibitory connections. We conclude that the self-optimization process can be applied to neural network topologies characterized by greater biological realism, and that long-range inhibitory connections can facilitate the generalization capacity of the process. |
format | Online Article Text |
id | pubmed-7805867 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78058672021-01-25 Unsupervised Learning Facilitates Neural Coordination Across the Functional Clusters of the C. elegans Connectome Morales, Alejandro Froese, Tom Front Robot AI Robotics and AI Modeling of complex adaptive systems has revealed a still poorly understood benefit of unsupervised learning: when neural networks are enabled to form an associative memory of a large set of their own attractor configurations, they begin to reorganize their connectivity in a direction that minimizes the coordination constraints posed by the initial network architecture. This self-optimization process has been replicated in various neural network formalisms, but it is still unclear whether it can be applied to biologically more realistic network topologies and scaled up to larger networks. Here we continue our efforts to respond to these challenges by demonstrating the process on the connectome of the widely studied nematode worm C. elegans. We extend our previous work by considering the contributions made by hierarchical partitions of the connectome that form functional clusters, and we explore possible beneficial effects of inter-cluster inhibitory connections. We conclude that the self-optimization process can be applied to neural network topologies characterized by greater biological realism, and that long-range inhibitory connections can facilitate the generalization capacity of the process. Frontiers Media S.A. 2020-04-02 /pmc/articles/PMC7805867/ /pubmed/33501208 http://dx.doi.org/10.3389/frobt.2020.00040 Text en Copyright © 2020 Morales and Froese. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Robotics and AI Morales, Alejandro Froese, Tom Unsupervised Learning Facilitates Neural Coordination Across the Functional Clusters of the C. elegans Connectome |
title | Unsupervised Learning Facilitates Neural Coordination Across the Functional Clusters of the C. elegans Connectome |
title_full | Unsupervised Learning Facilitates Neural Coordination Across the Functional Clusters of the C. elegans Connectome |
title_fullStr | Unsupervised Learning Facilitates Neural Coordination Across the Functional Clusters of the C. elegans Connectome |
title_full_unstemmed | Unsupervised Learning Facilitates Neural Coordination Across the Functional Clusters of the C. elegans Connectome |
title_short | Unsupervised Learning Facilitates Neural Coordination Across the Functional Clusters of the C. elegans Connectome |
title_sort | unsupervised learning facilitates neural coordination across the functional clusters of the c. elegans connectome |
topic | Robotics and AI |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7805867/ https://www.ncbi.nlm.nih.gov/pubmed/33501208 http://dx.doi.org/10.3389/frobt.2020.00040 |
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