Cargando…

Noise Helps Optimization Escape From Saddle Points in the Synaptic Plasticity

Numerous experimental studies suggest that noise is inherent in the human brain. However, the functional importance of noise remains unknown. n particular, from a computational perspective, such stochasticity is potentially harmful to brain function. In machine learning, a large number of saddle poi...

Descripción completa

Detalles Bibliográficos
Autores principales: Fang, Ying, Yu, Zhaofei, Chen, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7201302/
https://www.ncbi.nlm.nih.gov/pubmed/32410937
http://dx.doi.org/10.3389/fnins.2020.00343
_version_ 1783529518611300352
author Fang, Ying
Yu, Zhaofei
Chen, Feng
author_facet Fang, Ying
Yu, Zhaofei
Chen, Feng
author_sort Fang, Ying
collection PubMed
description Numerous experimental studies suggest that noise is inherent in the human brain. However, the functional importance of noise remains unknown. n particular, from a computational perspective, such stochasticity is potentially harmful to brain function. In machine learning, a large number of saddle points are surrounded by high error plateaus and give the illusion of the existence of local minimum. As a result, being trapped in the saddle points can dramatically impair learning and adding noise will attack such saddle point problems in high-dimensional optimization, especially under the strict saddle condition. Motivated by these arguments, we propose one biologically plausible noise structure and demonstrate that noise can efficiently improve the optimization performance of spiking neural networks based on stochastic gradient descent. The strict saddle condition for synaptic plasticity is deduced, and under such conditions, noise can help optimization escape from saddle points on high dimensional domains. The theoretical results explain the stochasticity of synapses and guide us on how to make use of noise. In addition, we provide biological interpretations of proposed noise structures from two points: one based on the free energy principle in neuroscience and another based on observations of in vivo experiments. Our simulation results manifest that in the learning and test phase, the accuracy of synaptic sampling with noise is almost 20% higher than that without noise for synthesis dataset, and the gain in accuracy with/without noise is at least 10% for the MNIST and CIFAR-10 dataset. Our study provides a new learning framework for the brain and sheds new light on deep noisy spiking neural networks.
format Online
Article
Text
id pubmed-7201302
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-72013022020-05-14 Noise Helps Optimization Escape From Saddle Points in the Synaptic Plasticity Fang, Ying Yu, Zhaofei Chen, Feng Front Neurosci Neuroscience Numerous experimental studies suggest that noise is inherent in the human brain. However, the functional importance of noise remains unknown. n particular, from a computational perspective, such stochasticity is potentially harmful to brain function. In machine learning, a large number of saddle points are surrounded by high error plateaus and give the illusion of the existence of local minimum. As a result, being trapped in the saddle points can dramatically impair learning and adding noise will attack such saddle point problems in high-dimensional optimization, especially under the strict saddle condition. Motivated by these arguments, we propose one biologically plausible noise structure and demonstrate that noise can efficiently improve the optimization performance of spiking neural networks based on stochastic gradient descent. The strict saddle condition for synaptic plasticity is deduced, and under such conditions, noise can help optimization escape from saddle points on high dimensional domains. The theoretical results explain the stochasticity of synapses and guide us on how to make use of noise. In addition, we provide biological interpretations of proposed noise structures from two points: one based on the free energy principle in neuroscience and another based on observations of in vivo experiments. Our simulation results manifest that in the learning and test phase, the accuracy of synaptic sampling with noise is almost 20% higher than that without noise for synthesis dataset, and the gain in accuracy with/without noise is at least 10% for the MNIST and CIFAR-10 dataset. Our study provides a new learning framework for the brain and sheds new light on deep noisy spiking neural networks. Frontiers Media S.A. 2020-04-29 /pmc/articles/PMC7201302/ /pubmed/32410937 http://dx.doi.org/10.3389/fnins.2020.00343 Text en Copyright © 2020 Fang, Yu and Chen. 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 Neuroscience
Fang, Ying
Yu, Zhaofei
Chen, Feng
Noise Helps Optimization Escape From Saddle Points in the Synaptic Plasticity
title Noise Helps Optimization Escape From Saddle Points in the Synaptic Plasticity
title_full Noise Helps Optimization Escape From Saddle Points in the Synaptic Plasticity
title_fullStr Noise Helps Optimization Escape From Saddle Points in the Synaptic Plasticity
title_full_unstemmed Noise Helps Optimization Escape From Saddle Points in the Synaptic Plasticity
title_short Noise Helps Optimization Escape From Saddle Points in the Synaptic Plasticity
title_sort noise helps optimization escape from saddle points in the synaptic plasticity
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7201302/
https://www.ncbi.nlm.nih.gov/pubmed/32410937
http://dx.doi.org/10.3389/fnins.2020.00343
work_keys_str_mv AT fangying noisehelpsoptimizationescapefromsaddlepointsinthesynapticplasticity
AT yuzhaofei noisehelpsoptimizationescapefromsaddlepointsinthesynapticplasticity
AT chenfeng noisehelpsoptimizationescapefromsaddlepointsinthesynapticplasticity