神经群体代码特性对神经形态电路设计的限制

S. Panzeri, Ella Janotte, Alejandro Pequeño-Zurro, Jacopo Bonato, C. Bartolozzi
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引用次数: 2

摘要

在大脑中,信息是在分布于神经元群的动作电位时序水平上进行编码、传输和用于指导行为的。要在硅学中实现类神经系统、模拟神经功能并成功与大脑对接,神经形态电路需要以与大脑中神经元群兼容的方式编码信息。为了促进神经形态工程与神经科学之间的交流,我们将在这篇综述中首先批判性地研究和总结有关神经元群如何编码和传输信息的最新发现。我们研究了神经群活动的不同特征对信息编码和读出的影响,即神经表征的稀疏性、神经特性的异质性、神经元之间的相关性,以及神经元编码信息并随时间持续保持信息的时标(从短到长)。最后,我们将批判性地阐述这些事实如何制约神经形态电路中的信息编码设计。我们主要关注设计与大脑交流的神经形态电路的影响,因为在这种情况下,人工神经元和生物神经元必须使用兼容的神经编码。不过,我们也讨论了设计神经形态系统以实现或模拟神经计算的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Constraints on the design of neuromorphic circuits set by the properties of neural population codes
In the brain, information is encoded, transmitted and used to inform behaviour at the level of timing of action potentials distributed over population of neurons. To implement neural-like systems in silico, to emulate neural function, and to interface successfully with the brain, neuromorphic circuits need to encode information in a way compatible to that used by populations of neuron in the brain. To facilitate the cross-talk between neuromorphic engineering and neuroscience, in this review we first critically examine and summarize emerging recent findings about how population of neurons encode and transmit information. We examine the effects on encoding and readout of information for different features of neural population activity, namely the sparseness of neural representations, the heterogeneity of neural properties, the correlations among neurons, and the timescales (from short to long) at which neurons encode information and maintain it consistently over time. Finally, we critically elaborate on how these facts constrain the design of information coding in neuromorphic circuits. We focus primarily on the implications for designing neuromorphic circuits that communicate with the brain, as in this case it is essential that artificial and biological neurons use compatible neural codes. However, we also discuss implications for the design of neuromorphic systems for implementation or emulation of neural computation.
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CiteScore
5.90
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