将稀疏和预测编码与分裂归一化联系起来。

IF 3.8 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
PLoS Computational Biology Pub Date : 2025-05-27 eCollection Date: 2025-05-01 DOI:10.1371/journal.pcbi.1013059
Yanbo Lian, Anthony N Burkitt
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引用次数: 0

摘要

稀疏编码、预测编码和分裂归一化都被发现是大脑许多部位神经回路功能的基础原则,并得到了大量实验证据的支持。然而,这些相关原则之间的联系仍然知之甚少。稀疏编码和预测编码可以协调成一个具有预测结构和稀疏响应的学习框架,称为稀疏/预测编码。然而,稀疏/预测编码(学习模型)如何与分裂归一化(不是学习模型)联系起来仍然没有得到很好的研究。在本文中,我们展示了如何在一个统一的框架内描述稀疏编码、预测编码和分裂归一化,并在稀疏/预测编码的双层神经学习模型的背景下明确地说明了这一点。该两层模型的构建方式是通过实现预测编码构建网络结构,实现稀疏编码。我们展示了调节模型中神经反应的稳态函数如何以复制不同形式的分裂归一化的方式塑造神经反应的非线性。仿真结果表明,该模型可以学习初级视觉皮层中具有对比度饱和度的简单细胞,这一特性之前被分裂归一化解释。综上所述,该研究表明,稀疏编码、预测编码和分裂归一化这三种原则可以联系起来,提供一个基于生物物理特性(如Hebbian学习和稳态)的学习框架,该框架结合了学习和实验观察到的更多样化的响应非线性。这个框架也有可能被用来解释大脑如何学习整合来自不同感觉模式的输入。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Relating sparse and predictive coding to divisive normalization.

Sparse coding, predictive coding and divisive normalization have each been found to be principles that underlie the function of neural circuits in many parts of the brain, supported by substantial experimental evidence. However, the connections between these related principles are still poorly understood. Sparse coding and predictive coding can be reconciled into a learning framework with predictive structure and sparse responses, termed as sparse/predictive coding. However, how sparse/predictive coding (a learning model) is connected with divisive normalization (not a learning model) is still not well investigated. In this paper, we show how sparse coding, predictive coding, and divisive normalization can be described within a unified framework, and illustrate this explicitly within the context of a two-layer neural learning model of sparse/predictive coding. This two-layer model is constructed in a way that implements sparse coding with a network structure that is constructed by implementing predictive coding. We demonstrate how a homeostatic function that regulates neural responses in the model can shape the nonlinearity of neural responses in a way that replicates different forms of divisive normalization. Simulations show that the model can learn simple cells in the primary visual cortex with the property of contrast saturation, which has previously been explained by divisive normalization. In summary, the study demonstrates that the three principles of sparse coding, predictive coding, and divisive normalization can be connected to provide a learning framework based on biophysical properties, such as Hebbian learning and homeostasis, and this framework incorporates both learning and more diverse response nonlinearities observed experimentally. This framework has the potential to also be used to explain how the brain learns to integrate input from different sensory modalities.

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来源期刊
PLoS Computational Biology
PLoS Computational Biology BIOCHEMICAL RESEARCH METHODS-MATHEMATICAL & COMPUTATIONAL BIOLOGY
CiteScore
7.10
自引率
4.70%
发文量
820
审稿时长
2.5 months
期刊介绍: PLOS Computational Biology features works of exceptional significance that further our understanding of living systems at all scales—from molecules and cells, to patient populations and ecosystems—through the application of computational methods. Readers include life and computational scientists, who can take the important findings presented here to the next level of discovery. Research articles must be declared as belonging to a relevant section. More information about the sections can be found in the submission guidelines. Research articles should model aspects of biological systems, demonstrate both methodological and scientific novelty, and provide profound new biological insights. Generally, reliability and significance of biological discovery through computation should be validated and enriched by experimental studies. Inclusion of experimental validation is not required for publication, but should be referenced where possible. Inclusion of experimental validation of a modest biological discovery through computation does not render a manuscript suitable for PLOS Computational Biology. Research articles specifically designated as Methods papers should describe outstanding methods of exceptional importance that have been shown, or have the promise to provide new biological insights. The method must already be widely adopted, or have the promise of wide adoption by a broad community of users. Enhancements to existing published methods will only be considered if those enhancements bring exceptional new capabilities.
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