Paper List
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Developing the PsyCogMetrics™ AI Lab to Evaluate Large Language Models and Advance Cognitive Science
This paper addresses the critical gap between sophisticated LLM evaluation needs and the lack of accessible, scientifically rigorous platforms that in...
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Equivalence of approximation by networks of single- and multi-spike neurons
This paper resolves the fundamental question of whether single-spike spiking neural networks (SNNs) are inherently less expressive than multi-spike SN...
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The neuroscience of transformers
提出了Transformer架构与皮层柱微环路之间的新颖计算映射,连接了现代AI与神经科学。
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Framing local structural identifiability and observability in terms of parameter-state symmetries
This paper addresses the core challenge of systematically determining which parameters and states in a mechanistic ODE model can be uniquely inferred ...
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Leveraging Phytolith Research using Artificial Intelligence
This paper addresses the critical bottleneck in phytolith research by automating the labor-intensive manual microscopy process through a multimodal AI...
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Neural network-based encoding in free-viewing fMRI with gaze-aware models
This paper addresses the core challenge of building computationally efficient and ecologically valid brain encoding models for naturalistic vision by ...
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Scalable DNA Ternary Full Adder Enabled by a Competitive Blocking Circuit
This paper addresses the core bottleneck of carry information attenuation and limited computational scale in DNA binary adders by introducing a scalab...
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ELISA: An Interpretable Hybrid Generative AI Agent for Expression-Grounded Discovery in Single-Cell Genomics
This paper addresses the critical bottleneck of translating high-dimensional single-cell transcriptomic data into interpretable biological hypotheses ...
Formation of Artificial Neural Assemblies by Biologically Plausible Inhibition Mechanisms
Neuroscience Graduate Program, Federal University of Rio Grande do Sul, Brazil | Department of Computer Science, University of Exeter, UK | Department of Computer Science, University of Sheffield, UK | Physics Department, Federal University of Rio Grande do Sul, Brazil
30秒速读
IN SHORT: This work addresses the core limitation of the Assembly Calculus model—its fixed-size, biologically implausible k-WTA selection process—by introducing a dynamic, gamma-oscillation-inspired E%-WTA mechanism and feedforward inhibition, enabling more realistic, self-determined assembly formation and superior retrieval.
核心创新
- Methodology Proposes the E%-Winners-Take-All (E%-WTA) selection mechanism, inspired by gamma oscillation dynamics, which allows a variable number of neurons to fire based on input strength, replacing the fixed-k selection of the original model.
- Methodology Integrates a biologically plausible feedforward inhibition mechanism based on the cortical excitatory-inhibitory neuron ratio (e.g., pi=0.2), enhancing network stability and assembly formation.
- Biology Defines a more rigorous, multi-condition criterion for assembly formation (stationary pattern, synchronization, higher synaptic density), moving beyond the original model's simpler 'no new winners' rule.
主要结论
- The E%-WTA model with feedforward inhibition (ωinh = -0.2, β ≤ 0.01) successfully forms neural assemblies where size is dynamically determined by network activity, not preset, addressing a key biological limitation.
- The new model achieves a superior assembly recovery rate (evocation accuracy) compared to the original AC model, demonstrating enhanced functional stability and memory retrieval capability.
- The introduced formation conditions (stationary pattern, synchronization, higher synaptic density) converge reliably in simulations, providing a robust framework for defining and identifying stable neural assemblies.
摘要: As proposed by Hebb’s theory, neural assemblies are groups of excitatory neurons that fire synchronously and exhibit high synaptic density, representing external stimuli and supporting cognitive functions such as language and decision-making. Recently, a model called Assembly Calculus (AC) was proposed, enabling the formation of artificial neural assemblies through the kk-winners-take-all selection process and Hebbian learning. Although the model is capable of forming assemblies according to Hebb’s theory, the adopted selection process does not incorporate essential aspects of biological neural computation, as neural activity, which is often governed by statistical distributions consistent with power-law scaling. Given this limitation, the present work aimed to bring the model’s dynamics closer to that observed in real cortical networks. To achieve this, a new selection mechanism inspired by the dynamics of gamma oscillation cycles, called E%-winners-take-all, was implemented, combined with an inhibition process based on the ratio between excitatory and inhibitory neurons observed in various regions of the cerebral cortex. The results obtained from our model (called E%-WTA model) were compared with those of the original model, and the analyses demonstrated that the introduced modifications allowed the network’s own dynamics to determine the size of the formed assemblies. Furthermore, the recovery rate of these groups, through the evocation of the stimuli that generated them, became superior to that obtained in the original model.