Neural networks present a fundamentally different model of computation from the conventional sequential digital model. Dedicated hardware may thus be more suitable for executing them. Given that there is no clear consensus on the model of computation in the brain, model flexibility is at least as important a characteristic of neural hardware as is performance acceleration. The SpiNNaker chip is an example of the emerging 'neuromimetic' architecture, a universal platform that specialises the hardware for neural networks but allows flexibility in model choice. It integrates four key attributes: native parallelism, event-driven processing, incoherent memory and incremental reconfiguration, in a system combining an array of general-purpose processors with a configurable asynchronous interconnect. Making such a device usable in practice requires an environment for instantiating neural models on the chip that allows the user to focus on model characteristics rather than on hardware details. The central part of this system is a library of predesigned, 'drop-in' event-driven neural components that specify their specific implementation on SpiNNaker. Three exemplar models: two spiking networks and a multilayer perceptron network, illustrate techniques that provide a basis for the library and demonstrate a reference methodology that can be extended to support third-party library components not only on SpiNNaker but on any configurable neuromimetic platform. Experiments demonstrate the capability of the library model to implement efficient on-chip neural networks, but also reveal important hardware limitations, particularly with respect to communications, that require careful design. The ultimate goal is the creation of a library-based development system that allows neural modellers to work in the high-level environment of their choice, using an automated tool chain to create the appropriate SpiNNaker instantiation. Such a system would enable the use of the hardware to explore abstractions of biological neurodynamics that underpin a functional model of neural computation.

Ces travaux de thèse, réalisés dans une équipe concevant des circuits analogiques neuromimétiques suivant le modèle d’Hodgkin-Huxley, concernent la modélisation de neurones biologiques, plus précisément, l’estimation des paramètres de modèles de neurones. Une première partie de ce manuscrit s’attache à faire le lien entre la modélisation neuronale et l’optimisation. L’accent est mis sur le modèle d’Hodgkin- Huxley pour lequel il existait déjà une méthode d’extraction des paramètres associée à une technique de mesures électrophysiologiques (le voltage-clamp) mais dont les approximations successives rendaient impossible la détermination précise de certains paramètres. Nous proposons dans une seconde partie une méthode alternative d’estimation des paramètres du modèle d’Hodgkin-Huxley s’appuyant sur l’algorithme d’évolution différentielle et qui pallie les limitations de la méthode classique. Cette alternative permet d’estimer conjointement tous les paramètres d’un même canal ionique. Le troisième chapitre est divisé en trois sections. Dans les deux premières, nous appliquons notre nouvelle technique à l’estimation des paramètres du même modèle à partir de données biologiques, puis développons un protocole automatisé de réglage de circuits neuromimétiques, canal ionique par canal ionique. La troisième section présente une méthode d’estimation des paramètres à partir d’enregistrements de la tension de membrane d’un neurone, données dont l’acquisition est plus aisée que celle des courants ioniques. Le quatrième et dernier chapitre, quant à lui, est une ouverture vers l’utilisation de petits réseaux d’une centaine de neurones électroniques : nous réalisons une étude logicielle de l’influence des propriétés intrinsèques de la cellule sur le comportement global du réseau dans le cadre des oscillations gamma. / These works, which were conducted in a research group designing neuromimetic integrated circuits based on the Hodgkin-Huxley model, deal with the parameter estimation of biological neuron models. The first part of the manuscript tries to bridge the gap between neuron modeling and optimization. We focus our interest on the Hodgkin-Huxley model because it is used in the group. There already existed an estimation method associated to the voltage-clamp technique. Nevertheless, this classical estimation method does not allow to extract precisely all parameters of the model, so in the second part, we propose an alternative method to jointly estimate all parameters of one ionic channel avoiding the usual approximations. This method is based on the differential evolution algorithm. The third chaper is divided into three sections : the first two sections present the application of our new estimation method to two different problems, model fitting from biological data and development of an automated tuning of neuromimetic chips. In the third section, we propose an estimation technique using only membrane voltage recordings – easier to mesure than ionic currents. Finally, the fourth and last chapter is a theoretical study preparing the implementation of small neural networks on neuromimetic chips. More specifically, we try to study the influence of cellular intrinsic properties on the global behavior of a neural network in the context of gamma oscillations.

Artificial neural network simulators are a research field which attracts the interest of researchers from various fields, from biology to computer science. The final objectives are the understanding of the mechanisms underlying the human brain, how to reproduce them in an artificial environment, and how drugs interact with them. Multiple neural models have been proposed, each with their peculiarities, from the very complex and biologically realistic Hodgkin-Huxley neuron model to the very simple 'leaky integrate-and-fire' neuron. However, despite numerous attempts to understand the learning behaviour of the synapses, few models have been proposed. Spike-Timing-Dependent Plasticity (STDP) is one of the most relevant and biologically plausible models, and some variants (such as the triplet-based STDP rule) have been proposed to accommodate all biological observations. The research presented in this thesis focuses on a novel learning rule, based on the spike-pair STDP algorithm, which provides a statistical approach with the advantage of being less computationally expensive than the standard STDP rule, and is therefore suitable for its implementation on stand-alone computational units. The environment in which this research work has been carried out is the SpiNNaker project, which aims to provide a massively parallel computational substrate for neural simulation. To support such research, two other topics have been addressed: the first is a way to inject spikes into the SpiNNaker system through a non-real-time channel such as the Ethernet link, synchronising with the timing of the SpiNNaker system. The second research topic is focused on a way to route spikes in the SpiNNaker system based on populations of neurons. The three topics are presented in sequence after a brief introduction to the SpiNNaker project. Future work could include structural plasticity (also known as synaptic rewiring); here, during the simulation of neural networks on the SpiNNaker system, axons, dendrites and synapses may be grown or pruned according to biological observations.