We study the dynamics of supervised learning in layered neural networks, in the regime where the size p of the training set is proportional to the number N of inputs. Here the local fields are no longer described by Gaussian distributions.

Graphical models provide a broad probabilistic framework with applications in speech recognition (Hidden Markov Models), medical diagnosis (Belief networks) and artificial intelligence (Boltzmann Machines). However, the computing time is typically exponential in the number of nodes in the graph. Within the variational framework for approximating these models, we present two classes of distributions, decimatable Boltzmann Machines and Tractable Belief Networks that go beyond the standard factorized approach. We give generalised mean-field equations for both these directed and undirected approximations. Simulation results on a small benchmark problem suggest using these richer approximations compares favorably against others previously reported in the literature. 1 Introduction Graphical models provide a powerful framework for probabilistic inference[l] but suffer intractability when applied to large scale problems.

Information from the senses must be compressed into the limited range of firing rates generated by spiking nerve cells. Optimal compression uses all firing rates equally often, implying that the nerve cell's response matches the statistics of naturally occurring stimuli. Since changing the voltage-dependent ionic conductances in the cell membrane alters the flow of information, an unsupervised, non-Hebbian, developmental learning rule is derived to adapt the conductances in Hodgkin-Huxley model neurons. By maximizing the rate of information transmission, each firing rate within the model neuron's limited dynamic range is used equally often. An efficient neuronal representation of incoming sensory information should take advantage of the regularity and scale invariance of stimulus features in the natural world. In the case of vision, this regularity is reflected in the typical probabilities of encountering particular visual contrasts, spatial orientations, or colors [1]. Given these probabilities, an optimized neural code would eliminate any redundancy, while devoting increased representation to commonly encountered features. At the level of a single spiking neuron, information about a potentially large range of stimuli is compressed into a finite range of firing rates, since the maximum firing rate of a neuron is limited. Optimizing the information transmission through a single neuron in the presence of uniform, additive noise has an intuitive interpretation: the most efficient representation of the input uses every firing rate with equal probability.

Lateral competition within a layer of neurons sharpens and localizes the response to an input stimulus. Here, we investigate a model for the activity dependent development of ocular dominance maps which allows to vary the degree of lateral competition. For weak competition, it resembles a correlation-based learning model and for strong competition, it becomes a self-organizing map. Thus, in the regime of weak competition the receptive fields are shaped by the second order statistics of the input patterns, whereas in the regime of strong competition, the higher moments and "features" of the individual patterns become important. When correlated localized stimuli from two eyes drive the cortical development we find (i) that a topographic map and binocular, localized receptive fields emerge when the degree of competition exceeds a critical value and (ii) that receptive fields exhibit eye dominance beyond a second critical value. For anti-correlated activity between the eyes, the second order statistics drive the system to develop ocular dominance even for weak competition, but no topography emerges. Topography is established only beyond a critical degree of competition.

Since every electrode is in a different position it will measure a different contribution from each of the different neurons. Simply stated, the problem is this: how can these complex signals be untangled to determine when each individual cell fired? This problem is difficult because, a) the objects being classified are very similar and often noisy, b) spikes coming from the same cell can ·Permanent address: Institute of Computer Science and Center for Neural Computation, The Hebrew University, Jerusalem, Israel.

Here we derive measures quantifying the information loss of a synaptic signal due to the presence of neuronal noise sources, as it electrotonically propagates along a weakly-active dendrite. We model the dendrite as an infinite linear cable, with noise sources distributed along its length. The noise sources we consider are thermal noise, channel noise arising from the stochastic nature of voltage-dependent ionic channels (K and Na) and synaptic noise due to spontaneous background activity. We assess the efficacy of information transfer using a signal detection paradigm where the objective is to detect the presence/absence of a presynaptic spike from the post-synaptic membrane voltage. This allows us to analytically assess the role of each of these noise sources in information transfer. For our choice of parameters, we find that the synaptic noise is the dominant noise source which limits the maximum length over which information be reliably transmitted. 1 Introduction This is a continuation of our efforts (Manwani and Koch, 1998) to understand the information capacity ofa neuronal link (in terms of the specific nature of neural "hardware") by a systematic study of information processing at different biophysical stages in a model of a single neuron. Here we investigate how the presence of neuronal noise sources influences the information transmission capabilities of a simplified model of a weakly-active dendrite. The noise sources we include are, thermal noise, channel noise arising from the stochastic nature of voltage-dependent channels (K and Na) and synaptic noise due to spontaneous background activity. We characterize the noise sources using analytical expressions of their current power spectral densities and compare their magnitudes for dendritic parameters reported in literature (Mainen and Sejnowski, 1998).

For example, a'Hebbian' (Hebb 1949) learning rule which is driven by the correlations between presynaptic and postsynaptic rates may be used to generate neuronal receptive fields (e.g., Linsker 1986, MacKay and Miller 1990, Wimbauer et al. 1997) with properties similar to those of real neurons. A rate-based description, however, neglects effects which are due to the pulse structure of neuronal signals.

Determining the relationship between the activity of a single nerve cell to that of an entire population is a fundamental question that bears on the basic neural computation paradigms. In this paper we apply an information theoretic approach to quantify the level of cooperative activity among cells in a behavioral context. It is possible to discriminate between synergetic activity of the cells vs. redundant activity, depending on the difference between the information they provide when measured jointly and the information they provide independently. We define a synergy value that is positive in the first case and negative in the second and show that the synergy value can be measured by detecting the behavioral mode of the animal from simultaneously recorded activity of the cells. We observe that among cortical cells positive synergy can be found, while cells from the basal ganglia, active during the same task, do not exhibit similar synergetic activity.

Cortical amplification has been proposed as a mechanism for enhancing the selectivity of neurons in the primary visual cortex. Less appreciated is the fact that the same form of amplification can also be used to de-tune or broaden selectivity. Using a network model with recurrent cortical circuitry, we propose that the spatial phase invariance of complex cell responses arises through recurrent amplification of feedforward input.

Visually-guided arm reaching movements are produced by distributed neural networks within parietal and frontal regions of the cerebral cortex. Experimental data indicate that (I) single neurons in these regions are broadly tuned to parameters of movement; (2) appropriate commands are elaborated by populations of neurons; (3) the coordinated action of neurons can be visualized using a neuronal population vector (NPV). However, the NPV provides only a rough estimate of movement parameters (direction, velocity) and may even fail to reflect the parameters of movement when arm posture is changed. We designed a model of the cortical motor command to investigate the relation between the desired direction of the movement, the actual direction of movement and the direction of the NPV in motor cortex. The model is a two-layer self-organizing neural network which combines broadly-tuned (muscular) proprioceptive and (cartesian) visual information to calculate (angular) motor commands for the initial part of the movement of a two-link arm. The network was trained by motor babbling in 5 positions. Simulations showed that (1) the network produced appropriate movement direction over a large part of the workspace; (2) small deviations of the actual trajectory from the desired trajectory existed at the extremities of the workspace; (3) these deviations were accompanied by large deviations of the NPV from both trajectories. These results suggest the NPV does not give a faithful image of cortical processing during arm reaching movements.