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John Hertz

Publications and source records attributed to John Hertz.

2 recordsLinked to original sources

Hebbian imprinting and retrieval in oscillatory neural networks.

We introduce a model of generalized Hebbian learning and retrieval in oscillatory neural networks modeling cortical areas such as hippocampus and olfactory cortex. Recent experiments have shown that synaptic plasticity depends on spike timing, especially on synapses from excitatory pyramidal cells, in hippocampus, and in sensory and cerebellar cortex. Here we study how such plasticity can be used to form memories and input representations when the neural dynamics are oscillatory, as is common in the brain (particularly in the hippocampus and olfactory cortex). Learning is assumed to occur in a phase of neural plasticity, in which the network is clamped to external teaching signals. By suitable manipulation of the nonlinearity of the neurons or the oscillation frequencies during learning, the model can be made, in a retrieval phase, either to categorize new inputs or to map them, in a continuous fashion, onto the space spanned by the imprinted patterns. We identify the first of these possibilities with the function of olfactory cortex and the second with the observed response characteristics of place cells in hippocampus. We investigate both kinds of networks analytically and by computer simulations, and we link the models with experimental findings, exploring, in particular, how the spike timing dependence of the synaptic plasticity constrains the computational function of the network and vice versa.

Hippocampus↗

Effective dimensionality of large-scale expression data using principal component analysis.

Large-scale expression data are today measured for thousands of genes simultaneously. This development is followed by an exploration of theoretical tools to get as much information out of these data as possible. One line is to try to extract the underlying regulatory network. The models used thus far, however, contain many parameters, and a careful investigation is necessary in order not to over-fit the models. We employ principal component analysis to show how, in the context of linear additive models, one can get a rough estimate of the effective dimensionality (the number of information-carrying dimensions) of large-scale gene expression datasets. We treat both the lack of independence of different measurements in a time series and the fact that that measurements are subject to some level of noise, both of which reduce the effective dimensionality and thereby constrain the complexity of models which can be built from the data.

Gene Expression Profiling↗