Topic: Network Models

Seminar
6 seminars
SeminarComputational NeuroscienceRecording

Theory of recurrent neural networks – from parameter inference to intrinsic timescales in spiking networks

Alexander van Meegen
Forschungszentrum Jülich
Jan 13, 2022
SeminarPsychiatryRecording

Computational Models of Compulsivity

Frederike Petzschner
Brown University
Nov 11, 2021
SeminarComputational NeuroscienceRecording

Finding the needle in the haystack – Functional circuit and network models for neuroscience

Friedemann Zenke
Friedrich Miescher Institute for Biomedical Research, Basel
May 12, 2021

Start of the talk will be 17:15h (CEST). This session is a double feature of the Cologne Theoretical Neuroscience Forum and the BCCN Berlin.

SeminarComputational NeuroscienceRecording

Neural network models – analysis of their spontaneous activity and their response to single-neuron stimulation

Benjamin Lindner
Humboldt University Berlin
Feb 11, 2021
SeminarElectrophysiologyRecording

Cellular mechanisms behind stimulus evoked quenching of variability

Brent Doiron
University of Chicago
Jan 27, 2021

A wealth of experimental studies show that the trial-to-trial variability of neuronal activity is quenched during stimulus evoked responses. This fact has helped ground a popular view that the variability of spiking activity can be decomposed into two components. The first is due to irregular spike timing conditioned on the firing rate of a neuron (i.e. a Poisson process), and the second is the trial-to-trial variability of the firing rate itself. Quenching of the variability of the overall response is assumed to be a reflection of a suppression of firing rate variability. Network models have explained this phenomenon through a variety of circuit mechanisms. However, in all cases, from the vantage of a neuron embedded within the network, quenching of its response variability is inherited from its synaptic input. We analyze in vivo whole cell recordings from principal cells in layer (L) 2/3 of mouse visual cortex. While the variability of the membrane potential is quenched upon stimulation, the variability of excitatory and inhibitory currents afferent to the neuron are amplified. This discord complicates the simple inheritance assumption that underpins network models of neuronal variability. We propose and validate an alternative (yet not mutually exclusive) mechanism for the quenching of neuronal variability. We show how an increase in synaptic conductance in the evoked state shunts the transfer of current to the membrane potential, formally decoupling changes in their trial-to-trial variability. The ubiquity of conductance based neuronal transfer combined with the simplicity of our model, provides an appealing framework. In particular, it shows how the dependence of cellular properties upon neuronal state is a critical, yet often ignored, factor. Further, our mechanism does not require a decomposition of variability into spiking and firing rate components, thereby challenging a long held view of neuronal activity.

SeminarComputational NeuroscienceRecording

Motor Cortex in Theory and Practice

Mark Churchland
Columbia University, New York
Nov 30, 2020

A central question in motor physiology has been whether motor cortex activity resembles muscle activity, and if not, why not? Over fifty years, extensive observations have failed to provide a concise answer, and the topic remains much debated. To provide a different perspective, we employed a novel behavioral paradigm that affords extensive comparison between time-evolving neural and muscle activity. Single motor-cortex neurons displayed many muscle-like properties, but the structure of population activity was not muscle-like. Unlike muscle activity, neural activity was structured to avoid ’trajectory tangling’: moments where similar activity patterns led to dissimilar future patterns. Avoidance of trajectory tangling was present across tasks and species. Network models revealed a potential reason for this consistent feature: low tangling confers noise robustness. Remarkably, we were able to predict motor cortex activity from muscle activity alone, by leveraging the hypothesis that muscle-like commands are embedded in additional structure that yields low tangling. Our results argue that motor cortex embeds descending commands in additional structure that ensure low tangling, and thus noise-robustness. The dominant structure in motor cortex may thus serve not a representational function (encoding specific variables) but a computational function: ensuring that outgoing commands can be generated reliably. Our results establish the utility of an emerging approach: understanding the structure of neural activity based on properties of population geometry that flow from normative principles such as noise robustness.

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