Abstract

Understanding information processing in the brain requires the ability to determine the functional connectivity between the different regions of the brain. We present a method using transfer entropy to extract this flow of information between brain regions from spike-train data commonly obtained in neurological experiments. Transfer entropy is a statistical measure based in information theory that attempts to quantify the information flow from one process to another, and has been applied to find connectivity in simulated spike-train data. Due to statistical error in the estimator, inferring functional connectivity requires a method for determining significance in the transfer entropy values. We discuss the issues with numerical estimation of transfer entropy and resulting challenges in determining significance before presenting the trial-shuffle method as a viable option. The trial-shuffle method, for spike-train data that is split into multiple trials, determines significant transfer entropy values independently for each individual pair of neurons by comparing to a created baseline distribution using a rigorous statistical test. This is in contrast to either globally comparing all neuron transfer entropy values or comparing pairwise values to a single baseline value. In establishing the viability of this method by comparison to several alternative approaches in the literature, we find evidence that preserving the inter-spike-interval timing is important. We then use the trial-shuffle method to investigate information flow within a model network as we vary model parameters. This includes investigating the global flow of information within a connectivity network divided into two well-connected subnetworks, going beyond local transfer of information between pairs of neurons.

Highlights

  • Understanding the flow of information in the brain is a key step in determining how the brain processes information

  • We show that the estimated transfer entropy (TE) values can drastically vary independent of the actual causal relation between the neurons

  • We use a pairwise comparison method to determine the significance of transfer entropy values in an objective way for spike-train data comprised of multiple trials

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Summary

Introduction

Understanding the flow of information in the brain is a key step in determining how the brain processes information Methods for observing this flow of information include non-invasive methods such as MEG or calcium imaging that produce a pseudo-continuous image of activity in a brain region [1, 2] but lack high spatial resolution. Another approach, multi-unit recording, is an invasive method that inserts electrode arrays into the brain to detect when nearby neurons fire [3, 4], producing a detailed measurement of the activity of a relatively small number of neurons. This data can be processed to produce a list of spike-times for each observed

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