Identifying functional connectivity between neuronal elements is an essential first step toward understanding how the brain orchestrates information processing at the single-cell and population levels to carry out biological computations. This letter suggests a new approach to identify functional connectivity between neuronal elements from their simultaneously recorded spike trains. In particular, we identify clusters of neurons that exhibit functional interdependency over variable spatial and temporal patterns of interaction. We represent neurons as objects in a graph and connect them using arbitrarily defined similarity measures calculated across multiple timescales. We then use a probabilistic spectral clustering algorithm to cluster the neurons in the graph by solving a minimum graph cut optimization problem. Using point process theory to model population activity, we demonstrate the robustness of the approach in tracking a broad spectrum of neuronal interaction, from synchrony to rate co-modulation, by systematically varying the length of the firing history interval and the strength of the connecting synapses that govern the discharge pattern of each neuron. We also demonstrate how activity-dependent plasticity can be tracked and quantified in multiple network topologies built to mimic distinct behavioral contexts. We compare the performance to classical approaches to illustrate the substantial gain in performance.
Coordination among cortical neurons is believed to be key element in mediating many high level cortical processes such as perception, attention, learning and memory formation. Inferring the topology of the neural circuitry underlying this coordination is important to characterize the highly non-linear, time-varying interactions between cortical neurons in the presence of complex stimuli. In this work, we investigate the applicability of Dynamic Bayesian Networks (DBNs) in inferring the effective connectivity between spiking cortical neurons from their observed spike trains. We demonstrate that DBNs can infer the underlying non-linear and time-varying causal interactions between these neurons and can discriminate between mono and polysynaptic links between them under certain constraints governing their putative connectivity. We analyzed conditionally-Poisson spike train data mimicking spiking activity of cortical networks of small and moderately-large sizes. The performance was assessed and compared to other methods under systematic variations of the network structure to mimic a wide range of responses typically observed in the cortex. Results demonstrate the utility of DBN in inferring the effective connectivity in cortical networks.
Analyzing the massive amounts of neural data collected using microelectrodes to extract biologically relevant information is a major challenge. Many scientific findings rest on the ability to overcome these challenges and to standardize experimental analysis across labs. This can be facilitated in part through comprehensive, efficient and practical software tools disseminated to the community at large. We have developed a comprehensive, MATLAB-based software package - entitled NeuroQuest - that bundles together a number of advanced neural signal processing algorithms in a user-friendly environment. Results demonstrate the efficiency and reliability of the software compared to other software packages, and versatility over a wide range of experimental conditions.
Correlation among neocortical neurons is thought to play an indispensable role in mediating sensory processing of external stimuli. The role of temporal precision in this correlation has been hypothesized to enhance information flow along sensory pathways. Its role in mediating the integration of information at the output of these pathways, however, remains poorly understood. Here, we examined spike timing correlation between simultaneously recorded layer V neurons within and across columns of the primary somatosensory cortex of anesthetized rats during unilateral whisker stimulation. We used Bayesian statistics and information theory to quantify the causal influence between the recorded cells with millisecond precision. For each stimulated whisker, we inferred stable, whisker-specific, dynamic Bayesian networks over many repeated trials, with network similarity of 83.3±6% within whisker, compared to only 50.3±18% across whiskers. These networks further provided information about whisker identity that was approximately 6 times higher than what was provided by the latency to first spike and 13 times higher than what was provided by the spike count of individual neurons examined separately. Furthermore, prediction of individual neurons' precise firing conditioned on knowledge of putative pre-synaptic cell firing was 3 times higher than predictions conditioned on stimulus onset alone. Taken together, these results suggest the presence of a temporally precise network coding mechanism that integrates information across neighboring columns within layer V about vibrissa position and whisking kinetics to mediate whisker movement by motor areas innervated by layer V.
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