ArticleFrontiers in computational neuroscience2015
Triplet correlations among similarly tuned cells impact population coding.
Article in Frontiers in computational neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
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12 citing papers in PubMed.
- Quantifying Information Stored in Synaptic Connections Rather Than in Firing Activities of Neural Networks.Neural computation · 2026Article
- Uncovering hidden network architecture from spiking activities using an exact statistical input-output relation of neurons.Communications biology · 2023Article
- High-order interactions explain the collective behavior of cortical populations in executive but not sensory areas.Neuron · 2021Article
- Cyclic transitions between higher order motifs underlie sustained asynchronous spiking in sparse recurrent networks.PLoS computational biology · 2020Article
- Autonomous emergence of connectivity assemblies via spike triplet interactions.PLoS computational biology · 2020Article
- Higher-Order Cumulants Drive Neuronal Activity Patterns, Inducing UP-DOWN States in Neural Populations.Entropy (Basel, Switzerland) · 2020Article
- Predicting how and when hidden neurons skew measured synaptic interactions.PLoS computational biology · 2018Article
- A Moment-Based Maximum Entropy Model for Fitting Higher-Order Interactions in Neural Data.Entropy (Basel, Switzerland) · 2018Article
- Robust information propagation through noisy neural circuits.PLoS computational biology · 2017Article
- Interplay between Graph Topology and Correlations of Third Order in Spiking Neuronal Networks.PLoS computational biology · 2016Article
- Article
- A Simple Mechanism for Beyond-Pairwise Correlations in Integrate-and-Fire Neurons.Journal of mathematical neuroscience · 2015Article
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3 authors.
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Abstract
Which statistical features of spiking activity matter for how stimuli are encoded in neural populations? A vast body of work has explored how firing rates in individual cells and correlations in the spikes of cell pairs impact coding. Recent experiments have shown evidence for the existence of higher-order spiking correlations, which describe simultaneous firing in triplets and larger ensembles of cells; however, little is known about their impact on encoded stimulus information. Here, we take a first step toward closing this gap. We vary triplet correlations in small (approximately 10 cell) neural populations while keeping single cell and pairwise statistics fixed at typically reported values. This connection with empirically observed lower-order statistics is important, as it places strong constraints on the level of triplet correlations that can occur. For each value of triplet correlations, we estimate the performance of the neural population on a two-stimulus discrimination task. We find that the allowed changes in the level of triplet correlations can significantly enhance coding, in particular if triplet correlations differ for the two stimuli. In this scenario, triplet correlations must be included in order to accurately quantify the functionality of neural populations. When both stimuli elicit similar triplet correlations, however, pairwise models provide relatively accurate descriptions of coding accuracy. We explain our findings geometrically via the skew that triplet correlations induce in population-wide distributions of neural responses. Finally, we calculate how many samples are necessary to accurately measure spiking correlations of this type, providing an estimate of the necessary recording times in future experiments.
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