ArticlePLoS computational biology2018
Functional triplet motifs underlie accurate predictions of single-trial responses in populations of tuned and untuned V1 neurons.
Article in PLoS computational biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.
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Who cites it
25 citing papers in PubMed, 40 citations in OpenAlex.
- Neurons embedded in loop-like motifs act as central hubs for brain-wide integration.The Journal of physiology · 2026Article
- Network Topography Alterations in Alzheimer's Disease: Insights From Motif Changes via Multisite Datasets (N = 3262).CNS neuroscience & therapeutics · 2025Article
- Temporal resolution of spike coding in feedforward networks with signal convergence and divergence.PLoS computational biology · 2025Article
- A dynamic subset of network interactions underlies tuning to natural movements in marmoset sensorimotor cortex.Nature communications · 2024Article
- A transthalamic pathway crucial for perception.Nature communications · 2024Article
- Stimulus type shapes the topology of cellular functional networks in mouse visual cortex.Nature communications · 2024Article
- Trial-by-trial variability in cortical responses exhibits scaling of spatial correlations predicted from critical dynamics.Cell reports · 2024Article
- Connecting the dots in the zona incerta: A study of neural assemblies and motifs of inter-area coordination in mice.iScience · 2024Article
- A dynamic subset of network interactions underlies tuning to natural movements in marmoset sensorimotor cortex.Research square · 2023Article
- Third-order motifs are sufficient to fully and uniquely characterize spatiotemporal neural network activity.Scientific reports · 2023Article
- Normalization in mouse primary visual cortex.PloS one · 2023Article
- Dynamic structure of motor cortical neuron coactivity carries behaviorally relevant information.Network neuroscience (Cambridge, Mass.) · 2023Article
- A deep learning framework for inference of single-trial neural population dynamics from calcium imaging with subframe temporal resolution.Nature neuroscience · 2022Article
- Large-Scale Algorithmic Search Identifies Stiff and Sloppy Dimensions in Synaptic Architectures Consistent With Murine Neocortical Wiring.Neural computation · 2022Article
- Edges in brain networks: Contributions to models of structure and function.Network neuroscience (Cambridge, Mass.) · 2022Review
- Article
- Partial information decomposition reveals that synergistic neural integration is greater downstream of recurrent information flow in organotypic cortical cultures.PLoS computational biology · 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
- Network Analysis of Murine Cortical Dynamics Implicates Untuned Neurons in Visual Stimulus Coding.Cell reports · 2020Article
Corrections and comments
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Authors and funding
2 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Visual stimuli evoke activity in visual cortical neuronal populations. Neuronal activity can be selectively modulated by particular visual stimulus parameters, such as the direction of a moving bar of light, resulting in well-defined trial averaged tuning properties. However, given any single stimulus parameter, a large number of neurons in visual cortex remain unmodulated, and the role of this untuned population is not well understood. Here, we use two-photon calcium imaging to record, in an unbiased manner, from large populations of layer 2/3 excitatory neurons in mouse primary visual cortex to describe co-varying activity on single trials in neuronal populations consisting of both tuned and untuned neurons. Specifically, we summarize pairwise covariability with an asymmetric partial correlation coefficient, allowing us to analyze the resultant population correlation structure, or functional network, with graph theory. Using the graph neighbors of a neuron, we find that the local population, including both tuned and untuned neurons, are able to predict individual neuron activity on a moment to moment basis, while also recapitulating tuning properties of tuned neurons. Variance explained in total population activity scales with the number of neurons imaged, demonstrating larger sample sizes are required to fully capture local network interactions. We also find that a specific functional triplet motif in the graph results in the best predictions, suggesting a signature of informative correlations in these populations. In summary, we show that unbiased sampling of the local population can explain single trial response variability as well as trial-averaged tuning properties in V1, and the ability to predict responses is tied to the occurrence of a functional triplet motif.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.