ArticlePLoS computational biology2021
Embedding optimization reveals long-lasting history dependence in neural spiking activity.
Article in PLoS computational biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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8 citing papers in PubMed, 11 citations in OpenAlex.
- Neural timescales from a computational perspective.Nature neuroscience · 2026Review
- Inferring effective networks of spiking neurons using a continuous-time estimator of transfer entropy.PLoS computational biology · 2025Article
- Signatures of hierarchical temporal processing in the mouse visual system.PLoS computational biology · 2024Article
- Information-theoretic analyses of neural data to minimize the effect of researchers' assumptions in predictive coding studies.PLoS computational biology · 2023Article
- An information theoretic method to resolve millisecond-scale spike timing precision in a comprehensive motor program.PLoS computational biology · 2023Article
- Information theoretic evidence for layer- and frequency-specific changes in cortical information processing under anesthesia.PLoS computational biology · 2023Article
- Early lock-in of structured and specialised information flows during neural development.eLife · 2022Article
- Bias-free estimation of information content in temporally sparse neuronal activity.PLoS computational biology · 2022Article
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4 authors at 3 institutions in 1 country.
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Abstract
Information processing can leave distinct footprints on the statistics of neural spiking. For example, efficient coding minimizes the statistical dependencies on the spiking history, while temporal integration of information may require the maintenance of information over different timescales. To investigate these footprints, we developed a novel approach to quantify history dependence within the spiking of a single neuron, using the mutual information between the entire past and current spiking. This measure captures how much past information is necessary to predict current spiking. In contrast, classical time-lagged measures of temporal dependence like the autocorrelation capture how long-potentially redundant-past information can still be read out. Strikingly, we find for model neurons that our method disentangles the strength and timescale of history dependence, whereas the two are mixed in classical approaches. When applying the method to experimental data, which are necessarily of limited size, a reliable estimation of mutual information is only possible for a coarse temporal binning of past spiking, a so-called past embedding. To still account for the vastly different spiking statistics and potentially long history dependence of living neurons, we developed an embedding-optimization approach that does not only vary the number and size, but also an exponential stretching of past bins. For extra-cellular spike recordings, we found that the strength and timescale of history dependence indeed can vary independently across experimental preparations. While hippocampus indicated strong and long history dependence, in visual cortex it was weak and short, while in vitro the history dependence was strong but short. This work enables an information-theoretic characterization of history dependence in recorded spike trains, which captures a footprint of information processing that is beyond time-lagged measures of temporal dependence. To facilitate the application of the method, we provide practical guidelines and a toolbox.
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