Evidence map›Paper›PMID 38557984›Full record

ArticlePLoS computational biology2024

Predictive coding networks for temporal prediction.

Beren Millidge, Mufeng Tang, Mahyar Osanlouy, Nicol S Harper, Rafal Bogacz

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
8.6field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
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  5. A neural mechanism for online discovery of latent contexts.bioRxiv : the preprint server for biology · 2026
    Article
  6. Review
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  9. Deep Hybrid Models: Infer and Plan in a Dynamic World.Entropy (Basel, Switzerland) · 2025
    Article
  10. Article
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  13. Review
  14. Article
  15. Article
  16. Article
  17. Sequential Memory with Temporal Predictive Coding.Advances in neural information processing systems · 2023
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 2 countries.

Beren MillidgeMRC Brain Network Dynamics Unit, University of Oxford, Oxford, United Kingdom.
Mufeng TangMRC Brain Network Dynamics Unit, University of Oxford, Oxford, United Kingdom.
Mahyar OsanlouyAuckland Bioengineering Institute, University of Auckland, Auckland, New Zealand.
Nicol S HarperDepartment of Physiology, Anatomy and Genetics, University of Oxford, Oxford, United Kingdom.
Rafal BogaczMRC Brain Network Dynamics Unit, University of Oxford, Oxford, United Kingdom.ORCID 0000-0002-8994-1661
University of Oxford · GBUniversity of Auckland · NZ

Funding

Wellcome Trust
6 · The paper itself

Abstract

One of the key problems the brain faces is inferring the state of the world from a sequence of dynamically changing stimuli, and it is not yet clear how the sensory system achieves this task. A well-established computational framework for describing perceptual processes in the brain is provided by the theory of predictive coding. Although the original proposals of predictive coding have discussed temporal prediction, later work developing this theory mostly focused on static stimuli, and key questions on neural implementation and computational properties of temporal predictive coding networks remain open. Here, we address these questions and present a formulation of the temporal predictive coding model that can be naturally implemented in recurrent networks, in which activity dynamics rely only on local inputs to the neurons, and learning only utilises local Hebbian plasticity. Additionally, we show that temporal predictive coding networks can approximate the performance of the Kalman filter in predicting behaviour of linear systems, and behave as a variant of a Kalman filter which does not track its own subjective posterior variance. Importantly, temporal predictive coding networks can achieve similar accuracy as the Kalman filter without performing complex mathematical operations, but just employing simple computations that can be implemented by biological networks. Moreover, when trained with natural dynamic inputs, we found that temporal predictive coding can produce Gabor-like, motion-sensitive receptive fields resembling those observed in real neurons in visual areas. In addition, we demonstrate how the model can be effectively generalized to nonlinear systems. Overall, models presented in this paper show how biologically plausible circuits can predict future stimuli and may guide research on understanding specific neural circuits in brain areas involved in temporal prediction.

Indexed as

BrainModels, NeurologicalLearningNeurons

Identifiers

PMID38557984
PMCPMC11008833
OpenAlexW4393392404

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.