Evidence map›Paper›PMID 39028957›Full record

ArticleNeural computation2024

Extended Poisson Gaussian-Process Latent Variable Model for Unsupervised Neural Decoding.

Della Daiyi Luo, Bapun Giri, Kamran Diba, Caleb Kemere

Abstract read
In one paragraph

Article in Neural computation, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Della Daiyi LuoDepartment of Electrical and Computer Engineering, Rice University, Houston, TX 77005, U.S.A. dl67@rice.edu.
Bapun GiriDepartment of Anesthesiology, Neuroscience Graduate Program, University of Michigan Medical School, Ann Arbor, MI 48109, U.S.A. bapung@umich.edu.
Kamran DibaDepartment of Anesthesiology, Neuroscience Graduate Program, University of Michigan Medical School, Ann Arbor, MI 48109, U.S.A. kdiba@umich.edu.
Caleb KemereDepartment of Electrical and Computer Engineering, Rice University, Houston, TX 77005, U.S.A. caleb.kemere@rice.edu.

Funding

Div Supp: Daniela del Rio Pulido CRCNS: Unsupervised Learning of Hippocampal Sequence Dynamic in SleepR01NS115233 · NINDS · RICE UNIVERSITY · PI DIBA, KAMRAN, KEMERE, CALEB · 2019 to 2023
$2.3M
NINDS NIH HHS R01 NS115233
6 · The paper itself

Abstract

Dimension reduction on neural activity paves a way for unsupervised neural decoding by dissociating the measurement of internal neural pattern reactivation from the measurement of external variable tuning. With assumptions only on the smoothness of latent dynamics and of internal tuning curves, the Poisson gaussian-process latent variable model (P-GPLVM; Wu et al., 2017) is a powerful tool to discover the low-dimensional latent structure for high-dimensional spike trains. However, when given novel neural data, the original model lacks a method to infer their latent trajectories in the learned latent space, limiting its ability for estimating the neural reactivation. Here, we extend the P-GPLVM to enable the latent variable inference of new data constrained by previously learned smoothness and mapping information. We also describe a principled approach for the constrained latent variable inference for temporally compressed patterns of activity, such as those found in population burst events during hippocampal sharp-wave ripples, as well as metrics for assessing the validity of neural pattern reactivation and inferring the encoded experience. Applying these approaches to hippocampal ensemble recordings during active maze exploration, we replicate the result that P-GPLVM learns a latent space encoding the animal's position. We further demonstrate that this latent space can differentiate one maze context from another. By inferring the latent variables of new neural data during running, certain neural patterns are observed to reactivate, in accordance with the similarity of experiences encoded by its nearby neural trajectories in the training data manifold. Finally, reactivation of neural patterns can be estimated for neural activity during population burst events as well, allowing the identification for replay events of versatile behaviors and more general experiences. Thus, our extension of the P-GPLVM framework for unsupervised analysis of neural activity can be used to answer critical questions related to scientific discovery.

Indexed as

HippocampusModels, NeurologicalNeuronsAction PotentialsAnimalsNormal DistributionPoisson DistributionRatsUnsupervised Machine Learning

Identifiers

PMID39028957
PMCPMC12492801

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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.