Evidence map›Paper›PMID 39774254›Full record

ArticlePLoS computational biology2024

Marked point process variational autoencoder with applications to unsorted spiking activities.

Ryohei Shibue, Tomoharu Iwata

Abstract 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. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Ryohei ShibueCommunication Science Laboratories, NTT Corporation, Kanagawa, Japan.ORCID 0009-0008-9494-2627
Tomoharu IwataCommunication Science Laboratories, NTT Corporation, Kyoto, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spike train modeling across large neural populations is a powerful tool for understanding how neurons code information in a coordinated manner. Recent studies have employed marked point processes in neural population modeling. The marked point process is a stochastic process that generates a sequence of events with marks. Spike train models based on such processes use the waveform features of spikes as marks and express the generative structure of the unsorted spikes without applying spike sorting. In such modeling, the goal is to estimate the joint mark intensity that describes how observed covariates or hidden states (e.g., animal behaviors, animal internal states, and experimental conditions) influence unsorted spikes. A major issue with this approach is that existing joint mark intensity models are not designed to capture high-dimensional and highly nonlinear observations. To address this limitation, we propose a new joint mark intensity model based on a variational autoencoder, capable of representing the dependency structure of unsorted spikes on observed covariates or hidden states in a data-driven manner. Our model defines the joint mark intensity as a latent variable model, where a neural network decoder transforms a shared latent variable into states and marks. With our model, we derive a new log-likelihood lower bound by exploiting the variational evidence lower bound and upper bound (e.g., the χ upper bound) and use this new lower bound for parameter estimation. To demonstrate the strength of this approach, we integrate our model into a state space model with a nonlinear embedding to capture the hidden state dynamics underlying the observed covariates and unsorted spikes. This enables us to reconstruct covariates from unsorted spikes, known as neural decoding. Our model achieves superior performance in prediction and decoding tasks for synthetic data and the spiking activities of place cells.

Indexed as

Action PotentialsComputational BiologyModels, NeurologicalNeuronsAlgorithmsAnimalsComputer SimulationHumansNeural Networks, ComputerStochastic Processes

Identifiers

PMID39774254
PMCPMC11684723

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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.