Evidence map›Paper›PMID 37572301›Full record

ArticleBioinformatics (Oxford, England)2023

The Deep Generative Decoder: MAP estimation of representations improves modelling of single-cell RNA data.

Viktoria Schuster, Anders Krogh

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Article in Bioinformatics (Oxford, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Viktoria SchusterCenter for Health Data Science, University of Copenhagen, 2200 Copenhagen, Denmark.ORCID 0000-0002-6016-8337
Anders KroghCenter for Health Data Science, University of Copenhagen, 2200 Copenhagen, Denmark.ORCID 0000-0002-5147-6282

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationLearning low-dimensional representations of single-cell transcriptomics has become instrumental to its downstream analysis. The state of the art is currently represented by neural network models, such as variational autoencoders, which use a variational approximation of the likelihood for inference.

resultsWe here present the Deep Generative Decoder (DGD), a simple generative model that computes model parameters and representations directly via maximum a posteriori estimation. The DGD handles complex parameterized latent distributions naturally unlike variational autoencoders, which typically use a fixed Gaussian distribution, because of the complexity of adding other types. We first show its general functionality on a commonly used benchmark set, Fashion-MNIST. Secondly, we apply the model to multiple single-cell datasets. Here, the DGD learns low-dimensional, meaningful, and well-structured latent representations with sub-clustering beyond the provided labels. The advantages of this approach are its simplicity and its capability to provide representations of much smaller dimensionality than a comparable variational autoencoder. AVAILABILITY AND IMPLEMENTATION: scDGD is available as a python package at https://github.com/Center-for-Health-Data-Science/scDGD. The remaining code is made available here: https://github.com/Center-for-Health-Data-Science/dgd.

Indexed as

Neural Networks, ComputerRNAGene Expression ProfilingNormal DistributionProbabilitySingle-Cell AnalysisRNA

Identifiers

PMID37572301
PMCPMC10483129

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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.