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Autori principali: Schuster, Viktoria, Krogh, Anders
Natura: Preprint
Pubblicazione: 2021
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Accesso online:https://arxiv.org/abs/2110.06672
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author Schuster, Viktoria
Krogh, Anders
author_facet Schuster, Viktoria
Krogh, Anders
contents Learning 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 (VAEs) which use a variational approximation of the likelihood for inference. We here present the Deep Generative Decoder (DGD), a simple generative model that computes model parameters and representations directly via maximum a posteriori (MAP) estimation. The DGD handles complex parameterized latent distributions naturally unlike VAEs 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 data sets. 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 VAE.
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publishDate 2021
record_format arxiv
spellingShingle The Deep Generative Decoder: MAP estimation of representations improves modeling of single-cell RNA data
Schuster, Viktoria
Krogh, Anders
Machine Learning
Learning 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 (VAEs) which use a variational approximation of the likelihood for inference. We here present the Deep Generative Decoder (DGD), a simple generative model that computes model parameters and representations directly via maximum a posteriori (MAP) estimation. The DGD handles complex parameterized latent distributions naturally unlike VAEs 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 data sets. 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 VAE.
title The Deep Generative Decoder: MAP estimation of representations improves modeling of single-cell RNA data
topic Machine Learning
url https://arxiv.org/abs/2110.06672