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Sparsely-connected autoencoder (SCA) for single cell RNAseq data mining

Single-cell RNA sequencing (scRNAseq) is an essential tool to investigate cellular heterogeneity. Thus, it would be of great interest being able to disclose biological information belonging to cell subpopulations, which can be defined by clustering analysis of scRNAseq data. In this manuscript, we r...

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Autores principales: Alessandri, Luca, Cordero, Francesca, Beccuti, Marco, Licheri, Nicola, Arigoni, Maddalena, Olivero, Martina, Di Renzo, Maria Flavia, Sapino, Anna, Calogero, Raffaele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7785742/
https://www.ncbi.nlm.nih.gov/pubmed/33402683
http://dx.doi.org/10.1038/s41540-020-00162-6
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author Alessandri, Luca
Cordero, Francesca
Beccuti, Marco
Licheri, Nicola
Arigoni, Maddalena
Olivero, Martina
Di Renzo, Maria Flavia
Sapino, Anna
Calogero, Raffaele
author_facet Alessandri, Luca
Cordero, Francesca
Beccuti, Marco
Licheri, Nicola
Arigoni, Maddalena
Olivero, Martina
Di Renzo, Maria Flavia
Sapino, Anna
Calogero, Raffaele
author_sort Alessandri, Luca
collection PubMed
description Single-cell RNA sequencing (scRNAseq) is an essential tool to investigate cellular heterogeneity. Thus, it would be of great interest being able to disclose biological information belonging to cell subpopulations, which can be defined by clustering analysis of scRNAseq data. In this manuscript, we report a tool that we developed for the functional mining of single cell clusters based on Sparsely-Connected Autoencoder (SCA). This tool allows uncovering hidden features associated with scRNAseq data. We implemented two new metrics, QCC (Quality Control of Cluster) and QCM (Quality Control of Model), which allow quantifying the ability of SCA to reconstruct valuable cell clusters and to evaluate the quality of the neural network achievements, respectively. Our data indicate that SCA encoded space, derived by different experimentally validated data (TF targets, miRNA targets, Kinase targets, and cancer-related immune signatures), can be used to grasp single cell cluster-specific functional features. In our implementation, SCA efficacy comes from its ability to reconstruct only specific clusters, thus indicating only those clusters where the SCA encoding space is a key element for cells aggregation. SCA analysis is implemented as module in rCASC framework and it is supported by a GUI to simplify it usage for biologists and medical personnel.
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spelling pubmed-77857422021-01-14 Sparsely-connected autoencoder (SCA) for single cell RNAseq data mining Alessandri, Luca Cordero, Francesca Beccuti, Marco Licheri, Nicola Arigoni, Maddalena Olivero, Martina Di Renzo, Maria Flavia Sapino, Anna Calogero, Raffaele NPJ Syst Biol Appl Brief Communication Single-cell RNA sequencing (scRNAseq) is an essential tool to investigate cellular heterogeneity. Thus, it would be of great interest being able to disclose biological information belonging to cell subpopulations, which can be defined by clustering analysis of scRNAseq data. In this manuscript, we report a tool that we developed for the functional mining of single cell clusters based on Sparsely-Connected Autoencoder (SCA). This tool allows uncovering hidden features associated with scRNAseq data. We implemented two new metrics, QCC (Quality Control of Cluster) and QCM (Quality Control of Model), which allow quantifying the ability of SCA to reconstruct valuable cell clusters and to evaluate the quality of the neural network achievements, respectively. Our data indicate that SCA encoded space, derived by different experimentally validated data (TF targets, miRNA targets, Kinase targets, and cancer-related immune signatures), can be used to grasp single cell cluster-specific functional features. In our implementation, SCA efficacy comes from its ability to reconstruct only specific clusters, thus indicating only those clusters where the SCA encoding space is a key element for cells aggregation. SCA analysis is implemented as module in rCASC framework and it is supported by a GUI to simplify it usage for biologists and medical personnel. Nature Publishing Group UK 2021-01-05 /pmc/articles/PMC7785742/ /pubmed/33402683 http://dx.doi.org/10.1038/s41540-020-00162-6 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Brief Communication
Alessandri, Luca
Cordero, Francesca
Beccuti, Marco
Licheri, Nicola
Arigoni, Maddalena
Olivero, Martina
Di Renzo, Maria Flavia
Sapino, Anna
Calogero, Raffaele
Sparsely-connected autoencoder (SCA) for single cell RNAseq data mining
title Sparsely-connected autoencoder (SCA) for single cell RNAseq data mining
title_full Sparsely-connected autoencoder (SCA) for single cell RNAseq data mining
title_fullStr Sparsely-connected autoencoder (SCA) for single cell RNAseq data mining
title_full_unstemmed Sparsely-connected autoencoder (SCA) for single cell RNAseq data mining
title_short Sparsely-connected autoencoder (SCA) for single cell RNAseq data mining
title_sort sparsely-connected autoencoder (sca) for single cell rnaseq data mining
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7785742/
https://www.ncbi.nlm.nih.gov/pubmed/33402683
http://dx.doi.org/10.1038/s41540-020-00162-6
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