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Shallow Sparsely-Connected Autoencoders for Gene Set Projection
When analyzing biological data, it can be helpful to consider gene sets, or predefined groups of biologically related genes. Methods exist for identifying gene sets that are differential between conditions, but large public datasets from consortium projects and single-cell RNA-Sequencing have opened...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6417803/ https://www.ncbi.nlm.nih.gov/pubmed/30963076 |
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author | Gold, Maxwell P. LeNail, Alexander Fraenkel, Ernest |
author_facet | Gold, Maxwell P. LeNail, Alexander Fraenkel, Ernest |
author_sort | Gold, Maxwell P. |
collection | PubMed |
description | When analyzing biological data, it can be helpful to consider gene sets, or predefined groups of biologically related genes. Methods exist for identifying gene sets that are differential between conditions, but large public datasets from consortium projects and single-cell RNA-Sequencing have opened the door for gene set analysis using more sophisticated machine learning techniques, such as autoencoders and variational autoencoders. We present shallow sparsely-connected autoencoders (SSCAs) and variational autoencoders (SSCVAs) as tools for projecting gene-level data onto gene sets. We tested these approaches on single-cell RNA-Sequencing data from blood cells and on RNA-Sequencing data from breast cancer patients. Both SSCA and SSCVA can recover known biological features from these datasets and the SSCVA method often outperforms SSCA (and six existing gene set scoring algorithms) on classification and prediction tasks. |
format | Online Article Text |
id | pubmed-6417803 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
record_format | MEDLINE/PubMed |
spelling | pubmed-64178032019-03-14 Shallow Sparsely-Connected Autoencoders for Gene Set Projection Gold, Maxwell P. LeNail, Alexander Fraenkel, Ernest Pac Symp Biocomput Article When analyzing biological data, it can be helpful to consider gene sets, or predefined groups of biologically related genes. Methods exist for identifying gene sets that are differential between conditions, but large public datasets from consortium projects and single-cell RNA-Sequencing have opened the door for gene set analysis using more sophisticated machine learning techniques, such as autoencoders and variational autoencoders. We present shallow sparsely-connected autoencoders (SSCAs) and variational autoencoders (SSCVAs) as tools for projecting gene-level data onto gene sets. We tested these approaches on single-cell RNA-Sequencing data from blood cells and on RNA-Sequencing data from breast cancer patients. Both SSCA and SSCVA can recover known biological features from these datasets and the SSCVA method often outperforms SSCA (and six existing gene set scoring algorithms) on classification and prediction tasks. 2019 /pmc/articles/PMC6417803/ /pubmed/30963076 Text en https://creativecommons.org/licenses/by-nc/4.0/Open Access chapter published by World Scientific Publishing Company and distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC) 4.0 License. |
spellingShingle | Article Gold, Maxwell P. LeNail, Alexander Fraenkel, Ernest Shallow Sparsely-Connected Autoencoders for Gene Set Projection |
title | Shallow Sparsely-Connected Autoencoders for Gene Set Projection |
title_full | Shallow Sparsely-Connected Autoencoders for Gene Set Projection |
title_fullStr | Shallow Sparsely-Connected Autoencoders for Gene Set Projection |
title_full_unstemmed | Shallow Sparsely-Connected Autoencoders for Gene Set Projection |
title_short | Shallow Sparsely-Connected Autoencoders for Gene Set Projection |
title_sort | shallow sparsely-connected autoencoders for gene set projection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6417803/ https://www.ncbi.nlm.nih.gov/pubmed/30963076 |
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