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Deep autoencoder for interpretable tissue-adaptive deconvolution and cell-type-specific gene analysis
Single-cell RNA-sequencing has become a powerful tool to study biologically significant characteristics at explicitly high resolution. However, its application on emerging data is currently limited by its intrinsic techniques. Here, we introduce Tissue-AdaPtive autoEncoder (TAPE), a deep learning me...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9641692/ https://www.ncbi.nlm.nih.gov/pubmed/36347853 http://dx.doi.org/10.1038/s41467-022-34550-9 |
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author | Chen, Yanshuo Wang, Yixuan Chen, Yuelong Cheng, Yuqi Wei, Yumeng Li, Yunxiang Wang, Jiuming Wei, Yingying Chan, Ting-Fung Li, Yu |
author_facet | Chen, Yanshuo Wang, Yixuan Chen, Yuelong Cheng, Yuqi Wei, Yumeng Li, Yunxiang Wang, Jiuming Wei, Yingying Chan, Ting-Fung Li, Yu |
author_sort | Chen, Yanshuo |
collection | PubMed |
description | Single-cell RNA-sequencing has become a powerful tool to study biologically significant characteristics at explicitly high resolution. However, its application on emerging data is currently limited by its intrinsic techniques. Here, we introduce Tissue-AdaPtive autoEncoder (TAPE), a deep learning method connecting bulk RNA-seq and single-cell RNA-seq to achieve precise deconvolution in a short time. By constructing an interpretable decoder and training under a unique scheme, TAPE can predict cell-type fractions and cell-type-specific gene expression tissue-adaptively. Compared with popular methods on several datasets, TAPE has a better overall performance and comparable accuracy at cell type level. Additionally, it is more robust among different cell types, faster, and sensitive to provide biologically meaningful predictions. Moreover, through the analysis of clinical data, TAPE shows its ability to predict cell-type-specific gene expression profiles with biological significance. We believe that TAPE will enable and accelerate the precise analysis of high-throughput clinical data in a wide range. |
format | Online Article Text |
id | pubmed-9641692 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96416922022-11-14 Deep autoencoder for interpretable tissue-adaptive deconvolution and cell-type-specific gene analysis Chen, Yanshuo Wang, Yixuan Chen, Yuelong Cheng, Yuqi Wei, Yumeng Li, Yunxiang Wang, Jiuming Wei, Yingying Chan, Ting-Fung Li, Yu Nat Commun Article Single-cell RNA-sequencing has become a powerful tool to study biologically significant characteristics at explicitly high resolution. However, its application on emerging data is currently limited by its intrinsic techniques. Here, we introduce Tissue-AdaPtive autoEncoder (TAPE), a deep learning method connecting bulk RNA-seq and single-cell RNA-seq to achieve precise deconvolution in a short time. By constructing an interpretable decoder and training under a unique scheme, TAPE can predict cell-type fractions and cell-type-specific gene expression tissue-adaptively. Compared with popular methods on several datasets, TAPE has a better overall performance and comparable accuracy at cell type level. Additionally, it is more robust among different cell types, faster, and sensitive to provide biologically meaningful predictions. Moreover, through the analysis of clinical data, TAPE shows its ability to predict cell-type-specific gene expression profiles with biological significance. We believe that TAPE will enable and accelerate the precise analysis of high-throughput clinical data in a wide range. Nature Publishing Group UK 2022-11-08 /pmc/articles/PMC9641692/ /pubmed/36347853 http://dx.doi.org/10.1038/s41467-022-34550-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Chen, Yanshuo Wang, Yixuan Chen, Yuelong Cheng, Yuqi Wei, Yumeng Li, Yunxiang Wang, Jiuming Wei, Yingying Chan, Ting-Fung Li, Yu Deep autoencoder for interpretable tissue-adaptive deconvolution and cell-type-specific gene analysis |
title | Deep autoencoder for interpretable tissue-adaptive deconvolution and cell-type-specific gene analysis |
title_full | Deep autoencoder for interpretable tissue-adaptive deconvolution and cell-type-specific gene analysis |
title_fullStr | Deep autoencoder for interpretable tissue-adaptive deconvolution and cell-type-specific gene analysis |
title_full_unstemmed | Deep autoencoder for interpretable tissue-adaptive deconvolution and cell-type-specific gene analysis |
title_short | Deep autoencoder for interpretable tissue-adaptive deconvolution and cell-type-specific gene analysis |
title_sort | deep autoencoder for interpretable tissue-adaptive deconvolution and cell-type-specific gene analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9641692/ https://www.ncbi.nlm.nih.gov/pubmed/36347853 http://dx.doi.org/10.1038/s41467-022-34550-9 |
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