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Single-cell gene regulatory network prediction by explainable AI
The molecular heterogeneity of cancer cells contributes to the often partial response to targeted therapies and relapse of disease due to the escape of resistant cell populations. While single-cell sequencing has started to improve our understanding of this heterogeneity, it offers a mostly descript...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9976884/ https://www.ncbi.nlm.nih.gov/pubmed/36629274 http://dx.doi.org/10.1093/nar/gkac1212 |
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author | Keyl, Philipp Bischoff, Philip Dernbach, Gabriel Bockmayr, Michael Fritz, Rebecca Horst, David Blüthgen, Nils Montavon, Grégoire Müller, Klaus-Robert Klauschen, Frederick |
author_facet | Keyl, Philipp Bischoff, Philip Dernbach, Gabriel Bockmayr, Michael Fritz, Rebecca Horst, David Blüthgen, Nils Montavon, Grégoire Müller, Klaus-Robert Klauschen, Frederick |
author_sort | Keyl, Philipp |
collection | PubMed |
description | The molecular heterogeneity of cancer cells contributes to the often partial response to targeted therapies and relapse of disease due to the escape of resistant cell populations. While single-cell sequencing has started to improve our understanding of this heterogeneity, it offers a mostly descriptive view on cellular types and states. To obtain more functional insights, we propose scGeneRAI, an explainable deep learning approach that uses layer-wise relevance propagation (LRP) to infer gene regulatory networks from static single-cell RNA sequencing data for individual cells. We benchmark our method with synthetic data and apply it to single-cell RNA sequencing data of a cohort of human lung cancers. From the predicted single-cell networks our approach reveals characteristic network patterns for tumor cells and normal epithelial cells and identifies subnetworks that are observed only in (subgroups of) tumor cells of certain patients. While current state-of-the-art methods are limited by their ability to only predict average networks for cell populations, our approach facilitates the reconstruction of networks down to the level of single cells which can be utilized to characterize the heterogeneity of gene regulation within and across tumors. |
format | Online Article Text |
id | pubmed-9976884 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-99768842023-03-02 Single-cell gene regulatory network prediction by explainable AI Keyl, Philipp Bischoff, Philip Dernbach, Gabriel Bockmayr, Michael Fritz, Rebecca Horst, David Blüthgen, Nils Montavon, Grégoire Müller, Klaus-Robert Klauschen, Frederick Nucleic Acids Res Methods Online The molecular heterogeneity of cancer cells contributes to the often partial response to targeted therapies and relapse of disease due to the escape of resistant cell populations. While single-cell sequencing has started to improve our understanding of this heterogeneity, it offers a mostly descriptive view on cellular types and states. To obtain more functional insights, we propose scGeneRAI, an explainable deep learning approach that uses layer-wise relevance propagation (LRP) to infer gene regulatory networks from static single-cell RNA sequencing data for individual cells. We benchmark our method with synthetic data and apply it to single-cell RNA sequencing data of a cohort of human lung cancers. From the predicted single-cell networks our approach reveals characteristic network patterns for tumor cells and normal epithelial cells and identifies subnetworks that are observed only in (subgroups of) tumor cells of certain patients. While current state-of-the-art methods are limited by their ability to only predict average networks for cell populations, our approach facilitates the reconstruction of networks down to the level of single cells which can be utilized to characterize the heterogeneity of gene regulation within and across tumors. Oxford University Press 2023-01-11 /pmc/articles/PMC9976884/ /pubmed/36629274 http://dx.doi.org/10.1093/nar/gkac1212 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Methods Online Keyl, Philipp Bischoff, Philip Dernbach, Gabriel Bockmayr, Michael Fritz, Rebecca Horst, David Blüthgen, Nils Montavon, Grégoire Müller, Klaus-Robert Klauschen, Frederick Single-cell gene regulatory network prediction by explainable AI |
title | Single-cell gene regulatory network prediction by explainable AI |
title_full | Single-cell gene regulatory network prediction by explainable AI |
title_fullStr | Single-cell gene regulatory network prediction by explainable AI |
title_full_unstemmed | Single-cell gene regulatory network prediction by explainable AI |
title_short | Single-cell gene regulatory network prediction by explainable AI |
title_sort | single-cell gene regulatory network prediction by explainable ai |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9976884/ https://www.ncbi.nlm.nih.gov/pubmed/36629274 http://dx.doi.org/10.1093/nar/gkac1212 |
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