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miRSCAPE - inferring miRNA expression from scRNA-seq data

Our understanding of miRNA activity at cellular resolution is thwarted by the inability of standard scRNA-seq protocols to capture miRNAs. We introduce a novel tool, miRSCAPE, to infer miRNA expression in a sample from its RNA-seq profile. We establish miRSCAPE’s accuracy in 10 tumor and normal coho...

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Autores principales: Olgun, Gulden, Gopalan, Vishaka, Hannenhalli, Sridhar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9437856/
https://www.ncbi.nlm.nih.gov/pubmed/36060076
http://dx.doi.org/10.1016/j.isci.2022.104962
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author Olgun, Gulden
Gopalan, Vishaka
Hannenhalli, Sridhar
author_facet Olgun, Gulden
Gopalan, Vishaka
Hannenhalli, Sridhar
author_sort Olgun, Gulden
collection PubMed
description Our understanding of miRNA activity at cellular resolution is thwarted by the inability of standard scRNA-seq protocols to capture miRNAs. We introduce a novel tool, miRSCAPE, to infer miRNA expression in a sample from its RNA-seq profile. We establish miRSCAPE’s accuracy in 10 tumor and normal cohorts demonstrating its superiority over alternatives. miRSCAPE accurately infers cell type-specific miRNA activities (predicted versus observed fold-difference correlation ∼0.81) in two independent scRNA-seq datasets. We apply miRSCAPE to infer miRNA activities in scRNA clusters in pancreatic and lung adenocarcinomas, as well as in 56 cell types in the human cell landscape (HCL). In pancreatic and breast cancer scRNA-seq data, miRSCAPE recapitulates miRNAs associated with stemness and epithelial-mesenchymal transition (EMT) cell states, respectively. Overall, miRSCAPE recapitulates and refines miRNA biology at cellular resolution. miRSCAPE is freely available and is easily applicable to scRNA-seq data to infer miRNA activities at cellular resolution.
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spelling pubmed-94378562022-09-03 miRSCAPE - inferring miRNA expression from scRNA-seq data Olgun, Gulden Gopalan, Vishaka Hannenhalli, Sridhar iScience Article Our understanding of miRNA activity at cellular resolution is thwarted by the inability of standard scRNA-seq protocols to capture miRNAs. We introduce a novel tool, miRSCAPE, to infer miRNA expression in a sample from its RNA-seq profile. We establish miRSCAPE’s accuracy in 10 tumor and normal cohorts demonstrating its superiority over alternatives. miRSCAPE accurately infers cell type-specific miRNA activities (predicted versus observed fold-difference correlation ∼0.81) in two independent scRNA-seq datasets. We apply miRSCAPE to infer miRNA activities in scRNA clusters in pancreatic and lung adenocarcinomas, as well as in 56 cell types in the human cell landscape (HCL). In pancreatic and breast cancer scRNA-seq data, miRSCAPE recapitulates miRNAs associated with stemness and epithelial-mesenchymal transition (EMT) cell states, respectively. Overall, miRSCAPE recapitulates and refines miRNA biology at cellular resolution. miRSCAPE is freely available and is easily applicable to scRNA-seq data to infer miRNA activities at cellular resolution. Elsevier 2022-08-17 /pmc/articles/PMC9437856/ /pubmed/36060076 http://dx.doi.org/10.1016/j.isci.2022.104962 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Olgun, Gulden
Gopalan, Vishaka
Hannenhalli, Sridhar
miRSCAPE - inferring miRNA expression from scRNA-seq data
title miRSCAPE - inferring miRNA expression from scRNA-seq data
title_full miRSCAPE - inferring miRNA expression from scRNA-seq data
title_fullStr miRSCAPE - inferring miRNA expression from scRNA-seq data
title_full_unstemmed miRSCAPE - inferring miRNA expression from scRNA-seq data
title_short miRSCAPE - inferring miRNA expression from scRNA-seq data
title_sort mirscape - inferring mirna expression from scrna-seq data
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9437856/
https://www.ncbi.nlm.nih.gov/pubmed/36060076
http://dx.doi.org/10.1016/j.isci.2022.104962
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