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scPower accelerates and optimizes the design of multi-sample single cell transcriptomic studies
Single cell RNA-seq has revolutionized transcriptomics by providing cell type resolution for differential gene expression and expression quantitative trait loci (eQTL) analyses. However, efficient power analysis methods for single cell data and inter-individual comparisons are lacking. Here, we pres...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8595682/ https://www.ncbi.nlm.nih.gov/pubmed/34785648 http://dx.doi.org/10.1038/s41467-021-26779-7 |
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author | Schmid, Katharina T. Höllbacher, Barbara Cruceanu, Cristiana Böttcher, Anika Lickert, Heiko Binder, Elisabeth B. Theis, Fabian J. Heinig, Matthias |
author_facet | Schmid, Katharina T. Höllbacher, Barbara Cruceanu, Cristiana Böttcher, Anika Lickert, Heiko Binder, Elisabeth B. Theis, Fabian J. Heinig, Matthias |
author_sort | Schmid, Katharina T. |
collection | PubMed |
description | Single cell RNA-seq has revolutionized transcriptomics by providing cell type resolution for differential gene expression and expression quantitative trait loci (eQTL) analyses. However, efficient power analysis methods for single cell data and inter-individual comparisons are lacking. Here, we present scPower; a statistical framework for the design and power analysis of multi-sample single cell transcriptomic experiments. We modelled the relationship between sample size, the number of cells per individual, sequencing depth, and the power of detecting differentially expressed genes within cell types. We systematically evaluated these optimal parameter combinations for several single cell profiling platforms, and generated broad recommendations. In general, shallow sequencing of high numbers of cells leads to higher overall power than deep sequencing of fewer cells. The model, including priors, is implemented as an R package and is accessible as a web tool. scPower is a highly customizable tool that experimentalists can use to quickly compare a multitude of experimental designs and optimize for a limited budget. |
format | Online Article Text |
id | pubmed-8595682 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-85956822021-11-19 scPower accelerates and optimizes the design of multi-sample single cell transcriptomic studies Schmid, Katharina T. Höllbacher, Barbara Cruceanu, Cristiana Böttcher, Anika Lickert, Heiko Binder, Elisabeth B. Theis, Fabian J. Heinig, Matthias Nat Commun Article Single cell RNA-seq has revolutionized transcriptomics by providing cell type resolution for differential gene expression and expression quantitative trait loci (eQTL) analyses. However, efficient power analysis methods for single cell data and inter-individual comparisons are lacking. Here, we present scPower; a statistical framework for the design and power analysis of multi-sample single cell transcriptomic experiments. We modelled the relationship between sample size, the number of cells per individual, sequencing depth, and the power of detecting differentially expressed genes within cell types. We systematically evaluated these optimal parameter combinations for several single cell profiling platforms, and generated broad recommendations. In general, shallow sequencing of high numbers of cells leads to higher overall power than deep sequencing of fewer cells. The model, including priors, is implemented as an R package and is accessible as a web tool. scPower is a highly customizable tool that experimentalists can use to quickly compare a multitude of experimental designs and optimize for a limited budget. Nature Publishing Group UK 2021-11-16 /pmc/articles/PMC8595682/ /pubmed/34785648 http://dx.doi.org/10.1038/s41467-021-26779-7 Text en © The Author(s) 2021 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 Schmid, Katharina T. Höllbacher, Barbara Cruceanu, Cristiana Böttcher, Anika Lickert, Heiko Binder, Elisabeth B. Theis, Fabian J. Heinig, Matthias scPower accelerates and optimizes the design of multi-sample single cell transcriptomic studies |
title | scPower accelerates and optimizes the design of multi-sample single cell transcriptomic studies |
title_full | scPower accelerates and optimizes the design of multi-sample single cell transcriptomic studies |
title_fullStr | scPower accelerates and optimizes the design of multi-sample single cell transcriptomic studies |
title_full_unstemmed | scPower accelerates and optimizes the design of multi-sample single cell transcriptomic studies |
title_short | scPower accelerates and optimizes the design of multi-sample single cell transcriptomic studies |
title_sort | scpower accelerates and optimizes the design of multi-sample single cell transcriptomic studies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8595682/ https://www.ncbi.nlm.nih.gov/pubmed/34785648 http://dx.doi.org/10.1038/s41467-021-26779-7 |
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