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Benchmarking of a Bayesian single cell RNAseq differential gene expression test for dose–response study designs

The application of single-cell RNA sequencing (scRNAseq) for the evaluation of chemicals, drugs, and food contaminants presents the opportunity to consider cellular heterogeneity in pharmacological and toxicological responses. Current differential gene expression analysis (DGEA) methods focus primar...

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Autores principales: Nault, Rance, Saha, Satabdi, Bhattacharya, Sudin, Dodson, Jack, Sinha, Samiran, Maiti, Tapabrata, Zacharewski, Tim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9071439/
https://www.ncbi.nlm.nih.gov/pubmed/35061903
http://dx.doi.org/10.1093/nar/gkac019
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author Nault, Rance
Saha, Satabdi
Bhattacharya, Sudin
Dodson, Jack
Sinha, Samiran
Maiti, Tapabrata
Zacharewski, Tim
author_facet Nault, Rance
Saha, Satabdi
Bhattacharya, Sudin
Dodson, Jack
Sinha, Samiran
Maiti, Tapabrata
Zacharewski, Tim
author_sort Nault, Rance
collection PubMed
description The application of single-cell RNA sequencing (scRNAseq) for the evaluation of chemicals, drugs, and food contaminants presents the opportunity to consider cellular heterogeneity in pharmacological and toxicological responses. Current differential gene expression analysis (DGEA) methods focus primarily on two group comparisons, not multi-group dose–response study designs used in safety assessments. To benchmark DGEA methods for dose–response scRNAseq experiments, we proposed a multiplicity corrected Bayesian testing approach and compare it against 8 other methods including two frequentist fit-for-purpose tests using simulated and experimental data. Our Bayesian test method outperformed all other tests for a broad range of accuracy metrics including control of false positive error rates. Most notable, the fit-for-purpose and standard multiple group DGEA methods were superior to the two group scRNAseq methods for dose–response study designs. Collectively, our benchmarking of DGEA methods demonstrates the importance in considering study design when determining the most appropriate test methods.
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spelling pubmed-90714392022-05-06 Benchmarking of a Bayesian single cell RNAseq differential gene expression test for dose–response study designs Nault, Rance Saha, Satabdi Bhattacharya, Sudin Dodson, Jack Sinha, Samiran Maiti, Tapabrata Zacharewski, Tim Nucleic Acids Res Methods Online The application of single-cell RNA sequencing (scRNAseq) for the evaluation of chemicals, drugs, and food contaminants presents the opportunity to consider cellular heterogeneity in pharmacological and toxicological responses. Current differential gene expression analysis (DGEA) methods focus primarily on two group comparisons, not multi-group dose–response study designs used in safety assessments. To benchmark DGEA methods for dose–response scRNAseq experiments, we proposed a multiplicity corrected Bayesian testing approach and compare it against 8 other methods including two frequentist fit-for-purpose tests using simulated and experimental data. Our Bayesian test method outperformed all other tests for a broad range of accuracy metrics including control of false positive error rates. Most notable, the fit-for-purpose and standard multiple group DGEA methods were superior to the two group scRNAseq methods for dose–response study designs. Collectively, our benchmarking of DGEA methods demonstrates the importance in considering study design when determining the most appropriate test methods. Oxford University Press 2022-01-21 /pmc/articles/PMC9071439/ /pubmed/35061903 http://dx.doi.org/10.1093/nar/gkac019 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methods Online
Nault, Rance
Saha, Satabdi
Bhattacharya, Sudin
Dodson, Jack
Sinha, Samiran
Maiti, Tapabrata
Zacharewski, Tim
Benchmarking of a Bayesian single cell RNAseq differential gene expression test for dose–response study designs
title Benchmarking of a Bayesian single cell RNAseq differential gene expression test for dose–response study designs
title_full Benchmarking of a Bayesian single cell RNAseq differential gene expression test for dose–response study designs
title_fullStr Benchmarking of a Bayesian single cell RNAseq differential gene expression test for dose–response study designs
title_full_unstemmed Benchmarking of a Bayesian single cell RNAseq differential gene expression test for dose–response study designs
title_short Benchmarking of a Bayesian single cell RNAseq differential gene expression test for dose–response study designs
title_sort benchmarking of a bayesian single cell rnaseq differential gene expression test for dose–response study designs
topic Methods Online
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9071439/
https://www.ncbi.nlm.nih.gov/pubmed/35061903
http://dx.doi.org/10.1093/nar/gkac019
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