| Literature DB >> 35061903 |
Rance Nault1,2, Satabdi Saha3, Sudin Bhattacharya4, Jack Dodson1, Samiran Sinha5, Tapabrata Maiti3, Tim Zacharewski1,2.
Abstract
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.Entities:
Mesh:
Year: 2022 PMID: 35061903 PMCID: PMC9071439 DOI: 10.1093/nar/gkac019
Source DB: PubMed Journal: Nucleic Acids Res ISSN: 0305-1048 Impact factor: 19.160