Plate IV.266 · Publications

scPower accelerates and optimizes the design of multi-sample single cell transcriptomic studies

Article in Nature Communications, 16 November 2021.

Open accessResearch area: Single Cell RNA, Gene Expression

Authors

  1. Katharina T. Schmid
  2. Barbara Höllbacher
  3. Cristiana Cruceanu
  4. Anika Böttcher
  5. Heiko Lickert
  6. Elisabeth B. Binder
  7. Fabian J. Theis
  8. Matthias Heinig

Abstract

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.

Versions3

  1. PublishedNature Communications10.1038/s41467-021-26779-7
  2. PreprintResearch Square10.21203/rs.3.rs-331370/v1
  3. PreprintbioRxiv10.1101/2020.04.01.019851

Cite

@article{schmid2021scpower,
  title = {{scPower accelerates and optimizes the design of multi-sample single cell transcriptomic studies}},
  author = {Schmid, Katharina T. and Höllbacher, Barbara and Cruceanu, Cristiana and Böttcher, Anika and Lickert, Heiko and Binder, Elisabeth B. and Theis, Fabian J. and Heinig, Matthias},
  journal = {Nature Communications},
  publisher = {Springer Science and Business Media LLC},
  year = {2021},
  month = nov,
  doi = {10.1038/s41467-021-26779-7},
  url = {https://doi.org/10.1038/s41467-021-26779-7},
  pmid = {34785648},
  pmcid = {PMC8595682}
}
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