propeller

propeller detects differences in cell type proportions across experimental conditions using single-cell RNA sequencing (scRNA-seq) data to identify statistically significant shifts in cellular composition.


Key Features:

  • Statistical testing for cell type proportions: Detects statistically significant shifts in cell type composition between experimental groups using scRNA-seq data.
  • Biological replication: Incorporates biological replication into the analysis framework to account for sample-level variability in scRNA-seq datasets.
  • Variability modeling: Accounts for different sources of variability inherent in scRNA-seq data to improve robustness of proportion estimates.
  • Validation by simulation: Performance and flexibility have been demonstrated through simulations with varied cell type proportion scenarios.
  • Implementation: Implemented within the speckle R package.
  • Support for complex designs: Designed to handle complex experimental designs that include multiple conditions or treatments.

Scientific Applications:

  • Human Heart Development: Applied to investigate changes in cell type proportions during heart development.
  • Aging Studies: Used to analyze how aging affects cell type composition.
  • COVID-19 Disease Severity: Applied to scRNA-seq data from COVID-19 patients to identify shifts in cell type proportions associated with disease severity.

Methodology:

Leverages biological replication and explicit modeling of scRNA-seq variability to test for differences in cell type proportions across groups, with performance evaluated using simulations of varied cell type proportion datasets.

Topics

Details

License:
Not licensed
Cost:
Free of charge
Tool Type:
workflow
Operating Systems:
Mac, Linux, Windows
Programming Languages:
R
Added:
11/5/2022
Last Updated:
11/5/2022

Operations

Publications

Phipson B, Sim CB, Porrello ER, Hewitt AW, Powell J, Oshlack A. <i>propeller:</i> testing for differences in cell type proportions in single cell data. Bioinformatics. 2022;38(20):4720-4726. doi:10.1093/bioinformatics/btac582. PMID:36005887. PMCID:PMC9563678.

PMID: 36005887
Funding: - National Health and Medical Research Council Investigator: GNT1175653, GNT1175781, GNT1196256, GNT2008376 - National Health and Medical Research Council: GNT1187748 - Royal Children’s Hospital Foundation and National Health and Medical Research Council Project: GNT1160257 - The Novo Nordisk Foundation Center for Stem Cell Medicine is supported by Novo Nordisk Foundation grants: NNF21CC0073729

Links