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BEARscc determines robustness of single-cell clusters using simulated technical replicates

Author

Listed:
  • D. T. Severson

    (University of Oxford)

  • R. P. Owen

    (University of Oxford
    Oxford University Hospital NHS Trust, John Radcliffe Hospital)

  • M. J. White

    (University of Oxford
    Oxford University Hospital NHS Trust, John Radcliffe Hospital)

  • X. Lu

    (University of Oxford)

  • B. Schuster-Böckler

    (University of Oxford)

Abstract

Single-cell messenger RNA sequencing (scRNA-seq) has emerged as a powerful tool to study cellular heterogeneity within complex tissues. Subpopulations of cells with common gene expression profiles can be identified by applying unsupervised clustering algorithms. However, technical variance is a major confounding factor in scRNA-seq, not least because it is not possible to replicate measurements on the same cell. Here, we present BEARscc, a tool that uses RNA spike-in controls to simulate experiment-specific technical replicates. BEARscc works with a wide range of existing clustering algorithms to assess the robustness of clusters to technical variation. We demonstrate that the tool improves the unsupervised classification of cells and facilitates the biological interpretation of single-cell RNA-seq experiments.

Suggested Citation

  • D. T. Severson & R. P. Owen & M. J. White & X. Lu & B. Schuster-Böckler, 2018. "BEARscc determines robustness of single-cell clusters using simulated technical replicates," Nature Communications, Nature, vol. 9(1), pages 1-7, December.
  • Handle: RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-03608-y
    DOI: 10.1038/s41467-018-03608-y
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    Cited by:

    1. Xiaotian Wu & Hao Wu & Zhijin Wu, 2021. "Penalized Latent Dirichlet Allocation Model in Single-Cell RNA Sequencing," Statistics in Biosciences, Springer;International Chinese Statistical Association, vol. 13(3), pages 543-562, December.

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