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A benchmark study of simulation methods for single-cell RNA sequencing data

Author

Listed:
  • Yue Cao

    (The University of Sydney
    The University of Sydney)

  • Pengyi Yang

    (The University of Sydney
    The University of Sydney
    Children’s Medical Research Institute)

  • Jean Yee Hwa Yang

    (The University of Sydney
    The University of Sydney)

Abstract

Single-cell RNA-seq (scRNA-seq) data simulation is critical for evaluating computational methods for analysing scRNA-seq data especially when ground truth is experimentally unattainable. The reliability of evaluation depends on the ability of simulation methods to capture properties of experimental data. However, while many scRNA-seq data simulation methods have been proposed, a systematic evaluation of these methods is lacking. We develop a comprehensive evaluation framework, SimBench, including a kernel density estimation measure to benchmark 12 simulation methods through 35 scRNA-seq experimental datasets. We evaluate the simulation methods on a panel of data properties, ability to maintain biological signals, scalability and applicability. Our benchmark uncovers performance differences among the methods and highlights the varying difficulties in simulating data characteristics. Furthermore, we identify several limitations including maintaining heterogeneity of distribution. These results, together with the framework and datasets made publicly available as R packages, will guide simulation methods selection and their future development.

Suggested Citation

  • Yue Cao & Pengyi Yang & Jean Yee Hwa Yang, 2021. "A benchmark study of simulation methods for single-cell RNA sequencing data," Nature Communications, Nature, vol. 12(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-27130-w
    DOI: 10.1038/s41467-021-27130-w
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    References listed on IDEAS

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    1. Beate Vieth & Swati Parekh & Christoph Ziegenhain & Wolfgang Enard & Ines Hellmann, 2019. "A systematic evaluation of single cell RNA-seq analysis pipelines," Nature Communications, Nature, vol. 10(1), pages 1-11, December.
    2. Xiuwei Zhang & Chenling Xu & Nir Yosef, 2019. "Simulating multiple faceted variability in single cell RNA sequencing," Nature Communications, Nature, vol. 10(1), pages 1-16, December.
    3. Mohamed Marouf & Pierre Machart & Vikas Bansal & Christoph Kilian & Daniel S. Magruder & Christian F. Krebs & Stefan Bonn, 2020. "Realistic in silico generation and augmentation of single-cell RNA-seq data using generative adversarial networks," Nature Communications, Nature, vol. 11(1), pages 1-12, December.
    4. Davide Risso & Fanny Perraudeau & Svetlana Gribkova & Sandrine Dudoit & Jean-Philippe Vert, 2018. "A general and flexible method for signal extraction from single-cell RNA-seq data," Nature Communications, Nature, vol. 9(1), pages 1-17, December.
    5. Robrecht Cannoodt & Wouter Saelens & Louise Deconinck & Yvan Saeys, 2021. "Spearheading future omics analyses using dyngen, a multi-modal simulator of single cells," Nature Communications, Nature, vol. 12(1), pages 1-9, December.
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    Cited by:

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    3. Xiaohang Fu & Yingxin Lin & David M. Lin & Daniel Mechtersheimer & Chuhan Wang & Farhan Ameen & Shila Ghazanfar & Ellis Patrick & Jinman Kim & Jean Y. H. Yang, 2024. "BIDCell: Biologically-informed self-supervised learning for segmentation of subcellular spatial transcriptomics data," Nature Communications, Nature, vol. 15(1), pages 1-17, December.

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