Skip to main content
bioRxiv
  • Home
  • About
  • Submit
  • ALERTS / RSS
Advanced Search
New Results

Integration, exploration, and analysis of high-dimensional single-cell cytometry data using Spectre

View ORCID ProfileThomas Myles Ashhurst, Felix Marsh-Wakefield, Givanna Haryono Putri, Alanna Gabrielle Spiteri, Diana Shinko, Mark Norman Read, Adrian Lloyd Smith, Nicholas Jonathan Cole King
doi: https://doi.org/10.1101/2020.10.22.349563
Thomas Myles Ashhurst
1Sydney Cytometry Core Research Facility, Charles Perkins Centre, Centenary Institute and The University of Sydney, NSW, Australia
2Marie Bashir Institute for Infectious Diseases and Biosecurity, The University of Sydney, NSW, Australia
3Charles Perkins Centre, The University of Sydney, NSW, Australia
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for Thomas Myles Ashhurst
  • For correspondence: thomas.ashhurst@sydney.edu.au
Felix Marsh-Wakefield
3Charles Perkins Centre, The University of Sydney, NSW, Australia
4School of Medical Sciences, Faculty of Medicine and Health, The University of Sydney, NSW, Australia
5Vascular Immunology Unit, Department of Pathology, The University of Sydney, NSW, Australia
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Givanna Haryono Putri
3Charles Perkins Centre, The University of Sydney, NSW, Australia
6School of Computer Science, The University of Sydney, NSW, Australia
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Alanna Gabrielle Spiteri
3Charles Perkins Centre, The University of Sydney, NSW, Australia
7Viral Immunopathology Laboratory, Discipline of Pathology, School of Medical Sciences, Faculty of Medicine and Health
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Diana Shinko
1Sydney Cytometry Core Research Facility, Charles Perkins Centre, Centenary Institute and The University of Sydney, NSW, Australia
3Charles Perkins Centre, The University of Sydney, NSW, Australia
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Mark Norman Read
3Charles Perkins Centre, The University of Sydney, NSW, Australia
6School of Computer Science, The University of Sydney, NSW, Australia
8The Westmead Initiative, Faculty of Engineering, The University of Sydney, NSW, Australia
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Adrian Lloyd Smith
1Sydney Cytometry Core Research Facility, Charles Perkins Centre, Centenary Institute and The University of Sydney, NSW, Australia
3Charles Perkins Centre, The University of Sydney, NSW, Australia
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Nicholas Jonathan Cole King
1Sydney Cytometry Core Research Facility, Charles Perkins Centre, Centenary Institute and The University of Sydney, NSW, Australia
2Marie Bashir Institute for Infectious Diseases and Biosecurity, The University of Sydney, NSW, Australia
3Charles Perkins Centre, The University of Sydney, NSW, Australia
7Viral Immunopathology Laboratory, Discipline of Pathology, School of Medical Sciences, Faculty of Medicine and Health
9Sydney Nano, The University of Sydney, NSW, Australia
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • Abstract
  • Full Text
  • Info/History
  • Metrics
  • Supplementary material
  • Data/Code
  • Preview PDF
Loading

ABSTRACT

As the size and complexity of high-dimensional cytometry data continue to expand, comprehensive, scalable, and methodical computational analysis approaches are essential. Yet, contemporary clustering and dimensionality reduction tools alone are insufficient to analyze or reproduce analyses across large numbers of samples, batches, or experiments. Moreover, approaches that allow for the integration of data across batches or experiments are not well incorporated into computational toolkits to allow for streamlined workflows. Here we present Spectre, an R package that enables comprehensive end-to-end integration and analysis of high-dimensional cytometry data from different batches or experiments. Spectre streamlines the analytical stages of raw data pre-processing, batch alignment, data integration, clustering, dimensionality reduction, visualization and population labelling, as well as quantitative and statistical analysis. Critically, the fundamental data structures used within Spectre, along with the implementation of machine learning classifiers, allow for the scalable analysis of very large high-dimensional datasets, generated by flow cytometry, mass cytometry (CyTOF), or spectral cytometry. Using open and flexible data structures, Spectre can also be used to analyze data generated by single-cell RNA sequencing (scRNAseq) or high-dimensional imaging technologies, such as Imaging Mass Cytometry (IMC). The simple, clear, and modular design of analysis workflows allow these tools to be used by bioinformaticians and laboratory scientists alike. Spectre is available as an R package or Docker container. R code is available on Github (https://github.com/immunedynamics/spectre).

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • https://github.com/ImmuneDynamics/Spectre

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
Back to top
PreviousNext
Posted October 23, 2020.
Download PDF

Supplementary Material

Data/Code
Email

Thank you for your interest in spreading the word about bioRxiv.

NOTE: Your email address is requested solely to identify you as the sender of this article.

Enter multiple addresses on separate lines or separate them with commas.
Integration, exploration, and analysis of high-dimensional single-cell cytometry data using Spectre
(Your Name) has forwarded a page to you from bioRxiv
(Your Name) thought you would like to see this page from the bioRxiv website.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Share
Integration, exploration, and analysis of high-dimensional single-cell cytometry data using Spectre
Thomas Myles Ashhurst, Felix Marsh-Wakefield, Givanna Haryono Putri, Alanna Gabrielle Spiteri, Diana Shinko, Mark Norman Read, Adrian Lloyd Smith, Nicholas Jonathan Cole King
bioRxiv 2020.10.22.349563; doi: https://doi.org/10.1101/2020.10.22.349563
Reddit logo Twitter logo Facebook logo LinkedIn logo Mendeley logo
Citation Tools
Integration, exploration, and analysis of high-dimensional single-cell cytometry data using Spectre
Thomas Myles Ashhurst, Felix Marsh-Wakefield, Givanna Haryono Putri, Alanna Gabrielle Spiteri, Diana Shinko, Mark Norman Read, Adrian Lloyd Smith, Nicholas Jonathan Cole King
bioRxiv 2020.10.22.349563; doi: https://doi.org/10.1101/2020.10.22.349563

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
  • Tweet Widget
  • Facebook Like
  • Google Plus One

Subject Area

  • Immunology
Subject Areas
All Articles
  • Animal Behavior and Cognition (4663)
  • Biochemistry (10320)
  • Bioengineering (7647)
  • Bioinformatics (26266)
  • Biophysics (13486)
  • Cancer Biology (10655)
  • Cell Biology (15372)
  • Clinical Trials (138)
  • Developmental Biology (8473)
  • Ecology (12787)
  • Epidemiology (2067)
  • Evolutionary Biology (16806)
  • Genetics (11374)
  • Genomics (15438)
  • Immunology (10586)
  • Microbiology (25099)
  • Molecular Biology (10176)
  • Neuroscience (54271)
  • Paleontology (399)
  • Pathology (1663)
  • Pharmacology and Toxicology (2884)
  • Physiology (4329)
  • Plant Biology (9216)
  • Scientific Communication and Education (1583)
  • Synthetic Biology (2547)
  • Systems Biology (6765)
  • Zoology (1459)