MATISSE: An analysis protocol for combining imaging mass cytometry with fluorescence microscopy to generate single-cell data

Daniëlle Krijgsman, Neeraj Sinha, Matthijs J.D. Baars, Stephanie van Dam, Mojtaba Amini, Yvonne Vercoulen*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Exploring tissue heterogeneity on a single-cell level by imaging mass cytometry (IMC) remains challenging because of its limiting resolution. We previously demonstrated that combining higher resolution fluorescence with IMC data in the analysis pipeline resulted in high-quality single-cell segmentation. Here, we provide a step-by-step workflow of this MATISSE pipeline, including instructions regarding the staining procedure, and the analysis route to generate single-cell data. For complete details on the use and execution of this protocol, please refer to Baars et al., 2021.

Original languageEnglish
Article number101034
Pages (from-to)1-36
JournalSTAR protocols
Volume3
Issue number1
DOIs
Publication statusPublished - 18 Mar 2022

Keywords

  • Antibody
  • Bioinformatics
  • Biotechnology and bioengineering
  • Cell Biology
  • Flow Cytometry/Mass Cytometry
  • Microscopy
  • Single Cell
  • Image Cytometry
  • Staining and Labeling
  • Workflow
  • Microscopy, Fluorescence

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