Semi‐automated background removal limits data loss and normalizes imaging mass cytometry data

Imaging mass cytometry (IMC) allows the detection of multiple antigens (approximately 40 markers) combined with spatial information, making it a unique tool for the evaluation of complex biological systems. Due to its widespread availability and retained tissue morphology, formalin‐fixed, paraffin‐e...

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Bibliographic Details
Published inCytometry. Part A Vol. 99; no. 12; pp. 1187 - 1197
Main Authors Ijsselsteijn, Marieke E., Somarakis, Antonios, Lelieveldt, Boudewijn P. F., Höllt, Thomas, Miranda, Noel F. C. C.
Format Journal Article
LanguageEnglish
Published Hoboken, USA John Wiley & Sons, Inc 01.12.2021
Wiley Subscription Services, Inc
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Summary:Imaging mass cytometry (IMC) allows the detection of multiple antigens (approximately 40 markers) combined with spatial information, making it a unique tool for the evaluation of complex biological systems. Due to its widespread availability and retained tissue morphology, formalin‐fixed, paraffin‐embedded (FFPE) tissues are often a material of choice for IMC studies. However, antibody performance and signal to noise ratios can differ considerably between FFPE tissues as a consequence of variations in tissue processing, including fixation. In contrast to batch effects caused by differences in the immunodetection procedure, variations in tissue processing are difficult to control. We investigated the effect of immunodetection‐related signal intensity fluctuations on IMC analysis and phenotype identification, in a cohort of 12 colorectal cancer tissues. Furthermore, we explored different normalization strategies and propose a workflow to normalize IMC data by semi‐automated background removal, using publicly available tools. This workflow can be directly applied to previously acquired datasets and considerably improves the quality of IMC data, thereby supporting the analysis and comparison of multiple samples.
Bibliography:Thomas Höllt and Noel F. C. C. de Miranda contributed equally to this study.
Funding information
Marieke E. Ijsselsteijn and Antonios Somarakis contributed equally to this study.
H2020 European Research Council, Grant/Award Number: 852832; Leiden university data science research program
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ISSN:1552-4922
1552-4930
1552-4930
DOI:10.1002/cyto.a.24480