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scROSHI - robust supervised hierarchical identification of single cells

View ORCID ProfileMichael Prummer, Anne Bertolini, View ORCID ProfileLars Bosshard, Florian Barkmann, View ORCID ProfileJosephine Yates, View ORCID ProfileValentina Boeva, The TumorProfiler Consortium, View ORCID ProfileDaniel Stekhoven, View ORCID ProfileFranziska Singer
doi: https://doi.org/10.1101/2022.04.05.487176
Michael Prummer
1Nexus Personalized Health Technologies, ETH Zurich, Zurich Switzerland
4Swiss Institute of Bioinformatics (SIB), Zurich, Switzerland
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  • For correspondence: michael.prummer@nexus.ethz.ch
Anne Bertolini
1Nexus Personalized Health Technologies, ETH Zurich, Zurich Switzerland
4Swiss Institute of Bioinformatics (SIB), Zurich, Switzerland
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Lars Bosshard
1Nexus Personalized Health Technologies, ETH Zurich, Zurich Switzerland
4Swiss Institute of Bioinformatics (SIB), Zurich, Switzerland
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Florian Barkmann
2Institute for Machine Learning, Department of Computer Science, ETH Zurich, Zurich Switzerland
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Josephine Yates
2Institute for Machine Learning, Department of Computer Science, ETH Zurich, Zurich Switzerland
4Swiss Institute of Bioinformatics (SIB), Zurich, Switzerland
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Valentina Boeva
2Institute for Machine Learning, Department of Computer Science, ETH Zurich, Zurich Switzerland
3Cochin Institute, Inserm U1016, CNRS UMR 8104, Paris Descartes University UMR-S1016, Paris 75014, France
4Swiss Institute of Bioinformatics (SIB), Zurich, Switzerland
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Daniel Stekhoven
1Nexus Personalized Health Technologies, ETH Zurich, Zurich Switzerland
4Swiss Institute of Bioinformatics (SIB), Zurich, Switzerland
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Franziska Singer
1Nexus Personalized Health Technologies, ETH Zurich, Zurich Switzerland
4Swiss Institute of Bioinformatics (SIB), Zurich, Switzerland
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Abstract

Identifying cell types based on expression profiles is a pillar of single cell analysis. Existing machine-learning methods identify predictive features from annotated training data, which are often not available in early-stage studies. This can lead to overfitting and inferior performance when applied to new data. To address these challenges we present scROSHI, which utilizes previously obtained cell type-specific gene sets and does not require training or the existence of annotated data. By respecting the hierarchical nature of cell type relationships and assigning cells consecutively to more specialized identities, excellent prediction performance is achieved. In a benchmark based on publicly available PBMC data sets, scROSHI outperforms competing methods when training data are limited or the diversity between experiments is large.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • ↵** Full author list provided in the supplements

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 4.0 International license.
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Posted April 08, 2022.
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scROSHI - robust supervised hierarchical identification of single cells
Michael Prummer, Anne Bertolini, Lars Bosshard, Florian Barkmann, Josephine Yates, Valentina Boeva, The TumorProfiler Consortium, Daniel Stekhoven, Franziska Singer
bioRxiv 2022.04.05.487176; doi: https://doi.org/10.1101/2022.04.05.487176
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scROSHI - robust supervised hierarchical identification of single cells
Michael Prummer, Anne Bertolini, Lars Bosshard, Florian Barkmann, Josephine Yates, Valentina Boeva, The TumorProfiler Consortium, Daniel Stekhoven, Franziska Singer
bioRxiv 2022.04.05.487176; doi: https://doi.org/10.1101/2022.04.05.487176

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