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Deep generative modeling for quantifying sample-level heterogeneity in single-cell omics

View ORCID ProfilePierre Boyeau, View ORCID ProfileJustin Hong, View ORCID ProfileAdam Gayoso, Michael I. Jordan, Elham Azizi, Nir Yosef
doi: https://doi.org/10.1101/2022.10.04.510898
Pierre Boyeau
1Department of Electrical Engineering and Computer Sciences, University of California, Berkeley
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Justin Hong
2Department of Computer Science, Columbia University
6Irving Institute for Cancer Dynamics, Columbia University
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Adam Gayoso
3Center for Computational Biology, University of California, Berkeley
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Michael I. Jordan
1Department of Electrical Engineering and Computer Sciences, University of California, Berkeley
3Center for Computational Biology, University of California, Berkeley
4Department of Statistics, University of California, Berkeley
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Elham Azizi
2Department of Computer Science, Columbia University
5Department of Biomedical Engineering, Columbia University
6Irving Institute for Cancer Dynamics, Columbia University
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Nir Yosef
1Department of Electrical Engineering and Computer Sciences, University of California, Berkeley
3Center for Computational Biology, University of California, Berkeley
7Department of Systems Immunology, Weizmann Institute of Science
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  • For correspondence: niryosef@berkeley.edu
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Abstract

Contemporary single-cell omics technologies have enabled complex experimental designs incorporating hundreds of samples accompanied by detailed information on sample-level conditions. Current approaches for analyzing condition-level heterogeneity in these experiments often rely on a simplification of the data such as an aggregation at the cell-type or cell-state-neighborhood level. Here we present MrVI, a deep generative model that provides sample-sample comparisons at a single-cell resolution, permitting the discovery of subtle sample-specific effects across cell populations. Additionally, the output of MrVI can be used to quantify the association between sample-level metadata and cell state variation. We benchmarked MrVI against conventional meta-analysis procedures on two synthetic datasets and one real dataset with a well-controlled experimental structure. This work introduces a novel approach to understanding sample-level heterogeneity while leveraging the full resolution of single-cell sequencing data.

Competing Interest Statement

N.Y. is an advisor and/or has equity in Cellarity, Celsius Therapeutics, and Rheos Medicine.

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 4.0 International license.
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Posted October 06, 2022.
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Deep generative modeling for quantifying sample-level heterogeneity in single-cell omics
Pierre Boyeau, Justin Hong, Adam Gayoso, Michael I. Jordan, Elham Azizi, Nir Yosef
bioRxiv 2022.10.04.510898; doi: https://doi.org/10.1101/2022.10.04.510898
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Deep generative modeling for quantifying sample-level heterogeneity in single-cell omics
Pierre Boyeau, Justin Hong, Adam Gayoso, Michael I. Jordan, Elham Azizi, Nir Yosef
bioRxiv 2022.10.04.510898; doi: https://doi.org/10.1101/2022.10.04.510898

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