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Learning Single-Cell Perturbation Responses using Neural Optimal Transport

Charlotte Bunne, View ORCID ProfileStefan G. Stark, View ORCID ProfileGabriele Gut, Jacobo Sarabia del Castillo, View ORCID ProfileKjong-Van Lehmann, View ORCID ProfileLucas Pelkmans, View ORCID ProfileAndreas Krause, View ORCID ProfileGunnar Rätsch
doi: https://doi.org/10.1101/2021.12.15.472775
Charlotte Bunne
1Department of Computer Science, ETH Zurich, Switzerland
2AI Center, ETH Zurich, Switzerland
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Stefan G. Stark
1Department of Computer Science, ETH Zurich, Switzerland
2AI Center, ETH Zurich, Switzerland
3Medical Informatics Unit, University Hospital Zurich, Switzerland
4Swiss Institute of Bioinformatics, Switzerland
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  • ORCID record for Stefan G. Stark
Gabriele Gut
5Department of Molecular Life Sciences, University of Zurich, Switzerland
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Jacobo Sarabia del Castillo
5Department of Molecular Life Sciences, University of Zurich, Switzerland
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Kjong-Van Lehmann
1Department of Computer Science, ETH Zurich, Switzerland
2AI Center, ETH Zurich, Switzerland
3Medical Informatics Unit, University Hospital Zurich, Switzerland
4Swiss Institute of Bioinformatics, Switzerland
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  • For correspondence: kjlehmann@ukaachen.de lucas.pelkmans@mls.uzh.ch krausea@inf.ethz.ch raetsch@inf.ethz.ch
Lucas Pelkmans
5Department of Molecular Life Sciences, University of Zurich, Switzerland
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  • For correspondence: kjlehmann@ukaachen.de lucas.pelkmans@mls.uzh.ch krausea@inf.ethz.ch raetsch@inf.ethz.ch
Andreas Krause
1Department of Computer Science, ETH Zurich, Switzerland
2AI Center, ETH Zurich, Switzerland
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  • For correspondence: kjlehmann@ukaachen.de lucas.pelkmans@mls.uzh.ch krausea@inf.ethz.ch raetsch@inf.ethz.ch
Gunnar Rätsch
1Department of Computer Science, ETH Zurich, Switzerland
2AI Center, ETH Zurich, Switzerland
3Medical Informatics Unit, University Hospital Zurich, Switzerland
4Swiss Institute of Bioinformatics, Switzerland
6Department of Biology, ETH Zurich, Switzerland
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  • For correspondence: kjlehmann@ukaachen.de lucas.pelkmans@mls.uzh.ch krausea@inf.ethz.ch raetsch@inf.ethz.ch
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Abstract

The ability to understand and predict molecular responses towards external perturbations is a core question in molecular biology. Technological advancements in the recent past have enabled the generation of high-resolution single-cell data, making it possible to profile individual cells under different experimentally controlled perturbations. However, cells are typically destroyed during measurement, resulting in unpaired distributions over either perturbed or non-perturbed cells. Leveraging the theory of optimal transport and the recent advents of convex neural architectures, we learn a coupling describing the response of cell populations upon perturbation, enabling us to predict state trajectories on a single-cell level. We apply our approach, CellOT, to predict treatment responses of 21,650 cells subject to four different drug perturbations. CellOT outperforms current state-of-the-art methods both qualitatively and quantitatively, accurately capturing cellular behavior shifts across all different drugs.

Competing Interest Statement

G.G. and L.P. have filed a patent on the 4i technology (patentWO2019207004A1).

Footnotes

  • http://tu-pro.ch/

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 December 15, 2021.
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Learning Single-Cell Perturbation Responses using Neural Optimal Transport
Charlotte Bunne, Stefan G. Stark, Gabriele Gut, Jacobo Sarabia del Castillo, Kjong-Van Lehmann, Lucas Pelkmans, Andreas Krause, Gunnar Rätsch
bioRxiv 2021.12.15.472775; doi: https://doi.org/10.1101/2021.12.15.472775
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Learning Single-Cell Perturbation Responses using Neural Optimal Transport
Charlotte Bunne, Stefan G. Stark, Gabriele Gut, Jacobo Sarabia del Castillo, Kjong-Van Lehmann, Lucas Pelkmans, Andreas Krause, Gunnar Rätsch
bioRxiv 2021.12.15.472775; doi: https://doi.org/10.1101/2021.12.15.472775

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