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 StatementG.G. and L.P. have filed a patent on the 4i technology (patentWO2019207004A1). Show more
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https://doi.org/10.3929/ethz-b-000524354Publication status
publishedExternal links
Journal / series
bioRxivPublisher
Cold Spring Harbor LaboratoryOrganisational unit
09568 - Rätsch, Gunnar / Rätsch, Gunnar
03908 - Krause, Andreas / Krause, Andreas
Funding
180544 - NCCR Catalysis (phase I) (SNF)
Related publications and datasets
Is supplemented by: https://doi.org/10.3929/ethz-b-000609681
Is previous version of: https://doi.org/10.3929/ethz-b-000637174
Has part: https://doi.org/10.3929/ethz-b-000612005
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