Learning and modeling the molecular response of single cells to drug perturbations
DeepCell aims to model cellular responses to drug perturbations using multiomics and deep learning, facilitating optimal treatment design and expediting drug discovery in clinical settings.
Projectdetails
Introduction
Advances in single-cell genomics (SCG) allow us to read out a cell's molecular state with unprecedented detail, increasingly so across perturbations. To fully understand a cellular system, one must be able to predict its internal state in response to all perturbations. Yet such modeling in SCG is currently limited to descriptive statistics.
Proposal
Building upon my expertise in machine learning, I propose to systematically model a cell's behavior under perturbation, focusing on the largely untouched area of drug-induced perturbations with multiomics SCG readouts. A sufficiently generic model will predict perturbed cellular states, enabling the design of optimal treatments in new cell types.
Pilot Study
In a pilot study, we predicted gene expression changes of a cell ensemble in response to stimuli. DeepCell builds upon this approach: Based on a multi-condition, multi-modal deep-learning approach for both normal and spatially-resolved genomics, we will set up a constrained, interpretable model for the cellular expression response to diverse perturbations.
Model Flexibility
The added flexibility of the DeepCell model versus classical small-scale systems biology models will allow us to:
- Interrogate the effects of combined drug stimuli.
- Characterize the gene regulatory landscape by interpretation of the learned deep network.
Unique Possibilities
DeepCell provides unique possibilities to capitalize on cell-based drug screens to address fundamental questions in gene regulation and predicting treatment outcomes. As a proof of concept, I will identify targets that regulate enteroendocrine lineage selection in the intestine.
Experimental Setup
I will set up a 500-compound single-cell organoid RNA-seq screen based on compounds from a spatial imaging screen across 200,000 intestinal organoids, both of which we will model with DeepCell. We will leverage those models to predict optimal treatment for obese mice.
Conclusion
DeepCell opens up the possibility of in silico drug screens, with the potential to expedite drug discovery and impact clinical settings.
Financiële details & Tijdlijn
Financiële details
Subsidiebedrag | € 2.497.298 |
Totale projectbegroting | € 2.497.298 |
Tijdlijn
Startdatum | 1-1-2023 |
Einddatum | 31-12-2027 |
Subsidiejaar | 2023 |
Partners & Locaties
Projectpartners
- HELMHOLTZ ZENTRUM MUENCHEN DEUTSCHES FORSCHUNGSZENTRUM FUER GESUNDHEIT UND UMWELT GMBHpenvoerder
- GENOME RESEARCH LIMITED
- GENOME RESEARCH LIMITED
Land(en)
Vergelijkbare projecten binnen European Research Council
Project | Regeling | Bedrag | Jaar | Actie |
---|---|---|---|---|
MANUNKIND: Determinants and Dynamics of Collaborative ExploitationThis project aims to develop a game theoretic framework to analyze the psychological and strategic dynamics of collaborative exploitation, informing policies to combat modern slavery. | ERC STG | € 1.497.749 | 2022 | Details |
Elucidating the phenotypic convergence of proliferation reduction under growth-induced pressureThe UnderPressure project aims to investigate how mechanical constraints from 3D crowding affect cell proliferation and signaling in various organisms, with potential applications in reducing cancer chemoresistance. | ERC STG | € 1.498.280 | 2022 | Details |
Uncovering the mechanisms of action of an antiviral bacteriumThis project aims to uncover the mechanisms behind Wolbachia's antiviral protection in insects and develop tools for studying symbiont gene function. | ERC STG | € 1.500.000 | 2023 | Details |
The Ethics of Loneliness and SociabilityThis project aims to develop a normative theory of loneliness by analyzing ethical responsibilities of individuals and societies to prevent and alleviate loneliness, establishing a new philosophical sub-field. | ERC STG | € 1.025.860 | 2023 | Details |
MANUNKIND: Determinants and Dynamics of Collaborative Exploitation
This project aims to develop a game theoretic framework to analyze the psychological and strategic dynamics of collaborative exploitation, informing policies to combat modern slavery.
Elucidating the phenotypic convergence of proliferation reduction under growth-induced pressure
The UnderPressure project aims to investigate how mechanical constraints from 3D crowding affect cell proliferation and signaling in various organisms, with potential applications in reducing cancer chemoresistance.
Uncovering the mechanisms of action of an antiviral bacterium
This project aims to uncover the mechanisms behind Wolbachia's antiviral protection in insects and develop tools for studying symbiont gene function.
The Ethics of Loneliness and Sociability
This project aims to develop a normative theory of loneliness by analyzing ethical responsibilities of individuals and societies to prevent and alleviate loneliness, establishing a new philosophical sub-field.
Vergelijkbare projecten uit andere regelingen
Project | Regeling | Bedrag | Jaar | Actie |
---|---|---|---|---|
Decoding the Multi-facets of Cellular Identity from Single-cell DataDevelop computational methods combining machine learning and dynamical systems to analyze single-cell data, uncovering cellular identities and interactions to enhance understanding of multicellular systems in health and disease. | ERC STG | € 1.484.125 | 2022 | Details |
Revealing cellular behavior with single-cell multi-omicsDevelop a single-cell multi-omics approach to analyze β-cell heterogeneity and metabolism, aiming to uncover insights into diabetes-related dysfunction and potential treatment targets. | ERC STG | € 2.499.864 | 2022 | Details |
Integration of single-cell multi-omics data across space and time to unlock cellular trajectoriesMULTIview-CELL aims to integrate multi-omics single-cell data using novel MML approaches to uncover spatiotemporal cell trajectories and molecular regulators, enhancing biological understanding and health outcomes. | ERC STG | € 1.285.938 | 2024 | Details |
Precision Lethality to overcome clonal heterogeneity in high-risk neuroblastomaThis project aims to develop precision lethality methodologies using cell barcoding to identify effective drug combinations for treating neuroblastoma, overcoming clonal heterogeneity. | ERC STG | € 1.497.981 | 2024 | Details |
Decoding the Multi-facets of Cellular Identity from Single-cell Data
Develop computational methods combining machine learning and dynamical systems to analyze single-cell data, uncovering cellular identities and interactions to enhance understanding of multicellular systems in health and disease.
Revealing cellular behavior with single-cell multi-omics
Develop a single-cell multi-omics approach to analyze β-cell heterogeneity and metabolism, aiming to uncover insights into diabetes-related dysfunction and potential treatment targets.
Integration of single-cell multi-omics data across space and time to unlock cellular trajectories
MULTIview-CELL aims to integrate multi-omics single-cell data using novel MML approaches to uncover spatiotemporal cell trajectories and molecular regulators, enhancing biological understanding and health outcomes.
Precision Lethality to overcome clonal heterogeneity in high-risk neuroblastoma
This project aims to develop precision lethality methodologies using cell barcoding to identify effective drug combinations for treating neuroblastoma, overcoming clonal heterogeneity.