Summary
The advent of single cell technologies has enabled the characterization of cell types and developmental processes. Observations from different cells allow one to identify underlying patterns at higher resolution than convoluted bulk data, and integration of different omics data can yield a more differentiated picture of mechanistic connections. In this proposal, Gene REgulatory Cell States (GReCS) from multi-modal data, I plan to develop a computational method that combines these aspects to generate insights into gene regulation at the level of single cells.
Measurements of chromatin accessibility in single cells are becoming increasingly common. The method I propose to develop combines sc/sn-ATAC- and scRNA-sequencing data to characterize gene regulation. My approach will integrate and use transcriptomics and open chromatin data to filter comprehensive prior information about candidate interactions and predict cell-specific gene regulatory network versions using machine learning, while sparse single cell measurements are imputed using local cell similarities. In this way, rare measurements across cell types and a larger condition space for network inference can be exploited, using the natural potential of chromatin accessibility data as a filter to map interactions into a cell-specific context.
A distinguishing feature of the proposed method is the characterization of local gene regulatory states, which allows the observation of continuous changes throughout a cell-cell similarity embedding. This will be useful to examine changes during cell differentiation and along gradients in spatial reconstructions, for example of embryonic development. The developed methods will be made available to the community as a computational toolkit to improve the characterization of gene regulation by combining different types of data.
Measurements of chromatin accessibility in single cells are becoming increasingly common. The method I propose to develop combines sc/sn-ATAC- and scRNA-sequencing data to characterize gene regulation. My approach will integrate and use transcriptomics and open chromatin data to filter comprehensive prior information about candidate interactions and predict cell-specific gene regulatory network versions using machine learning, while sparse single cell measurements are imputed using local cell similarities. In this way, rare measurements across cell types and a larger condition space for network inference can be exploited, using the natural potential of chromatin accessibility data as a filter to map interactions into a cell-specific context.
A distinguishing feature of the proposed method is the characterization of local gene regulatory states, which allows the observation of continuous changes throughout a cell-cell similarity embedding. This will be useful to examine changes during cell differentiation and along gradients in spatial reconstructions, for example of embryonic development. The developed methods will be made available to the community as a computational toolkit to improve the characterization of gene regulation by combining different types of data.
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More information & hyperlinks
| Web resources: | https://cordis.europa.eu/project/id/101026233 |
| Start date: | 15-11-2021 |
| End date: | 14-11-2023 |
| Total budget - Public funding: | 224 933,76 Euro - 224 933,00 Euro |
Cordis data
Original description
The advent of single cell technologies has enabled the characterization of cell types and developmental processes. Observations from different cells allow one to identify underlying patterns at higher resolution than convoluted bulk data, and integration of different omics data can yield a more differentiated picture of mechanistic connections. In this proposal, Gene REgulatory Cell States (GReCS) from multi-modal data, I plan to develop a computational method that combines these aspects to generate insights into gene regulation at the level of single cells.Measurements of chromatin accessibility in single cells are becoming increasingly common. The method I propose to develop combines sc/sn-ATAC- and scRNA-sequencing data to characterize gene regulation. My approach will integrate and use transcriptomics and open chromatin data to filter comprehensive prior information about candidate interactions and predict cell-specific gene regulatory network versions using machine learning, while sparse single cell measurements are imputed using local cell similarities. In this way, rare measurements across cell types and a larger condition space for network inference can be exploited, using the natural potential of chromatin accessibility data as a filter to map interactions into a cell-specific context.
A distinguishing feature of the proposed method is the characterization of local gene regulatory states, which allows the observation of continuous changes throughout a cell-cell similarity embedding. This will be useful to examine changes during cell differentiation and along gradients in spatial reconstructions, for example of embryonic development. The developed methods will be made available to the community as a computational toolkit to improve the characterization of gene regulation by combining different types of data.
Status
CLOSEDCall topic
MSCA-IF-2020Update Date
28-04-2024
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EU-Programme-Call
Horizon 2020
H2020-EU.1. EXCELLENT SCIENCE
H2020-EU.1.3. EXCELLENT SCIENCE - Marie Skłodowska-Curie Actions (MSCA)
H2020-EU.1.3.2. Nurturing excellence by means of cross-border and cross-sector mobility
H2020-MSCA-IF-2020
MSCA-IF-2020 Individual Fellowships
