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JUMPn: A Streamlined Application for Protein Co-Expression Clustering and Network Analysis in Proteomics
Published on: October 19, 2021
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Bayesian hierarchical models for protein networks in single-cell mass cytometry
Riten Mitra1, Peter Müller2, Peng Qiu3
1Department of Bioinformatics and Biostatistics, University of Louisville, Louisville, KY, USA.
Cancer Informatics
|January 10, 2015
Summary
We developed new Bayesian models to analyze single-cell proteomics data, revealing protein functional networks and identifying differences between experimental conditions. This approach helps uncover molecular interactions within individual cells.
Area of Science:
- Proteomics
- Systems Biology
- Cellular Biology
Background:
- Understanding protein functional networks is crucial for deciphering cellular mechanisms.
- Single-cell proteomics offers high-resolution insights into protein expression within individual cells.
- Mass cytometry generates large-scale, multi-marker protein expression data from single cells.
Purpose of the Study:
- To develop and apply hierarchical Bayesian models for analyzing single-cell proteomics data.
- To investigate protein functional networks and identify differential networks across experimental conditions.
- To visualize and interpret the links between experimental agents and targeted proteins.
Main Methods:
- Utilized a novel dataset from single-cell mass cytometry experiments.
- Applied hierarchical Bayesian models to model protein expression in tens of thousands of single cells.
- Developed a method for novel visualization of differential networks based on posterior inference.
Main Results:
- Successfully constructed protein functional networks under various experimental conditions.
- Identified and characterized differential networks, highlighting condition-specific molecular interactions.
- Presented a novel visualization method for direct observation of agent-target protein relationships.
Conclusions:
- The proposed Bayesian models provide a powerful tool for studying molecular interactions at the single-cell level.
- The method enables the identification of differential protein functional networks.
- The novel visualization facilitates the understanding of experimental agent effects on protein targets.
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