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- W4319791230 abstract "Abstract Cell-cell interaction networks are pivotal in cancer development and treatment response. These networks can be inferred from data; however, this process often combines data from multiple patients, and/or creates networks on a cell-types level. It creates a good average overview of cell-cell interaction networks but fails to capture patient heterogeneity and/or masks potentially relevant local network structures. We propose a mathematical model based on random graphs (called RaCInG) to alleviate these issues using prior knowledge on potential cellular interactions and patient’s bulk RNA-seq data. We have applied RaCInG to extract 444 network features related to the tumor microenvironment, unveiled associations with immune response and subtypes, and identified cancer-type specific differences in inter-cellular signaling. Additionally, we have used RaCInG to explain how immune phenotypes regulated by context-specific intercellular communication affect immunotherapy response. RaCInG is a modular pipeline, and we envision its application for cell-cell interaction reconstruction in different contexts." @default.
- W4319791230 created "2023-02-11" @default.
- W4319791230 creator A5016886168 @default.
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- W4319791230 creator A5082488664 @default.
- W4319791230 date "2023-02-04" @default.
- W4319791230 modified "2023-10-14" @default.
- W4319791230 title "Mathematically mapping the network of cells in the tumor microenvironment" @default.
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- W4319791230 doi "https://doi.org/10.1101/2023.02.03.526946" @default.
- W4319791230 hasPublicationYear "2023" @default.
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