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10.1101/2022.02.04.479209

http://scihub22266oqcxt.onion/10.1101/2022.02.04.479209
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35169794!8845414!35169794
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suck abstract from ncbi


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pmid35169794      bioRxiv 2022 ; ä (ä): ä
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  • Comparative analysis of cell-cell communication at single-cell resolution #MMPMID35169794
  • Wilk AJ; Shalek AK; Holmes S; Blish CA
  • bioRxiv 2022[Jul]; ä (ä): ä PMID35169794show ga
  • Inference of cell-cell communication (CCC) from single-cell RNA-sequencing data is a powerful technique to uncover putative axes of multicellular coordination, yet existing methods perform this analysis at the level of the cell type or cluster, discarding single-cell level information. Here we present Scriabin aeuro" a flexible and scalable framework for comparative analysis of CCC at single-cell resolution. We leverage multiple published datasets to show that Scriabin recovers expected CCC edges and use spatial transcriptomic data, genetic perturbation screens, and direct experimental manipulation of receptor-ligand interactions to validate that the recovered edges are biologically meaningful. We then apply Scriabin to uncover co-expressed programs of CCC from atlas-scale datasets, validating known communication pathways required for maintaining the intestinal stem cell niche and revealing species-specific communication pathways. Finally, we utilize single-cell communication networks calculated using Scriabin to follow communication pathways that operate between timepoints in longitudinal datasets, highlighting bystander cells as important initiators of inflammatory reactions in acute SARS-CoV-2 infection. Our approach represents a broadly applicable strategy to leverage single-cell resolution data maximally toward uncovering CCC circuitry and rich niche-phenotype relationships in health and disease.
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