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10.1093/bib/bbab372

http://scihub22266oqcxt.onion/10.1093/bib/bbab372
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34535795!ä!34535795

suck abstract from ncbi


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pmid34535795      Brief+Bioinform 2022 ; 23 (1): ä
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  • Network-based analysis revealed significant interactions between risk genes of severe COVID-19 and host genes interacted with SARS-CoV-2 proteins #MMPMID34535795
  • Qi HX; Shen QD; Zhao HY; Qi GZ; Gao L
  • Brief Bioinform 2022[Jan]; 23 (1): ä PMID34535795show ga
  • Whether risk genes of severe coronavirus disease 2019 (COVID-19) from genome-wide association study could play their regulatory roles by interacting with host genes that were interacted with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) proteins was worthy of exploration. In this study, we implemented a network-based approach by developing a user-friendly software Network Calculator (https://github.com/Haoxiang-Qi/Network-Calculator.git). By using Network Calculator, we identified a network composed of 13 risk genes and 28 SARS-CoV-2 interacted host genes that had the highest network proximity with each other, with a hub gene HNRNPK identified. Among these genes, 14 of them were identified to be differentially expressed in RNA-seq data from severe COVID-19 cases. Besides, by expression enrichment analysis in single-cell RNA-seq data, compared with mild COVID-19, these genes were significantly enriched in macrophage, T cell and epithelial cell for severe COVID-19. Meanwhile, 74 pathways were significantly enriched. Our analysis provided insights for the underlying genetic etiology of severe COVID-19 from the perspective of network biology.
  • |*COVID-19/genetics/metabolism[MESH]
  • |*RNA-Seq[MESH]
  • |*SARS-CoV-2/genetics/metabolism[MESH]
  • |*Viral Proteins/genetics/metabolism[MESH]
  • |Genome-Wide Association Study[MESH]
  • |Humans[MESH]
  • |Patient Acuity[MESH]


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