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10.1016/j.csbj.2020.11.054

http://scihub22266oqcxt.onion/10.1016/j.csbj.2020.11.054
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33312454!7719280!33312454
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suck abstract from ncbi


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pmid33312454      Comput+Struct+Biotechnol+J 2020 ; 18 (ä): 3947-3949
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  • L1000 connectivity map interrogation identifies candidate drugs for repurposing as SARS-CoV-2 antiviral therapies #MMPMID33312454
  • Sendama W
  • Comput Struct Biotechnol J 2020[]; 18 (ä): 3947-3949 PMID33312454show ga
  • Adaptive clinical trials are underway to determine the efficacy of potential therapies for COVID-19, with flexibility to include emerging therapies if there is sufficient preclinical evidence for their potential utility. In silico screening of connectivity maps, which link gene expression profiles to libraries of perturbagens, may facilitate the identification of such emerging therapies. The L1000 Connectivity Map is built from samples of transcripts taken from gene expression profiles of cells in various experimental conditions followed by computational inferences of the remainder of the transcriptome. Searching the L1000 Connectivity Map for modulators of a protease that facilitates coronavirus infection identifies plausible candidate drugs for repurposing as antiviral agents against SARS-CoV-2 following further investigation.
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