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10.1038/s41598-021-83105-3 http://scihub22266oqcxt.onion/10.1038/s41598-021-83105-3 33568759!7876117!33568759     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=33568759&cmd=llinks): Failed to open stream: HTTP request failed! 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Genomic mutations and changes in protein secondary structure and solvent accessibility of SARS-CoV-2 (COVID-19 virus) |pdf=|usr=}}{{33568759}} gab.com Text Genomic mutations and changes in protein secondary structure and solvent accessibility of SARS-CoV-2 (COVID-19 virus) JO: Sci Rep http://www.kidney.de/pget.php?&tw=1&pmid=33568759 #FOAvip Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a highly pathogenic virus that has caused the global COVID-19 pandemic. Tracing the evolution and transmission of the virus is crucial to respond to and control the pandemic through appropriate intervention strategies. This paper reports and analyses genomic mutations in the coding regions of SARS-CoV-2 and their probable protein secondary structure and solvent accessibility changes, which are predicted using deep learning models. Prediction results suggest that mutation D614G in the virus spike protein, which has attracted much attention from researchers, is unlikely to make changes in protein secondary structure and relative solvent accessibility. Based on 6324 viral genome sequences, we create a spreadsheet dataset of point mutations that can facilitate the investigation of SARS-CoV-2 in many perspectives, especially in tracing the evolution and worldwide spread of the virus. Our analysis results also show that coding genes E, M, ORF6, ORF7a, ORF7b and ORF10 are most stable, potentially suitable to be targeted for vaccine and drug development. Twit Text FOAVip Genomic mutations and changes in protein secondary structure and solvent accessibility of SARS-CoV-2 (COVID-19 virus) ????Sci Rep http://www.kidney.de/pget.php?&tw=1&pmid=33568759 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=33568759 #FOAvip English Wikipedia <ref>{{Cite pmid|33568759}}</ref> Genomic mutations and changes in protein secondary structure and solvent accessibility of SARS-CoV-2 (COVID-19 virus) #MMPMID33568759 Nguyen TT; Pathirana PN; Nguyen T; Nguyen QVH; Bhatti A; Nguyen DC; Nguyen DT; Nguyen ND; Creighton D; Abdelrazek M Sci Rep 2021[Feb]; 11 (1): 3487 PMID33568759show ga Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a highly pathogenic virus that has caused the global COVID-19 pandemic. Tracing the evolution and transmission of the virus is crucial to respond to and control the pandemic through appropriate intervention strategies. This paper reports and analyses genomic mutations in the coding regions of SARS-CoV-2 and their probable protein secondary structure and solvent accessibility changes, which are predicted using deep learning models. Prediction results suggest that mutation D614G in the virus spike protein, which has attracted much attention from researchers, is unlikely to make changes in protein secondary structure and relative solvent accessibility. Based on 6324 viral genome sequences, we create a spreadsheet dataset of point mutations that can facilitate the investigation of SARS-CoV-2 in many perspectives, especially in tracing the evolution and worldwide spread of the virus. Our analysis results also show that coding genes E, M, ORF6, ORF7a, ORF7b and ORF10 are most stable, potentially suitable to be targeted for vaccine and drug development. |*Genome, Viral[MESH] |*Mutation[MESH] |*Protein Structure, Secondary[MESH] |COVID-19/*virology[MESH] |DNA, Viral[MESH] |Genomics[MESH] |Humans[MESH] |SARS-CoV-2/*genetics/metabolism[MESH]Genomic mutations and changes in protein secondary structure and solve(epmc).pdf DeepDyve Pubget Overpricing