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10.1016/j.ygeno.2020.09.019 http://scihub22266oqcxt.onion/10.1016/j.ygeno.2020.09.019 32920121!7500163!32920121     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=32920121&cmd=llinks): Failed to open stream: HTTP request failed! 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SARS-CoV-2 transcriptome analysis and molecular cataloguing of immunodominant epitopes for multi-epitope based vaccine design |pdf=|usr=}}{{32920121}} gab.com Text SARS-CoV-2 transcriptome analysis and molecular cataloguing of immunodominant epitopes for multi-epitope based vaccine design JO: Genomics http://www.kidney.de/pget.php?&tw=1&pmid=32920121 #FOAvip Genomics-led researches are engaged in tracing virus expression pattern, and induced immune responses in human to develop effective vaccine against COVID-19. In this study, targeted expression profiling and differential gene expression analysis of major histocompatibility complexes and innate immune system genes were performed through SARS-CoV-2 infected RNA-seq data of human cell line, and virus transcriptome was generated for T-and B-cell epitope prediction. Docking studies of epitopes with MHC and B-cell receptors were performed to identify potential T-and B-cell epitopes. Transcriptome analysis revealed the specific multiple allele expressions in cell line, genes for elicited induce immune response, and virus gene expression. Proposed T- and B-cell epitopes have high potential to elicit equivalent immune responses caused by SARS-CoV-2 infection which can be useful to provide links between elicited immune response and virus gene expression. This study will facilitate in vitro and in vivo vaccine related research studies in disease control. Twit Text FOAVip SARS-CoV-2 transcriptome analysis and molecular cataloguing of immunodominant epitopes for multi-epitope based vaccine design ????Genomics http://www.kidney.de/pget.php?&tw=1&pmid=32920121 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=32920121 #FOAvip English Wikipedia <ref>{{Cite pmid|32920121}}</ref> SARS-CoV-2 transcriptome analysis and molecular cataloguing of immunodominant epitopes for multi-epitope based vaccine design #MMPMID32920121 Kushwaha SK; Kesarwani V; Choudhury S; Gandhi S; Sharma S Genomics 2020[Nov]; 112 (6): 5044-5054 PMID32920121show ga Genomics-led researches are engaged in tracing virus expression pattern, and induced immune responses in human to develop effective vaccine against COVID-19. In this study, targeted expression profiling and differential gene expression analysis of major histocompatibility complexes and innate immune system genes were performed through SARS-CoV-2 infected RNA-seq data of human cell line, and virus transcriptome was generated for T-and B-cell epitope prediction. Docking studies of epitopes with MHC and B-cell receptors were performed to identify potential T-and B-cell epitopes. Transcriptome analysis revealed the specific multiple allele expressions in cell line, genes for elicited induce immune response, and virus gene expression. Proposed T- and B-cell epitopes have high potential to elicit equivalent immune responses caused by SARS-CoV-2 infection which can be useful to provide links between elicited immune response and virus gene expression. This study will facilitate in vitro and in vivo vaccine related research studies in disease control. |*COVID-19 Vaccines[MESH] |B-Lymphocytes/immunology[MESH] |COVID-19/genetics/*immunology[MESH] |Computational Biology[MESH] |Epitopes, T-Lymphocyte/genetics/immunology[MESH] |Gene Expression Profiling[MESH] |Genes, MHC Class I[MESH] |Genes, MHC Class II[MESH] |Humans[MESH] |Immunity, Innate/genetics[MESH] |Immunodominant Epitopes/chemistry/*genetics/metabolism[MESH] |Molecular Docking Simulation[MESH]SARS-CoV-2 transcriptome analysis and molecular cataloguing of immunod(epmc).pdf DeepDyve Pubget Overpricing