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10.1101/gr.268961.120

http://scihub22266oqcxt.onion/10.1101/gr.268961.120
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33602693!8015855!33602693
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suck abstract from ncbi


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pmid33602693      Genome+Res 2021 ; 31 (4): 635-644
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  • SARS-CoV-2 genomic diversity and the implications for qRT-PCR diagnostics and transmission #MMPMID33602693
  • Sapoval N; Mahmoud M; Jochum MD; Liu Y; Elworth RAL; Wang Q; Albin D; Ogilvie HA; Lee MD; Villapol S; Hernandez KM; Maljkovic Berry I; Foox J; Beheshti A; Ternus K; Aagaard KM; Posada D; Mason CE; Sedlazeck FJ; Treangen TJ
  • Genome Res 2021[Apr]; 31 (4): 635-644 PMID33602693show ga
  • The COVID-19 pandemic has sparked an urgent need to uncover the underlying biology of this devastating disease. Though RNA viruses mutate more rapidly than DNA viruses, there are a relatively small number of single nucleotide polymorphisms (SNPs) that differentiate the main SARS-CoV-2 lineages that have spread throughout the world. In this study, we investigated 129 RNA-seq data sets and 6928 consensus genomes to contrast the intra-host and inter-host diversity of SARS-CoV-2. Our analyses yielded three major observations. First, the mutational profile of SARS-CoV-2 highlights intra-host single nucleotide variant (iSNV) and SNP similarity, albeit with differences in C > U changes. Second, iSNV and SNP patterns in SARS-CoV-2 are more similar to MERS-CoV than SARS-CoV-1. Third, a significant fraction of insertions and deletions contribute to the genetic diversity of SARS-CoV-2. Altogether, our findings provide insight into SARS-CoV-2 genomic diversity, inform the design of detection tests, and highlight the potential of iSNVs for tracking the transmission of SARS-CoV-2.
  • |*Genetic Variation[MESH]
  • |*Genome, Viral[MESH]
  • |COVID-19/*diagnosis/*transmission/virology[MESH]
  • |Host-Pathogen Interactions[MESH]
  • |Humans[MESH]
  • |Polymorphism, Single Nucleotide[MESH]
  • |Real-Time Polymerase Chain Reaction/*methods[MESH]


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