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  1. Article: Mutational Frequencies of SARS-CoV-2 Genome during the Beginning Months of the Outbreak in USA.

    Kaushal, Neha / Gupta, Yogita / Goyal, Mehendi / Khaiboullina, Svetlana F / Baranwal, Manoj / Verma, Subhash C

    Pathogens (Basel, Switzerland)

    2020  Volume 9, Issue 7

    Abstract: ... accumulation over a period of 11 weeks (submitted between 19th January to 15 April 2020) in USA SARS-CoV-2 ... SARS-CoV-2 has spread very quickly from its first reported case on 19 January 2020 ... a basis for a better understanding of the genetic variation in SARS-CoV-2 circulating ...

    Abstract SARS-CoV-2 has spread very quickly from its first reported case on 19 January 2020 in the United Stated of America, leading WHO to declare pandemic by 11 March 2020. RNA viruses accumulate mutations following replication and passage in human population, which prompted us to determine the rate and the regions (hotspots) of the viral genome with high rates of mutation. We analyzed the rate of mutation accumulation over a period of 11 weeks (submitted between 19th January to 15 April 2020) in USA SARS-CoV-2 genome. Our analysis identified that majority of the viral genes accumulated mutations, although with varying rates and these included NSP2, NSP3, RdRp, helicase, Spike, ORF3a, ORF8, and Nucleocapsid protein. Sixteen mutations accumulated in Spike protein in which four mutations are located in the receptor binding domain. Intriguingly, we identified a fair number of viral proteins (NSP7, NSP9, NSP10, NSP11, Envelop, ORF6, and ORF7b proteins), which did not accumulate any mutation. Limited changes in these proteins may suggest that they have conserved functions, which are essential for virus propagation. This provides a basis for a better understanding of the genetic variation in SARS-CoV-2 circulating in the US, which could help in identifying potential therapeutic targets for controlling COVID-19.
    Keywords covid19
    Language English
    Publishing date 2020-07-13
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2695572-6
    ISSN 2076-0817
    ISSN 2076-0817
    DOI 10.3390/pathogens9070565
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Mutational Frequencies of SARS-CoV-2 Genome during the Beginning Months of the Outbreak in USA

    Neha Kaushal / Yogita Gupta / Mehendi Goyal / Svetlana F. Khaiboullina / Manoj Baranwal / Subhash C. Verma

    Pathogens, Vol 9, Iss 565, p

    2020  Volume 565

    Abstract: ... accumulation over a period of 11 weeks (submitted between 19 th January to 15 th April 2020) in USA SARS-CoV-2 ... SARS-CoV-2 has spread very quickly from its first reported case on January 19 th , 2020 ... a basis for a better understanding of the genetic variation in SARS-CoV-2 circulating ...

    Abstract : SARS-CoV-2 has spread very quickly from its first reported case on January 19 th , 2020 in the United Stated of America, leading WHO to declare pandemic by March 11 th , 2020. RNA viruses accumulate mutations following replication and passage in human population, which prompted us to determine the rate and the regions (hotspots) of the viral genome with high rates of mutation. We analyzed the rate of mutation accumulation over a period of 11 weeks (submitted between 19 th January to 15 th April 2020) in USA SARS-CoV-2 genome. Our analysis identified that majority of the viral genes accumulated mutations, although with varying rates and these included NSP2, NSP3, RdRp, helicase, Spike, ORF3a, ORF8, and Nucleocapsid protein. Sixteen mutations accumulated in Spike protein in which four mutations are located in the receptor binding domain. Intriguingly, we identified a fair number of viral proteins (NSP7, NSP9, NSP10, NSP11, Envelop, ORF6, and ORF7b proteins), which did not accumulate any mutation. Limited changes in these proteins may suggest that they have conserved functions, which are essential for virus propagation. This provides a basis for a better understanding of the genetic variation in SARS-CoV-2 circulating in the US, which could help in identifying potential therapeutic targets for controlling COVID-19.
    Keywords SARS-CoV2 ; genome ; mutation ; bioinformatics ; Medicine ; R ; covid19
    Subject code 333
    Language English
    Publishing date 2020-07-01T00:00:00Z
    Publisher MDPI AG
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  3. Article: Mutational Frequencies of SARS-CoV-2 Genome during the Beginning Months of the Outbreak in USA

    Kaushal, N. / Gupta, Y. / Goyal, M. / Khaiboullina, S. F. / Baranwal, M. / Verma, S. C.

    Pathogens (Basel, Switzerland)

    Abstract: ... accumulation over a period of 11 weeks (submitted between 19th January to 15 April 2020) in USA SARS-CoV-2 ... SARS-CoV-2 has spread very quickly from its first reported case on 19 January 2020 ... a basis for a better understanding of the genetic variation in SARS-CoV-2 circulating ...

    Abstract SARS-CoV-2 has spread very quickly from its first reported case on 19 January 2020 in the United Stated of America, leading WHO to declare pandemic by 11 March 2020 RNA viruses accumulate mutations following replication and passage in human population, which prompted us to determine the rate and the regions (hotspots) of the viral genome with high rates of mutation We analyzed the rate of mutation accumulation over a period of 11 weeks (submitted between 19th January to 15 April 2020) in USA SARS-CoV-2 genome Our analysis identified that majority of the viral genes accumulated mutations, although with varying rates and these included NSP2, NSP3, RdRp, helicase, Spike, ORF3a, ORF8, and Nucleocapsid protein Sixteen mutations accumulated in Spike protein in which four mutations are located in the receptor binding domain Intriguingly, we identified a fair number of viral proteins (NSP7, NSP9, NSP10, NSP11, Envelop, ORF6, and ORF7b proteins), which did not accumulate any mutation Limited changes in these proteins may suggest that they have conserved functions, which are essential for virus propagation This provides a basis for a better understanding of the genetic variation in SARS-CoV-2 circulating in the US, which could help in identifying potential therapeutic targets for controlling COVID-19
    Keywords covid19
    Publisher WHO
    Document type Article
    Note WHO #Covidence: #646540
    Database COVID19

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