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Assessing transmissibility of SARS-CoV-2 lineage B.1.1.7 in England
by
Gonçalves, Sónia
, Volz, Erik
, Chand, Meera
, Johnson, Robert
, Jackson, Ben
, Flaxman, Seth
, Hinsley, Wes R.
, Myers, Richard
, Loman, Nicholas J.
, Harrison, Ian
, Amato, Robert
, Gandy, Axel
, Laydon, Daniel J.
, Mishra, Swapnil
, Groves, Natalie
, Bhatt, Samir
, Barrett, Jeffrey C.
, Gaythorpe, Katy
, Rambaut, Andrew
, Geidelberg, Lily
, Jackson, David K.
, Kwiatkowski, Dominic P.
, McCrone, John T.
, Dabrera, Gavin
, Ragonnet-Cronin, Manon
, Ariani, Cristina V.
, Boyd, Olivia
, Ratmann, Oliver
, Ferguson, Neil M.
, Jorgensen, David
, Hopkins, Susan
, O’Toole, Áine
, Hill, Verity
, Sillitoe, John
in
45
/ 631/181/457
/ 631/326/596/4130
/ 692/699/255/2514
/ Adolescent
/ Adult
/ Age
/ Age composition
/ Age Distribution
/ Age groups
/ Aged
/ Aged, 80 and over
/ Autumn
/ Basic Reproduction Number
/ Biomarkers
/ Child
/ Child, Preschool
/ Coronaviruses
/ COVID-19
/ COVID-19 - diagnosis
/ COVID-19 - epidemiology
/ COVID-19 - transmission
/ COVID-19 - virology
/ COVID-19 diagnostic tests
/ Diagnostic systems
/ Disease transmission
/ England - epidemiology
/ Evolution, Molecular
/ Genome, Viral - genetics
/ Genomes
/ Humanities and Social Sciences
/ Humans
/ Infant
/ Infant, Newborn
/ Latent period
/ Middle Aged
/ multidisciplinary
/ Nucleotide sequence
/ Phylogeny
/ Proteins
/ Public health
/ S gene
/ SARS-CoV-2 - classification
/ SARS-CoV-2 - genetics
/ SARS-CoV-2 - isolation & purification
/ SARS-CoV-2 - pathogenicity
/ Science
/ Science (multidisciplinary)
/ Severe acute respiratory syndrome coronavirus 2
/ Spike Glycoprotein, Coronavirus - analysis
/ Spike Glycoprotein, Coronavirus - genetics
/ Time Factors
/ Trends
/ Young Adult
2021
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Assessing transmissibility of SARS-CoV-2 lineage B.1.1.7 in England
by
Gonçalves, Sónia
, Volz, Erik
, Chand, Meera
, Johnson, Robert
, Jackson, Ben
, Flaxman, Seth
, Hinsley, Wes R.
, Myers, Richard
, Loman, Nicholas J.
, Harrison, Ian
, Amato, Robert
, Gandy, Axel
, Laydon, Daniel J.
, Mishra, Swapnil
, Groves, Natalie
, Bhatt, Samir
, Barrett, Jeffrey C.
, Gaythorpe, Katy
, Rambaut, Andrew
, Geidelberg, Lily
, Jackson, David K.
, Kwiatkowski, Dominic P.
, McCrone, John T.
, Dabrera, Gavin
, Ragonnet-Cronin, Manon
, Ariani, Cristina V.
, Boyd, Olivia
, Ratmann, Oliver
, Ferguson, Neil M.
, Jorgensen, David
, Hopkins, Susan
, O’Toole, Áine
, Hill, Verity
, Sillitoe, John
in
45
/ 631/181/457
/ 631/326/596/4130
/ 692/699/255/2514
/ Adolescent
/ Adult
/ Age
/ Age composition
/ Age Distribution
/ Age groups
/ Aged
/ Aged, 80 and over
/ Autumn
/ Basic Reproduction Number
/ Biomarkers
/ Child
/ Child, Preschool
/ Coronaviruses
/ COVID-19
/ COVID-19 - diagnosis
/ COVID-19 - epidemiology
/ COVID-19 - transmission
/ COVID-19 - virology
/ COVID-19 diagnostic tests
/ Diagnostic systems
/ Disease transmission
/ England - epidemiology
/ Evolution, Molecular
/ Genome, Viral - genetics
/ Genomes
/ Humanities and Social Sciences
/ Humans
/ Infant
/ Infant, Newborn
/ Latent period
/ Middle Aged
/ multidisciplinary
/ Nucleotide sequence
/ Phylogeny
/ Proteins
/ Public health
/ S gene
/ SARS-CoV-2 - classification
/ SARS-CoV-2 - genetics
/ SARS-CoV-2 - isolation & purification
/ SARS-CoV-2 - pathogenicity
/ Science
/ Science (multidisciplinary)
/ Severe acute respiratory syndrome coronavirus 2
/ Spike Glycoprotein, Coronavirus - analysis
/ Spike Glycoprotein, Coronavirus - genetics
/ Time Factors
/ Trends
/ Young Adult
2021
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Assessing transmissibility of SARS-CoV-2 lineage B.1.1.7 in England
by
Gonçalves, Sónia
, Volz, Erik
, Chand, Meera
, Johnson, Robert
, Jackson, Ben
, Flaxman, Seth
, Hinsley, Wes R.
, Myers, Richard
, Loman, Nicholas J.
, Harrison, Ian
, Amato, Robert
, Gandy, Axel
, Laydon, Daniel J.
, Mishra, Swapnil
, Groves, Natalie
, Bhatt, Samir
, Barrett, Jeffrey C.
, Gaythorpe, Katy
, Rambaut, Andrew
, Geidelberg, Lily
, Jackson, David K.
, Kwiatkowski, Dominic P.
, McCrone, John T.
, Dabrera, Gavin
, Ragonnet-Cronin, Manon
, Ariani, Cristina V.
, Boyd, Olivia
, Ratmann, Oliver
, Ferguson, Neil M.
, Jorgensen, David
, Hopkins, Susan
, O’Toole, Áine
, Hill, Verity
, Sillitoe, John
in
45
/ 631/181/457
/ 631/326/596/4130
/ 692/699/255/2514
/ Adolescent
/ Adult
/ Age
/ Age composition
/ Age Distribution
/ Age groups
/ Aged
/ Aged, 80 and over
/ Autumn
/ Basic Reproduction Number
/ Biomarkers
/ Child
/ Child, Preschool
/ Coronaviruses
/ COVID-19
/ COVID-19 - diagnosis
/ COVID-19 - epidemiology
/ COVID-19 - transmission
/ COVID-19 - virology
/ COVID-19 diagnostic tests
/ Diagnostic systems
/ Disease transmission
/ England - epidemiology
/ Evolution, Molecular
/ Genome, Viral - genetics
/ Genomes
/ Humanities and Social Sciences
/ Humans
/ Infant
/ Infant, Newborn
/ Latent period
/ Middle Aged
/ multidisciplinary
/ Nucleotide sequence
/ Phylogeny
/ Proteins
/ Public health
/ S gene
/ SARS-CoV-2 - classification
/ SARS-CoV-2 - genetics
/ SARS-CoV-2 - isolation & purification
/ SARS-CoV-2 - pathogenicity
/ Science
/ Science (multidisciplinary)
/ Severe acute respiratory syndrome coronavirus 2
/ Spike Glycoprotein, Coronavirus - analysis
/ Spike Glycoprotein, Coronavirus - genetics
/ Time Factors
/ Trends
/ Young Adult
2021
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Assessing transmissibility of SARS-CoV-2 lineage B.1.1.7 in England
Journal Article
Assessing transmissibility of SARS-CoV-2 lineage B.1.1.7 in England
2021
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Overview
The SARS-CoV-2 lineage B.1.1.7, designated variant of concern (VOC) 202012/01 by Public Health England
1
, was first identified in the UK in late summer to early autumn 2020
2
. Whole-genome SARS-CoV-2 sequence data collected from community-based diagnostic testing for COVID-19 show an extremely rapid expansion of the B.1.1.7 lineage during autumn 2020, suggesting that it has a selective advantage. Here we show that changes in VOC frequency inferred from genetic data correspond closely to changes inferred by
S
gene target failures (SGTF) in community-based diagnostic PCR testing. Analysis of trends in SGTF and non-SGTF case numbers in local areas across England shows that B.1.1.7 has higher transmissibility than non-VOC lineages, even if it has a different latent period or generation time. The SGTF data indicate a transient shift in the age composition of reported cases, with cases of B.1.1.7 including a larger share of under 20-year-olds than non-VOC cases. We estimated time-varying reproduction numbers for B.1.1.7 and co-circulating lineages using SGTF and genomic data. The best-supported models did not indicate a substantial difference in VOC transmissibility among different age groups, but all analyses agreed that B.1.1.7 has a substantial transmission advantage over other lineages, with a 50% to 100% higher reproduction number.
Genetic and testing data from England show that the SARS-CoV-2 variant of concern B.1.1.7 has a transmission advantage over other lineages.
Publisher
Nature Publishing Group UK,Nature Publishing Group
Subject
/ Adult
/ Age
/ Aged
/ Autumn
/ Child
/ COVID-19
/ Genomes
/ Humanities and Social Sciences
/ Humans
/ Infant
/ Proteins
/ S gene
/ SARS-CoV-2 - isolation & purification
/ Science
/ Severe acute respiratory syndrome coronavirus 2
/ Spike Glycoprotein, Coronavirus - analysis
/ Spike Glycoprotein, Coronavirus - genetics
/ Trends
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