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About:
Accommodating individual travel history, global mobility, and unsampled diversity in phylogeography: a SARS-CoV-2 case study
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research paper
schema:ScholarlyArticle
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Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
title
Accommodating individual travel history, global mobility, and unsampled diversity in phylogeography: a SARS-CoV-2 case study
Creator
Colizza, Vittoria
Poletto, Chiara
Rambaut, Andrew
Lemey, Philippe
Baele, Guy
Nelson, Martha
Andersen, Kristian
Mccrone, John
Suchard, Marc
Hill, Verity
Worobey, Michael
Hong, Samuel
O'toole, Áine
source
BioRxiv; Medline
abstract
Spatiotemporal bias in genome sequence sampling can severely confound phylogeographic inference based on discrete trait ancestral reconstruction. This has impeded our ability to accurately track the emergence and spread of SARS-CoV-2, the virus responsible for the COVID-19 pandemic. Despite the availability of unprecedented numbers of SARS-CoV-2 genomes on a global scale, evolutionary reconstructions are hindered by the slow accumulation of sequence divergence over its relatively short transmission history. When confronted with these issues, incorporating additional contextual data may critically inform phylodynamic reconstructions. Here, we present a new approach to integrate individual travel history data in Bayesian phylogeographic inference and apply it to the early spread of SARS-CoV-2, while also including global air transportation data. We demonstrate that including travel history data for each SARS-CoV-2 genome yields more realistic reconstructions of virus spread, particularly when travelers from undersampled locations are included to mitigate sampling bias. We further explore methods to ameliorate the impact of sampling bias by augmenting the phylogeographic analysis with lineages from undersampled locations in the analyses. Our reconstructions reinforce specific transmission hypotheses suggested by the inclusion of travel history data, but also suggest alternative routes of virus migration that are plausible within the epidemiological context but are not apparent with current sampling efforts. Although further research is needed to fully examine the performance of our travel-aware phylogeographic analyses with unsampled diversity and to further improve them, they represent multiple new avenues for directly addressing the colossal issue of sample bias in phylogeographic inference.
has issue date
2020-06-23
(
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)
bibo:doi
10.1101/2020.06.22.165464
bibo:pmid
32596695
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biorxiv
sha1sum (hex)
cf162f18bef0530f30fc336929b540873c3c7fa4
schema:url
https://doi.org/10.1101/2020.06.22.165464
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Accommodating individual travel history, global mobility, and unsampled diversity in phylogeography: a SARS-CoV-2 case study
has PubMed identifier
32596695
schema:publication
bioRxiv
resource representing a document's body
covid:cf162f18bef0530f30fc336929b540873c3c7fa4#body_text
is
schema:about
of
named entity 'virus'
named entity 'history'
named entity 'phylogeographic'
named entity 'genomes'
named entity 'SARS-CoV-2'
named entity 'genome'
named entity 'needed'
named entity 'SARS-CoV-2'
named entity 'IMPEDED'
named entity 'ACCUMULATION'
covid:arg/cf162f18bef0530f30fc336929b540873c3c7fa4
named entity 'availability'
named entity 'history'
named entity 'suggested'
named entity 'Spatiotemporal'
named entity 'Iran'
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named entity 'basal'
named entity 'SARS-CoV-2'
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named entity 'epidemiological data'
named entity 'taxa'
named entity 'pathogen'
named entity 'Beijing'
named entity 'phylogeographic'
named entity 'sampling'
named entity 'epidemiological data'
named entity 'inference'
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named entity 'hypotheses'
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named entity 'incorporating'
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named entity 'Canadian'
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named entity 'taxa'
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named entity 'incubation time'
named entity 'nucleotide substitution'
named entity 'SARS-CoV-2 virus'
named entity 'diffusion'
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named entity 'genome'
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named entity 'Bayesian inference'
named entity 'sequence data'
named entity 'West Africa'
named entity 'Hubei'
named entity 'data sets'
named entity 'Iran'
named entity 'clade'
named entity 'sampling'
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