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The proximal origin of SARS-CoV-2.

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TLDR
It is shown that SARS-CoV-2 is not a laboratory construct or a purposefully manipulated virus, and scenarios by which they could have arisen are discussed.
Abstract
SARS-CoV-2 is the seventh coronavirus known to infect humans; SARSCoV, MERS-CoV and SARS-CoV-2 can cause severe disease, whereas HKU1, NL63, OC43 and 229E are associated with mild symptoms6. Here we review what can be deduced about the origin of SARS-CoV-2 from comparative analysis of genomic data. We offer a perspective on the notable features of the SARS-CoV-2 genome and discuss scenarios by which they could have arisen. Our analyses clearly show that SARS-CoV-2 is not a laboratory construct or a purposefully manipulated virus.

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Face coverings for the public: Laying straw men to rest.

TL;DR: This article responds to one by Graham Martin and colleagues, who offered a critique of my previous publications on face coverings for the lay public in the Covid‐19 pandemic, and sets out some key findings from basic science, epidemiology, mathematical modelling, case studies, and natural experiments as the backdrop for a rebuttal of their narrowly framed objections.
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Emerging genetic diversity among clinical isolates of SARS-CoV-2: Lessons for today.

TL;DR: In this article, the role of molecular divergence in SARS-CoV-2 with time, due to clinical and epidemiological concerns, has been investigated, and the authors identify mutational hotspots which appear to be major drivers of diversity among strains, with RBD of spike protein emerging as the key region involved in interaction with ACE2.
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Land-use change and the livestock revolution increase the risk of zoonotic coronavirus transmission from rhinolophid bats

TL;DR: It is indicated that human–livestock–wildlife interactions in China may form hotspots with the potential to increase SARS-related coronavirus transmission from animals to humans, and that horseshoe bats occur in hotspots of forest fragmentation, livestock density and human populations—particularly in China—increasing the risk of Sars-related zoonotic pathogen spillover.
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Transmission of SARS-CoV-2, Required Developments in Research and Associated Public Health Concerns

TL;DR: The features, entry mechanism, infectiousness, and health consequences related to the COVID-19 outbreak are discussed and proper strategies addressing the infection control and clinical supplies are implemented.
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Report on Electroencephalographic Findings in Critically Ill Patients with COVID-19.

TL;DR: Of the 26 patients studied, 5 patients had EEGs that showed Periodic Discharges (PD) consisting of high amplitude frontal monomorphic delta waves with absence of epileptic activity, which may suggest CNS injury potentially related to COVID‐19 in these patients.
References
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Journal ArticleDOI

A pneumonia outbreak associated with a new coronavirus of probable bat origin

TL;DR: Identification and characterization of a new coronavirus (2019-nCoV), which caused an epidemic of acute respiratory syndrome in humans in Wuhan, China, and it is shown that this virus belongs to the species of SARSr-CoV, indicates that the virus is related to a bat coronav virus.
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A new coronavirus associated with human respiratory disease in China.

TL;DR: Phylogenetic and metagenomic analyses of the complete viral genome of a new coronavirus from the family Coronaviridae reveal that the virus is closely related to a group of SARS-like coronaviruses found in bats in China.
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An interactive web-based dashboard to track COVID-19 in real time.

TL;DR: The outbreak of the 2019 novel coronavirus disease (COVID-19) has induced a considerable degree of fear, emotional stress and anxiety among individuals around the world.
Journal ArticleDOI

Cryo-EM structure of the 2019-nCoV spike in the prefusion conformation.

TL;DR: The authors show that this protein binds at least 10 times more tightly than the corresponding spike protein of severe acute respiratory syndrome (SARS)–CoV to their common host cell receptor, and test several published SARS-CoV RBD-specific monoclonal antibodies found that they do not have appreciable binding to 2019-nCoV S, suggesting that antibody cross-reactivity may be limited between the two RBDs.
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