Asset Details
MbrlCatalogueTitleDetail
Do you wish to reserve the book?
Using big sequencing data to identify chronic SARS-Coronavirus-2 infections
by
Miller, Danielle
, Harari, Sheri
, Burstein, David
, Stern, Adi
, Fleishon, Shay
in
631/114/1305
/ 631/181/735
/ 631/326/596/4130
/ 692/700/478/174
/ Chronic infection
/ Coronaviruses
/ COVID-19
/ Disease transmission
/ Gene sequencing
/ Genomes
/ Humanities and Social Sciences
/ Infections
/ Metadata
/ multidisciplinary
/ Mutation
/ Phylogeny
/ Science
/ Science (multidisciplinary)
/ Severe acute respiratory syndrome coronavirus 2
/ Viral diseases
/ Whole genome sequencing
2024
Hey, we have placed the reservation for you!
By the way, why not check out events that you can attend while you pick your title.
You are currently in the queue to collect this book. You will be notified once it is your turn to collect the book.
Oops! Something went wrong.
Looks like we were not able to place the reservation. Kindly try again later.
Are you sure you want to remove the book from the shelf?
Using big sequencing data to identify chronic SARS-Coronavirus-2 infections
by
Miller, Danielle
, Harari, Sheri
, Burstein, David
, Stern, Adi
, Fleishon, Shay
in
631/114/1305
/ 631/181/735
/ 631/326/596/4130
/ 692/700/478/174
/ Chronic infection
/ Coronaviruses
/ COVID-19
/ Disease transmission
/ Gene sequencing
/ Genomes
/ Humanities and Social Sciences
/ Infections
/ Metadata
/ multidisciplinary
/ Mutation
/ Phylogeny
/ Science
/ Science (multidisciplinary)
/ Severe acute respiratory syndrome coronavirus 2
/ Viral diseases
/ Whole genome sequencing
2024
Oops! Something went wrong.
While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Using big sequencing data to identify chronic SARS-Coronavirus-2 infections
by
Miller, Danielle
, Harari, Sheri
, Burstein, David
, Stern, Adi
, Fleishon, Shay
in
631/114/1305
/ 631/181/735
/ 631/326/596/4130
/ 692/700/478/174
/ Chronic infection
/ Coronaviruses
/ COVID-19
/ Disease transmission
/ Gene sequencing
/ Genomes
/ Humanities and Social Sciences
/ Infections
/ Metadata
/ multidisciplinary
/ Mutation
/ Phylogeny
/ Science
/ Science (multidisciplinary)
/ Severe acute respiratory syndrome coronavirus 2
/ Viral diseases
/ Whole genome sequencing
2024
Please be aware that the book you have requested cannot be checked out. If you would like to checkout this book, you can reserve another copy
We have requested the book for you!
Your request is successful and it will be processed during the Library working hours. Please check the status of your request in My Requests.
Oops! Something went wrong.
Looks like we were not able to place your request. Kindly try again later.
Using big sequencing data to identify chronic SARS-Coronavirus-2 infections
Journal Article
Using big sequencing data to identify chronic SARS-Coronavirus-2 infections
2024
Request Book From Autostore
and Choose the Collection Method
Overview
The evolution of SARS-Coronavirus-2 (SARS-CoV-2) has been characterized by the periodic emergence of highly divergent variants. One leading hypothesis suggests these variants may have emerged during chronic infections of immunocompromised individuals, but limited data from these cases hinders comprehensive analyses. Here, we harnessed millions of SARS-CoV-2 genomes to identify potential chronic infections and used language models (LM) to infer chronic-associated mutations. First, we mined the SARS-CoV-2 phylogeny and identified chronic-like clades with identical metadata (location, age, and sex) spanning over 21 days, suggesting a prolonged infection. We inferred 271 chronic-like clades, which exhibited characteristics similar to confirmed chronic infections. Chronic-associated mutations were often high-fitness immune-evasive mutations located in the spike receptor-binding domain (RBD), yet a minority were unique to chronic infections and absent in global settings. The probability of observing high-fitness RBD mutations was 10-20 times higher in chronic infections than in global transmission chains. The majority of RBD mutations in BA.1/BA.2 chronic-like clades bore predictive value, i.e., went on to display global success. Finally, we used our LM to infer hundreds of additional chronic-like clades in the absence of metadata. Our approach allows mining extensive sequencing data and providing insights into future evolutionary patterns of SARS-CoV-2.
Chronic SARS-CoV-2 infections have been hypothesised to be sources of new variants. Here, the authors use large-scale genome sequencing data to identify mutations predictive of chronic infections, which may therefore be relevant in future variants.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
This website uses cookies to ensure you get the best experience on our website.