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About:
Evaluation of COVID-19 RT-qPCR test in multi-sample pools
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covidontheweb.inria.fr
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Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Evaluation of COVID-19 RT-qPCR test in multi-sample pools
Creator
Aharony, Noga
Argoetti, Amir
Berenbaum, Dina
Gandali, Nagam
Geffen, Yuval
Halberthal, Michael
Hashimshony, Tamar
Kishony,
Kuzli, Areen
Mandel-Gutfreund, Yael
Messer, Esther
Shafran, Einat
Szwarcwort-Cohen, Moran
Tamar, Shaer
Yelin, Idan
Source
MedRxiv
abstract
The recent emergence of SARS-CoV-2 lead to a current pandemic of unprecedented levels. Though diagnostic tests are fundamental to the ability to detect and respond, many health systems are already experiencing shortages of reagents associated with this test. Here, testing a pooling approach for the standard RT-qPCR test, we find that a single positive sample can be detected even in pools of up to 32 samples, with an estimated false negative rate of 10%. Detection of positive samples diluted in even up to 64 samples may also be attainable, though may require additional amplification cycles. As it uses the standard protocols, reagents and equipment, this pooling method can be applied immediately in current clinical testing laboratories. We hope that such implementation of a pool test for COVID-19 would allow expanding current screening capacities thereby enabling the expansion of detection in the community, as well as in close integral groups, such as hospital departments, army units, or factory shifts.
has issue date
2020-03-27
(
xsd:dateTime
)
bibo:doi
10.1101/2020.03.26.20039438
has license
medrxiv
sha1sum (hex)
0ba71b8ced117cf824c3675bbbb5ae51c12719b9
schema:url
https://doi.org/10.1101/2020.03.26.20039438
resource representing a document's title
Evaluation of COVID-19 RT-qPCR test in multi-sample pools
resource representing a document's body
covid:0ba71b8ced117cf824c3675bbbb5ae51c12719b9#body_text
is
schema:about
of
named entity 'laboratory'
named entity 'Correspondence'
named entity 'correspondence'
named entity 'R. K.'
named entity 'data analysis'
named entity 'Rambam Health Care Campus'
named entity 'MEDICAL'
named entity 'INTERPRETATION'
named entity 'CORRESPONDENCE'
named entity 'sample collection'
named entity 'Bacteriology'
named entity 'technion.ac.il'
named entity 'experimental procedure'
named entity 'CAMPUS'
named entity 'LABORATORY'
named entity 'rambam'
named entity 'sample'
named entity 'equally'
named entity 'procedure'
named entity 'authors'
named entity 'data analysis'
named entity 'set'
named entity 'experimental'
named entity 'EXPERIMENTAL PROCEDURE'
named entity 'Bacteriology'
named entity 'Rambam Health Care Campus'
named entity 'THESE'
named entity 'AUTHORS'
named entity 'GOV'
named entity 'SENT'
named entity 'SAMPLE COLLECTION'
named entity 'SET'
named entity 'DATA ANALYSIS'
named entity 'HEALTH CARE'
named entity 'HEALTH'
named entity 'BACTERIOLOGY'
is
part of
of
Evaluation of COVID-19 RT-qPCR test in multi-sample pools
The recent emergence of SARS-CoV-2 lead to a current pandemic of unprecedented levels. Though diagnostic tests are fundamental to the ability to detect and respond, many health systems are already experiencing shortages of reagents associated with this test. Here, testing a pooling approach for the standard RT-qPCR test, we find that a single positive sample can be detected even in pools of up to 32 samples, with an estimated false negative rate of 10%. Detection of positive samples diluted in even up to 64 samples may also be attainable, though may require additional amplification cycles. As it uses the standard protocols, reagents and equipment, this pooling method can be applied immediately in current clinical testing laboratories. We hope that such implementation of a pool test for COVID-19 would allow expanding current screening capacities thereby enabling the expansion of detection in the community, as well as in close integral groups, such as hospital departments, army units, or factory shifts.
covid:0ba71b8ced117cf824c3675bbbb5ae51c12719b9#body_text
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