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About:
SARS-CoV2 quantification using RT-dPCR: a faster and safer alternative to assist viral genomic copies assessment using RT-qPCR
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An Entity of Type :
schema:ScholarlyArticle
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covidontheweb.inria.fr
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Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
title
SARS-CoV2 quantification using RT-dPCR: a faster and safer alternative to assist viral genomic copies assessment using RT-qPCR
Creator
Karolina, Ana
Rodrigues De Almeida, Paula
Demoliner¹, Meriane
Eisen¹, Antunes
Fleck¹, Juliane
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source
BioRxiv
abstract
In this study, serial dilutions of SARS-CoV 2 RNA extract were tested using RT-dPCR using three different primer-probe assays aiming SARS-CoV 2 nucleocapsid coding region. Narrower confidence intervals, indicating high quantification precision were obtained in 100 and 1000-fold serial dilution and RT-dPCR results were equivalent between different assays in the same dilution. High accuracy of this test allowed conclusions regarding the ability of this technique to evaluate precisely the amount of genomic copies present in a sample. We believe that this fast and safe method can assist other researchers in titration of SARS-CoV2 controls used in RT-qPCR without the need of virus isolation.
has issue date
2020-05-01
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bibo:doi
10.1101/2020.05.01.072728
has license
biorxiv
sha1sum (hex)
7364613efdf21241a54ae67572eb0a2e39c76683
schema:url
https://doi.org/10.1101/2020.05.01.072728
resource representing a document's title
SARS-CoV2 quantification using RT-dPCR: a faster and safer alternative to assist viral genomic copies assessment using RT-qPCR
schema:publication
bioRxiv
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covid:7364613efdf21241a54ae67572eb0a2e39c76683#body_text
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schema:about
of
named entity 'nucleocapsid'
named entity 'researchers'
named entity 'GENOMIC'
named entity 'SERIAL'
named entity '1000'
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