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About:
Rapid colorimetric detection of COVID-19 coronavirus using a reverse tran-scriptional loop-mediated isothermal amplification (RT-LAMP) diagnostic plat-form: iLACO
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research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Rapid colorimetric detection of COVID-19 coronavirus using a reverse tran-scriptional loop-mediated isothermal amplification (RT-LAMP) diagnostic plat-form: iLACO
Creator
Li, Xin
Liu, Na
Yu, Lin
Chen, Wei-Hua
Dong, Xue
Han, Heng
Hao, Xiaowen
Li, Jiyao
Li, Xuelong
Liu, Jianmin
Liu, Xiyang
Pelechano, Vicent
Wu, Shanshan
Ye, Shenglong
Yin, Xiushan
Zhang, Wanzhong
Source
MedRxiv
abstract
The recent outbreak of a novel coronavirus SARS-CoV-2 (also known as 2019-nCoV) threatens global health, given serious cause for concern. SARS-CoV-2 is a human-to-human pathogen that caused fever, severe respiratory disease and pneumonia (known as COVID-19). By press time, more than 70,000 infected people had been confirmed worldwide. SARS-CoV-2 is very similar to the severe acute respiratory syndrome (SARS) coronavirus broke out 17 years ago. However, it has increased transmissibility as compared with the SARS-CoV, e.g. very often infected individuals without any symptoms could still transfer the virus to others. It is thus urgent to develop a rapid, accurate and onsite diagnosis methods in order to effectively identify these early infects, treat them on time and control the disease spreading. Here we developed an isothermal LAMP based method-iLACO (isothermal LAMP based method for COVID-19) to amplify a fragment of the ORF1ab gene using 6 primers. We assured the species-specificity of iLACO by comparing the sequences of 11 related viruses by BLAST (including 7 similar coronaviruses, 2 influenza viruses and 2 normal coronaviruses). The sensitivity is comparable to Taqman based qPCR detection method, detecting synthesized RNA equivalent to 10 copies of 2019-nCoV virus. Reaction time varied from 15-40 minutes, depending on the loading of virus in the collected samples. The accuracy, simplicity and versatility of the new developed method suggests that iLACO assays can be conveniently applied with for 2019-nCoV threat control, even in those cases where specialized molecular biology equipment is not available.
has issue date
2020-02-24
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xsd:dateTime
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bibo:doi
10.1101/2020.02.20.20025874
has license
medrxiv
sha1sum (hex)
bd8f57ea4aadeda075d557f566a1909d68e658c4
schema:url
https://doi.org/10.1101/2020.02.20.20025874
resource representing a document's title
Rapid colorimetric detection of COVID-19 coronavirus using a reverse tran-scriptional loop-mediated isothermal amplification (RT-LAMP) diagnostic plat-form: iLACO
resource representing a document's body
covid:bd8f57ea4aadeda075d557f566a1909d68e658c4#body_text
is
schema:about
of
named entity 'PLAT'
named entity 'The'
named entity '2019-nCoV'
named entity 'SARS-CoV-2'
named entity 'Taqman'
named entity 'cases'
named entity 'RNA'
named entity 'develop'
named entity '40 minutes'
named entity 'based'
named entity 'assays'
named entity 'SIMILAR'
named entity 'ACCURACY'
named entity 'TRANSFER'
named entity 'YEARS'
named entity 'REVERSE'
named entity 'BLAST'
named entity 'COLLECTED'
named entity 'INFLUENZA VIRUSES'
named entity 'VERY OFTEN'
named entity 'VIRUS'
named entity 'RAPID'
named entity 'MOLECULAR BIOLOGY'
named entity 'THREAT'
named entity 'EARLY'
named entity 'CORONAVIRUS'
named entity 'NORMAL'
named entity 'CONCERN'
covid:arg/bd8f57ea4aadeda075d557f566a1909d68e658c4
named entity 'GLOBAL HEALTH'
named entity 'SEVERE'
named entity '70%'
named entity 'CASES'
named entity 'SPECIALIZED'
named entity 'OUTBREAK'
named entity 'EQUIPMENT'
named entity 'ANY SYMPTOMS'
named entity 'SPECIFICITY'
named entity 'COMPARED'
named entity 'RECENT'
named entity 'PRIMERS'
named entity 'TRAN'
named entity 'DIAGNOSTIC'
named entity 'TIME'
named entity 'BASED'
named entity 'DIAGNOSIS'
named entity 'EQUIVALENT'
named entity 'LOADING'
named entity 'HERE'
named entity 'LAMP'
named entity 'FORM'
named entity 'COVID-19'
named entity 'USING'
named entity 'CORONAVIRUS'
named entity 'SARS-COV'
named entity 'AMPLIFY'
named entity 'WHERE'
named entity 'DETECTING'
named entity 'GIVEN'
named entity 'RESPIRATORY DISEASE'
named entity 'CONFIRMED'
named entity 'CAUSE'
named entity 'PNEUMONIA'
named entity 'FRAGMENT OF'
named entity 'VIRUSES'
named entity 'DETECTION METHOD'
named entity 'GENE'
named entity 'SARS-COV-2'
named entity 'QPCR'
named entity 'URGENT'
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