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10.1038/s41467-021-21627-0

http://scihub22266oqcxt.onion/10.1038/s41467-021-21627-0
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suck abstract from ncbi


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pmid33674580      Nat+Commun 2021 ; 12 (1): 1467
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  • Point-of-care bulk testing for SARS-CoV-2 by combining hybridization capture with improved colorimetric LAMP #MMPMID33674580
  • Bokelmann L; Nickel O; Maricic T; Paabo S; Meyer M; Borte S; Riesenberg S
  • Nat Commun 2021[Mar]; 12 (1): 1467 PMID33674580show ga
  • Efforts to contain the spread of SARS-CoV-2 have spurred the need for reliable, rapid, and cost-effective diagnostic methods which can be applied to large numbers of people. However, current standard protocols for the detection of viral nucleic acids while sensitive, require a high level of automation and sophisticated laboratory equipment to achieve throughputs that allow whole communities to be tested on a regular basis. Here we present Cap-iLAMP (capture and improved loop-mediated isothermal amplification) which combines a hybridization capture-based RNA extraction of gargle lavage samples with an improved colorimetric RT-LAMP assay and smartphone-based color scoring. Cap-iLAMP is compatible with point-of-care testing and enables the detection of SARS-CoV-2 positive samples in less than one hour. In contrast to direct addition of the sample to improved LAMP (iLAMP), Cap-iLAMP prevents false positives and allows single positive samples to be detected in pools of 25 negative samples, reducing the reagent cost per test to ~1 Euro per individual.
  • |*Point-of-Care Testing[MESH]
  • |COVID-19 Testing/*methods[MESH]
  • |COVID-19/*diagnosis/*virology[MESH]
  • |Colorimetry/*methods[MESH]
  • |Coronavirus Nucleocapsid Proteins/genetics[MESH]
  • |Humans[MESH]
  • |Molecular Diagnostic Techniques/*methods[MESH]
  • |Nucleic Acid Amplification Techniques/*methods[MESH]
  • |Nucleic Acid Hybridization/*methods[MESH]
  • |Phosphoproteins/genetics[MESH]
  • |RNA, Viral/genetics[MESH]
  • |SARS-CoV-2/genetics/*isolation & purification[MESH]


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