Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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Materials Map under construction

The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (2/2 displayed)

  • 2022Reverse-transcription loop-mediated isothermal amplification has high accuracy for detecting severe acute respiratory syndrome coronavirus 2 in saliva and nasopharyngeal/oropharyngeal swabs from asymptomatic and symptomatic individuals15citations
  • 2016Investigation into the Corrosion Mechanisms and Effective Inhibitor Additions for Zinc-Magnesium-Aluminium (ZMA) Alloys1citations

Places of action

Chart of shared publication
Prosek, Tomas
1 / 6 shared
Elvins, Jonathon
1 / 2 shared
Gallagher, Callum
1 / 1 shared
Sullivan, James
1 / 3 shared
Thierry, Dominique
1 / 12 shared
Cooze, Nathan
1 / 1 shared
Chart of publication period
2022
2016

Co-Authors (by relevance)

  • Prosek, Tomas
  • Elvins, Jonathon
  • Gallagher, Callum
  • Sullivan, James
  • Thierry, Dominique
  • Cooze, Nathan
OrganizationsLocationPeople

article

Reverse-transcription loop-mediated isothermal amplification has high accuracy for detecting severe acute respiratory syndrome coronavirus 2 in saliva and nasopharyngeal/oropharyngeal swabs from asymptomatic and symptomatic individuals

  • Love, Hannah
  • Gretton, Cosima
  • Houghton, Rebecca
  • Burns, Dan
  • Grippon, Seden
  • Whalley, Celina
  • Patrick, Helen
  • Douglas, Angela
  • Wise, Emma L.
  • Skinner, Paul
  • Beggs, Andrew D.
  • Fouch, Sarah
  • Hill, Sue L.
  • Reid, Scott M.
  • Kidd, Michael
  • Deans, Zandra
  • Sawyer, Jason
  • Ferguson, Jack
  • Moore, Nathan
  • Parker, Joe
  • Goring, Alice
  • Banyard, Ashley
  • Howson, Emma L. A.
  • Slater-Jefferies, Joanne
  • Kidd, Stephen P.
  • Davies, Kerrie
  • Andreou, Michael
  • Tillyer, Claire
  • Porter, Deborah
  • Cassar, Claire
  • Bryer, Claire
  • Vincent-Mistiaen, Zoe
  • Williams, Anthony
  • Rivers, Samantha
  • Lewis, Thomas
  • Brown, Ian
  • Poxon, Charlie
  • Godfrey, Keith
  • Morant, Nick
  • Fowler, Veronica L.
  • James, Joe
  • Ptasinska, Anetta
  • Sowood, Amy
  • Cortes, Nicholas J.
  • Cross, David
  • Bosworth, Andrew
  • Burton, Jane
  • Snell, Gemma
  • Armson, Bryony
  • Richter, Alex
Abstract

Previous studies have described reverse-transcription loop-mediated isothermal amplification (RT-LAMP) for the rapid detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in nasopharyngeal/oropharyngeal swab and saliva samples. This multisite clinical evaluation describes the validation of an improved sample preparation method for extraction-free RT-LAMP and reports clinical performance of four RT-LAMP assay formats for SARS-CoV-2 detection. Direct RT-LAMP was performed on 559 swabs and 86,760 saliva samples and RNA RT-LAMP on extracted RNA from 12,619 swabs and 12,521 saliva samples from asymptomatic and symptomatic individuals across health care and community settings. For direct RT-LAMP, overall diagnostic sensitivity (DSe) was 70.35% (95% CI, 63.48%-76.60%) on swabs and 84.62% (95% CI, 79.50%-88.88%) on saliva, with diagnostic specificity of 100% (95% CI, 98.98%-100.00%) on swabs and 100% (95% CI, 99.72%-100.00%) on saliva, compared with quantitative RT-PCR (RT-qPCR); analyzing samples with RT-qPCR ORF1ab C T values of ≤25 and ≤33, DSe values were 100% (95% CI, 96.34%-100%) and 77.78% (95% CI, 70.99%-83.62%) for swabs, and 99.01% (95% CI, 94.61%-99.97%) and 87.61% (95% CI, 82.69%-91.54%) for saliva, respectively. For RNA RT-LAMP, overall DSe and diagnostic specificity were 96.06% (95% CI, 92.88%-98.12%) and 99.99% (95% CI, 99.95%-100%) for swabs, and 80.65% (95% CI, 73.54%-86.54%) and 99.99% (95% CI, 99.95%-100%) for saliva, respectively. These findings demonstrate that RT-LAMP is applicable to a variety of use cases, including frequent, interval-based direct RT-LAMP of saliva from asymptomatic individuals who may otherwise be missed using symptomatic testing alone.

Topics
  • impedance spectroscopy
  • extraction
  • chemical ionisation