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| Name | Authors | DOI | Group |
Summary |
Associated Publications |
RRIDs used | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
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Open Isothermal Platform Protocal Resource Report Resource Website |
Andrew Buultjens, Koen Vandelannoote, Tim Stinear | DOI:10.17504/protocols.io.bk3nkyme | XPRIZE Rapid Covid Testing, Open-Isothermal-Platforms Dx, Open-Isothermal-Platforms Dx | The University of Melbourne, The University of Melbourne, The University of Melbourne | 1 | 2020 | Andrew Buultjens, Koen Vandelannoote, Tim Stinear 2020. Open Isothermal Platform Protocal. protocols.io https://dx.doi.org/10.17504/protocols.io.bk3nkyme | 2021-04-15 09:16:29 | ||||
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Find SARS-CoV-2 testing protocol Resource Report Resource Website |
jose.nuno | DOI:10.17504/protocols.io.bk5aky2e | XPRIZE Rapid Covid Testing | Unima Inc | 1 | 2020 | jose.nuno 2020. Find SARS-CoV-2 testing protocol. protocols.io https://dx.doi.org/10.17504/protocols.io.bk5aky2e | 2021-04-15 09:16:59 | ||||
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Sampleholder preparation Resource Report Resource Website |
philippe.bechtold | DOI:10.17504/protocols.io.bky4kxyw | XPRIZE Rapid Covid Testing | ETHZ - ETH Zurich | 1 | 2020 | philippe.bechtold 2020. Sampleholder preparation. protocols.io https://dx.doi.org/10.17504/protocols.io.bky4kxyw | 2021-04-15 09:16:41 | ||||
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SUPER rapid kit Resource Report Resource Website |
Hyeon Jin Kim, Seong T. Hong | DOI:10.17504/protocols.io.bkqvkvw6 | Coronavirus Method Development Community, XPRIZE Rapid Covid Testing | We developed a supersensitive capillary reaction kit intended for the direct and qualitative detection of SARS-CoV-2 virus in saliva and nasal swabs. It enables sensitive and specific detection of the SARS-CoV-2 spike antigens in respiratory specimens more accurately than most PCR method within 5 minutes. Our rapid capillary kit will help not only fight but also end COVID-19 by providing the first sensitive self-diagnosis at home as well as POC clinical diagnosis at the health care facilities. | SNJ Pharma Inc, Jeonbuk National University | 1 | 2020 | Hyeon Jin Kim, Seong T. Hong 2020. SUPER rapid kit. protocols.io https://dx.doi.org/10.17504/protocols.io.bkqvkvw6 | 2021-04-15 09:16:45 | |||
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Coronavirus Lateral Flow Assay (LFA) operation protocol v2 Resource Report Resource Website |
peijun he | DOI:10.17504/protocols.io.bqvpmw5n | Coronavirus Method Development Community, XPRIZE Rapid Covid Testing, Highfield Diagnostics | Coronavirus Lateral Flow Assay (LFA) operation protocol | Highfield Diagnostics, UK | 2 | 2020 | peijun he 2020. Coronavirus Lateral Flow Assay (LFA) operation protocol v2. protocols.io https://dx.doi.org/10.17504/protocols.io.bqvpmw5n | 2021-04-15 09:16:57 | |||
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PCR-cDNA Barcoding (SQK-PCB109) Resource Report Resource Website |
Oxford Nanopore Technologies | DOI:10.17504/protocols.io.bkypkxvn | XPRIZE Rapid Covid Testing, XENOGENE | Barcoding or multiplexing is useful when the amount of data required per sample is less than the total amount of data that can be generated from a single flow cell: it allows a user to pool multiple samples and sequence them together, making more efficient use of the flow cell.The PCR-cDNA Barcoding Kit is used to prepare cDNA for nanopore sequencing for up to 12 samples, from an input of as low as 1 ng poly-A+ RNA. Users who do not have poly-A+ enriched RNA can use 50 ng of total RNA but additional optimisation may be required.Taking full-length poly-A+ RNA, complementary strand synthesis and strand switching are performed using kit-supplied oligonucleotides. The kit contains 12 primer pairs which are used to generate and then amplify double-stranded cDNA by PCR amplification: each primer pair contains a barcode and 5’ tag which facilitates the ligase-free attachment of Rapid Sequencing Adapters. Amplified and barcoded samples are then pooled together, and Rapid Sequencing Adapters are added to the pooled mix. | nanoporetech.com | 1 | 2020 | Oxford Nanopore Technologies 2020. PCR-cDNA Barcoding (SQK-PCB109). protocols.io https://dx.doi.org/10.17504/protocols.io.bkypkxvn | 2021-04-15 09:17:04 | |||
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Copy of Corona Detective User Protocol V1.0 Resource Report Resource Website |
Rachel Aronoff, Guy Aidelberg | DOI:10.17504/protocols.io.bk43kyyn | XPRIZE Rapid Covid Testing, Guy Aidelberg | Corona Detective is based upon a molecular amplification strategy inspired by the ‘GMO Detective’ method, in order to detect the virus causing Covid-19. Done not only without complicated equipment, but with a simple +/- readout, the Corona Detective is very specific. Furthermore, controls to ensure sensitive detection, without false positives or negatives, are intrinsic to this solution. The final product, strips/plates of tubes with dry reagents, specific for Corona and a control gene (extraction control), can be shipped anywhere, without cold-chain dependence. Critically, monitoring tests could be run by ordinary people, by following this protocol. (Even kids have successfully participated in GMO detective workshops, also soldering their own fluor detectors.)This user guide will allow you to test samples with this system, provided as freeze-dried reaction components in 0.2ml tubes (formats possible, 8-tube strips, 96-well plates).Human or clinical samples should only be run in settings with access to appropriate biosafety facilities, of course.Acknowledging the JOGL Open Covid 19 Initiative and all the #proj nucleic-acid-amplification team for support. | Hackuarium, CRI (Center for research and interdisciplinarity) Paris | 1 | 2020 | Rachel Aronoff, Guy Aidelberg 2020. Copy of Corona Detective User Protocol V1.0. protocols.io https://dx.doi.org/10.17504/protocols.io.bk43kyyn | 2021-04-15 09:17:07 | |||
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FLASH amp Resource Report Resource Website |
eesha.sharma.phd | DOI:10.17504/protocols.io.bk2hkyb6 | XPRIZE Rapid Covid Testing | FLASH amp is a method that allows for room temperature detection and amplification of a viral RNA sequence of interest submitted as part of the Xprize competition. The main components of the reaction are not included here and are given generic names such as enzyme X as they are currently not protected under IP. The steps outlined with tubes labeled with the generic names would allow any lab to reproduce the method. Version 1 of this method outlines the protocol for a fluorescence-based readout that can be used with a qPCR machine or TECAN style plate reader. Version 2 (to be released shortly) will be a colorimetric readout that can be assessed by eye. The outlined protocol assumes the user performing this in a laboratory setting will setup reactions in a clean room and analyze results in a seperate post-amplification room. In addition, since our amplification is rapid and at room temperature, care but be taken to add ligand to the master mix quickly and the reactions be sealed. | Quantification by Design, Stanford University | 1 | 2020 | eesha.sharma.phd 2020. FLASH amp. protocols.io https://dx.doi.org/10.17504/protocols.io.bk2hkyb6 | 2021-04-15 09:17:05 |
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