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Name Authors DOI Group Summary Associated Publications RRIDs used Affiliations External URL Version Publication Date Proper Citation Record Last Update
nCoV-2019 McGill Artic PCR Protocol, 5 ul RT and V3 only + LA1 at 63C
 
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Sarah Reiling, Josh Quick, Ioannis Ragoussis DOI:10.17504/protocols.io.bjkrkkv6 Coronavirus Method Development Community, McGill Genome Centre V3 only primers can be found here:https://github.com/sarahreiling/artic-ncov2019/blob/master/primer_schemes/nCoV-2019/V3/nCoV-2019_V3only.scheme.bed McGill University, University of Birmingham, McGill University 1 2020 Sarah Reiling, Josh Quick, Ioannis Ragoussis 2020. nCoV-2019 McGill Artic PCR Protocol, 5 ul RT and V3 only + LA1 at 63C. protocols.io https://dx.doi.org/10.17504/protocols.io.bjkrkkv6 2021-04-15 09:15:38
Coronavirus Lateral Flow Assay (LFA) sample preparation protocol v2
 
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peijun he DOI:10.17504/protocols.io.bqvnmw5e Coronavirus Method Development Community, XPRIZE Rapid Covid Testing, Highfield Diagnostics Coronavirus Lateral Flow Assay (LFA) sample preparation protocol Highfield Diagnostics, UK 2 2020 peijun he 2020. Coronavirus Lateral Flow Assay (LFA) sample preparation protocol v2. protocols.io https://dx.doi.org/10.17504/protocols.io.bqvnmw5e 2021-04-15 09:15:38
RNA Extraction of SARS-CoV-2 from Wastewater
 
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Neha Mittal, Vbarua , Nick Stark, Cynthia Gibas, jschluet , Mariya Munir Coronavirus Method Development Community, UNC Charlotte COVID WBE UNC Charlotte Department of Bioinformatics and Genomics, UNC Charlotte Department of Civil and Environmental Engineering, UNC Charlotte Department of Bioinformatics and Genomics, UNC Charlotte Department of Bioinformatics and Genomics, UNC Charlotte Department of Bioinformatics and Genomics, UNC Charlotte Department of Civil and Environmental Engineering 1 2021 Neha Mittal, Vbarua , Nick Stark, Cynthia Gibas, jschluet , Mariya Munir 2021. RNA Extraction of SARS-CoV-2 from Wastewater. protocols.io https:// 2021-04-15 09:15:14
Amplicon clean-up using SPRI beads for RAPID nanopore kit RBK004
 
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Nikki Freed, Olin Silander DOI:10.17504/protocols.io.bgsrjwd6 Coronavirus Method Development Community Massey University, Massey University 3 2020 Nikki Freed, Olin Silander 2020. Amplicon clean-up using SPRI beads for RAPID nanopore kit RBK004. protocols.io https://dx.doi.org/10.17504/protocols.io.bgsrjwd6 2021-04-15 09:15:14
Starting a MinION sequencing run using MinKNOW
 
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Muhammad Faisal, Olin Silander, Nikki Freed DOI:10.17504/protocols.io.bfwqjpdw Coronavirus Method Development Community Massey University, Massey University, Massey University 1 2020 Muhammad Faisal, Olin Silander, Nikki Freed 2020. Starting a MinION sequencing run using MinKNOW. protocols.io https://dx.doi.org/10.17504/protocols.io.bfwqjpdw 2021-04-15 09:15:14
Saliva Vapor Tests in a Home Environment for Point-of-care COVID-19 Tests
 
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Shadi Emam, nasrollahpourmotla.m , n.sun DOI:10.17504/protocols.io.bkwrkxd6 Coronavirus Method Development Community, XPRIZE Rapid Covid Testing Northeastern University, Northeastern University, Northeastern University 1 2020 Shadi Emam, nasrollahpourmotla.m , n.sun 2020. Saliva Vapor Tests in a Home Environment for Point-of-care COVID-19 Tests. protocols.io https://dx.doi.org/10.17504/protocols.io.bkwrkxd6 2021-04-15 09:15:16
Preliminary Evaluation of RNA Extraction Methods
 
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Aniela Wozniak, Catalina Ibarra-Henriquez, Valentina Sebastian, Grace Armijo, Liliana Lamig, Carolina Miranda, Marcela Lagos, Sandra Solari, Ana María Guzmán, Teresa Quiroga, Susan Hitschfeld, Eleodoro Riveras, Marcela Ferres, Rodrigo A. Gutiérrez, Patricia García, Ariel Cerda Coronavirus Method Development Community, Reclone.org (The Reagent Collaboration Network) Departamento de Laboratorios Clínicos. Escuela de Medicina. Facultad de Medicina. Pontificia Universidad Católica de chile, FONDAP Center for Genome Regulation. Millennium Institute for Integrative Biology (iBio), Departamento de Genética Molecular y Microbiología, Pontificia Universidad Católica de Chile, Santiago, 8331150, Chile, Laboratorio de Microbiología. Servicio de laboratorios Clínicos. Red de Salud UC-CHRISTUS, FONDAP Center for Genome Regulation. Millennium Institute for Integrative Biology (iBio), Departamento de Genética Molecular y Microbiología, Pontificia Universidad Católica de Chile, Santiago, 8331150, Chile, FONDAP Center for Genome Regulation. Millennium Institute for Integrative Biology (iBio), Departamento de Genética Molecular y Microbiología, Pontificia Universidad Católica de Chile, Santiago, 8331150, Chile, Laboratorio de Microbiología. Servicio de laboratorios Clínicos. Red de Salud UC-CHRISTUS, Departamento de Laboratorios Clínicos. Escuela de Medicina. Facultad de Medicina. Pontificia Universidad Católica de chile, Departamento de Laboratorios Clínicos. Escuela de Medicina. Facultad de Medicina. Pontificia Universidad Católica de chile, Departamento de Laboratorios Clínicos. Escuela de Medicina. Facultad de Medicina. Pontificia Universidad Católica de chile, Departamento de Laboratorios Clínicos. Escuela de Medicina. Facultad de Medicina. Pontificia Universidad Católica de chile, FONDAP Center for Genome Regulation. Millennium Institute for Integrative Biology (iBio), Departamento de Genética Molecular y Microbiología, Pontificia Universidad Católica de Chile, Santiago, 8331150, Chile, FONDAP Center for Genome Regulation. Millennium Institute for Integrative Biology (iBio), Departamento de Genética Molecular y Microbiología, Pontificia Universidad Católica de Chile, Santiago, 8331150, Chile, Departamento de Laboratorios Clínicos. Escuela de Medicina. Facultad de Medicina. Pontificia Universidad Católica de chile, FONDAP Center for Genome Regulation. Millennium Institute for Integrative Biology (iBio), Departamento de Genética Molecular y Microbiología, Pontificia Universidad Católica de Chile, Santiago, 8331150, Chile, Departamento de Laboratorios Clínicos. Escuela de Medicina. Facultad de Medicina. Pontificia Universidad Católica de chile, FONDAP Center for Genome Regulation. Millennium Institute for Integrative Biology (iBio), Departamento de Genética Molecular y Microbiología, Pontificia Universidad Católica de Chile, Santiago, 8331150, Chile https://doi.org/10.1101/2020.05.07.083048 1 2020 Aniela Wozniak, Catalina Ibarra-Henriquez, Valentina Sebastian, Grace Armijo, Liliana Lamig, Carolina Miranda, Marcela Lagos, Sandra Solari, Ana María Guzmán, Teresa Quiroga, Susan Hitschfeld, Eleodoro Riveras, Marcela Ferres, Rodrigo A. Gutiérrez, Patricia García, Ariel Cerda 2020. Preliminary Evaluation of RNA Extraction Methods. protocols.io https:// 2021-04-15 09:15:17
Opentrons COVID-19 testing (RT-qPCR path, Station C, 24+3+1 sample special)
 
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Max Marrone DOI:10.17504/protocols.io.beqajdse Coronavirus Method Development Community, Opentrons COVID-19 Testing Opentrons Labworks 2 2020 Max Marrone 2020. Opentrons COVID-19 testing (RT-qPCR path, Station C, 24+3+1 sample special). protocols.io https://dx.doi.org/10.17504/protocols.io.beqajdse 2021-04-15 09:15:46
Protocol for Extraction of Viral RNA with added DNase treatment
 
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Megan Folkerts, Ashlyn Pfeiffer, mnguyen , Danielle Vazquez, Amber Jones DOI:10.17504/protocols.io.bnkhmct6 Coronavirus Method Development Community This protocol is modified from the MagMAX MVP II protocol from Thermo Fisher, and the MagMAX mirVana protocol from Thermo Fisher. Modifications were necessary to include a DNAse treatment step, which improves viral recovery in low-burden samples. Translational Genomics Research Institute, Flagstaff AZ, Translational Genomics Research Institute, Flagstaff AZ, Translational Genomics Research Institute, Flagstaff AZ, Translational Genomics Research Institute, Flagstaff AZ, Translational Genomics Research Institute, Flagstaff AZ 1 2020 Megan Folkerts, Ashlyn Pfeiffer, mnguyen , Danielle Vazquez, Amber Jones 2020. Protocol for Extraction of Viral RNA with added DNase treatment. protocols.io https://dx.doi.org/10.17504/protocols.io.bnkhmct6 2021-04-15 09:15:19
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) real-time RT-PCR ORF1ab 2020 (Wuhan-ORF1ab; 2019-nCoV-related test)
 
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Judy Northill, Ian Mackay DOI:10.17504/protocols.io.bchvit66 protocols.io Ambassadors, Public Health Virology, Forensic and Scientific Services, Coronavirus Method Development Community A real-time RT-PCR to specifically detect SARS-CoV-2 betacoronavirus also called nCoV-2019 or Wuhan seafood market pneumonia virus. Based on sequence MN908947 made available by Professor Yong-Zhen Zhang, Fudan University, Shanghai, China. The target region is within the ORF1ab sequence.NotesAssay is fully optimised (as of 24Jan2020).This test has identified a clinical positive case of coronavirus disease (COVID-19) Public Health Virology, Forensic and Scientific Services, Public Health Virology, Forensic and Scientific Services 3 2020 Judy Northill, Ian Mackay 2020. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) real-time RT-PCR ORF1ab 2020 (Wuhan-ORF1ab; 2019-nCoV-related test). protocols.io https://dx.doi.org/10.17504/protocols.io.bchvit66 2021-04-15 09:15:19
Culture of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2; f.2019-nCoV)
 
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Alyssa Pyke, Ian Mackay, Frederick Moore, Andrew Van Den Hurk, Judy Northill, Mitchell Finger, Natalie Simpson, Neelima Nair, Peter Burtonclay, Peter Moore, Sarah Wheatley, Sean Moody, Sonja Hall-Mendelin, Elisabeth Gamez, Amanda De Jong, Ben Huang, Carmel Taylor, David Warrilow, Doris Genge, Glen Hewitson, Inga Sultana, Jamie McMahon, Jean Barcelon DOI:10.17504/protocols.io.bcduis6w protocols.io Ambassadors, Public Health Virology, Forensic and Scientific Services, Coronavirus Method Development Community We briefly describe a method to inoculate a susceptible cell line with a human patient sample in order to culture the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the cause of coronavirus disease, COVID-19.Clinical samples including nasopharyngeal swabs and aspirates were inoculated onto confluent monolayers of African green monkey kidney Vero C1008, clone E6 cells (ATCC®-CRL-1586) grown in Opti-Mem reduced serum growth medium supplemented with 3% foetal bovine serum in polystyrene, flat-sided, screw-cap 3 mL cell culture tubes.This work was conducted in Queensland under PC3 laboratory conditions by experienced scientists. Public Health Virology, Forensic and Scientific Services, Public Health Virology, Forensic and Scientific Services, Public Health Virology, Forensic and Scientific Services, Public Health Virology, Forensic and Scientific Services, Public Health Virology, Forensic and Scientific Services, Public Health Virology, Forensic and Scientific Services, Public Health Virology, Forensic and Scientific Services, Public Health Virology, Forensic and Scientific Services, Public Health Virology, Forensic and Scientific Services, Public Health Virology, Forensic and Scientific Services, Public Health Virology, Forensic and Scientific Services, Public Health Virology, Forensic and Scientific Services, Public Health Virology, Forensic and Scientific Services, Public Health Virology, Forensic and Scientific Services, Public Health Virology, Forensic and Scientific Services, Public Health Virology, Forensic and Scientific Services, Public Health Virology, Forensic and Scientific Services, Public Health Virology, Forensic and Scientific Services, Public Health Virology, Forensic and Scientific Services, Public Health Virology, Forensic and Scientific Services, Public Health Virology, Forensic and Scientific Services, Public Health Virology, Forensic and Scientific Services, Public Health Virology, Forensic and Scientific Services 1 2020 Alyssa Pyke, Ian Mackay, Frederick Moore, Andrew Van Den Hurk, Judy Northill, Mitchell Finger, Natalie Simpson, Neelima Nair, Peter Burtonclay, Peter Moore, Sarah Wheatley, Sean Moody, Sonja Hall-Mendelin, Elisabeth Gamez, Amanda De Jong, Ben Huang, Carmel Taylor, David Warrilow, Doris Genge, Glen Hewitson, Inga Sultana, Jamie McMahon, Jean Barcelon 2020. Culture of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2; f.2019-nCoV). protocols.io https://dx.doi.org/10.17504/protocols.io.bcduis6w 2021-04-15 09:15:24
BSCI:414 Lab 8 Transform and Miniprep Plasmid Containing SARS-CoV-2 Spike Gene
 
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Harley King Coronavirus Method Development Community, USG Fall 2020 BSCI:414, protocols.io for Educators LuminUltra 1 2020 Harley King 2020. BSCI:414 Lab 8 Transform and Miniprep Plasmid Containing SARS-CoV-2 Spike Gene. protocols.io https:// 2021-04-15 09:15:23
Antibody neutralization assay with SARS-CoV-2 and SARS-CoV pseudovirus
 
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Bei Wang, Wen-Hsin Sandy Lee, Cheng-I Wang DOI:10.17504/protocols.io.biztkf6n Coronavirus Method Development Community Singapore Immunology Network, A*STAR, Singapore, Singapore Immunology Network, A*STAR, Singapore, Singapore Immunology Network, A*STAR, Singapore 1 2020 Bei Wang, Wen-Hsin Sandy Lee, Cheng-I Wang 2020. Antibody neutralization assay with SARS-CoV-2 and SARS-CoV pseudovirus. protocols.io https://dx.doi.org/10.17504/protocols.io.biztkf6n 2021-04-15 09:15:24
Wastewater Concentration by Adsorption and Direct Extraction for SARS-CoV-2 RNA Detection and Quantification by RT-ddPCR
 
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Aaron Bivins, Warish Ahmed, Devin North, Kyle Bibby Coronavirus Method Development Community, 2019-nCoV Wastewater Epidemiology University of Notre Dame, CSIRO, University of Notre Dame, University of Notre Dame https://www.sciencedirect.com/science/article/pii/S004896972033480X 1 2020 Aaron Bivins, Warish Ahmed, Devin North, Kyle Bibby 2020. Wastewater Concentration by Adsorption and Direct Extraction for SARS-CoV-2 RNA Detection and Quantification by RT-ddPCR. protocols.io https:// 2021-04-15 09:15:48
Manual Silane magnetic bead-based high throughput protocol for SARS-CoV-2 RNA extraction
 
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Ainhoa Goñi-Salaverri, Jose A. Rodriguez, Nicholas Weber, Juan Pablo Unfried, Josepmaria Argemi, , David Lara Astiaso, DOI:10.17504/protocols.io.bfmajk2e Coronavirus Method Development Community The COVID-19 pandemic has presented an unprecedent challenge to develop and validate testing tools for urgent disease diagnosis. Current testing for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) via molecular diagnostics is woefully inadequate due to myriad issues with cross-entity coordination, reagent availability, and labor- and time-intensive protocols. The bottleneck in the workflow from patient sampling to diagnosis is not in the identification of viral genetic material (RT-qPCR) but in the collection, processing, and purification of the viral genetic material (patient sampling and RNA extraction). The majority of tests performed in laboratories lacking sophisticated automation require individual sample processing that severely limits the possibilities of scale-up. Thus, throughput depends on the availability of trained operator person-hours. We have developed a protocol for SARS-CoV-2 RNA extraction based on silane ferrimagnetic beads that is easily scaled up to multiwell culture plates with the processing done using multichannel pipettes. This protocol significantly reduces the hands-on time per sample and increases throughput such that an individual operator can process 100-200 samples per hour. Cima Universidad de Navarra, Pamplona, Spain, Cima Universidad de Navarra, Pamplona, Spain, Vivet Therapeutics SL, Pamplona, Spain, Cima Universidad de Navarra, Pamplona, Spain, Liver Unit. Internal Medicine Department. Clinica Universidad de Navarra, Pamplona, Spain, Division of Medicine - Gastroenterology and Hepatology Department, University of Pittsburgh, PA, USA, Cima Universidad de Navarra, Pamplona, Spain, Cambridge Stem Cell Institute, Cambridge, England 2 2020 Ainhoa Goñi-Salaverri, Jose A. Rodriguez, Nicholas Weber, Juan Pablo Unfried, Josepmaria Argemi, , David Lara Astiaso, 2020. Manual Silane magnetic bead-based high throughput protocol for SARS-CoV-2 RNA extraction. protocols.io https://dx.doi.org/10.17504/protocols.io.bfmajk2e 2021-04-15 09:15:32
One-Step RT-ddPCR for Detection of SARS-CoV-2, Bovine Coronavirus, and PMMoV RNA in RNA Derived from Wastewater or Primary Settled Solids v2 
 
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Stephanie Loeb, Katy Graham, David Catoe, Marlene Wolfe, Alexandria Boehm, Krista Wigginton DOI:10.17504/protocols.io.br96m99e Coronavirus Method Development Community, Wastewater-based epidemiology working group This protocol is an updated version of the original protocols.io protocol for these procedures from this group, with changes in the cycling conditions for the BCoV/PMMoV assay and the concentration of the PMMoV probe.Goal: Quantify concentration of N1, N2, BCoV, and PMMoV in RNA extractions using RT-ddPCR. Stanford University, Stanford University, Stanford University, Stanford University, Stanford University, University of Michigan 1 2021 Stephanie Loeb, Katy Graham, David Catoe, Marlene Wolfe, Alexandria Boehm, Krista Wigginton 2021. One-Step RT-ddPCR for Detection of SARS-CoV-2, Bovine Coronavirus, and PMMoV RNA in RNA Derived from Wastewater or Primary Settled Solids v2 . protocols.io https://dx.doi.org/10.17504/protocols.io.br96m99e 2021-04-15 09:15:29
ENNOLIFE SARS-CoV-2 Antigen Test Kit Protocol
 
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Hsiao-Chung Tsai DOI:10.17504/protocols.io.bke3ktgn Coronavirus Method Development Community, ProtectLife-AnTaimmu, XPRIZE Rapid Covid Testing General manager, ProtectLife International Biomedical Inc. 1 2020 Hsiao-Chung Tsai 2020. ENNOLIFE SARS-CoV-2 Antigen Test Kit Protocol. protocols.io https://dx.doi.org/10.17504/protocols.io.bke3ktgn 2021-04-15 09:15:50
AAU-nCoV-2019_Tailed_Long_Amplicon_Sequncing
 
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Emil Aarre Sorensen, Søren M. Karst, Simon Knutsson DOI:10.17504/protocols.io.bfc3jiyn AlbertsenLab, Coronavirus Method Development Community This protocol describes the preparation of long read amplicon libraries of nCoV-2019 for sequencing with the Oxford Nanopore MinION platform. The protocol is based on samples of rRNA extracts of the nCoV-2019 virus.Sequences for primers can be found under guidelines, currently using V3.1 from CJ020. The protocol is based on the ARTIC Networks nCoV-2019 sequencing protocol and modified to our lab at Aalborg Univeristy. https://www.protocols.io/view/ncov-2019-sequencing-protocol-bbmuik6w Center for Microbial Communities, Department of Chemistry and Bioscience, Aalborg University, Denmark, Center for Microbial Communities, Department of Chemistry and Bioscience, Aalborg University, Denmark, Center for Microbial Communities, Department of Chemistry and Bioscience, Aalborg University, Denmark 2 2020 Emil Aarre Sorensen, Søren M. Karst, Simon Knutsson 2020. AAU-nCoV-2019_Tailed_Long_Amplicon_Sequncing. protocols.io https://dx.doi.org/10.17504/protocols.io.bfc3jiyn 2021-04-15 09:15:32
GM Covid-19 saliva test (v2)
 
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Coronavirus Method Development Community, Narwhale for XPrize GM Biosciences 2 2020 2020. GM Covid-19 saliva test (v2). protocols.io https:// 2021-04-15 09:15:42
nCoV-2019 McGill Nanopore LibPrep Protocol, 5 ng NB
 
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Sarah Reiling, Anne-Marie Roy, Shu-Huang Chen, Josh Quick, Ioannis Ragoussis DOI:10.17504/protocols.io.bjkvkkw6 Coronavirus Method Development Community, McGill Genome Centre Artic nCoV-2019 McGill modified Lunascript Reverse Transcriptase nanopore sequencing protocol. McGill University, McGill University, McGill University, University of Birmingham, McGill University 1 2020 Sarah Reiling, Anne-Marie Roy, Shu-Huang Chen, Josh Quick, Ioannis Ragoussis 2020. nCoV-2019 McGill Nanopore LibPrep Protocol, 5 ng NB. protocols.io https://dx.doi.org/10.17504/protocols.io.bjkvkkw6 2021-04-15 09:15:40

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