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arXiv | Vol., Issue. | 2020-06-08 | Pages

arXiv

A Public Website for the Automated Assessment and Validation of SARS-CoV-2 Diagnostic PCR Assays

Flynn, Mark   Li, Po-E   Lo, Chien-Chi   Gutiérrez, Adán Myers y   Xu, Yan   Gans, Jason   Chain, Patrick S. G.   Shakya, Migun   Davenport, Karen   Hu, Bin   Jackson, Elais Player  
Abstract

Summary: Polymerase chain reaction-based assays are the current gold standard for detecting and diagnosing SARS-CoV-2. However, as SARS-CoV-2 mutates, we need to constantly assess whether existing PCR-based assays will continue to detect all known viral strains. To enable the continuous monitoring of SARS-CoV-2 assays, we have developed a web-based assay validation algorithm that checks existing PCR-based assays against the ever-expanding genome databases for SARS-CoV-2 using both thermodynamic and edit-distance metrics. The assay screening results are displayed as a heatmap, showing the number of mismatches between each detection and each SARS-CoV-2 genome sequence. Using a mismatch threshold to define detection failure, assay performance is summarized with the true positive rate (recall) to simplify assay comparisons. Availability: https://covid19.edgebioinformatics.org/#/assayValidation. Contact: Jason Gans (jgans@lanl.gov) and Patrick Chain (pchain@lanl.gov)

Original Text (This is the original text for your reference.)

A Public Website for the Automated Assessment and Validation of SARS-CoV-2 Diagnostic PCR Assays

Summary: Polymerase chain reaction-based assays are the current gold standard for detecting and diagnosing SARS-CoV-2. However, as SARS-CoV-2 mutates, we need to constantly assess whether existing PCR-based assays will continue to detect all known viral strains. To enable the continuous monitoring of SARS-CoV-2 assays, we have developed a web-based assay validation algorithm that checks existing PCR-based assays against the ever-expanding genome databases for SARS-CoV-2 using both thermodynamic and edit-distance metrics. The assay screening results are displayed as a heatmap, showing the number of mismatches between each detection and each SARS-CoV-2 genome sequence. Using a mismatch threshold to define detection failure, assay performance is summarized with the true positive rate (recall) to simplify assay comparisons. Availability: https://covid19.edgebioinformatics.org/#/assayValidation. Contact: Jason Gans (jgans@lanl.gov) and Patrick Chain (pchain@lanl.gov)

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Flynn, Mark,Li, Po-E, Lo, Chien-Chi, Gutiérrez, Adán Myers y, Xu, Yan, Gans, Jason, Chain, Patrick S. G., Shakya, Migun, Davenport, Karen, Hu, Bin, Jackson, Elais Player,.A Public Website for the Automated Assessment and Validation of SARS-CoV-2 Diagnostic PCR Assays. (),.

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