Available COVID-19 serial seroconversion panel for validation of SARS-CoV-2 antibody assays.
This article has been Reviewed by the following groups
Listed in
- Evaluated articles (ScreenIT)
Abstract
No abstract available
Article activity feed
-
-
SciScore for 10.1101/2020.09.08.20190256: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Institutional Review Board Statement Consent: The samples were collected with informed consent, under an approved IRB protocol (Advarra, Columbia MD, USA) and in compliance with all applicable regulatory guidelines. Randomization not detected. Blinding not detected. Power Analysis not detected. Sex as a biological variable not detected. Table 2: Resources
Antibodies Sentences Resources Five anti-SARS-CoV-2 antibody tests were used in this study to characterize a COVID-19 seroconversion panel (COVID-19 Seroconversion Panel: CVD19SCP, Access Biologicals, Vista, CA, USA). anti-SARS-CoV-2suggested: NoneThe antibody tests used were: the Gold Standard™ Diagnostics SARS-CoV-2 IgG ELISA and SARS-CoV-2 IgM ELISA test … SciScore for 10.1101/2020.09.08.20190256: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Institutional Review Board Statement Consent: The samples were collected with informed consent, under an approved IRB protocol (Advarra, Columbia MD, USA) and in compliance with all applicable regulatory guidelines. Randomization not detected. Blinding not detected. Power Analysis not detected. Sex as a biological variable not detected. Table 2: Resources
Antibodies Sentences Resources Five anti-SARS-CoV-2 antibody tests were used in this study to characterize a COVID-19 seroconversion panel (COVID-19 Seroconversion Panel: CVD19SCP, Access Biologicals, Vista, CA, USA). anti-SARS-CoV-2suggested: NoneThe antibody tests used were: the Gold Standard™ Diagnostics SARS-CoV-2 IgG ELISA and SARS-CoV-2 IgM ELISA test kits (Gold Standard™ Diagnostics (GSD), Davis, CA, USA; CE-IVD certified immunoassays, emergency use authorization (EUA) submission pending), Vitros® anti-SARS-CoV-2 IgG and anti-SARS-CoV-2 total Ig tests (Vitros® Immunodiagnostic Products, Ortho-Clinical Diagnostics, Inc., Rochester, NY, USA; EUA approved) and Liaison® SARS-CoV-2 S1/S2 IgG assay (Diasorin, Inc., Saluggia, Italy; EUA approved). SARS-CoV-2 IgMsuggested: Noneanti-SARS-CoV-2 IgGsuggested: NonePlasma from this single donor was screened and found to be negative for syphilis and antibodies to HIV-1/2 HCV and non-reactive for hepatitis B surface antigen (HBsAg). HIV-1/2suggested: NoneHCVsuggested: Noneantigen (HBsAg).suggested: NoneResults from OddPub: We did not detect open data. We also did not detect open code. Researchers are encouraged to share open data when possible (see Nature blog).
Results from LimitationRecognizer: An explicit section about the limitations of the techniques employed in this study was not found. We encourage authors to address study limitations.Results from TrialIdentifier: No clinical trial numbers were referenced.
Results from Barzooka: We did not find any issues relating to the usage of bar graphs.
Results from JetFighter: We did not find any issues relating to colormaps.
Results from rtransparent:- Thank you for including a conflict of interest statement. Authors are encouraged to include this statement when submitting to a journal.
- Thank you for including a funding statement. Authors are encouraged to include this statement when submitting to a journal.
- No protocol registration statement was detected.
-
-