Diagnostic accuracy comparison of three fully automated chemiluminescent immunoassay platforms for the detection of SARS-CoV-2 antibodies
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SciScore for 10.1101/2020.10.07.20207696: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Institutional Review Board Statement Consent: COVID-19 patients were informed about the serological test with proper written consent.
IRB: The study was approved by Institutional Ethics Committee.Randomization not detected. Blinding not detected. Power Analysis not detected. Sex as a biological variable not detected. Table 2: Resources
Antibodies Sentences Resources Test method: All three different automated machines can qualitatively detect anti-SARS-CoV-2 antibodies based on the two-step immunoassay principle. anti-SARS-CoV-2suggested: NoneAbbott made ARCHITECT i2000SR platform uses chemiluminescent microparticle immunoassay (CMIA) technology for the detection of immunoglobulin class G (IgG) antibodies … SciScore for 10.1101/2020.10.07.20207696: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Institutional Review Board Statement Consent: COVID-19 patients were informed about the serological test with proper written consent.
IRB: The study was approved by Institutional Ethics Committee.Randomization not detected. Blinding not detected. Power Analysis not detected. Sex as a biological variable not detected. Table 2: Resources
Antibodies Sentences Resources Test method: All three different automated machines can qualitatively detect anti-SARS-CoV-2 antibodies based on the two-step immunoassay principle. anti-SARS-CoV-2suggested: NoneAbbott made ARCHITECT i2000SR platform uses chemiluminescent microparticle immunoassay (CMIA) technology for the detection of immunoglobulin class G (IgG) antibodies against the nucleocapsid protein of SARS-CoV-2 from human serum. immunoglobulin class G (IgGsuggested: NoneThe third one, Yhlo Biotech manufactured iFlash-SARS-CoV-2 IgG was a paramagnetic particle based chemiluminescent immunoassay (CLIA) to determine the IgG antibodies against SARS-CoV-2 nucleocapsid and spike protein. SARS-CoV-2 nucleocapsid and spike protein.suggested: NoneSoftware and Algorithms Sentences Resources Statistical analysis: Descriptive statistical analyses were performed by SPSS software (IBM SPSS statistics for Windows, version 24.0, Armonk, NY). SPSSsuggested: (SPSS, RRID:SCR_002865)Results 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.
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