SARS-CoV-2 antibodies in the Southern Region of New Zealand, 2020

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Abstract

No abstract available

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  1. SciScore for 10.1101/2020.10.20.20215616: (What is this?)

    Please note, not all rigor criteria are appropriate for all manuscripts.

    Table 1: Rigor

    Institutional Review Board StatementIRB: It was approved by the Health and Disability Ethics Committee (20/NTB/101).
    Randomizationnot detected.
    Blindingnot detected.
    Power Analysisnot detected.
    Sex as a biological variablenot detected.

    Table 2: Resources

    Software and Algorithms
    SentencesResources
    The primary assay was the Abbott Architect SARS-CoV-2 IgG chemiluminescent microparticle immunoassay (CMIA) (Abbott, Chicago, USA).
    Abbott
    suggested: (Abbott, RRID:SCR_010477)
    Samples were analysed on the Abbott Architect i2000SR Immunoassay Analyzer following manufacturer’s instructions.
    Abbott Architect
    suggested: (Abbott ARCHITECT i1000sr System, RRID:SCR_019328)
    Statistical analysis: Statistical analysis was performed using Prism 8 (GraphPad) or R (version 3.6.3) within R Studio (version 1.2.5033); a P-value of ≤0.05 was considered statistically significant.
    GraphPad
    suggested: (GraphPad Prism, RRID:SCR_002798)

    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: We detected the following sentences addressing limitations in the study:
    Our study has some limitations. Firstly, the delay in specimen collection after the outbreak likely had an impact on the Abbott assay sensitivity. We cannot be certain that undiagnosed cases were not missed using the Abbott assay as our screening test. However, every effort was made to mitigate against this by lowering the cut-off for the initial Abbott screening assay. Lastly, it is important to note that this is not a sero-prevalence study. Participants who self-identified as higher risk were actively recruited, therefore the sero-positivity rate calculated in this group in the SDHB region cannot be extrapolated to the general population.

    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.

    About SciScore

    SciScore is an automated tool that is designed to assist expert reviewers by finding and presenting formulaic information scattered throughout a paper in a standard, easy to digest format. SciScore checks for the presence and correctness of RRIDs (research resource identifiers), and for rigor criteria such as sex and investigator blinding. For details on the theoretical underpinning of rigor criteria and the tools shown here, including references cited, please follow this link.