Next generation plasma proteome profiling of COVID-19 patients with mild to moderate symptoms
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SciScore for 10.1101/2021.06.15.21258940: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Ethics Consent: Written informed consent was obtained from all participants before the initiation of any trial-related procedures.
IRB: The study was approved by the ethics committee of Istanbul Medipol University, Istanbul, Turkey, and retrospectively registered at https://clinicaltrials.gov/ with Clinical Trial ID: NCT04573153.
IACUC: The study protocol conforms to the ethical guidelines of the 1975 Declaration of Helsinki.Sex as a biological variable not detected. Randomization Participants: A total of 50 patients were randomly selected from a clinical trial cohort of 93 patients over 18 years of age, who had a PCR-confirmed COVID-19 test within the previous 24 h and were in stable condition not … SciScore for 10.1101/2021.06.15.21258940: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Ethics Consent: Written informed consent was obtained from all participants before the initiation of any trial-related procedures.
IRB: The study was approved by the ethics committee of Istanbul Medipol University, Istanbul, Turkey, and retrospectively registered at https://clinicaltrials.gov/ with Clinical Trial ID: NCT04573153.
IACUC: The study protocol conforms to the ethical guidelines of the 1975 Declaration of Helsinki.Sex as a biological variable not detected. Randomization Participants: A total of 50 patients were randomly selected from a clinical trial cohort of 93 patients over 18 years of age, who had a PCR-confirmed COVID-19 test within the previous 24 h and were in stable condition not requiring hospitalization. Blinding not detected. Power Analysis not detected. Table 2: Resources
Software and Algorithms Sentences Resources The study was approved by the ethics committee of Istanbul Medipol University, Istanbul, Turkey, and retrospectively registered at https://clinicaltrials.gov/ with Clinical Trial ID: NCT04573153. https://clinicaltrials.gov/suggested: (ClinicalTrials.gov, RRID:SCR_002309)The analytical performance of each of the protein assays included in the panel is carefully validated based on specificity, sensitivity, dynamic range, precision, scalability, endogenous interference and detectability (http://www.olink.com). http://www.olink.comsuggested: (Olink Bioscience, RRID:SCR_003899)Statistical Analysis: All data analysis and visualization was performed using R (v3.6.3)(R Development Core Team, 2021) R Development Coresuggested: (R Project for Statistical Computing, RRID:SCR_001905)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: We found the following clinical trial numbers in your paper:
Identifier Status Title NCT04573153 Recruiting Metabolic Cofactor Supplementation and Hydroxychloroquine Co… 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.
Results from scite Reference Check: We found no unreliable references.
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