A direct capture method for purification and detection of viral nucleic acid enables epidemiological surveillance of SARS-CoV-2
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SciScore for 10.1101/2021.05.06.21256753: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Ethics not detected. Sex as a biological variable not detected. Randomization For the purpose of comparing performance between libraries, random subsampling was performed to obtain the same number of input reads for each library using seqtk v1.2. Blinding not detected. Power Analysis not detected. Table 2: Resources
Recombinant DNA Sentences Resources The SARS-CoV-2 quantification standard was created by inserting the envelope gene (NCBI: 43740570) and the nucleocapsid gene (NCBI: 43740575) of SARS-CoV-2 into the pGEM-3z vector (Promega Corp.) using the BamH I site. pGEM-3zsuggested: RRID:Addgene_26665)Software and Algorithms Sentences Resources Manufacturer’s instructions were followed with one exception: … SciScore for 10.1101/2021.05.06.21256753: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Ethics not detected. Sex as a biological variable not detected. Randomization For the purpose of comparing performance between libraries, random subsampling was performed to obtain the same number of input reads for each library using seqtk v1.2. Blinding not detected. Power Analysis not detected. Table 2: Resources
Recombinant DNA Sentences Resources The SARS-CoV-2 quantification standard was created by inserting the envelope gene (NCBI: 43740570) and the nucleocapsid gene (NCBI: 43740575) of SARS-CoV-2 into the pGEM-3z vector (Promega Corp.) using the BamH I site. pGEM-3zsuggested: RRID:Addgene_26665)Software and Algorithms Sentences Resources Manufacturer’s instructions were followed with one exception: incubation time at 50°C was increased from 10 minutes to 30 minutes, as recommended by the Swift Biosciences SARS-CoV-2 Additional Genome Coverage amplicon panel library preparation protocol. Swift Biosciencessuggested: NoneAmplicon sequencing analysis: Compressed, demultiplexed reads were obtained from the Illumina MiniSeq instrument and assessed for sequencing quality using FastQC 0.11.9-0 (https://www.bioinformatics.babraham.ac.uk/projects/fastqc/). FastQCsuggested: (FastQC, RRID:SCR_014583)Adapter trimming was done using Fastp v0.20.132 (sequences AGATCGGAAGAGCACACGTCTGAACTCCAGTCA and AGATCGGAAGAGCGTCGTGTAGGGAAAGAGTGT). Fastpsuggested: (fastp, RRID:SCR_016962)Trimmed reads were mapped to the SARS-CoV-2 reference genome (NC_045512.2) using BWA v 0.7.17. BWAsuggested: (BWA, RRID:SCR_010910)QC metrics were generated using Picard (v 2.9.2; http://broadinstitute.github.io/picard) BedToIntervalList, CollectTargetedPcrMetrics, CollectGcBiasMetrics. Picardsuggested: (Picard, RRID:SCR_006525)Snakemake v5.17.0 was used for workflow management on a Microsoft Azure CycleCloud instance. Snakemakesuggested: (Snakemake, RRID:SCR_003475)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.
Results from scite Reference Check: We found no unreliable references.
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