Barely Significant
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Genomic surveillance of Nevada patients revealed prevalence of unique SARS-CoV-2 variants bearing mutations in the RdRp gene.

J Genet Genomics · 2021 · PMC7891100 · PMID 33820739

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highly significantno p-value reported
This is highly significant and shows the power of our workflow in sequencing of SARS-CoV-2 genome from a spectrum of samples, including the ones having inadequate amounts of specimen (due to the variability in collection) or lower viral loads in nasal secretions.

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Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.