Barely Significant
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Genome-wide analysis of the role of copy-number variation in pancreatic cancer risk.

Front Genet · 2014 · PMC3923159 · PMID 24592275

Europe PMCDOI
1
hedged sentence
0.0500
closest p · 1.0× alpha
0.0500
boldest claim

The sentences

nominally significantp-value < 0.05actually significant
A nominally significant ( p-value < 0.05) association was observed when counting duplications only (OR = 1.10, p = 0.02).

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