Barely Significant
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Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart Defects.

G3 (Bethesda) · 2018 · PMC5765339 · PMID 29141989

Europe PMCDOI
1
hedged sentence
0.0540
closest p · 1.1× alpha
0.0540
boldest claim

The sentences

marginally significantp-values = 0.054so close (0.05 < p ≤ 0.1)
(2013 ) were marginally significant in our data set (p-values = 0.054 and 0.056).

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