Barely Significant
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A pedigree-based prediction model identifies carriers of deleterious de novo mutations in families with Li-Fraumeni syndrome.

Genome Res · 2020 · PMC7462073 · PMID 32817165

Europe PMCDOI
1
hedged sentence
0.0900
closest p · 1.8× alpha
0.0900
boldest claim

The sentences

marginally significantP -value = 0.09so close (0.05 < p ≤ 0.1)
The observation of n = 0 out of 82 DNMs for p.R248W was marginally significant ( P -value = 0.09, based on a Poisson distribution).

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