Barely Significant
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Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorder.

Sci Rep · 2020 · PMC7441318 · PMID 32820185

Europe PMCDOI
1
hedged sentence
0.0090
closest p · 0.2× alpha
0.0090
boldest claim

The sentences

highly significantp < 0.009actually significant
The joint probability to observe a more extreme enrichment/depletion pattern is highly significant ( p < 0.009, Fig. 2 d).

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