Barely Significant
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Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome.

G3 (Bethesda) · 2015 · PMC4632064 · PMID 26384369

Europe PMCDOI
1
hedged sentence
0.1000
closest p · 2.0× alpha
0.1000
boldest claim

The sentences

nominally significantP < 0.10so close (0.05 < p ≤ 0.1)
Gene-sets with nominally significant burden for at least one variant category ( P < 0.10 for LoF and splicing regulatory, and P < 0.05 for missense variants) were then tested for the joint burden of the three variant categories with a multivariate, two-sample Hotelling’s T-Square test ( Hotelling 1931 ).

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