Barely Significant
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Comprehensive analysis of coding variants highlights genetic complexity in developmental and epileptic encephalopathy.

Nat Commun · 2019 · PMC6555845 · PMID 31175295

Europe PMCDOI
2
hedged sentences
0.0001
closest p · 0.0× alpha
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boldest claim

The sentences

highly significantP = 0.0000643actually significant
We observed highly significant excess of CD missense URVs in EE/DEE (Fig. 1a , P = 0.0000643, OR = 1.09), whereas there was no significant excess of the other missense/inframe URVs ( P = 0.0861, OR = 1.01).

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nominally significantno p-value reported
Regarding synonymous URVs, we observed nominally significant excess in EE/DEE (Fig. 1a ).

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