Barely Significant
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NGS and phenotypic ontology-based approaches increase the diagnostic yield in syndromic retinal diseases.

Hum Genet · 2021 · PMC8553673 · PMID 34448047

Europe PMCDOI
1
hedged sentence
0.0544
closest p · 1.1× alpha
0.0544
boldest claim

The sentences

showed a trendp = 0.0544so close (0.05 < p ≤ 0.1)
The characterization rate between the familial and sporadic cases showed a trend to be significant ( p = 0.0544).

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