Barely Significant
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Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing.

Nat Genet · 2023 · PMC10632132 · PMID 37904051

2
hedged sentences
0.1000
closest p · 2.0× alpha
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boldest claim

The sentences

marginal significanceP < 0.1so close (0.05 < p ≤ 0.1)
For mCA types with marginal significance ( P < 0.1), we then conducted logistic regression to test for association using a Bonferroni correction to account for the 156 independent tests.

also in 5,069 other papers

marginally significantno p-value reported
We make a similar observation for the IDH2 oncogene (15q gain and IDH2 somatic mutation); however, it is marginally significant.

also in 26,082 other papers

Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.