Barely Significant
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A maternal germline mutator phenotype in a family affected by heritable colorectal cancer.

Genetics · 2024 · PMC11631438 · PMID 39403956

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closest p · 1.0× alpha
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The sentences

nominally significantP < 0.05actually significant
To give readers an accurate sense of data heterogeneity and noise, we perform more tests than the minimum number required, computing C>A enrichments individual by individual and observing nominally significant enrichments in only a few children ( P < 0.05 in a 1-tailed test without multiple testing correction).

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