Barely Significant
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Exome-wide analysis of bi-allelic alterations identifies a Lynch phenotype in The Cancer Genome Atlas.

Genome Med · 2018 · PMC6138910 · PMID 30217226

Europe PMCDOI
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hedged sentence
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closest p · 1.0× alpha
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boldest claim

The sentences

nominally significantp ≤ 0.05actually significant
Only sites with a nominally significant ( p ≤ 0.05) increase in the germline allelic fraction were retained.

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