Barely Significant
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Marked variation in predicted and observed variability of tandem repeat loci across the human genome.

BMC Genomics · 2008 · PMC2364633 · PMID 18416815

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1
hedged sentence
0.0001
closest p · 0.0× alpha
0.0001
boldest claim

The sentences

highly significantp < 0.0001actually significant
27/30 (90%) of their variants were also reported as such by our model and 29/40 (73%) were reported as invariant by our model, a highly significant correlation (Fisher's exact test p < 0.0001).

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