Barely Significant
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Sequence artefacts in a prospective series of formalin-fixed tumours tested for mutations in hotspot regions by massively parallel sequencing.

BMC Med Genomics · 2014 · PMC4032349 · PMID 24885028

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

The sentences

highly significantp < 0.0001actually significant
The relative proportion of C>T/G>A changes was highly significant compared to other nucleotide changes (p < 0.0001, Kruskal–Wallis one-way analysis of variance) and formed 32% of all nucleotide changes overall, a proportion that was double what was expected due to chance.

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