Predicting human genes susceptible to genomic instability associated with <i>Alu</i>/<i>Alu</i>-mediated rearrangements.

Genome Res · 2018 · PMC6071635 · PMID 29907612

Europe PMC DOI

hedged sentence

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closest p · 0.0× alpha

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boldest claim

The sentences

highly significantP < 1 × 10 −16actually significant

Overall, a test of independence between the risk score tertiles and the potentially AAMR CNV count classes shows a highly significant association ( P < 1 × 10 −16 ) for both Fisher's exact test and a χ 2 test.

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