Whole genome sequencing identifies rare genetic variants in familial pancreatic cancer patients.

Ann Hum Genet · 2022 · PMC9313800 · PMID 35312039

Europe PMC DOI

hedged sentences

0.0000

closest p · 0.0× alpha

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boldest claim

The sentences

highly significantp < 1.45e‐07actually significant

As shown by Figure S1 , most of the PTVs have high PHRED scores of over 20, and there is a highly significant positive correlation between PHRED score and the number of votes for being predicted as damaging using dbNSFP ( p < 1.45e‐07).

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extremely significantno p-value reported

Extremely significant overlaps of our detected PTV genes have been found in cancer driver genes and previously reported cancer genes.

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Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.