Whole genome sequencing identifies rare germline variants enriched in cancer related genes in first degree relatives of familial pancreatic cancer patients.

Clin Genet · 2021 · PMC9291090 · PMID 34313325

Europe PMC DOI

hedged sentence

0.0000

closest p · 0.0× alpha

0.0000

boldest claim

The sentences

highly significantp < 1.53e‐33actually significant

PALD1 (paladin) on chromosome 10 is highly significant ( p < 1.53e‐33) as it stands out from the other genes in Figures 3 , 4 .

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