In silico and in vitro comparative analysis to select, validate and test SNPs for human identification.

BMC Genomics · 2007 · PMC2222643 · PMID 18076761

Europe PMC DOI

hedged sentence

0.0000

closest p · 0.0× alpha

0.0000

boldest claim

The sentences

highly significantp = 2 × 10 -5actually significant

We also observed a highly significant difference in allele frequency between the Benin and Yoruba samples (HapMap Project) for the SNP rs3130315 (p = 2 × 10 -5 ) and between the Mongolian and Han Chinese samples (HapMap project) for two SNPs: rs9562080 (p = 0.047) and rs4116821 (7.36 × 10 -11 ).

also in 132,142 other papers

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.