Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants.

HGG Adv · 2023 · PMC9772568 · PMID 36568030

Europe PMC DOI

hedged sentence

—

closest p

—

boldest claim

The sentences

nominally significantno p-value reported

We further evaluated the significance of the excess of nominally significant variants (with 5% expected) using one-sided binomial tests.

also in 7,732 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.