Barely Significant
← all excerpts

Whole Exome Sequencing Study Uncovers Novel Candidate Genes and Protein-Coding Variants for Cataract.

Invest Ophthalmol Vis Sci · 2025 · PMC12366868 · PMID 40801674

1
hedged sentence
0.0001
closest p · 0.0× alpha
0.0001
boldest claim

The sentences

nominally significantP < 1.00 × 10 − 4actually significant
3 , 12 Among the 32 nominally significant gene-based associations ( P < 1.00 × 10 − 4 ), six (18.75%) were issued from a missense|LC (i.e., low-confidence LoF variants) burden set, 19 (59.38%) were issued from a pLoF burden set, and seven (21.88%) were issued from a synonymous burden set ( Supplementary Figure S1 ).

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.