Barely Significant
← all excerpts

Annotation of functional variation in personal genomes using RegulomeDB.

Genome Res · 2012 · PMC3431494 · PMID 22955989

1
hedged sentence
closest p
boldest claim

The sentences

likely to be significantno p-value reported
As such, we consider variants that are known eQTLs for genes, and thus have been shown to be associated with expression, as most likely to be significant and label these variants as Category 1.

also in 993 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.