Barely Significant
← all excerpts

EMQN best practice guidelines for genetic testing in hereditary breast and ovarian cancer.

Eur J Hum Genet · 2024 · PMC11061103 · PMID 38443545

1
hedged sentence
closest p
boldest claim

The sentences

may be significantno p-value reported
Adequate test sensitivity may be achieved with lower NGS coverage depth in the case of deceased index patient testing on non-neoplastic tissue; however, failure rates due to technical challenges associated with FFPE tissue analysis may be significant [ 46 ]. 4.2 Specific Variant Testing (predictive testing) Where a causative PV has been identified in an index case, predictive testing for at-risk family members can be offered.

also in 13,097 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.