Custom multi‑tumor next‑generation sequencing panel for routine molecular diagnosis of solid tumors: Validation and results from three‑year clinical use.

Int J Mol Med · 2022 · PMC8920498 · PMID 35244186

Europe PMC DOI

hedged sentence

0.0634

closest p · 1.3× alpha

0.0634

boldest claim

The sentences

almost significantlyP=0.0634so close (0.05 < p ≤ 0.1)

Mutant allele frequencies in EGFR and RAS/BRAF/MAPK1 genes were almost significantly different (6.778 and 2.445%, P=0.0634).

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