Barely Significant
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Whole-genome sequencing and gene network modules predict gemcitabine/carboplatin-induced myelosuppression in non-small cell lung cancer patients.

NPJ Syst Biol Appl · 2020 · PMC7445166 · PMID 32839457

Europe PMCDOI
1
hedged sentence
0.0010
closest p · 0.0× alpha
0.0010
boldest claim

The sentences

nominally significantp ≤ 1 × 10 −3actually significant
SNV/INDEL association analysis Fisher’s exact test identified 4594 (5743), 5019 (6063), and 5066 (5959) autosomal (total numbers in parentheses) nominally significant ( p ≤ 1 × 10 −3 ) genetic variants (SNVs/INDELs) for neutropenia, leukopenia, and thrombocytopenia, respectively.

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