Barely Significant
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Gene editing of NCF1 loci is associated with homologous recombination and chromosomal rearrangements.

Commun Biol · 2024 · PMC11464842 · PMID 39384978

Europe PMCDOI
1
hedged sentence
0.0001
closest p · 0.0× alpha
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The sentences

highly significantp value < 10 −4actually significant
Because the sequence homology was highly significant (98% vs. 50% in random sequences, p value < 10 −4 ), NCF1B was selected as the surrogate for any chromosomal rearrangements detected in this study.

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