Barely Significant
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Antisense Oligonucleotide Screening to Optimize the Rescue of the Splicing Defect Caused by the Recurrent Deep-Intronic <i>ABCA4</i> Variant c.4539+2001G>A in Stargardt Disease.

Genes (Basel) · 2019 · PMC6628380 · PMID 31197102

1
hedged sentence
0.0611
closest p · 1.2× alpha
0.0611
boldest claim

The sentences

nearly significantp = 0.0611so close (0.05 < p ≤ 0.1)
The differences in Tm between groups was statistically different ( p = 0.0292, nonparametric one-way ANOVA), while the GC content was nearly significant ( p = 0.0611).

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