Barely Significant
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Validation of predicted mRNA splicing mutations using high-throughput transcriptome data.

F1000Res · 2014 · PMC3983938 · PMID 24741438

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hedged sentence
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closest p · 0.8× alpha
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boldest claim

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marginally statistically significantp = 0.04actually significant
These results are consistent with an imbalance of expression of the two alleles, as expected for a leaky variant. Figure 5 shows that for the distribution of read-abundance-based intron inclusion is marginally statistically significant ( p = 0.04).

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