Barely Significant
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Reference-informed prediction of alternative splicing and splicing-altering mutations from sequences.

Genome Res · 2024 · PMC11368187 · PMID 39060028

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closest p · 0.1× alpha
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The sentences

highly significantP = 0.006actually significant
This overlap is highly significant based on a permutation test ( P = 0.006; see Methods).

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