Barely Significant
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Systematically developing a registry of splice-site creating variants utilizing massive publicly available transcriptome sequence data.

Nat Commun · 2025 · PMC11718197 · PMID 39788962

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modest significanceno p-value reported
Furthermore, compared with SSCVs identified by juncmut, the variant chosen by SpliceAI 23 , a machine learning-based splicing effect predictor, showed modest significance (Fig. 1e , see “Methods” section for details).

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