Barely Significant
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Genomic characterisation of Chinese myeloid malignancies and its clinical correlates: insights from targeted next-generation sequencing.

Front Med (Lausanne) · 2026 · PMC13173672 · PMID 42145737

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nominally significantno p-value reported
Because a large number of statistical tests were performed, particularly in the co-occurrence and SNP-related analyses, and not all exploratory analyses were adjusted for multiple comparisons, some nominally significant findings may reflect false-positive associations.

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