Barely Significant
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The genomic landscape across 474 surgically accessible epileptogenic human brain lesions.

Brain · 2023 · PMC10115236 · PMID 36226386

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nominally significantno p-value reported
52 A global false discovery rate adjusted P -value q ≤ 0.1 was used to identify statistically significant non-synonymous variant-enriched genes and an unadjusted P ≤ 0.005 to identify nominally significant non-synonymous variant-enriched genes.

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