Barely Significant
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“marginal significance”

5,069 sentences · 5,069 papers · 6,913 search hits before verification · confirmed specimen

Sighted at

p=0.07

Listed by Hankins (2013) · Otte et al. (2022)

In the literature

marginal significanceP ≤ 0.010.2× alphagold
To identify cancer-specific regulatory variants, we compared our eQTLs to eQTLs from the Genotype-Tissue Expression (GTEx) project 10 , adopting previous strategies to assess eQTL replication 11 , and probed lead eQTL variants for marginal significance in GTEx tissues ( P ≤ 0.01, Bonferroni-adjusted).
marginal significancep < 0.010.2× alphagold
Interpretation thresholds followed standard normal distribution critical values: ±1.96 ( p > 0.05) = Nonsignificant deviation; ±1.96 to ± 2.58 (0.01 < p < 0.05) = Marginal significance and ±2.58 to ± 3.29 (0.001 < p < 0.01): Strong evidence against independence.
marginal significanceP < 0.010.2× alphagold
highly significantqualifiedgold
Differences were deemed statistically significant based on stringent criteria, specifically, * P < 0.05 for marginal significance, ** P < 0.01 for moderate significance, *** P < 0.001 for strong significance, and **** P < 0.0001 for highly significant differences, or as not significant.
marginal significanceP = 0.010.2× alphagold
Although we found marginal significance between two SNPs, rs7013278 and rs7014346 (HR = 2.20, P = 0.01 and HR = 1.96, P = 0.03 respectively), with inferior CRC survival by multivariate regression analysis, none of these variants showed study-wide association with survival after correction for multiple testing.
marginal significancep = 0.0140.3× alphagold
Although the latency difference between stimulation and non-stimulation trials reached marginal significance at the population level ( n = 56 sites, z = -2.45, p = 0.014; two-tailed Wilcoxon signed-rank test), the difference was small, and only one of the 56 stimulation sites showed a significant effect ( p < 0.05; two-tailed Wilcoxon rank-sum test).
marginal significancep = 0.0170.3× alphagold
A lack of an association between each SNP and MIH was found in analyses performed for frequency distributions of major homozygotes, heterozygotes, and minor homozygotes (except for the rs4811117 polymorphism, for which the p -value reached marginal significance at p = 0.017, which is on the borderline if the Bonferroni-corrected significance level of p = 0.05/3 = 0.017 is used for the global chi-squared test with the further tests treated as post-hoc tests).