Barely Significant

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highly significantp-values <2×10 −160.0× alphaqualifiedgold
The variation in ancestry seen in the admixture maps of Figure 1 also result in highly significant correlations of the three ancestries with altitude of birthplace (p-values <2×10 −16 for the three ancestries): African and European ancestry decreases with altitude (r of −0.24 and −0.39, respectively), while Native American ancestry increases (r = 0.48).
highly significantP <2×10 −160.0× alphaqualifiedgold
The association between miR-100 and EMT markers was further validated in human tumors: from the Cancer Genome Atlas (TCGA) breast cancer data [17] , we observed a moderate but significant inverse correlation between miR-100 and E-cadherin expression levels ( Rs = −0.1, P = 0.006, Figure 1F ) and a highly significant positive correlation between miR-100 and vimentin expression levels ( Rs = 0.43, P <2×10 −16 , Figure 1G ). miR-100 suppresses tumor growth and is downregulated in human breast cancer We performed TCGA data analysis to determine the expression levels of miR-100 and miR-22 in human breast cancer.
highly significantp ≤ 2E-160.0× alphaqualifiedgold
Vials of APSA stored on ice in the fridge for up to 22 months and then sampled at a dilution factor of 1/250,000 (DF 250,000) prior to assay showed extreme sample to sample variation in enzyme activity and a trend to lower OD values over time with a highly significant effect of the storage time on the detection limit (ANOVA p ≤ 2E-16, Regression p < 0.043) ( Fig. 2 A).
an increasing trendp < 2e-160.0× alphagold
Across the 38 weeks of the study, the percentage of reactive cases per week showed an increasing trend (value of p < 2e-16), ranging from 0.4% (95% C.I.: 0.11–1.47%) in the second week to 41.9% (95% C.I.: 26.4–59.2%) in the last week ( Figure 1 ).
highly significantp < 2 x 10 ‐160.0× alphaqualifiedgold
Result After controlling for baseline age, sex, education, APOE ε4 dosage, and self‐reported race, IFI44L genotype strongly associated with clinical trajectories in clinically normal (CN) individuals and those with mild cognitive impairment (MCI) in the ADNI cohort, with the rs273259 alternate (G) allele displaying a highly significant, dose‐dependent relationship with worse clinical trajectories (for CDR‐SB, in CN, p < 2 x 10 ‐16 ; in MCI, p = 1.1 x 10 ‐6 ; Figure 1A‐B).