Barely Significant

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514,629 sentences

highly significantp<2e-160.0× alphaqualifiedgold
t-PGCS DNMs and likely post-zygotic DNMs) we first fit a simple Poisson regression model that calculated the effect of paternal age on total autosomal DNM counts in the R statistical language (v3.5.1) as follows: glm(autosomal_dnms ~ dad_age, family = poisson(link='identity’)) This model returned a highly significant effect of paternal age on total DNM counts (1.72 DNMs per year of paternal age, p<2e-16), but was agnostic to the family from which each third-generation individual was ‘sampled.’ Importantly, a number of third-generation individuals in the CEPH/Utah cohort share grandparents, and may therefore be considered members of the same family, despite having unique second-generation parents ( Figure 3—figure supplement 1 ).
highly significantP<2x10 -160.0× alphaqualifiedgold
marginally significantP=0.051.0× alphagold
Specifically, adjusting for African ancestry in a multiple regression model largely eliminated the highly significant effect of Black ethnicity on serum creatinine levels (decreased from P<2x10 -16 to a marginally significant P=0.05) whilst the highly significant effect of African ancestry on creatinine remained essentially unchanged when adjusted for Black ethnicity (P<2x10 -16 before and after adjustment).
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).
highly significantp ‐value < 2e−160.0× alphaqualifiedgold
All pairwise comparisons were highly significant ( p ‐value < 2e−16), indicating that the distribution of Tajima's D values differs between every pair of populations. 3 Results From the DNA extracted from the six toe pads, we sequenced between 135,310,794 and 208,948,341 Illumina pair reads per sample.