Barely Significant
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“highly significant”

132,143 sentences · 132,143 papers · 160,126 search hits before verification · confirmed specimen

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p=0.09

Listed by Hankins (2013)

In the literature

highly significantp<9e−050.0× alphaqualifiedgold
To estimate probability of error, we sampled 10 sets of 40 predicted genes and 10 equally-sized control sets, matched by expression; the comparison of the mean bias in the 10 sampled sets showed highly significant difference (p<9e−05; non-paired t test).
highly significantP ‐value < 9 × 10 –50.0× alphaqualifiedgold
Genes that have previously been identified as containing SNPs that are genome‐wide significantly associated with obesity‐related phenotypes (Ensembl; http://www.ensembl.org/index.html ) are labeled with a double asterisk in Table 3 , whereas those that have been observed as highly significant ( P ‐value < 9 × 10 –5 ) have a single asterisk.
highly significantP = 9.43 × 10 −50.0× alphaqualifiedgold
We used a fixed-effects model to validate this observation (“Methods”) and detected a highly significant difference ( P = 9.43 × 10 −5 ) in mean effect between pre-natal ( \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{d
highly significantp = 9.482 × 10 −50.0× alphaqualifiedgold
This was again confirmed by a highly significant interaction between the factors “expected time” and “probed time” ( F (1,23) = 22.27; p = 9.482 × 10 −5 , η p 2 = 0.49), or, equivalently, a highly significant benefit for valid compared with invalid trials ( t (23) = −4.71; p = 9.590 × 10 −5 ; d = −0.96).
highly significantp = 9.485 × 10 − 50.0× alphaqualifiedgold
Conversely, we observed a highly significant difference ( p = 9.485 × 10 − 5 ; paired t ‐test) in self‐described interest when comparing the post‐introductory lecture responses to responses after the practical session with DadApp (mean = 4.746 ± 0.489 SD; Figure 4a ).
highly significantp-value < 9.7979e-050.0× alphaqualifiedgold
Interestingly, in our study, both the pangenome- and SNP- based GWAS analyses indicated that the rimI gene, encoding a ribosomal protein S18-alanine N-acetyltransferase, is linked to clinical traits displayed by the isolates, as indicated by a significant pangenome locus (adjusted p-value < 0.00033) and two highly significant SNPs (adjusted p-value < 9.7979e-05).