Barely Significant
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“highly significant”

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

Sighted at

p=0.09

Listed by Hankins (2013)

In the literature

highly significant−log( p ) = 13.720.0× alphaqualifiedgold
Two linkage blocks within the Waxy locus (5034 bp in length) reflected an unusual LD decay within the gene, and the first block contained a highly significant T→G splice variant at 1 765 761 bp (−log( p ) = 13.72, β = −0.74) lying in 5′end of intron 1 (LOC_Os06g04200.1) (Figures 3 a and S4 a,b).
highly significantp = 2E−140.0× alphaqualifiedgold
We subjected the top 200 variant genes to GO (gene ontology) term analysis and found a highly significant over-representation of terms such as spermatogenesis ( p = 2E−14), mitosis ( p = 5E−6) and meiosis ( p = 1E−3).
highly significantP = 2.4×10 −140.0× alphaqualifiedgold
Only one locus, IL23R , demonstrated true independence of the psoriasis SNP; the PsA-associated SNP rs12044149 remained highly significant ( P = 2.4×10 −14 ) after conditioning on the psoriasis SNP, rs9988642, and the addition of rs9988642 did not improve the model fit with LRT ( P = 0.21).
highly significantp = 3.1 × 10 −140.0× alphaqualifiedgold
6 B ), along with the highly significant positive correlation (Pearson's correlation, r = 0.98; p = 3.1 × 10 −14 ; N = 19) between them, confirms the model's reliability as a KE estimator for any trajectory defined in either the hand space or the joint space, within the context of the current 2D movement setup.
highly significantp = 3.7 × 10 −140.0× alphaqualifiedgold
A GWAS for LSK cells revealed several suggestively associated loci, including those on chromosomes 2, 4, 6, and 18, as well as a highly significant (p = 3.7 × 10 −14 ) locus on chromosome 15 ( Figure 2 B; Table 1 ), where the lead SNP (rs31675052) is located approximately 100 kb downstream of Ly6f ( Figure 3 B).
highly significantP =3.8e-140.0× alphaqualifiedgold
A highly significant correlation was observed between SETD2 and H3K36me3 immunohistochemical staining ( P =3.8e-14, Cochran-Armitage test, Supplementary Figure S3a ), suggesting that absence of H3K36me3 staining is a good surrogate for SETD2 loss-of-function. 8 DNA damage was assessed by staining for phosphorylated his
highly significantP = 3.8 × 10 −140.0× alphaqualifiedgold
For T1D, the white UK Biobank British PRS models was highly significant ( P = 3.8 × 10 −14 ) with outstanding predictive performance in white British ancestry; however, the predictive performance was significantly worse when transferred to individuals of African or South Asian ancestry.