Barely Significant
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“modestly significant”

258 sentences · 258 papers · 308 search hits before verification · confirmed specimen

Sighted at

p=0.09

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

In the literature

modestly significantp < 0.051.0× alphaqualifiedgold
Clinical information of these patients was provided in Supplementary Data 1 , with no significant differences in HBsAg, antiviral treatment, liver cirrhosis status, tumor number; modestly significant bias in gender, age and tumor size ( p < 0.05); and significantly lower microvascular invasion (MVI), Barcelona Clinic Liver Cancer (BCLC) stages and Edmondson-Steiner (E-S) grades in AFP − HCC versus AFP + HCC ( p < 0.001).
modestly significantp < 0.051.0× alphaqualifiedgold
The mean 3D CT–CN–CT angle obtained for the five largest chromosomes was not significantly different from the mean angle for the small metacentric and submetacentric chromosomes, while a modestly significant difference ( p < 0.05) was noted in mean angle between the latter and the acrocentric chromosomes ( Table 1 ).
modestly significantp<0.051.0× alphaqualifiedgold
In the Cox-PH analysis, along with a focused MMS, the ages of the patients at the initial diagnosis and a binary measurement variable indicating the presence of somatic mutation on TP53 gene, which had a modestly significant (p<0.05) effect on the patient survival as shown in our preliminary analysis of the same data, were included as covariates.
modestly significantp < 0.051.0× alphaqualifiedgold
We chose variants that a) surpassed multiple testing in the pooled sequencing based case-control comparison (p < 10 −5 ), b) were modestly significant in the pooled sequencing based case-control comparison (p < 0.05) and had a low allele frequency (MAF < 5%), c) had functional consequence (within 20bp of a splice acceptor or donor site or non-synonymous variant), and were novel or low frequency (< 1%), d) were absent from one group (either controls or cases) and had a functional consequence (within 20bp of a splice acceptor or donor site or non-synonymous variant).