Barely Significant
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highly significant

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p=0.09

Listed by Hankins (2013)

In the literature

highly significantP =8.6 × 10 −290.0× alphaqualifiedgold
When we performed a gene-set enrichment analysis of these 1,341 genes using the Database for Annotation, Visualization and Integrated Discovery 20 , we found highly significant enrichment of ‘SP_PIR_KEYWORDS: alternative splicing' (Benjamini-corrected P =8.6 × 10 −29 ) and ‘UP_SEQ_FEATURE: splice variants' (Benjamini-corrected P =1.1 × 10 28 ), which denote genes with known splicing isoforms ( Supplementary Data 2 ).
highly significantP = 9.3 × 10 −290.0× alphaqualifiedgold
This genotyping revealed that in 56 of 57 cases, orange and mosaic individuals were homozygous for one allele (hereafter o ) at the SPR locus, whereas yellow and white individuals, with one exception, were either heterozygous ( n = 41) or homozygous ( n = 16) for the alternative allele (hereafter O ): a highly significant association (recessive model, P = 9.3 × 10 −29 ).
highly significantp < 10 -280.0× alphaqualifiedgold
The resulting Manhattan plot ( Figure 5B ) identified several highly significant metabolic hubs: 3.6.1 Stress-induced lipid amide accumulation The tentative lipid amide (m/z 338.33) was the most significant feature ( p < 10 -28 ), showing prominent accumulation in T3 and T4 samples as a marker for biotic stress. 3.6.2 Phenolic partitioning and correlation with lipid derivatives Quantitative analysis showed that Benzoic acid (GC_BA-TMS) levels were significantly higher in T2 compared to all other treatments.
highly significantp -value = 1.29E-280.0× alphaqualifiedgold
Pathways showing highly significant results include the MAPK signalling pathway ( p -value = 1.29E-28), the FoxO signalling pathway ( p -value = 8.09E-19), the HIF-1 signalling pathway ( p -value = 9.65E-19), the PI3K-Akt signalling pathway ( p -value = 1.09E-18), and the insulin signalling pathway ( p -value = 2.87E-16).
highly significantP = 1·3 × 10 −280.0× alphaqualifiedgold
8 , 9 The strongest and most highly significant associations have been reported with early-onset, persistent eczema 10 , 11 (odds ratio 5·6, 95% confidence interval 4·1–7·8, P = 1·3 × 10 −28 ) and asthma occurring in individuals with atopic eczema 12 – 14 (odds ratio 3·49, 95% confidence interval 2·00–6·08, P = 1·0 × 10 −5 ).
highly significantp value = 3.1 × 10 −280.0× alphaqualifiedgold
An Amino Acid Permease gene, CsAAP2A (gene ID: Csa4M573860), was selected as a promising candidate gene based on the finding that this gene was down‐regulated by a factor of 100 in NIL DM4.1.3 compared to HS279, which was highly significant (Benjamini–Hochberg corrected p value = 3.1 × 10 −28 ). 2.2 Lack of CsAAP2A expression is due to the insertion of a CUMULE transposon To investigate the reason why CsAAP2A was very poorly expressed in NIL DM4.1.3, we resequenced the whole genomes of genotype NIL DM4.1 (an NIL with an introgression spanning subQTL DM4.1.1, DM4.1.2, and DM4.1.3) as well as susceptible parent HS279.