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Metacore maps with p-value < 0.05 were considered significant.
GeneMAPP maps with p-value <0.1 were considered significant.
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First, in total, we tabulated 2236 unique genes associated that mapped to a variant with P-value ≤1×10−6 and all of these 2236 genes had some documented relationship in the CTD.
All DEGs mapped in the KEGG pathways with P-value ≤ 0.05 were considered statistically significantly enriched.
Based on the transcriptome data, genes that were significantly regulated by mercury were identified at different time points (8 h, 24 h, 48 h and 96 h) with p-value < 0.05 and mapped to human homologous genes (See Additional file 2).
In both datasets from Σ DTree, MixDTrees MAP has higher mean values than MixDTrees MLE, which indicates a higher robustness of the MAP estimates (paired t-tests indicate superiority of MixDTrees MAP with P-values <0.05 in both Σ DTree − and Σ DTree +).
Markers with P-value < = 0.05 are called "Somatic".
7,643 failed to map with a p-value ≤ 0.05, 605 reads mapped most strongly to human sequences and 587 reads were mapped to other organisms (Table 5).
6 SNPs map within the HLA-G gene itself with p-Values ≤1×10−4.
Pathway maps with a p value < 0.05 and at least two genes or metabolites present were considered significantly modulated.
In this analysis no background list could be used and pathway maps with a p value < 0.05 and at least two genes or metabolites present were considered significantly modulated.
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