Sentence examples for multiple fold change from inspiring English sources

Gene list was created with threshold of false discovery rate (FDR) ≤0.05, multiple fold change (FC) ≥1.5 or FC ≤ −1.5 (to detect as many genes as possible that is different between the mutant and WT) and subsequently merged with the above generated annotation file with the common column of D. tertiolecta contig names (results were reported in Additional file 2).

Only one gene, IL31RA remained significant following correction for multiple testing, fold change 3.85, p = 1.56 × 10−6, q = 0.025.

Since most cytotoxic drugs have a low therapeutic index, additive effects of multiple low fold changes in drug resistance may be sufficient to cause clinical treatment failure.

When a gene was represented by multiple sequences, the fold change with q value of only one sequence was selected to represent this gene.

For supervised statistical detection of genes differentially expressed between NS and NS/LAH samples and controls, a multiple test including fold change (absolute Log2 ratio > 0.5), t-test (P < 0.01), and signal-to-noise ratio (SNR > 0.5; see also Supp.

Significance of DEG was determined using the Fisher's exact test (P-value < 0.05) with the Benjamini-Hochberg multiple testing correction and fold change >1.5.

The output of XBSeq contains p value, adjusted p value for multiple test correction, log2 fold change and other statistical merits for each gene.

Peaks with a P-value <0.05 were assigned active-multiple sclerosis: C and inactive-multiple sclerosis: C ratios equal to the fold change between the active-multiple sclerosis or inactive-multiple sclerosis and control.

We selected high confidence genes with a P-value of <0.01 (ANOVA one-way, Bonferroni Step-Up multiple-test correction) and fold change ⩾+2 or ⩽−2.

Significantly expressed genes (p < 0.05) was obtained by Tukey HSD post-hoc test followed by Bonferroni multiple testing correction with a fold change set at ≥2. GO enrichment and KEGG pathway analysis were conducted with STRING (version 10.5) and the significance was set at a p-value < 0.05.

Transcripts with ≥ 2 fold change and multiple testing adjusted P-value ≤ 0.01 were identified as differentially expressed.