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A P-value of 1.6 × 10−9 provides a Bonferroni corrected P-value of 0.05 and a P-value of ∼1 × 10−06 provides a false-discovery rate of ∼5% given the number of cis-eQTLs we identified at that threshold (1314).
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Four additional targets – TGFBR1, CSNK1A1, CHD6 and FAM83G – were also identified at this threshold.
In both sharp regression discontinuity and fuzzy regression discontinuity designs, causal treatment effects are identified at the threshold.
In all, 41 significant associations with all nine phenotypic traits were identified at the threshold of P < 0.05, representing 24 SNPs from different regions within PtoCesA4 (see Table S2).
However, when testing the rest of the datasets (S4 down-regulated, AS13 up-regulated, AS13 down-regulated), no enriched terms could be identified at the threshold of False Discovery Rate (FDR) 0.05.
Table 3 shows the fraction of TSRs of each class that is identified at the optimal threshold.
Differentially expressed genes were identified at a threshold for significance of α<0.01 and a FDR<5%.
Assessed separately, the typical Alzheimer's disease and PCA groups showed no significant grey matter associations of performance on either spatial task at the prescribed threshold nor were any significant intergroup differences in regional grey matter associations of auditory spatial performance identified at this corrected threshold.
Due to the preliminary and localization goals of this analysis, areas of significant co-activation were identified at an uncorrected threshold of p<0.005, k>5 voxels.
No high-level amplifications were identified at the 1.5 threshold.
Twenty-six microorganisms were identified at a significant threshold in patients with VAP.
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com