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In contrast, only 40.1% of uniquely bound Dichaete intervals are conserved in D. simulans, and 33.7% of uniquely bound SoxN intervals are conserved (Table 4), a highly significant difference between common and unique binding (χ = 3398.3, d.f. = 2, p < 2.2e-16 [approaches 0]).
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We therefore developed a method for correcting for the bias introduced when combining statistically dependent data with a Bayesian approach in order to create a continuous scale confidence score that is comparable between interactions with common and unique evidences (Figure 2).
In light of our finding of the differences between common subset and unique AD discriminative signature, we suggest that in addition to the common set of the core proliferative genes, our ECD signature includes a subset of genes encoding proteins that often undergo mutagenesis, provide a regulation of proliferation and the transition steps in the AC development.
This aim will focus on implementing in community practices and hospitals, with one of the goals being to identify the challenges that are common and unique between the UF Health implementations, and implementation in other setting.
The various twin studies to date that have investigated the aetiological relationship between hyperactivity impulsivity and inattention therefore indicate that there are both common and unique genetic effects between the two symptoms domains.
We compared the quality of life issues between the two groups to identify common and unique issues.
This package gives the heritabilities and confidence intervals as well as the P values for statistical differences between the additive genetic and the common and unique environments, based on maximum likelihood estimation [36].
To estimate the sequence divergence between the two data sets, the common and unique sequences were extracted from the two repeat-masked WGS data sets by BLAST-searching between them (e-value: 1e-50).
A Venn diagram analysis was also performed to identify common and unique canonical pathways between different U concentrations.
The additive genetic, common, and unique environmental contributions to the association between brain volumes and risk for Sz were estimated by structural equation modeling.
In this model the factor loadings for the common and unique factors, and the twin correlations between the unique factors were constrained at the estimates obtained in the first step (see Table 4).
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