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Since the strain still had the PoxB path to acetate production, its contribution was tested by deleting the poxB gene (Fig. 4).
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These contributions are tested by coherence analysis for each ZO sample, and the set of attributes, which yield the highest coherency, is accepted as the optimum operator parameters to perform the actual stack (Höcht et al. 2009).
We use an elastic predictor plastic corrector scheme as a base and divide any predictor step into the contributions from the elastic and plastic components, where the elastic and plastic damage contributions are tested separately.
The contribution of adiponectin was tested by injecting bFKB1 into wild type (WT) and Adiponectin (Adipoq) KO mice on HFD.
Significant contribution of separate factors was tested with ANOVA (χ 2).
The contribution of each explanatory term was tested sequentially, with non-significant terms removed from the model to produce the minimal model following standard stepwise deletion [43].
Randomness of the parent contribution to the offspring population was tested by bootstrapping with 95%% confidence.
The contribution of a given explanatory variable was tested by the Wald test.
CD36 which plays a major role for the acquisition of excess cellular cholesterol in tissue macrophages in mice [ 17] was tested for its contribution to the increased uptake of oxLDL and nLDL by FH monocytes.
Contribution of the variables to the model was tested using the likelihood ratio X2 test.
The null hypothesis of no genetic contribution (i.e., h2 = 0) was tested with a likelihood ratio test, comparing the full model likelihood with that of the restricted model where h2 = 0. Heritability is expressed as the mean ± standard error of the mean.
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