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Several compounds with a high probability for exhibiting polymorphism in the analysis were chosen for a limited experimental crystal form screening.
Basically, independent variables with a P-value of <0.1 in the univariate analysis were chosen for the multivariate analysis.
A set of genes of interest from the microarray analysis were chosen for validation using semi-quantitative real-time PCR and/or immunoblotting.
Seven and five somaclones of 'Chardonnay 96' and 'Syrah 174', respectively, which covered at least all polymorphic loci found in the EcoRI/ MspI fragment analysis were chosen for digestion with the isoschizomer HpaII.
A total of 18 genes were randomly selected among the 1319 transcript clusters whose expression was commonly up- or downregulated in liver and kidneys as shown by microarray analysis, were chosen for validation by RT-qPCR.
To examine whether Zn2+ and nZnO have the same underlying molecular mechanisms, two genes, Tnfa and Orm1, which were determined to be up-regulated in the nZnO-treated rats by microarray analysis, were chosen for gene expression analysis.
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The significant variables from the correlation analysis are chosen for the final prediction model.
Finite element analysis was chosen for model development because of its robustness in capturing the changes in material coordinates during large strain tailings consolidation.
Here, the more highly abundant transcript from the RNAseq analysis was chosen for the matched dataset.
Editing style analysis was chosen for its ability to open for new and unexpected themes during the analysis.
A framework analysis was chosen for this study; this approach allows for a combined deductive and inductive approach to data analysis [ 23].
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