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The GST-tagged β-catenin and GST-tagged mGS-CTD were expressed by transforming expression plasmids into BL21 (DE3) cells, grown in LB Broth, and induced by 0.5 mM IPTG.
Transforming expression data into a "per cell" database is an effective way of normalizing expression data across samples and platforms.
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Maclellan [24] argued that mental computation entails transforming expressions into others that look different but are not changed in value (our emphasis).
Several variance-stabilization and normalization transformation methods, which try to transform expression values to be equal variance and normally distributed for each gene, have been proposed [ 19- 23].
The signal warping can be carried out before transformation or directly embedded in the transform expression [11]: (6).
Differentially expressed genes were determined by fold change (fc) calculation of log2 transformed expression data.
The basic idea consists in using a combination of an incremental method with the usual Hough transform expression to join circuit performances and accuracy requirements.
Log 2 transformed expression values were annotated with HUGO symbols.
Logarithmically transformed expression values were used to implement GSEA.
Next quantile normalization was applied to the log2 transformed expression values (Bolstad BM Bioinformatics 19: 195–193).
The transformed expression data, corresponding to 66 ratios, were then used for Fisher's Exact Test.
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