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For the tumor/normal parenchyma pairs, fold changes were calculated for each pair.
Fold changes were calculated for each transcripts between 3 weeks stored and heat-killed samples and 3 weeks stored positive controls (non heat-killed).
Values for RNA abundance were normalized for each gene with respect to the endogenous control in that sample (β-Actin), mean values for fold changes were calculated for each gene, and statistical testing was performed with the unpaired t-test.
Fold changes were calculated for each sample.
Mean values for fold changes were calculated for each gene.
Therefore, fold changes were calculated for each gene comparing tumors from the two patients.
Similar(50)
Geometric mean titers (GMTs) and fold changes were calculated for HI with 95% CIs.
The mean log2 fold changes were calculated for the spikes detected in all combinations of condition and compared to the log2 fold change expected (Fig. 3c).
Fold change was calculated for each strain relative to the uninfected control.
For each one-on-one comparison, log based fold changes are calculated for all genes.
The log2 (fold change) was calculated for both the microarray and qRT-PCR data.
More suggestions(11)
fold ratios were calculated for each
fold expressions were calculated for each
fold changes were determined for each
fold differences were calculated for each
fold changes were screened for each
fold changes were selected for each
fold changes were shown for each
fold changes were generated for each
fold changes were observed for each
fold changes were obtained for each
fold changes were extracted for each
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