Figure 2 shows mRNA expression profiles of all 31 carcinomas employing SNO as a control group, depicted as heat-maps of normalized log2 transformed original fold change (FC) values.
Figure 1 shows a map of normalized population densities.
We used the meta-analyzer program, which performs a heat map of normalized signal intensity values, corresponding to the different organs of the plant, for each gene.
Using single-color Agilent custom whole-transcriptome microarrays, we analyzed the expression of 88 CYP genes over the course of early development in zebrafish (plot, Figure 4; heat map of normalized values, Figure 5).
Averaged photocurrents evoked at each stimulation point were superimposed (B, upper left) and shown with an expanded time scale (B, upper right) and as a corresponding color map of normalized peak amplitudes (B, right; scale bar, 0 = min amplitude, and 1 = max amplitude).
These histology derived ROIs were then transferred onto extracted ion maps of tamoxifen (normalized on TIC) in monochromic MS images.
Maps of the normalized equivalent current function ({varPsi }_1) at different universal times and seasons (Figs. 8, 9, 10, 11) provide a convenient way to visualize the DIFI model and its temporal evolution.
The multispectral FLIM maps of the normalized fluorescence intensity and the lifetime of the thick cap fibroatheroma are shown in Fig. 4 d-e).
To generate smoothed texture coding maps of the normalized barrel each cell was assigned set of point coordinates c k (x i, y i ) with i = 1…N k, N k —number of cells found for texture k, and c k —color assigned to a texture k and x i, y i are the spatial coordinates of cell i.
Heat map construction of normalized expression of differentially expressed genes was performed using hierarchical cluster analysis with uncentered correlation used as similarity metric and complete linkage as clustering method.
