Noise elimination and scaling down to extract essential features of the data is therefore required in visualization: even if we could visualize everything, there would be too much information for efficient processing.
Not only could we think about genetics, we could visualize and analyze actual DNA molecules.
We could visualize that the bulk of free ending nerve fibers ramified within 25μm of the dermo-epidermal junction, whereas below that only larger nerve bundles were present.
If these plots were superimposed in a single image (not shown here), we could visualize the overlap between electron and hole wave functions.
Extending our work from model membranes to intact E. coli ATCC 11775 in scanning electron micrographs we could visualize different patterns of surface perturbation caused by peptide SA-3 and SA-4.
Even though we could visualize a tumor in PC-3 xenograft mouse model by ex vivo surface fluorescent imaging as well as whole-body PET imaging, further studies with different and potentially more stable BODIPY dyes will be conducted to reduce the off target bone uptake.
