It would also be interesting to use the duckweed model to further analysis how bacterial pathogens subvert host-cell pathways, which is central to understanding infectious disease.
It would also be interesting to use our approach in the context of complex diseases like cancer to study pathological modifications of such biological pathways.
In the future, it would also be interesting to use methods which provide quantitative information for the comparison of data from both cellular levels.
Concerning latency III EBV cells, it will also be interesting to use in vivo models to assess the efficiency of ABT-737 alone, as we found that, even at very low doses, this compound promoted apoptosis in LCL cells.
It would also be interesting to use other methods for image generation, for example, new non-invasive photonic techniques such as the FD measurements in light scattering microscopy and look for the equivalence of the results [165 167].
Also, it is interesting to use the face graph, instead of the square graph.
It will also be very interesting to use our method for making ligand predictions for the structurally distinct receptors such as olfactory ionotropic glutamate receptors (IRs), and gustatory receptors (Grs) in insects, and olfactory and taste GPCRs in vertebrates.
It is also interesting to note that using a longer block size appears to improve the performance.
It is also interesting to note how using the three geographic alternatives for EEJ, changes the correlation, when only European populations are included.
