It allows to detect common temporal features of two even distant neural populations, due to weak reciprocal interactions or shared influence of a third variable [10].
It allows to detect predefined events in real time and therefore the camera is capable to change its own operation or to give warnings e.g. to the safety system of the experiment.
It allows to detect protein interactions in all cellular compartments, it is fast and quantitative, non-invasive and highly reproducible.
It allows to detect unknown geriatric problems and to adapt treatment regimens accordingly [ 2, 30- 32].
Real-time RT-PCR technology is more sensitive, as it allows to detect a very small number of cells in larger volumes of previously pulverized (or homogenized) tissues.
In addition, it is shown that this approach allows to detect and exclude experimental points that are not fully equilibrated due to diffusion problems in narrow micropores.
The unique identifier approach might seem redundant to the SHA512 checksum, but it allowed us to detect duplicates for which the files were different, because of differences in the CEL file format used (i.e. CEL format version 3 and 4 generated with MAS5 and Gene Chip Operating Software, respectively).
First, it allowed us to detect subtle associations of phthalate exposure with child behavior.
Additionally, peaks corresponding to cancrinite and W zeolite phases have been detected; it allows to infer that the thickness of the coating Ca P is thin.
Its limitation is that it allows one to detect only the fact of regulation but, due to the absence of mapped promoters in the studied genomes, does not predict the type of regulation, such as repression or activation.
