Using a new method of wavelet filtering broadband sub-second pulses with a frequency width of 0.48 GHz and narrowband millisecond spikes with a frequency width 0.13 GHz were recognized and analysed in detail.
As no systematic variation could be recognized, we analysed all the subgroups together.
The observed immunogenic antigen of M. leprae present specifically only in leprosy sera would then be recognized and analysed statistically.
Age is not explicitly recognized; cohort analyses, where time reflects age, can readily be done.
Ser-SLiMs (since we only had motif with a central Serine residue, only Ser-SLiMs but not Thr-SLiMs were analysed) recognized by Ser/Thr kinases are conserved in both ordered and disordered protein regions but are more conserved in disordered regions.
The desirable sub-group analyses (cf. exposure groups) are listed in advance for transparency, although it is recognized that some analyses will lack statistical power.
Furthermore, the monophyly of Pentatomidae is also strongly supported in all analyses, and a phylogenetic relationship of (Carpocorini, (Cappaeini, (Strachiini + Pentatomini))) within Pentatominae is recognized in most analyses (Fig. 8, Additional files 9, 10 and 11).
However, a generally recognized model of analysing how short the pulse width should be is not yet created.
In the change blindness literature, the influence of response bias is recognized and thus analyses typically report performance based on SDT measures of sensitivity in addition to accuracy measures (e.g., Mitroff et al., 2004).
The purified protein was recognized in Western analyses by monoclonal antibodies specific for the 6× His tag as well as the 3H5 neutralizing epitope known to reside in domain III.
