Allport [58], for instance, has conducted experiments on phenomenal simultaneity, which seem to contradict the Discrete Moment Hypothesis – they are, however, compatible with LIDAs consciousness model, as can be seen from the Results section, in which we replicated the data from Allport's experiment using a LIDA-based agent.
10.7554/eLife.04811.020 Figure 8. Simulation results replicating the data from McFarland (1969) on learning the reinforcing effect of oral vs. intragastric delivery of water.
We conducted five additional behavioral measurements for those odorants (citral and l-carvone, respectively) that showed significant differences from the control in the initial screen, for sexes separately, at four different odorant concentrations and replicated the data from our initial screen at 1% (v/v) odorant concentration (Fig. S2).
Thus, we could not replicate the data from the recently published report by Wolmer-Solberg and colleagues 3. Based on our previous study 2 and the present results, we remain skeptical towards the prevalence of HCMV DNA in a majority of neuroblastomas.
For example, if a complete Gaussian window is used, it is not until time instant A+15 that the estimated value can be available for time instant A. However, Half-Window replicates the past data from time instant A-15 to time instant A as the future data from time instant A+1 to A+16, and immediately generates an estimated value for time instant A without any delay (Figure 10).
All aforementioned results were replicated with the data from discharge, except for one insignificant mean score difference.
The data from the Cal Tech (CC and CO) showed the highest agreement among the replicates, and the data from GNF and KAV showed a low level of agreement between replicates.
Technical variation in our methodology was tested by selecting a subset of strains for replicate hybridizations, and treating the data from replicates separately throughout the various analyses.
Because of the high overall reproducibility between the replicates, we tested whether the data from the three biological replicates could be combined to increase sequencing depth of the markers using repeated G-tests (McDonald 2009).
The developed model was robust and replicated the features of the data from which it was built in simulations.
