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To investigate whether other mammalian neural stem cells express CD133 in a similar pattern, we applied similar staining and flow cytometry analysis to mouse NS cells [27].
Based on the phage-selected binding pattern we applied a simple scoring system combined with an untraditional baseline correction approach to identify novel natural binding partners in the human proteome.
To restrict mCD8-GFP expression to single or few cells of the complete dvGlutCNSIII-Gal4 expression pattern, we applied mild heat shocks (37°C) to larvae that in addition carry the transgenes UAS-FRT-CD2y+- FRT-mCD8-GFP [35] and a heat-shock inducible flipase (hs-flp).
For each ℓ and each pattern, we applied our single-pattern approach and then calculated the average RF distances of the obtained trees to the respective reference trees.
To seek for such a pattern, we applied a segmented regression model on simulated data Z jk (1 ≤ k ≤ 10), with one breakpoint occurring at generation G b (2 ≤ b ≤ 7).
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So, to generate a multiple-scale DoG representation for the pattern we apply DoG filter at different scales to the pattern.
Also, given a structural weekly admission pattern, we apply a time-dependent analysis to determine the mean offered load per day.
Following observation of natural patterns, we applied this knowledge by experimentally drilling pits at varying densities and sizes in a seawall that had been constructed with simple topographical complexity.
For the study of occlusal wear patterns we applied the OFA method [54] [55], using three-dimensional digital models originated from the surface scanning of dental casts.
To test whether the timing of spikes was important on a given timescale for patterns, we applied jittering to the original spike trains.
To dynamically monitor the population firing patterns, we applied a sliding-window technique to the MDA method which enabled us to directly visualize the real-time network-level memory encoding dynamics [10], [12], [22].
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