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We analyze for each step (i.e. MRI acquisition, network building and network statistical analysis) the advantages and potential limitations.
For the two scenarios of ideal (i.e., without traps) and non-ideal (with traps) buffer/absorber interface, we vary ΔAB and ΔBW in the range −0.5 eV to 0.5 eV, and analyze, for each combination, the physical mechanisms limiting the cell performance and the way to optimize it by choosing optimal buffer doping and thickness.
Our main goal was to analyze for each species the effect of climate, local factors (i.e. light availability, stand structure and ground cover) and the interactions among them to identify the main drivers leading the regeneration process, assessed in terms of presence, abundance and mean annual growth of juveniles.
To limit redundancy in our analyses, we a priori chose a single probe set to analyze for each of the 20026 human genes.
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At least 10,000 cells were analyzed for each sample.
Three random fields were analyzed for each chamber.
A total of 10,000 cells were analyzed for each curve.
A total of 5 intestinal sections were analyzed for each animal at each time point.
The factors affecting enantioselectivity results are analyzed for each substituent.
A minimum of 20 neurons per culture were analyzed for each experiment.
A dissociation curve was analyzed for each PCR experiment to assess primer dimer formation or contamination.
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