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Supporting information includes supplementary tables and figures, methods for molecular dynamics simulation, synthetic procedures, experimental details, analytical data for all new synthetic compounds, NMR spectra.
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Additional tables and figures, detailed methods for protein purification, assay conditions (including a table summarizing all of the reaction conditions used for dose response), methods for isothermal titration calorimetry and cellular assays.
Figure 2 Methods for including a measurement study and (rice growth) model study to understand a real phenomenon or anticipate a future situation.
Figure 9 Different methods for frame detection and estimation using the core algorithms discussed.
Specific data are cited in the Figures, and the methods for their production are listed in the source documents.
Open image in new window Figure 1 Exact methods for QAP.
To construct a model that reproduces the distinct stages of the migration process (as illustrated in Figure 1A), we specified the interaction scheme shown in Figure 1B (see Methods for details of model formulation, construction and simulation).
Similarly, Figure 3B considers methods for assessing translocation and ADME properties in acellular, cellular (in vitro) and in vivo systems, whereas Figure 3C considers methods for assessing special chemistry of nanoparticles both in vivo and ex vivo.
What makes ROBOCHOP so promising is that it uses "smart" programming to figure out cutting methods for itself.
A schematic of the BMI is provided in Figure 1 (see Methods for details).
The results are summarized in Figure 5. Methods for functional connectivity analysis usually require one BOLD signal intensity time courses per ROI.
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