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Our method therefore yields completely automated synthesis of (globally) optimal CMOS amplifiers, directly from specifications.
Our method, therefore, correctly identified ERRB2 as an EMF and assigned it to its different and unrelated real functions.
Our method therefore represents a simple and practical method that can be incorporated into control schemes for intermittently mixed solid-state fermentation bioreactors with forced aeration.
Our method therefore also fosters the intercomparison and interpretation of the differences with these past models.
Our method therefore eliminates potential effects due to VPA uptake and phosphoinositide degradation.
Our method therefore has the considerable advantage of generating more realistic, detailed diets for the UK.
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Our methods therefore enabled us to identify and measure dynamic correlations between lipid droplet formation and cell metabolic state, while providing insight on the spatial heterogeneity of the observed signals.
Our methods, therefore, can be used for developing stable and reproducible models with good performances.
For the characterization of candidate epitopes for peptide-based cancer vaccines and ultimately also for monitoring of vaccination success in CTL from patients, our microarray-based method therefore enables functional studies that were not possible before.
Our method is therefore called a pseudo-spectral multiscale method.
Our method may, therefore, also be applicable to the de novo design of protein nanostructures.
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