A bootstrap method for sum-of-poles approximations

A bootstrap method is presented for finding efficient sum-of-poles approximations of causal functions. The method is based on a recursive application of the nonlinear least squares optimization scheme developed in (Alpert et al. in SIAM J. Numer. Anal. 37:1138–1164, 2000), followed by the balanced truncation method for model reduction in computational control theory as a final optimization step. The method is expected to be useful for a fairly large class of causal functions encountered in engineering and applied physics. The performance of the method and its application to computational physics are illustrated via several numerical examples

Projection Based Model Reduction for Optimal Design of the Time-Dependent Stokes System

The optimal design of structures and systems described by partial differential equations (PDEs) often gives rise to large-scale optimization problems, in particular if the underlying system of PDEs represents a multi-scale, multi-physics problem. Therefore, reduced order modeling techniques such as balanced truncation model reduction, proper orthogonal decomposition, or reduced basis methods are used to significantly decrease the computational complexity while maintaining the desired accuracy of the approximation. In particular, we are interested in such shape optimization problems where the design issue is restricted to a relatively small portion of the computational domain. In this case, it appears to be natural to rely on a full order model only in that specific part of the domain and to use a reduced order model elsewhere. A convenient methodology to realize this idea consists in a suitable combination of domain decomposition techniques and balanced truncation model reduction. We will consider such an approach for shape optimization problems associated with the time-dependent Stokes system and derive explicit error bounds for the modeling error. As an application in life sciences, we will be concerned with the optimal design of capillary barriers as part of a network of microchannels and reservoirs on microfluidic biochips that are used in clinical diagnostics, pharmacology, and forensics for high-throughput screening and hybridization in genomics and protein profiling in proteomics