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A reordering algorithm is applied on one portion of the matrix to minimize fill-ins.
In the second stage, we aim to find a unimodular matrix to minimize the PEPs as described above.
Secondly, we target to find a unimodular matrix to minimize the second largest PEP, which is also crucial to the BER performance, while keeping the largest PEP unchanged.
The totally MIMO approach is based on the optimization of an open-loop diagonal transfer matrix to minimize the stability margin variations of the perturbed diagonal elements of the closed-loop transfer matrix.
Here we describe the selection of four new pools isolated on a disulfide-linked CoA affinity matrix to minimize context-dependent recognition imposed by the attachment to the solid support.
We, furthermore, also assessed seed voxel clustering using the spectral reordering approach (Johansen-Berg et al. 2004) which involved computing the cross-correlation matrix of the whole brain co-activation profiles obtained for the individual seed voxels and reordering the matrix to minimize the cross-correlation values off the diagonal.
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This technology can be extended to extract organic compounds in different solid matrices to minimize time extraction and solvent consumption.
To find y1 and y2 for the estimates of s1 and s2, IVA instead estimates the unmixing matrices to minimize the dependency between different sources while maintaining strong dependency across frequency bins.
In [9], an iterative algorithm has been proposed to optimize the source beamforming vector and the relay precoding matrices to minimize the total source and relay transmit power such that a minimum signal-to-interference-plus-noise ratio (SINR) threshold is maintained at each receiver.
It then iteratively updates the matrices to minimize a cost function (usually related to the measure: V − W H ). At each iteration, W and H are updated by multiplying them by some factor which improves the quality of the approximation in Equation 1.
We aimed for a chromatographic system that results in sufficient retention for all compounds and adequate separation of the antiviral drugs from the matrix constituents to minimize matrix effects.
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