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The 64×4 matrices derived from human-chimp/baboon non-genic DNA were each based on at least 18,000 substitutions but since substitutions of complementary bases were pooled, these matrices are equivalent to full-structure 64×4 ones estimated on the basis of about 36,000 substitutions.
Two matrices are equivalent if one can be obtained from the other by a permutation of its columns.
These X and y matrices are equivalent to those of Kinghorn et al. [ 31], except that we add a vector of weights w.
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Since mode shape vectors have already been normalized by the mass matrix as φ u T M u φ u = I, multiplication of undamaged mode shape matrices is equivalent to the inverse intact mass matrix.
where A ∈ C rd R ( T, M n ( R ) ), n ∈ N and M n ( R ) is the family of all n × n real matrices is equivalent to the boundedness of all its solutions.
Hence, computing the GM of the covariance matrices is equivalent to computing the GM between the precision matrices, which is a particularly attractive idea in the case of Gaussian distributions, and may thus be a valuable property when fusing kernels.
Sensing matrix is equivalent to random measurement matrix, i.e., X = W.
Please be noted that weight matrix is equivalent to a weight vector.
Therefore, the th column of matrix is equivalent to the effective spreading sequence of the symbol.
Clearly, the M × N ′ matrix A' is equivalent to the original matrix A ~ under the row/column rearrangement.
The sensitivities are verified to be accurate, while the computational cost to compute the entire sensitivity matrix is equivalent to only one additional plasma edge simulation for each output quantity of interest.
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