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Each column in the state transition matrix was repeated R times to generate replicates.
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This signature or the initial matrix is repeated four times into an intermediate matrix which is again repeated according to the image capacity.
The matrix filling was repeated up to five cycles, and the efficiency of the matrix filling was examined.
The matrix multiplication was repeated multiple times until the spectrum matches the observed spectrum.
Matrix-Lysis was repeated making use of the adapted protocol (this study) to achieve more efficient tissue lysis.
During the extraction process, 500 μg/kg of each target analyte was spiked in three replicates for barley and wheat matrices; the process was repeated twice.
After adjusting the pairwise comparison matrices for consistency, ranking was repeated using the AHP and TOPSIS.
The transformation matrix between these two fibrinogens was repeated and used in a Chimera command to generate more monomers, attaching one monomer per iteration onto one end of the chain.
The process was repeated until the matrix was completed.
This calculation was repeated for each TRANSFAC matrix.
This operation was repeated 10,000 times, providing a random distribution of matrix correlations with which to assess the significance of the observed matrix correlation.
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