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To better reflect the current status of energy dissipation of sensor nodes, we give higher weight to the new REDR i sample by setting α to 0.3.
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The genomic/proteomic profile for a second target, which splits samples into groups, is limited to mutation and copy number; it is not feasible to split samples by setting an arbitrary cutoff for expression levels.
Figure3b shows an XRD {211} pole figure of the as-grown sample measured by setting 2θ = 57.92°.
Many studies have considered an upper limit of 4% as acceptable, 5 15 but we were conservative in our a priori sample size by setting it at 2%.
The observed autocorrelation in samples disappeared by setting the "thinning" to 50.
The binding energies for the sample were calibrated by setting the measured binding energy of C1s to 284.60 eV.
The recorded absorbance of each sample was normalized by setting the mean absorbance of the internal reference to 1 (450 nm; Cary 50 MPR microplate reader, Varian).
The binding energies for the samples were calibrated by setting the measured binding energy of C 1s to 284.60 eV.
Hence, the use of molecular beacon detection of M. tuberculosis and M. bovis in clinical samples is feasible by setting up two asymmetric PCRs concurrently.
The charging of samples was corrected by setting the binding energy of the adventitious carbon (C 1 s) at 284.6 eV.
The copy number of unknown samples was calculated by setting their PCR cycle number to the standard curve.
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