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The proposed method involves second order information.
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One fundamental consideration regarding our proposed method involves first distinguishing whether a signal onset occurs.
The method involves first dissolving the starch by the ZnCl2 aqueous solution then adding NaOH.
The method involves first performing sensitivity analysis based on a reasonable kinetic model to identify the species dominated by a target reaction.
The method involves first obtaining effective CFRs, in which irrelevant contributions from scattered paths and the uncertainty of the OFDM time synchronizer are minimal, and then searching for the most likely location.
This method involves first calculating the apparent strong ion difference (SIDa): SIDa = [Na+] + [K+] + [Mg2+] + [Ca2+] - [Cl- ] - [lactate- ] (all concentrations in meq/l).
Briefly, the method involves first segmenting the arrays to identify the locations of at most one copy number gain or loss on a chromosome arm [ 21].
The fundamental approach utilized in this non-parametric method involves first trimming (removing) small sample studies that cause funnel plot asymmetries.
This method involves first fitting a cubic smoothing spline to the data and then identifying the inflection points of the fitted spline, which serve as the boundaries of adjacent windows.
An alternative method involves first creating a de novo assembly to obtain a set of contigs and then selecting only those contigs that are highly similar to the reference.
This method involves, first, identifying an "initial analysis sample" based on appropriately sized sample sizes and second, defining the "stopping criterion" – e.g., how many additional interviews will be carried out with no new themes emerging, at which point data saturation can be declared.
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