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We begin by evaluating the selective approach of attributing a confidence-measure to each matched pair.
To this end, we begin by evaluating the performance of SDN-enabled switches and controller.
We begin by evaluating the types of relevant historical information available from contemporary forests, then evaluate common paleoecological techniques, namely dendrochronology, pollen, macrofossil, charcoal, and fossil insect and wood analyses.
We begin by evaluating the norm of the difference between both points of iteration n + 1: A n + 1 - B n + 1 = γ ∑ k = 1 K λ k · a k A n A n + λ k - B n B n + λ k (34) = γ A n - B n ∑ k = 1 K a k λ k 2 A n + λ k B n + λ k (35).
We begin by evaluating the first potential explanation for non-detects by examining the distribution of Ct values including non-detects coded as 40 (Fig. 5).
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We began by evaluating the phenotype of transferred effector T cells at multiple time points during tumor regression.
We began by evaluating the redox status of Trx in RKO colon cancer cells where endogenous TR1 levels were attenuated with siRNA.
To determine which of these could potentially participate in proventricular biofilm formation in the flea, we began by evaluating the effect each of these genes had on in vitro biofilm formation.
To generate each nMDS plot, we began by evaluating the number of dimensions required to appropriately present the bacterial communities using a stress plot, which was generated using n = 10 iterations of nMDS for dimensions n = 1 through n = 5.
We began by evaluating the clustering and reshaping stages of our algorithm (Section 3.6).
We began by evaluating the expression profile of a breast tumour specimen that had high-PLD1 mRNA levels (shown in Figure 2).
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