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In the IA design described previously, the achievable DoF per user can be obtained using the following combinations: d 1 = m ∗ + M + 1 M and d 3 = m ∗ + M M, where M is a parameter depending on the user number, M=(K−1)(K−2)−1, d i is the DoF of the i th user, i.e., the number of transmitted symbols, and N the number of symbols in each IA vector is defined as N=d1+d2.
To measure SREBP2 activity in HeLa cells, a luciferase reporter plasmid was created using a design described previously (47).
We determined our sample size based on the experimental design described previously to investigate the acute phase protein response in an experimental model of ovine caseous lymphadenitis [ 10].
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The experimental setup was analyzed based on the reference design as described previously [9], [10], [11].
Therefore, these P values and the associated confidence intervals were estimated based on a bootstrapping method that was developed for the case-cohort design, as described previously [53].
The trial is based on a randomized phase II screening design as described previously [ 20].
Gene-specific assays were amplified using a universal primer design as described previously.
Animals which were used in this study and experimental design were described previously [ 8].
The MH experiments were performed in a 2 × 2 design, as described previously.
The experimental setup was analyzed based on the reference-design as described previously [14], [15], [16] as presented in Figure S1A.
A microarray was designed as described previously and manufactured by Agilent Technology (Santa Clara, CA, USA) (Kim et al. 2009).
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