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Several studies have stated that these arrays may not be efficient due to high wake losses for some wind directions.
Therefore, normalization methods used for mRNA expression arrays may not be appropriate for miRNA arrays.
Under certain circumstances, however, the density of some tiling arrays may not be high enough to use the Wilcoxon method.
Therefore, researchers have generally concluded that off-the-shelf normalization methods for mRNA arrays may not be appropriate for miRNA arrays [ 11, 13, 15].
For example, information on array design description for commercially available arrays may not be necessary, but specifications should be provided for custom arrays.
Many bacterial genome sequences are deposited only in contig-state where long CRISPR arrays may not be assembled correctly onto a single contig.
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Generally, the microlens array may not be perfectly aligned to the imaging system, so some amount of manual rectification is required.
Further it is deduced that (1) selection of the RUCs for a fixed periodic array may not be unique, however, the solution is independent on the choice of the different RUCs; (2) boundary traction continuity conditions can be guaranteed by the application of the proposed unified displacement-difference periodic boundary conditions.
The higher diffuse reflectance indicates the surface without hole array may not be flat.
The RFIs are usually colored both spatially and temporally, and hence exploiting only the spatial diversity of the antenna array may not give the best performance.
Yet many real-world applications require a two-dimensional (2-D) AOA estimation (e.g., azimuth and elevation) because the sources and receive array may not lie in a single plane.
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