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PCR product sufficient for printing 1200 arrays was generated during July-September, 2004.
Additionally, a background dataset containing the promoters of all 8,125 genes present on both arrays was generated and used.
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Two independent extended families (A and B) of 31 × 31 arrays were generated.
Using this method, arrays are generated with average micro-dimple dimensions of 106 μm diameter and 10 μm depth, with a low standard deviation (STDEV).
The different noise arrays were generated by an algorithm given in Little, McSharry, Roberts, Costello, and Moroz (2007), the output values were then normalized (mean = 0, standard deviation = 1), and then their fractal property remeasured.
Utilizing an improved metal-assisted electroless etching (MAEE) of silicon in KMnO4/AgNO3/HF solution and silicon composite nanostructure of the long MPs erected in the short NWs arrays were generated on the silicon substrate.
Arrays were generated at the LLNL Microarray Center.
Arrays were analyzed using GenePix Pro 6.0, and.gpr files for individual arrays were generated.
Next, a set of 413 number arrays (pointer arrays) are generated.
Three biological replicated were performed per time point and 9 arrays were generated in total.
Strains carrying extragenic tba-1 arrays were generated as described below.
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