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A random dot motion stimulus was used as a control (random, Figure 1(g)).
As a control, random shuffling of donor segment locations found 3 overlapping segments in <5% of 1000 permutations.
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2% BSA in DMEM alone was added in the bottom of the chamber as a negative control (random chemotaxis).
As a negative control, random beacons were delivered into cells before and after differentiation and showed very weak signal in both cell types (red signal in the top panel), in contrast to the SSEA-1 signal.
As a control, 1,000 random sets of 275 DNA fragments (random ARSs) were generated genome wide.
As a control, a random sample of 50 non-responding genes was also analyzed.
As a control, a random sample of 50 genes was also analysed.
As a control, a random predictor was built that randomly assigns genes to three categories.
As a control, 12 random promoters that were not targets of CREB were also fused to luciferase reporters.
As control, random PPIs were used for AS-inter (Section 2.1).
As a control, we used random ECoG events selected within the same data files as the EEEs.
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