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Uncertainties of ultrasound guidance included tissue inhomogeneities, speckle noise, probe pressure, and inter-observer variation.
Today, the sensitivity, dynamic range, and resolution of DNA microarrays are limited by interference, noise, probe saturation, and other sources of errors in the analyte detection procedure.
A 97-dB white noise probe lasting 100 msec was presented binaurally via headphones.
To reduce noise, probe sets and transcript clusters which fell into the lowest quartile of the expression signal distribution across all samples were excluded from the dataset.
The fear acquisition phase consisted of three blocks with four trials of each type (a reinforced conditioned stimulus, CS+; a nonreinforced conditioned stimulus, CS−; and the noise probe alone, NA).
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The electrical characteristics were measured on a low-noise probe station in air using an Agilent parameter analyzer 4156C controlled by a Labview programme.
Several factors might contribute to this, including noise of probe hybridisation, MNase bias correction, and the specific methods used for peak calling/detecting.
We removed from analysis samples that were outliers with respect to any one of the internal control probes (excluding probes designed to evaluate the background noise and probes designed to normalize the data) and samples that were not of non-Hispanic white ancestry, either self-declared or by investigation of genetic ancestry using genome-wide SNP data.
The differential design of the two detectors eliminates both the fluctuation of light source and the electronic noise from probes, and increases the axial resolution as well.
To study this question in a realistic setting, we used ecological noises to probe environmental sensitivity throughout sleep, simultaneously monitoring subjects' brain activity with EEG.
To eliminate background noise, miRNA probes with signal intensities < 40 (i.e., the median signal) across all replicates were removed.
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