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To perform an analysis, diluted saliva, urine or blood samples are simply placed in a disposable thin-film sample holder using a dropper.
The existing spectral estimation algorithms designed for uniformly sampled complete-data sequences perform poorly when applied to data sequences with missing samples if the missing samples are simply set to zero.
The sequential nature of SMC methods can be exploited to design a fully sequential version of the EM, where the samples are simply updated from one iteration to the next rather than resampled from scratch.
In our approach, the plasma samples are simply diluted 30 times, which results in good crystallization and highly sensitive measurements.
Environmental and biological samples are simply too complex.
Most study samples are simply too small to give robust results.
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By using the pigment production which responded to exogenous BHL as biosensor output, BHL quantification in samples was simply done spectrophotometrically.
The trabecular samples were simply drilled out as found, as no mechanical de-contamination is possible on this type of tissue.
While for "bump-like" nanostructures the average residual reflection could be minimized with increasing thickness of the protective layers, the reflectance curves of "sponge-like" samples were simply shifted to longer wavelengths.
In this approach cellular samples were simply diluted 1 10 with 2% HNO3 prior to injection into the system.
Dry samples were simply placed on the ellipsometer stage for measurement, and hydrated samples were placed inside of the water-filled ellipsometry liquid cell described above.
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