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In the first spell, we randomly assign each individual in the sample a value of the individual unobserved heterogeneity coefficient (i.e. we determine of which type the individual is).
This signal is smoothed by computing for each sample a value that averages the membrane potential through a given time window.
When summing up the estimated relative frequency of all variants within a DNA sample, a value different from 100% was most often observed.
We employed a combination of Se, Sp, and PPV to arrive at the optimum CES-D cutoff score for probable major depression in our sample, a value that was between 16 and 17.
Measured values of prepared QC samples were within two standard deviations of the calibration standards (e.g., for the 5 μg/L QC sample a value between 4.67 μg/L and 5.33 μg/L was acceptable, given the standard deviation of 0.166).
The topology induced by a distance matrix can be described by a filter function, which assigns to every sample a value (phenotypic outcome, viral load, etc).. First, the topological space is decomposed into overlapping subsets using level sets of the filter function.
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Each response X ni was generated by sampling a value from a uniform distribution across the interval [0, 1].
By applying the Hoffman-Weeks method to the melting temperatures of isothermally crystallized samples, a value of 192 °C for the equilibrium melting temperature of CTB was obtained.
For our samples, a value of 0.0 would represent a pure cutthroat and a value of 1.0 would represent a pure steelhead.
For each measurement < LOD, we randomly sampled a value from the appropriate log-normal distribution as the imputed value.
As in prior studies (Whyatt et al. 2001), we assigned nondetectable samples a value midway between the limit of detection and zero.
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CEO of Professional Science Editing for Scientists @ prosciediting.com