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The running time and CPU time of these methods are measured by LSF.
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Other methods are measuring estrogen, FSH, and inhibin B serum levels with some restrictions such as time limitation for evaluation of the serum levels [ 7, 8].
(e.g., refs (20− 23)) Size spectra of bubbles produced using the two methods were measured using a mini-BMS (bubble measurement system).
The performance and cost of each of the methods were measured in a 9228-ha test area.
Accuracy of these methods was measured using an F1-score (harmonic mean of precision and recall).
The volumes of formed cylindrical spur gear calculated by above three methods were measured with Archimedes drainage method.
Gene expression, histology, immunohistology, and real-time PCR methods were measured on days 21 after cell induction.
The time required to calculate the absorbed dose for each of the three methods was measured from start of calculation until the report was completed.
For the sake of testing, the entire data stream was clustered in one pass; precision and recall of the two methods were measured.
The interobserver accuracy and the agreement between both methods were measured by the coefficient of intraclass correlation (CIC) and a Bland-Altman plotting (BAP).
Description: The prediction accuracies of all tested methods were measured using the structure benchmark set.
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