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The test was controlled by means of crack mouth opening displacement (CMOD), using a clip-on extensometer with a ±2.5 mm range and 10 mm gauge length.
The rate of increase of the CMOD during the flexure test was controlled in two stages, at 0.05 mm/min for CMOD less than 0.1 mm and at 0.1 mm/min for CMOD greater than 0.1 mm.
NAP test was controlled using ATCC strains.
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The quality of the test is controlled by applying Westgard QC-rules on 3 different QC-samples [ 33].
These limited simulations indicate that the size of the test is controlled at the nominal genome-wide P ≤ 0.05 level.
The ambient air temperature for the dry tests was controlled to ∼23 °C, and the mean skin temperatures averaged ∼35 °C.
The magnitude of cyclic strains imparted to each cable tested was controlled via the use of different diameter mandrels.
The data acquisition set-up used in the tests was controlled by a PHO 200 LDS (signal acquisition Photon II), which is a plug and play, multifunction analog, digital and timing I/O board for USB bus computers (Figure 3).
Empirical P values were calculated after permutations, and multiple testing was controlled by using the adaptive FDR.
Multiple hypotheses testing was controlled by applying the false discovery rate (FDR) algorithm [ 16].
False discovery in the multiple testing was controlled with the false discovery rate (FDR) procedure (23).
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