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Two successive pulses may not be detected depending on the received pulse intensities; therefore, some pulses failed to be detected before the second pulse was detected.
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If a trait of interest is controlled by multiple QTLs, whether the QTL under consideration can be detected depends on the proportions of phenotypic variance explained by both this QTL and background QTLs.
Determining at which interface a particular membrane will be detected depends on the lipid to protein content ratio.
The type of genetic variations that can be detected depends on the array design and the sequence similarity of reference and query genomes.
The amount of visual field change that can be detected depends on the variability and number of available examinations, as described above.
Figure 3 shows that the difference in growth rate that may be detected depends on the quality of the experimental data.
This observed conformation change associated with the binding of NADH at one active site is similar to the phenomenon that was observed in the EPR studies looking at cobinamide binding, where two different coordination states were detected depending on the whether one or both of the active sites in the dimer were occupied.
Different types of pressure traces were detected depending on the solid properties.
Considerable differences in wind amplitudes of up to 20 m/s were detected depending on latitudes and altitudes.
Several flow patterns have been detected depending on the density ratio between the non-permeating and the permeating component in the mixture.
Unlike the PA14 LPS, only small amounts or no QuiNAc was detected, depending on the preparation.
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