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In Figure21, the mean transmitted power along the second and third paths have been set to −20 dB, while that on the fourth path has been progressively increased.
Consequently, this principle also provides the second and third paths and the entire hierarchy of structural causes successively triggering the investigated endpoint effect with the observed actions.
In Figure15, we have fixed a very small power in the second and third paths (−20 dB, with respect to the first path), while the power on the fourth path has been progressively increased by steps of 2 dB.
As expected, the situation is more critical in the presence of multipaths: Figure17 shows the average BER, for the APSK and QAM systems, by considering, for the first path, the same Rice fading as in Figure16, but with the addition of the second and third paths, for which | α ~ i ( t, τ ) |, i = 1,2, has a Rayleigh distribution.
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Since path 2 and path 3 both contain 3 links before the schedule, (textbf {P}_{muh}^{1}) contains 2 paths: the second and third path.
Note that in Figure 2 we have, and, so that the separation between the first and second paths is close to the resolution limit.
In Figures 5 and 6, as the speed s set to 2 m/s and sampling time set to 1 s, the results demonstrate that more than 9060percentcent of the non-tracking method had error distances of less than 8.67 (5.40) m for the first and second paths; the estimates of KF-based tracking scheme had error distances of less than 4.80 (2.98) m for the first path and less than 4.72 (2.94) m for the second path.
Extensive simulations (not shown for space limitations) indicate that the floor of the SAGE estimator becomes smaller and smaller as the difference between the powers of the first and second path increases.
And similarly, the fraction of drug targets is enriched at the first, second and third shortest path distances in the neighborhood of disease genes (18, 30).
Previous studies suggested that the fraction of disease genes is enriched at the first, second and third shortest path distances in the neighborhood of drug targets.
The second and third cases pertain to path generation, with and without prescribed timing.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com