Exact(1)
Table 1 also shows that a DIR network has a lower delay than an OMN network since (frac {1}{left.frac {thetan ^{2}{rac {theta }{2}}right)^{frac {2}{alpha }}}) is always less than 1 since the beamwidth (theta < frac {pi }{2}).
Similar(59)
The topological tree showed that IiDIRs are divided into DIR-a, DIR-b/d, and DIR-e subfamilies.
The topology analyses of the IiDIRs showed that they contribute to DIR-a, DIR-b/d, and DIR-e subfamilies.
Therefore, to minimize the occurrences of IDIR, we embed a function that invokes DIR only for the first touch.
We then show that each cell in a DIR network has a constant number of interfering neighbors, which is independent of the number of nodes n.
The phylogenetic tree indicated that IiDIRs cluster into three groups, DIR-a, DIR-b/d and DIR-e.
Phylogenetic analysis of the 19 proteins indicated that the IiDIR genes cluster into three distinct subfamilies, DIR-a, DIR-b/d, and DIR-e, of a larger plant DIR and DIR-like gene family.
Ralph and coworkers [ 16] suggest that the DIR proteins are subdivided into five groups: the DIR-a, DIR-b, DIR-c, DIR-d and DIR-e subfamilies.
In order to evaluate the impacts of directional antennas on the antenna factor component, we define the directional improvement factor B DIR as the ratio of the antenna factor component of an DIR network to that one of an OMN network.
Phylogenetic analysis indicates the spruce DIR and DIR-like genes cluster into three distinct subfamilies, DIR-a, DIR-b/d, and DIR-f, of a larger plant DIR and DIR-like gene family.
However, only DIR-a, DIR-c and DIR-f subfamilies were clustered separately.
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