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The value of average degree for each connected component.
The first thing we should do is to determine the value of node number and average degree for each connected components.
Instead, for each time step period ((t_{i-1},t_i)) with (E_{t_i}) being the number of active links in ((t_{i-1},t_i)), the dynamic average degree for
Just as differences in average degree for binary graphs, the differences in weights do influence graph measures.
Taken together with the degree distributions, also displayed in Figure 2 with the gray shaded curves, the variation of C with k is even less significant in the regions within one-standard deviation of the average degree for these three systems.
We find that the average degree for both S. pombe and O. sativa are much lower than that of human or S. cerevisiae for both binary and co-complex data.
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The average degrees for WHPN and CASN were 4.51 and 5.44, respectively, showing that CASN was much closer than WHPN.
Then, we calculated degree distributions and average degrees for three drug sets and all drugs in DDIs. Figure 1 displays their degree distributions and average degrees.
This difference, however, is not significant among ancient genes (average degrees for proteins encoded by duplicated and singleton genes: 5.06 and 4.41 interactions, respectively; P = 0.484).
For maternal kinship, we used the average degree of relatedness for kin categories (mothers and daughters, r = 0.5, maternal sisters: r = 0.25, grandmother and granddaughters, r = 0.25; aunts and nieces, r = 0.125; cousins: r = 0.0625; great-aunts and nieces, r = 0.0625; nonkin, all others: r = 0).
In comparison, the average degree of neutrality for random units of replication is λ r = 0.33 and for a typical unit of replication obtained by optimizing replication rate is even larger (λ opt > 0.40, fig. 4, top row).
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com