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Alternatively, the focal network may be a module of a larger genetic network, and organismal fitness may depend on the network's ability to respond appropriately to signals from other modules.
The focal network may also be a module within the total genetic network of an organism [3], in which case its environment includes other components of that larger network.
However, if we assume that our environment provides a constant set of products, not produced by the focal network itself, but still able to bind and regulate the functioning of the network, the state space for any single network now depends on the particular environment of exogenous products in which the network operates (Fig. 12).
When sampling a small percentage of start nodes (e.g., below 40%%), <60 % of the nodes in the final focal network were obtained.
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The focal traditional network had a 20.8 average degree compared to an average degree of approximately 3 for the other focal networks.
To compare networks with more similar bounding, Table 2 also presents the network metrics for the base focal networks (no snowballing).
The sensitivity analysis indicated that the final focal networks were contingent on the identities and number of start nodes used to initialize the network (Fig. 3).
This high connectedness is also reflected in the high link density of the traditional network (0.18 and 0.16 for focal) and lower connectedness for all other focal networks (0.01).
Both variance components tend to be lower for all networks larger than the focal species' network (Figure S1).
More specifically, this study proposes the derivation of a focal mobility network, i.e. the network of most likely paths towards a given destination, and explores several of its applications within a landscape archaeology framework.
Thus, the focal combined network was not simply additive of the focal hyperlink and focal relatedness networks.
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