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Such a view is fully confirmed by the analysis of modularity: Although modular organization is a desirable and functionally key property of cellular maps, it can arise as a by-product of the rules driving network growth.
A thorough understanding of the modular organization is a prerequisite for lymphoid organ tissue-engineering.
Such modular organization is a characteristic feature of electronic designs, where integrated circuits (such as the one shown in d e) are fixed combinations of simpler gates.
As depicted in Figure 12 modular organization is evident.
On the one hand, while the term "modular organization" is fairly intuitive, anyone who is familiar with the structure of real-world networks understands that this intuitive notion can only be applied approximately, and with a good amount of prudence.
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Interestingly, a shared modular organization was also evidenced between the AA4 and AA7 families that feature an N-terminal FAD-binding-4 module (pfam01565).
Yet, core properties such as small-world topology and modular organization were retained throughout development (Fair et al. 2009; Gong et al. 2009; Supekar et al. 2009; Hagmann et al. 2010; Dennis et al. 2013).
In conclusion, diverse modular organizations are frequently detected in the AA families.
Due to its modular organization, it is straightforward to change different parts of the data processing.
Together with the other two leg pairs (T1 and T2), insect hind legs exhibit a modular organization and are composed of five segments (coxa, trochanter, femur, tibia, and tarsus, followed by claws).
In biological networks, such modular organization has been observed across many length scales, from the intra-cellular protein-protein interaction system [10], [11] to food webs comprising various species populations [12].
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