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Furthermore, a maximal clique distinct from C but inducing I C cannot exist because each of its vertices must be compatible in the interval [ l, r], which is in violation of the maximality of C. It follows that no maximal clique other than C can induce I C ; thus, each maximal clique uniquely defines an interval.
A clique-colouring of a graph is a colouring of its vertices such that no maximal clique of size at least two is monocoloured.
In other words: a clique-colouring of a graph is a colouring of its vertices such that no maximal clique of size at least two is monocoloured.
No maximal clique of size at least 2 is monocoloured since every maximal clique of G contains an induced subgraph isomorphic to a maximal clique of G′ that is not monocoloured by hypothesis.
It is easy to see that the the both arithmetic conditions (qequiv -varepsilon 7pmod {48}) in (2a) and (qequiv varepsilon 7,varepsilon 31pmod {72}) in (2b) imply that (qequiv pm 1pmod 8), so S has no maximal subgroup isomorphic to (A_4).
This process is known as no maximal suppression.
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We evaluate five chosen algorithms: Block Matching, Semi-Global Matching, No-Maximal Disparity, Cross-Based Local Approach, Adaptive Aggregation with Dynamic Programming.
Table 1 Algorithm abbreviation reference BLOCK Block matching [1] SEMI Semi-global block matching [2] NOMD No-maximal disparity algorithm [3] CROSS Cross-based local algorithm [4] ADAPT Adaptive aggregation with dynamic programming [5].
The cleaning continues until the activation level of the module is no longer maximal, at which point the transition of cleaning to the new maximally active module occurs.
When studied in a cell-free environment, the α1β1 and α2β1 NO receptor isoforms are similarly sensitive to NO, half-maximal activity being evoked at a concentration of ∼1 n m (Wykes & Garthwaite, 2004).
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