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The over-representation of reciprocally connected doublets in C. elegans has been explained [ 6] as a consequence of correlation between adjacency and connectivity of neurons.
A consequence of these definitions is that π comprises a disjoint collection of paths and cycles, where each connected component alternates between black genes and blue adjacencies.
(4) Here, x is an eigenvector of the adjacency matrix A with eigenvalue λ.
In particular, when we apply optimal DCJs internal to a single component of the adjacency graph, we can accumulate an entire run into a single adjacency [ 7].
Let (A(G)) be the adjacency matrix.
We present a heuristic algorithm based on the eigenvalue decomposition of the adjacency matrix of a graph.
In this article, we study whether the above conclusion holds in high-dimensional genotype space without the assumption of the adjacency of mutations, where the consequences of mutation-selection dynamics can be qualitatively different.
In definition 1, we employ the powers of the adjacency matrix A to sequentially diffuse the reconstructed residuals associated with the sampled vertices to the adjacency unsampled vertices.
For each pair of connected molecular objects, there is a record in the adjacency.
The spectrum of the adjacency matrix of a scale-free network was studied in [25].
Therefore we can use upper right triangle of the adjacency matrix to fully represent a graph.
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