177 research outputs found
Maximum flow and topological structure of complex networks
The problem of sending the maximum amount of flow between two arbitrary
nodes and of complex networks along links with unit capacity is
studied, which is equivalent to determining the number of link-disjoint paths
between and . The average of over all node pairs with smaller degree
is for large with a constant implying that the statistics of is related to the
degree distribution of the network. The disjoint paths between hub nodes are
found to be distributed among the links belonging to the same edge-biconnected
component, and can be estimated by the number of pairs of edge-biconnected
links incident to the start and terminal node. The relative size of the giant
edge-biconnected component of a network approximates to the coefficient .
The applicability of our results to real world networks is tested for the
Internet at the autonomous system level.Comment: 7 pages, 4 figure
Recommended from our members
Forests, Frames and Games: Algorithms for Matroid Sums and Applications ; CU-CS-446-89
On -Simple -Path
An -simple -path is a {path} in the graph of length that passes
through each vertex at most times. The -SIMPLE -PATH problem, given a
graph as input, asks whether there exists an -simple -path in . We
first show that this problem is NP-Complete. We then show that there is a graph
that contains an -simple -path and no simple path of length greater
than . So this, in a sense, motivates this problem especially
when one's goal is to find a short path that visits many vertices in the graph
while bounding the number of visits at each vertex.
We then give a randomized algorithm that runs in time that solves the -SIMPLE -PATH on a graph with
vertices with one-sided error. We also show that a randomized algorithm
with running time with gives a
randomized algorithm with running time \poly(n)\cdot 2^{cn} for the
Hamiltonian path problem in a directed graph - an outstanding open problem. So
in a sense our algorithm is optimal up to an factor
Balancing Minimum Spanning and Shortest Path Trees
This paper give a simple linear-time algorithm that, given a weighted
digraph, finds a spanning tree that simultaneously approximates a shortest-path
tree and a minimum spanning tree. The algorithm provides a continuous
trade-off: given the two trees and epsilon > 0, the algorithm returns a
spanning tree in which the distance between any vertex and the root of the
shortest-path tree is at most 1+epsilon times the shortest-path distance, and
yet the total weight of the tree is at most 1+2/epsilon times the weight of a
minimum spanning tree. This is the best tradeoff possible. The paper also
describes a fast parallel implementation.Comment: conference version: ACM-SIAM Symposium on Discrete Algorithms (1993
Ninth and Tenth Order Virial Coefficients for Hard Spheres in D Dimensions
We evaluate the virial coefficients B_k for k<=10 for hard spheres in
dimensions D=2,...,8. Virial coefficients with k even are found to be negative
when D>=5. This provides strong evidence that the leading singularity for the
virial series lies away from the positive real axis when D>=5. Further analysis
provides evidence that negative virial coefficients will be seen for some k>10
for D=4, and there is a distinct possibility that negative virial coefficients
will also eventually occur for D=3.Comment: 33 pages, 12 figure
A general approach to connected-component labeling for arbitrary image representations
Automated data interpretation based on the concept of “negative signature mass” for mass-mapping disulfide structures of cystinyl proteins
Polycystin-1 Surface Localization Is Stimulated by Polycystin-2 and Cleavage at the G Protein-coupled Receptor Proteolytic Site
The localization of polycystin (PC)1) to the plasma membrane requires coexpression with PC2 and cleavage at the PC1 G protein-coupled receptor proteolytic site. Neither the PC1 binding capacity of PC2 nor its channel function is required for this effect
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