Abstract:
A method for balancing traffic across paths connecting a network to the Internet using a fractional allocation strategy for distributing the traffic from a congested selected path. The strategy includes: (a) associating the paths j with a counter i; (b) calculating the total initial selected path overload; (c) calculating the selected path load, wherein the load is equal to the initial selected path overload less the sum of the low capacity boundary for i path(s); (d) calculating the portion of the traffic on the selected path to be distributed using a bi-sectional search strategy; (e) distributing a portion of the traffic on the selected path to the other paths; and (f) stopping if there are no more paths (i=j), otherwise increasing the numerical value of the counter by one (1) and go to step (c).
Abstract:
Compounds are provided that act as potent modulators of one or more of the CCR1, CCR2 and CCR3 receptors. The compounds are generally fused-, spiro- or bridged-nitrogen heterocycles having an aryl and heteroaryl component and are useful in pharmaceutical compositions, methods for the treatment of CCR1-, CCR2- and/or CCR3-mediated diseases, and as controls in assays for the identification of competitive receptor antagonists for the above chemokine receptors.
Abstract:
The present invention develops an efficient streaming method for detecting multidimensional hierarchical heavy hitters from massive data streams and enables near real time detection of anomaly behavior in networks.
Abstract:
Compounds are provided that act as potent modulators of one or more of the CCR1, CCR2 and CCR3 receptors. The compounds are generally fused-, spiro- or bridged-nitrogen heterocycles having an aryl and heteroaryl component and are useful in pharmaceutical compositions, methods for the treatment of CCR1-, CCR2- and/or CCR3-mediated diseases, and as controls in assays for the identification of competitive receptor antagonists for the above chemokine receptors.
Abstract:
Compounds are provided that act as potent antagonists of the CCR1 receptor, and have in vivo anti-inflammatory activity. The compounds are generally aryl piperazine derivatives and are useful in pharmaceutical compositions, methods for the treatment of CCR1-mediated diseases, and as controls in assays for the identification of competitive CCR1 antagonists.
Abstract:
Compounds are provided that act as potent modulators of one or more of the CCR1, CCR2 and CCR3 receptors. The compounds are generally fused-, spiro- or bridged-nitrogen heterocycles having an aryl and heteroaryl component and are useful in pharmaceutical compositions, methods for the treatment of CCR1-, CCR2- and/or CCR3-mediated diseases, and as controls in assays for the identification of competitive receptor antagonists for the above chemokine receptors.
Abstract:
A method of multicasting video to multiple client nodes via intermediate nodes that includes accessing video information descriptive of the video to be multicast, accessing information describing a distribution tree of nodes from a source of the video to the multiple clients nodes via one or more internetwork nodes, accessing rate constraints of nodes in the distribution tree, accessing buffer allocations of the nodes in the distribution tree, and determining one or more smoothed transmission schedules for each node in the distribution tree based on the accessed video information, the accessed information describing the distribution tree, the accessed rate constraints of nodes in the distribution tree, and the accessed buffer allocations of the nodes in the distribution tree, the one or more transmission schedules describing the transmission of video data to one or more children nodes.