Network Information Mining for Content Delivery Route Control in P2P Network

Author(s):  
Yoshikatsu Fujita ◽  
Jun Yoshida ◽  
Kenichi Yoshida ◽  
Kazuhiko Tsuda
2021 ◽  
Author(s):  
Yijun Ran ◽  
Tianyu Liu ◽  
Tao Jia ◽  
Xiao-Ke Xu

Abstract Network information mining is the study of the network topology, which may answer a large number of application-based questions towards the structural evolution and the function of a real system. The question can be related to how the real system evolves or how individuals interact with each other in social networks. Although the evolution of the real system may seem to be found regularly, capturing patterns on the whole process of evolution is not trivial. Link prediction is one of the most important technologies in network information mining, which can help us understand the evolution mechanism of real-life network. Link prediction aims to uncover missing links or quantify the likelihood of the emergence of nonexistent links from known network structures. Currently, widely existing methods of link prediction almost focus on short-path networks that usually have a myriad of close triangular structures. However, these algorithms on highly sparse or long-path networks have poor performance. Here, we propose a new index that is associated with the principles of Structural Equivalence and Shortest Path Length (SESPL) to estimate the likelihood of link existence in long-path networks. Through 548 real networks test, we find that SESPL is more effective and efficient than other similarity-based predictors in long-path networks. Meanwhile, we also exploit the performance of SESPL predictor and of embedding-based approaches via machine learning techniques. The results show that the performance of SESPL can achieve a gain of 44.09% over GraphWave and 7.93% over Node2vec. Finally, according to the matrix of Maximal Information Coefficient (MIC) between all the similarity-based predictors, SESPL is a new independent feature in the space of traditional similarity features.


2014 ◽  
Author(s):  
Binyang Li ◽  
Lanjun Zhou ◽  
Zhongyu Wei ◽  
Kam-fai Wong ◽  
Ruifeng Xu ◽  
...  

2020 ◽  
Vol 132 (4) ◽  
pp. 1234-1242 ◽  
Author(s):  
Paolo Belardinelli ◽  
Ramin Azodi-Avval ◽  
Erick Ortiz ◽  
Georgios Naros ◽  
Florian Grimm ◽  
...  

Deep brain stimulation (DBS) of the subthalamic nucleus (STN) is an effective treatment for symptomatic Parkinson’s disease (PD); the clinical benefit may not only mirror modulation of local STN activity but also reflect consecutive network effects on cortical oscillatory activity. Moreover, STN-DBS selectively suppresses spatially and spectrally distinct patterns of synchronous oscillatory activity within cortical-subcortical loops. These STN-cortical circuits have been described in PD patients using magnetoencephalography after surgery. This network information, however, is currently not available during surgery to inform the implantation strategy.The authors recorded spontaneous brain activity in 3 awake patients with PD (mean age 67 ± 14 years; mean disease duration 13 ± 7 years) during implantation of DBS electrodes into the STN after overnight withdrawal of dopaminergic medication. Intraoperative propofol was discontinued at least 30 minutes prior to the electrophysiological recordings. The authors used a novel approach for performing simultaneous recordings of STN local field potentials (LFPs) and multichannel electroencephalography (EEG) at rest. Coherent oscillations between LFP and EEG sensors were computed, and subsequent dynamic imaging of coherent sources was performed.The authors identified coherent activity in the upper beta range (21–35 Hz) between the STN and the ipsilateral mesial (pre)motor area. Coherence in the theta range (4–6 Hz) was detected in the ipsilateral prefrontal area.These findings demonstrate the feasibility of detecting frequency-specific and spatially distinct synchronization between the STN and cortex during DBS surgery. Mapping the STN with this technique may disentangle different functional loops relevant for refined targeting during DBS implantation.


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