New adaptive counter based broadcast using neighborhood information in MANETS

Author(s):  
M. Bani Yassein ◽  
A. Al-Dubai ◽  
M. Ould Khaoua ◽  
Omar M. Al-jarrah
2010 ◽  
Vol 20 (7) ◽  
pp. 1931-1942 ◽  
Author(s):  
Yan-Jun LI ◽  
Zhi WANG ◽  
You-Xian SUN

2002 ◽  
Vol 19 (3) ◽  
pp. 307-310
Author(s):  
Ning Huang ◽  
Minhui Zhu ◽  
Shourong Zhang

Ultra wideband (UWB) radio is ascending as an attracting physical layer for adaptable uncommonly picked structure (MANET). Overseeing in MANET is a test inferable from the dynamic thought of framework topology and resource blocks. A steady arranging structure is proposed for UWB sort out in this paper, focusing on the flimsiness issue got from correspondence foggy zone. This instrument is a cross-layer change of outstandingly doled out on-demand vector (AODV) controlling custom, which is named as CLS_AODV. The guiding disclosure computation is connected by displaying source coordinating and exceptionally selected on-ask for multipath expels vector coordinating. A preparing model is developed to portray signal characteristics into interface constancy factor and course soundness factor which fills in as a coordinating metric for way decision. Rather than the open path in AODV, the got sign quality can be utilized to uncover the affiliation state data for shady zone want, and for course state viewing. A HELLO-based preemptive neighborhood course fix estimation is familiar with keep the event of affiliation breakage. Welcome message is broadened not only for neighbor perceiving and neighborhood information exchanging, yet moreover as an ON/OFF charge to control the position territory structure and HELLO plan of neighbor centers. The multiplication happens show the movements of CLS_AODV to the degree bundle occurrence degree and run of the mill start to finish yield without trading off the throughput execution separated and AODV


2021 ◽  
Author(s):  
Lin Yuan ◽  
Jing Zhao ◽  
Tao Sun ◽  
Zhen Shen

Abstract Background: LncRNAs (Long non-coding RNAs) are a type of non-coding RNA molecule with transcript length longer than 200 nucleotides. LncRNA has been novel candidate biomarkers in cancer diagnosis and prognosis. However, it is difficult to discover the true association mechanism between lncRNAs and complex diseases. The unprecedented enrichment of multi-omics data and the rapid development of machine learning technology provide us with the opportunity to design a machine learning framework to study the relationship between lncRNAs and complex diseases. Results: In this article, we proposed a new machine learning approach, namely LGDLDA (LncRNA-Gene-Disease association networks based LncRNA-Disease Association prediction), for disease-related lncRNAs association prediction based multi-omics data, machine learning methods and neural network neighborhood information aggregation. Firstly, LGDLDA calculates the similarity matrix of lncRNA, gene and disease respectively. LGDLDA calculates the similarity between lncRNAs through the lncRNA expression profile matrix, lncRNA-miRNA interaction matrix and lncRNA-protein interaction matrix. LGDLDA obtains gene similarity matrix by calculating the lncRNA-gene association matrix and the gene-disease association matrix. LGDLDA obtains disease similarity matrix by calculating the disease ontology, the disease-miRNA association matrix, and Gaussian interaction profile kernel similarity. Secondly, LGDLDA integrates the neighborhood information in similarity matrices by using nonlinear feature learning of neural network. Thirdly, LGDLDA uses embedded node representations to approximate the observed matrices. Finally, LGDLDA ranks candidate lncRNA-disease pairs and then selects potential disease-related lncRNAs. Conclusions: Compared with lncRNA-disease prediction methods, IHI-BMLLR takes into account more critical information and obtains the performance improvement cancer-related lncRNA predictions. Randomly split data experiment results show that the stability of LGDLDA is better than IDHI-MIRW, NCPLDA, LncDisAP and NCPHLDA. The results on different simulation data sets show that LGDLDA can accurately and effectively predict the disease-related lncRNAs. Furthermore, we applied LGDLDA to three real cancer data including gastric cancer, colorectal cancer and breast cancer to predict potential cancer-related lncRNAs.


Sign in / Sign up

Export Citation Format

Share Document