Pilot-based Sequence Design to Overcome a Blockage in mmWave Cellular Systems

Author(s):  
Yeong Jun Kim ◽  
Qasim Sultan ◽  
Yong Soo Cho
Electronics ◽  
2021 ◽  
Vol 10 (19) ◽  
pp. 2413
Author(s):  
Yeong Jun Kim ◽  
Muhammad Asim ◽  
Tae Ho Im ◽  
Yong Soo Cho

In underwater acoustic cellular (UWAC) systems, underwater equipment or sensor nodes (UE/SN) should perform downlink synchronisation and a cell search during the initial access stage using the preambles received from adjacent underwater base stations (UWBSs). The UE/SN needs to estimate accurate timing and cell ID (CID) using the received preambles, and synchronise with a serving UWBS, even in high-Doppler environments. In this paper, a sequence design technique for joint estimation of accurate timing and CID in UWAC systems with a high Doppler is proposed to decrease the receiver complexity and processing time. A generalised Zadoff–Chu sequence is proposed for the preamble design. This sequence is decomposed into multiple short sub-sequences to reduce the effect of Doppler shift on the timing and CID estimation. The performance loss caused by the short sequence length is compensated by combining the sub-sequences using the repetition property of the ZC sequence. The properties (autocorrelation and cross-correlation) of the proposed sequence are derived analytically in the presence of Doppler shift and compared with the simulation results. The simulation results reveal that the proposed technique performs better than existing techniques in both additive white Gaussian noise and multipath channels with a high-Doppler. It is concluded that the proposed technique is suitable for accurate timing estimation and CID detection in UWAC systems with a high Doppler.


2021 ◽  
pp. 100358
Author(s):  
Mohammed Saquib Khan ◽  
Chang Hwan Park ◽  
Jingon Joung ◽  
Yong Soo Cho

IEEE Access ◽  
2020 ◽  
Vol 8 ◽  
pp. 80454-80467
Author(s):  
Yeong Jun Kim ◽  
Qasim Sultan ◽  
Yong Soo Cho

2020 ◽  
Author(s):  
Nikolas Hundt

Abstract Single-molecule imaging has mostly been restricted to the use of fluorescence labelling as a contrast mechanism due to its superior ability to visualise molecules of interest on top of an overwhelming background of other molecules. Recently, interferometric scattering (iSCAT) microscopy has demonstrated the detection and imaging of single biomolecules based on light scattering without the need for fluorescent labels. Significant improvements in measurement sensitivity combined with a dependence of scattering signal on object size have led to the development of mass photometry, a technique that measures the mass of individual molecules and thereby determines mass distributions of biomolecule samples in solution. The experimental simplicity of mass photometry makes it a powerful tool to analyse biomolecular equilibria quantitatively with low sample consumption within minutes. When used for label-free imaging of reconstituted or cellular systems, the strict size-dependence of the iSCAT signal enables quantitative measurements of processes at size scales reaching from single-molecule observations during complex assembly up to mesoscopic dynamics of cellular components and extracellular protrusions. In this review, I would like to introduce the principles of this emerging imaging technology and discuss examples that show how mass-sensitive iSCAT can be used as a strong complement to other routine techniques in biochemistry.


2012 ◽  
Vol E95-B (4) ◽  
pp. 1190-1197
Author(s):  
Hiromasa FUJII ◽  
Hiroki HARADA ◽  
Shunji MIURA ◽  
Hidetoshi KAYAMA

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