A threshold-based MIMO TOA location estimation for cellular systems

Author(s):  
Tomofumi Yabu ◽  
Shinsuke Hara ◽  
Radim Zemek ◽  
Thomas Derham
Energies ◽  
2019 ◽  
Vol 12 (9) ◽  
pp. 1668 ◽  
Author(s):  
Sajina Pradhan ◽  
Youngchul Bae ◽  
Jae-Young Pyun ◽  
Nak Yong Ko ◽  
Suk-seung Hwang

The ever-growing mobile station (MS) localization technologies provide an increasingly important role in all aspects of the wireless cellular systems and Internet of Things (IoT). The accurate MS location information is the basis in connection of different devices in IoT. The MS localization techniques based on time of arrival (TOA) trilateration algorithm, which determines the location of MS using an intersection point of three circles based on distances between MS and base stations (BS) and coordinates of BSs, have been actively studied. In general, the distance between the MS and BS is calculated by counting the number of delay samples or measuring the power of the received signal. Since the estimated distance (radius of a circle) between MS and BS is commonly increased, three circles may not meet at a single point, resulting in the estimation error of MS localization. In order to improve this problem, in this paper, we propose the hybrid TOA trilateration algorithm based on the line intersection algorithm for the general case for intersection of three circles and the comparison approach of intersection distances for the specific case where a small circle is located inside the area of two large circles. The line intersection algorithm has an excellent location estimation performance in the general case, but it does not work in the specific case. The comparison approach of intersection distances has good performance only for the specific case. In addition, we propose the mode selection algorithm to efficiently select a proper mode between the general and specific cases. The representative computer simulation examples are provided to verify the localization performance of the proposed algorithm.


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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