Multi-cell interference coordinated scheduling in mmWave 5G cellular systems

2016 ◽  
Author(s):  
Chun-Yen Chen ◽  
Yin-Yi Chen ◽  
Hung-Yu Wei
Keyword(s):  
Cellular Systems ◽  
Coordinated Scheduling

scholarly journals Real-time Coordinated Scheduling for Cloud Radio Access Networks in a Software-only Environment using the OpenAirInterface Platform

2021 ◽  
Vol 25 ◽  
Author(s):  
Luis Felipe Ariza-Vesga ◽  
Johan Sebastian Eslava-Garzon
Keyword(s):  
Frequency Domain ◽  
Real Time ◽  
Software Defined Radio ◽  
General Purpose ◽  
Cellular Systems ◽  
Access Networks ◽  
Coordinated Scheduling ◽  
Cloud Radio Access Networks ◽  
Radio Access Networks ◽  
Radio Access

The objective of this paper is to extend into the OpenAirInterface platform the Coordinated Scheduling (CS) technique to allocate resource blocks among User Equipment (UE) in a wisely way and to control the energy efficiency, the throughput, and the inter-cell interference for Cloud Radio Access Networks (C-RANs). It is achieved by modifying the OpenAirInterface scheduler code, increasing the Remote Radio Unit (RRU) scalability, and employing some component carriers of the Radio Cloud Center (RCC), each one them with one or more UEs. The hardware utilized is composed of general-purpose processors and fast Ethernet transport ports, and the software is recent frequency-domain methodologies in a software-only environment where the use of radio units are not required. However, the USRP B200 mini-i radio unit and the UE (Samsung Galaxy S8) were considered only for validation purposes. The emulations using frequency-domain methodologies, compatible with fourth and fifth-generation cellular systems, allowed real-time emulations and reduced 10-fold the multipath channel’s signal processing complexity compared to time-domain methodologies. The results show we can emulate a real-time static coordinated scheduling proof-of-concept for one C-RAN composed of one RCC, three RRUs, and three UEs. In the end, it is evaluated the reproducibility and the scalability of synthetic networks composed of one RRU and at least one UE, without using software-defined radio units, reducing prototyping uncertainties of the physical hardware and the total price of the experiment.

Label-free, mass-sensitive single-molecule imaging using interferometric scattering microscopy

2020 ◽  
Author(s):  
Nikolas Hundt
Keyword(s):  
Single Molecule ◽  
Cellular Systems ◽  
Single Molecule Imaging ◽  
Label Free ◽  
Measurement Sensitivity ◽  
Mass Distributions ◽  
Quantitative Measurements ◽  
Contrast Mechanism ◽  
Cellular Components ◽  
Scattering Signal

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.

Achievable Capacity of Closed/Open-Access Cognitive Radio Systems Coexisting with a Macro Cellular Systems

2012 ◽  
Vol E95-B (4) ◽  
pp. 1190-1197
Author(s):  
Hiromasa FUJII ◽  
Hiroki HARADA ◽  
Shunji MIURA ◽  
Hidetoshi KAYAMA
Keyword(s):  
Cognitive Radio ◽  
Open Access ◽  
Cellular Systems ◽  
Cognitive Radio Systems ◽  
Radio Systems ◽  
Macro Cellular

Zero Forcing Beamforming Based Coordinated Scheduling Algorithm for Downlink Coordinated Multi-Point Transmission System

2015 ◽  
Vol E98.B (2) ◽  
pp. 352-359 ◽  
Author(s):  
Ping WANG ◽  
Lei DING ◽  
Huifang PANG ◽  
Fuqiang LIU ◽  
Nguyen Ngoc VAN
Keyword(s):  
Scheduling Algorithm ◽  
Transmission System ◽  
Zero Forcing ◽  
Coordinated Scheduling

A Photoactivable Formaldehyde Donor with Fluorescence Monitoring Reveals Threshold to Arrest Cell Migration

2019 ◽  
Author(s):  
Lukas P Smaga ◽  
Nicholas W Pino ◽  
Gabriela E Ibarra ◽  
Vishnu Krishnamurthy ◽  
Jefferson Chan
Keyword(s):  
Wound Healing ◽  
Cell Migration ◽  
Fluorescence Enhancement ◽  
Biological Effects ◽  
Cellular Systems ◽  
Live Cells ◽  
First Report ◽  
Cell Lysate ◽  
Intracellular Release ◽  
Biological Analytes

Controlled light-mediated delivery of biological analytes enables the investigation of highly reactivity molecules within cellular systems. As many biological effects are concentration dependent, it is critical to determine the location, time, and quantity of analyte donation. In this work, we have developed the first photoactivatable donor for formaldehyde (FA). Our optimized photoactivatable donor, photoFAD-3, is equipped with a fluorescence readout that enables monitoring of FA release with a concomitant 139-fold fluorescence enhancement. Tuning of photostability and cellular retention enabled quantification of intracellular FA release through cell lysate calibration. Application of photoFAD-3 uncovered the concentration range necessary for arresting wound healing in live cells. This marks the first report where a photoactivatable donor for any analyte has been used to quantify intracellular release.

A Review on 3GPP 5G Security Aspects

2019 ◽  
Author(s):  
Rajavelsamy R ◽  
Debabrata Das
Keyword(s):  
Network Architecture ◽  
Base Station ◽  
Cellular Systems ◽  
Core Network ◽  
User Privacy ◽  
Wireless Backhaul ◽  
Level Of Use ◽  
Unified Authentication ◽  
3Rd Generation Partnership Project ◽  
5G Security

5G promises to support new level of use cases that will deliver a better user experience. The 3rd Generation Partnership Project (3GPP) [1] defined 5G system introduced fundamental changes on top of its former cellular systems in several design areas, including security. Unlike in the legacy systems, the 5G architecture design considers Home control enhancements for roaming customer, tight collaboration with the 3rd Party Application servers, Unified Authentication framework to accommodate various category of devices and services, enhanced user privacy, and secured the new service based core network architecture. Further, 3GPP is investigating the enhancements to the 5G security aspects to support longer security key lengths, False Base station detection and wireless backhaul in the Phase-2 of 5G standardization [2]. This paper provides the key enhancements specified by the 3GPP for 5G system, particularly the differences to the 4G system and the rationale behind the decisions.

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