scholarly journals Evaluating the Performance of Novel JWT Revocation Strategy

2021 ◽  
Author(s):  
László Viktor Jánoky ◽  
Péter Ekler ◽  
János Levendovszky

JSON Web Tokens (JWT) provide a scalable, distributed way of user access control for modern web-based systems. The main advantage of the scheme is that the tokens are valid by themselves – through the use of digital signing – also imply its greatest weakness. Once issued, there is no trivial way to revoke a JWT token. In our work, we present a novel approach for this revocation problem, overcoming some of the problems of currently used solutions. To compare our solution to the established solutions, we also introduce the mathematical framework of comparison, which we ultimately test using real-world measurements.

2012 ◽  
Vol 127 (5) ◽  
pp. 373-380 ◽  
Author(s):  
G. Parker ◽  
K. Fletcher ◽  
B. Blanch ◽  
L. Greenfield

Author(s):  
Ahmed Haroun Sabry ◽  
Jamal Benhra ◽  
Abdelkabir Bacha

The present article describes a contribution to solve transportation problems with green constraints. The aim is to solve an urban traveling salesman problem where the objective function is the total emitted CO2. We start by adapting ASIF approach for calculating CO2 emissions to the urban logistics problem. Then, we solve it using ant colony optimization metaheuristic. The problem formulation and solving will both work under a web-based mapping platform. The selected problem is a real-world NP-hard transportation problem in the city of Casablanca.


2011 ◽  
Vol 279 (1732) ◽  
pp. 1327-1334 ◽  
Author(s):  
R. Kanai ◽  
B. Bahrami ◽  
R. Roylance ◽  
G. Rees

The increasing ubiquity of web-based social networking services is a striking feature of modern human society. The degree to which individuals participate in these networks varies substantially for reasons that are unclear. Here, we show a biological basis for such variability by demonstrating that quantitative variation in the number of friends an individual declares on a web-based social networking service reliably predicted grey matter density in the right superior temporal sulcus, left middle temporal gyrus and entorhinal cortex. Such regions have been previously implicated in social perception and associative memory, respectively. We further show that variability in the size of such online friendship networks was significantly correlated with the size of more intimate real-world social groups. However, the brain regions we identified were specifically associated with online social network size, whereas the grey matter density of the amygdala was correlated both with online and real-world social network sizes. Taken together, our findings demonstrate that the size of an individual's online social network is closely linked to focal brain structure implicated in social cognition.


10.2196/11566 ◽  
2019 ◽  
Vol 21 (1) ◽  
pp. e11566 ◽  
Author(s):  
Hugh Cameron McCall ◽  
Fjola Dogg Helgadottir ◽  
Ross G Menzies ◽  
Heather D Hadjistavropoulos ◽  
Frances S Chen

2021 ◽  
Author(s):  
Anne M Luescher ◽  
Julian Koch ◽  
Wendelin J Stark ◽  
Robert N Grass

Aerosolized particles play a significant role in human health and environmental risk management. The global importance of aerosol-related hazards, such as the circulation of pathogens and high levels of air pollutants, have led to a surging demand for suitable surrogate tracers to investigate the complex dynamics of airborne particles in real-world scenarios. In this study, we propose a novel approach using silica particles with encapsulated DNA (SPED) as a tracing agent for measuring aerosol distribution indoors. In a series of experiments with a portable setup, SPED were successfully aerosolized, re-captured and quantified using quantitative polymerase chain reaction (qPCR). Position-dependency and ventilation effects within a confined space could be shown in a quantitative fashion achieving detection limits below 0.1 ng particles per m3 of sampled air. In conclusion, SPED show promise for a flexible, cost-effective and low-impact characterization of aerosol dynamics in a wide range of settings.


2008 ◽  
Vol 10 (5) ◽  
pp. e41 ◽  
Author(s):  
Susan M Zbikowski ◽  
Jenny Hapgood ◽  
Sara Smucker Barnwell ◽  
Tim McAfee

2020 ◽  
Vol 19 (2) ◽  
pp. 21-35
Author(s):  
Ryan Beal ◽  
Timothy J. Norman ◽  
Sarvapali D. Ramchurn

AbstractThis paper outlines a novel approach to optimising teams for Daily Fantasy Sports (DFS) contests. To this end, we propose a number of new models and algorithms to solve the team formation problems posed by DFS. Specifically, we focus on the National Football League (NFL) and predict the performance of real-world players to form the optimal fantasy team using mixed-integer programming. We test our solutions using real-world data-sets from across four seasons (2014-2017). We highlight the advantage that can be gained from using our machine-based methods and show that our solutions outperform existing benchmarks, turning a profit in up to 81.3% of DFS game-weeks over a season.


Author(s):  
Katrina A. Lythgoe ◽  
Sheila F. Lumley ◽  
Jane A. McKeating ◽  
Philippa C. Matthews

AbstractHepatitis B virus (HBV) infection is a major global health problem with over 240 million infected individuals at risk of developing progressive liver disease and hepatocellular carcinoma. HBV is an enveloped DNA virus that establishes its genome as an episomal, covalently closed circular DNA (cccDNA) in the nucleus of infected hepatocytes. Currently available standard-of-care treatments for chronic hepatitis B (CHB) include nucleos(t)ide analogues (NA) that suppress HBV replication but do not target the cccDNA and hence rarely cure infection. There is considerable interest in determining the lifespan of cccDNA molecules to design and evaluate new curative treatments. We took a novel approach to this problem by developing a new mathematical framework to model changes in evolutionary rates during infection which, combined with previously determined within-host evolutionary rates of HBV, we used to determine the lifespan of cccDNA. We estimate that during HBe-antigen positive (HBeAgPOS) infection the cccDNA lifespan is 61 (36-236) days, whereas during the HBeAgNEG phase of infection it is only 26 (16-81) days. We found that cccDNA replicative capacity declined by an order of magnitude between HBeAgPOS and HBeAgNEG phases of infection. Our estimated lifespan of cccDNA is too short to explain the long durations of chronic infection observed in patients on NA treatment, suggesting that either a sub-population of long-lived hepatocytes harbouring cccDNA molecules persists during therapy, or that NA therapy does not suppress all viral replication. These results provide a greater understanding of the biology of the cccDNA reservoir and can aid the development of new curative therapeutic strategies for treating CHB.


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