The topic of big data has attracted increasing interest in recent years. The emergence of big data leads to new difficulties in terms of protection models used for data privacy, which is of necessity for sharing and processing data. Protecting individuals' sensitive information while maintaining the usability of the data set published is the most important challenge in privacy preserving. In this regard, data anonymization methods are utilized in order to protect data against identity disclosure and linking attacks. In this study, a novel data anonymization algorithm based on chaos and perturbation has been proposed for privacy and utility preserving in big data. The performance of the proposed algorithm is evaluated in terms of Kullback-Leibler divergence, probabilistic anonymity, classification accuracy, F-measure and execution time. The experimental results have shown that the proposed algorithm is efficient and performs better in terms of Kullback-Leibler divergence, classification accuracy and F-measure compared to most of the existing algorithms using the same data set. Resulting from applying chaos to perturb data, such successful algorithm is promising to be used in privacy preserving data mining and data publishing.
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http://dx.doi.org/10.3390/e20050373 | DOI Listing |
Soc Stud Sci
January 2025
Science, Technology and Innovation Studies, The University of Edinburgh, Edinburgh, Scotland, UK.
Accounts of the origins of the genomic commons typically focus on the development of public repositories and data-sharing agreements. This article tells a different story. During the 1990s in the United States, efforts of private companies to prevent the patenting of certain kinds of DNA sequences were essentially a conservative response to shifts in the sociotechnical constitution of the pharmaceutical innovation system, and to the operation of intellectual property as one of the key knowledge control regimes that regulate that system.
View Article and Find Full Text PDFInt J Cancer
January 2025
Jockey Club School of Public Health and Primary Care, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong, Hong Kong SAR.
Long-term use of low-dose aspirin has been demonstrated to reduce cancer risk, but the duration of necessary medication use remains uncertain. This study aimed to investigate the long-term chemoprotective effect of aspirin among the Chinese population. This population-based study included all aspirin users between 2000 and 2019.
View Article and Find Full Text PDFBMC Public Health
January 2025
Emerging Diseases Epidemiology Unit, Institut Pasteur, 25-28 Rue du Docteur Roux, Bâtiment Laveran, Paris, 75015, France.
Background: The capacity of the 7C model's psychological antecedents, which include confidence in vaccines, complacency, convenience, calculation, collective responsibility, confidence in the wider system, and social conformism, to explain variance in COVID-19 vaccine intentions and behaviours has been documented. However, it remains unclear whether the attitudes represented by the 7C psychological antecedents are specific to vaccination or if they are, in fact, an expression of underlying personality traits.
Methods: From February to June 2022, French adults completed self-administered questionnaires assessing COVID-19 vaccination history, the 7C antecedents, and personality traits ("ComCor" and "Cognitiv" studies).
Sci Rep
January 2025
College of Mathematics and Statistics, Chongqing University, Chongqing, 401331, China.
In this study, we introduce a coupled fractional system consisting of two fluctuating-mass oscillators with time delay and investigate their collective resonant behaviors. First, we achieve complete synchronization between the average behaviors of these oscillators. We then derive the exact analytical expression for the output amplitude gain, and based on this, we observe generalized stochastic resonance (GSR) in the system.
View Article and Find Full Text PDFAm J Hum Genet
January 2025
Shenzhen Research Institute of Big Data, Shenzhen 518172, China. Electronic address:
Genome-wide association studies (GWASs) have identified numerous genetic variants associated with complex traits, yet the biological interpretation remains challenging, especially for variants in non-coding regions. Expression quantitative trait locus (eQTL) studies have linked these variations to gene expression, aiding in identifying genes involved in disease mechanisms. Traditional eQTL analyses using bulk RNA sequencing (bulk RNA-seq) provide tissue-level insights but suffer from signal loss and distortion due to unaddressed cellular heterogeneity.
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