Fingerprinting localization approach is widely used in indoor positioning applications owing to its high reliability. However, the learning procedure of radio signals in fingerprinting is time-consuming and labor-intensive. In this paper, an affinity propagation clustering (APC)-based fingerprinting localization system with Gaussian process regression (GPR) is presented for a practical positioning system with the reduced offline workload and low online computation cost. The proposed system collects sparse received signal strength (RSS) data from the deployed Bluetooth low energy beacons and trains them with the Gaussian process model. As the signal estimation component, GPR predicts not only the mean RSS but also the variance, which indicates the uncertainty of the estimation. The predicted RSS and variance can be employed for probabilistic-based fingerprinting localization. As the clustering component, the APC minimizes the searching space of reference points on the testbed. Consequently, it also helps to reduce the localization estimation error and the computational cost of the positioning system. The proposed method is evaluated through real field deployments. Experimental results show that the proposed method can reduce the offline workload and increase localization accuracy with less computational cost. This method outperforms the existing methods owing to RSS prediction using GPR and RSS clustering using APC.
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http://dx.doi.org/10.3390/s18124267 | DOI Listing |
J Cell Sci
January 2025
Laboratory of Cell Death & Cell Survival, Centre for DNA Fingerprinting and Diagnostics (CDFD), Uppal, Hyderabad 500039, India.
PPTC7 is a mitochondrial phosphatase that is essential for mitochondrial biogenesis, metabolism, protein content maintenance and transport. While the mitochondrial roles of PPTC7 are well-characterized, its roles outside the mitochondria are unclear. Here we identified a non-mitochondrial role for PPTC7 in regulating epidermal growth factor receptor (EGFR) trafficking.
View Article and Find Full Text PDFMicrobiol Spectr
January 2025
UMR7245 MCAM MNHN-CNRS, Muséum National d'Histoire Naturelle, Paris, France.
Unlabelled: can colonize a wide variety of environments (e.g., freshwater, brackish, alkaline, or alkaline-saline water) and develop dominant and even permanent blooms that overshadow and limit the diversity of adjacent phototrophs, especially in alkaline and saline environments.
View Article and Find Full Text PDFInt J Mol Sci
December 2024
ISEL-Instituto Superior de Engenharia de Lisboa, Instituto Politécnico de Lisboa, Rua Conselheiro Emídio Navarro 1, 1959-007 Lisbon, Portugal.
Predicting mortality in intensive care units (ICUs) is essential for timely interventions and efficient resource use, especially during pandemics like COVID-19, where high mortality persisted even after the state of emergency ended. Current mortality prediction methods remain limited, especially for critically ill ICU patients, due to their dynamic metabolic changes and heterogeneous pathophysiological processes. This study evaluated how the serum metabolomic fingerprint, acquired through Fourier-Transform Infrared (FTIR) spectroscopy, could support mortality prediction models in COVID-19 ICU patients.
View Article and Find Full Text PDFBrain functional connectivity patterns exhibit distinctive, individualized characteristics capable of distinguishing one individual from others, like fingerprint. Accurate and reliable depiction of individualized functional connectivity patterns during infancy is crucial for advancing our understanding of individual uniqueness and variability of the intrinsic functional architecture during dynamic early brain development, as well as its role in neurodevelopmental disorders. However, the highly dynamic and rapidly developing nature of the infant brain presents significant challenges in capturing robust and stable functional fingerprint, resulting in low accuracy in individual identification over ages during infancy using functional connectivity.
View Article and Find Full Text PDFJ Chem Inf Model
January 2025
Department of Chemistry, University of Rome, Sapienza, P.le A. Moro 5, 00185 Rome, Italy.
The oxidation of Met residues in proteins is a complex process, where protein-specific structural and dynamical features play a relevant role in determining the reaction kinetics. Aiming to a full-side perspective, we report here a comprehensive characterization of Met oxidation kinetics by hydrogen peroxide in a leptin protein case study. To do that, we estimated the reaction-free energy profile of the Met oxidation via a QM/MM approach, while the kinetics of the formation of the reactive species were calculated using classical molecular dynamics (MD) simulations.
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