The 'simultaneous maximum-likelihood attenuation correction factors' (sMLACF) algorithm presented here, is an iterative algorithm to calculate the maximum-likelihood estimate of the activity λ and the attenuation factors a in time-of-flight positron emission tomography, and this from emission data only. Hence sMLACF is an alternative to the MLACF algorithm. sMLACF is derived using the generalized expectation-maximization principle by introducing an appropriate set of complete data. The resulting iteration step yields a simultaneous update of λ and a which, in addition, enforces in a natural way the constraints [Formula: see text] where [Formula: see text] is a fixed lower bound that ensures the boundedness of the reconstructed activities. Some properties-like the monotonic increase of the likelihood and the asymptotic regularity of the estimated [Formula: see text]-of sMLACF are proven. Comparison of sMLACF with MLACF for two data sets reveals that both algorithms show very similar results, although sMLACF converges slower.
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http://dx.doi.org/10.1088/1361-6560/aa82ea | DOI Listing |
PNAS Nexus
January 2025
Department of Mathematics, Aston University, Birmingham B4 7ET, United Kingdom.
Understanding the relation between cortical neuronal network structure and neuronal activity is a fundamental unresolved question in neuroscience, with implications to our understanding of the mechanism by which neuronal networks evolve over time, spontaneously or under stimulation. It requires a method for inferring the structure and composition of a network from neuronal activities. Tracking the evolution of networks and their changing functionality will provide invaluable insight into the occurrence of plasticity and the underlying learning process.
View Article and Find Full Text PDFFront Immunol
January 2025
Department of Computer Science, University of Victoria, Victoria, BC, Canada.
Introduction: Accurate genotyping of Killer cell Immunoglobulin-like Receptor (KIR) genes plays a pivotal role in enhancing our understanding of innate immune responses, disease correlations, and the advancement of personalized medicine. However, due to the high variability of the KIR region and high level of sequence similarity among different KIR genes, the generic genotyping workflows are unable to accurately infer copy numbers and complete genotypes of individual KIR genes from next-generation sequencing data. Thus, specialized genotyping tools are needed to genotype this complex region.
View Article and Find Full Text PDFAsia Ocean J Nucl Med Biol
January 2025
Department of Radiology, Faculty of Medicine, Shimane University, Izumo, Japan.
Objectives: We investigated image quality and standardized uptake values (SUVs) for different lesion sizes using clinical data generated by F-FDG-prone breast silicon photomultiplier (SiPM)-based positron emission tomography/computed tomography (PET/CT).
Methods: We evaluated the effect of point-spread function (PSF) modeling and Gaussian filtering (Gau) and determined the optimal reconstruction conditions. We compared the signal-to-noise ratio (SNR), contrast, %coefficient of variation (%CV), SUV, and Likert scale score between ordered-subset expectation maximization (OSEM) time-of-flight (TOF) and OSEM+TOF+PSF in phantom and clinical studies.
Front Psychol
December 2024
Natural and Artificial Cognition Laboratory, Department of Humanistic Studies, University of Naples "Federico II", Naples, Italy.
Introduction: Missing data in psychometric research presents a substantial challenge, impacting the reliability and validity of study outcomes. Various factors contribute to this issue, including participant non-response, dropout, or technical errors during data collection. Traditional methods like mean imputation or regression, commonly used to handle missing data, rely upon assumptions that may not hold on psychological data and can lead to distorted results.
View Article and Find Full Text PDFBiometrics
October 2024
INSERM, Centre de recherche des Cordeliers, Univ. Sorbonne, Univ. Paris Cité, Paris F-75006, France.
This paper introduces a prognostic method called FLASH that addresses the problem of joint modeling of longitudinal data and censored durations when a large number of both longitudinal and time-independent features are available. In the literature, standard joint models are either of the shared random effect or joint latent class type. Combining ideas from both worlds and using appropriate regularization techniques, we define a new model with the ability to automatically identify significant prognostic longitudinal features in a high-dimensional context, which is of increasing importance in many areas such as personalized medicine or churn prediction.
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