Estimating the reproduction number of an emerging infectious disease from an epidemiological data is becoming more essential in evaluating the current status of an outbreak. However, these studies are lacking the fundamental prerequisite in parameter estimation problem, namely the structural identifiability of the epidemic model, which determines the possibility of uniquely determining the model parameters from the epidemic data. In this paper, we perform both structural and practical identifiability analysis to classical epidemic models such as SIR (Susceptible-Infected-Recovered), SEIR (Susceptible-Exposed-Infected-Recovered) and an epidemic model with the treatment class (SITR). We performed structural identifiability analysis on these epidemic models using a differential algebra approach to investigate the well-posedness of the parameter estimation problem. Parameters of these models are estimated from different data types, namely prevalence, cumulative incidences and treated individuals. Furthermore, we carried out practical identifiability analysis on these models using Monte Carlo simulations and Fisher's Information Matrix. Our study shows that the SIR model is both structurally and practically identifiable from the prevalence data. It is also structurally identifiable to cumulative incidence observations, but due to high correlations of the parameters, it is practically unidentifiable from the cumulative incidence data. Furthermore, we found that none of these simple epidemic models are practically identifiable from the cumulative incidence data which is the standard type of epidemiological data provided by CDC or WHO. Our analysis with simple SIR model suggest that the health agencies, if possible, should report prevalence rather than incidence data.
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http://dx.doi.org/10.1016/j.mbs.2018.02.004 | DOI Listing |
Practical identifiability is a critical concern in data-driven modeling of mathematical systems. In this paper, we propose a novel framework for practical identifiability analysis to evaluate parameter identifiability in mathematical models of biological systems. Starting with a rigorous mathematical definition of practical identifiability, we demonstrate its equivalence to the invertibility of the Fisher Information Matrix.
View Article and Find Full Text PDFJ Mach Learn Res
January 2024
Division of Biostatistics, University of Minnesota, Minneapolis, MN 55455, USA.
This article presents a novel method for causal discovery with generalized structural equation models suited for analyzing diverse types of outcomes, including discrete, continuous, and mixed data. Causal discovery often faces challenges due to unmeasured confounders that hinder the identification of causal relationships. The proposed approach addresses this issue by developing two peeling algorithms (bottom-up and top-down) to ascertain causal relationships and valid instruments.
View Article and Find Full Text PDFAnal Chem
January 2025
School of Chemistry and Chemical Engineering University of Jinan, Jinan 250022, People's Republic of China.
Mitochondrial DNA (mtDNA) damage is a prevalent phenomenon that has been proven to be implicated in a wide spectrum of diseases. However, the progressive attenuation of probe signals in response to mtDNA damage within living cells inherently limits the sensitivity and precision of current probes for detecting mtDNA damage. Herein, we employ an innovative organelle signal ratio imaging approach, utilizing the mitochondria-nucleus migration probe MCQ, to achieve unparalleled sensitivity in detecting mtDNA damage in living cells.
View Article and Find Full Text PDFFront Neurosci
December 2024
Institut de Neurosciences des Systèmes, Aix-Marseille Université, Marseille, France.
Background: Brain connectome fingerprinting represents a recent and valid approach in assessing individual identifiability on the basis of the subject-specific brain functional connectome. Although this methodology has been tested and validated in several neurological diseases, its performance, reliability and reproducibility in healthy individuals has been poorly investigated. In particular, the impact of the changes in brain connectivity, induced by the different phases of the menstrual cycle (MC), on the reliability of this approach remains unexplored.
View Article and Find Full Text PDFEur Radiol
December 2024
Department of Radiology, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Objectives: To develop and validate deep learning (DL)-models that denoise late iodine enhancement (LIE) images and enable accurate extracellular volume (ECV) quantification.
Methods: This study retrospectively included patients with chest discomfort who underwent CT myocardial perfusion + CT angiography + LIE from two hospitals. Two DL models, residual dense network (RDN) and conditional generative adversarial network (cGAN), were developed and validated.
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