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1.
Mar Pollut Bull ; 173(Pt B): 113053, 2021 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-34678548

RESUMEN

As an important part of the global shipping industry, hazardous cargo transportation at ports is concerned by countries around the world due to the great hazards and high risks during its operations. However, multiple hazardous cargo accidents have occurred at ports in recent years. The explosion accident of hazardous cargoes at Tianjin Port, China, in 2015 is a typical case. It is a topic worth in-depth study to figure out how to analyze the causation factors of such accident and propose effective governance strategies against them. This article takes the hazardous cargo explosion at Tianjin Port of China as the subject and systematically analyzes the causation factors of the accident based on the Fault Tree Analysis (FTA) method. It proposes a strategy for governing hazardous cargoes at the port. The analysis results show that the hazardous cargo explosion at the port has complicated causation factors, among which management and human factors play a predominant role in the overall accident causation structure. Other factors include environmental factors and cargo & facility factors. Finally, the corresponding safety governance strategy is proposed based on the structural relationship of various accident causation factors in the above analysis. This study can offer guidance for port enterprises to reduce hazardous cargo accidents at ports and provide an important basis for port authorities to formulate strategies on emergency management and emergency decision-making of hazardous cargo accidents at ports.


Asunto(s)
Explosiones , Sustancias Peligrosas , Accidentes , China , Humanos , Transportes
2.
J Comput Graph Stat ; 26(3): 569-578, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-29217963

RESUMEN

A number of classical approaches to nonparametric regression have recently been extended to the case of functional predictors. This paper introduces a new method of this type, which extends intermediate-rank penalized smoothing to scalar-on-function regression. In the proposed method, which we call principal coordinate ridge regression, one regresses the response on leading principal coordinates defined by a relevant distance among the functional predictors, while applying a ridge penalty. Our publicly available implementation, based on generalized additive modeling software, allows for fast optimal tuning parameter selection and for extensions to multiple functional predictors, exponential family-valued responses, and mixed-effects models. In an application to signature verification data, principal coordinate ridge regression, with dynamic time warping distance used to define the principal coordinates, is shown to outperform a functional generalized linear model.

3.
Biometrics ; 71(3): 812-20, 2015 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-25939365

RESUMEN

Associating genetic markers with a multidimensional phenotype is an important yet challenging problem. In this work, we establish the equivalence between two popular methods: kernel-machine regression (KMR), and kernel distance covariance (KDC). KMR is a semiparametric regression framework that models covariate effects parametrically and genetic markers non-parametrically, while KDC represents a class of methods that include distance covariance (DC) and Hilbert-Schmidt independence criterion (HSIC), which are nonparametric tests of independence. We show that the equivalence between the score test of KMR and the KDC statistic under certain conditions can lead to a novel generalization of the KDC test that incorporates covariates. Our contributions are 3-fold: (1) establishing the equivalence between KMR and KDC; (2) showing that the principles of KMR can be applied to the interpretation of KDC; (3) the development of a broader class of KDC statistics, where the class members are statistics corresponding to different kernel combinations. Finally, we perform simulation studies and an analysis of real data from the Alzheimer's Disease Neuroimaging Initiative (ADNI) study. The ADNI study suggest that SNPs of FLJ16124 exhibit pairwise interaction effects that are strongly correlated to the changes of brain region volumes.


Asunto(s)
Enfermedad de Alzheimer/epidemiología , Enfermedad de Alzheimer/genética , Estudios de Asociación Genética/métodos , Modelos Estadísticos , Polimorfismo de Nucleótido Simple/genética , Análisis de Regresión , Enfermedad de Alzheimer/diagnóstico , Análisis de Varianza , Simulación por Computador , Interpretación Estadística de Datos , Marcadores Genéticos/genética , Predisposición Genética a la Enfermedad/epidemiología , Predisposición Genética a la Enfermedad/genética , Prevalencia , Reproducibilidad de los Resultados , Factores de Riesgo , Sensibilidad y Especificidad
4.
Biostatistics ; 16(1): 17-30, 2015 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-24963012

RESUMEN

Recent research in neuroimaging has focused on assessing associations between genetic variants that are measured on a genomewide scale and brain imaging phenotypes. A large number of works in the area apply massively univariate analyses on a genomewide basis to find single nucleotide polymorphisms that influence brain structure. In this paper, we propose using various dimensionality reduction methods on both brain structural MRI scans and genomic data, motivated by the Alzheimer's Disease Neuroimaging Initiative (ADNI) study. We also consider a new multiple testing adjustment method and compare it with two existing false discovery rate (FDR) adjustment methods. The simulation results suggest an increase in power for the proposed method. The real-data analysis suggests that the proposed procedure is able to find associations between genetic variants and brain volume differences that offer potentially new biological insights.


Asunto(s)
Encéfalo/patología , Interpretación Estadística de Datos , Estudio de Asociación del Genoma Completo/métodos , Imagen por Resonancia Magnética/métodos , Neuroimagen/métodos , Enfermedad de Alzheimer/genética , Enfermedad de Alzheimer/patología , Disfunción Cognitiva/genética , Disfunción Cognitiva/patología , Variación Genética , Humanos , Fenotipo
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