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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
1

Regulation der Synthese der Glukosamin-6-Phosphat Synthase GlmS in Escherichia coli durch das neuartige Protein YhbJ / Regulation of the synthesis of the glucosamine-6-phosphate Synthase GlmS in Escherichia coli by the novel protein YhbJ

Kalamorz, Falk 19 January 2009 (has links)
No description available.
2

MULTIVARIATE MULTISITE STATISTICAL DOWNSCALING OF ATMOSPHERE-OCEAN GENERAL CIRCULATION MODEL OUTPUTS OVER THE CANADIAN PRAIRIE PROVINCES

2015 December 1900 (has links)
Atmosphere-Ocean General Circulation Models (AOGCMs) are the primary tool for modelling global climate change in the future. However, their coarse spatial resolution does not permit direct application for local scale impact studies. Therefore, either dynamical or statistical downscaling techniques are used for translating AOGCM outputs to local scale climatic variables. The main goal of this study was to improve our understanding of the historical and future climate change at local-scale in the Canadian Prairie Provinces (CPPs) of Alberta, Saskatchewan and Manitoba, comprising 47 diverse watersheds. Given the vast nature of the study area and paucity of recorded data, a novel approach for identifying homogeneous regions for regionalization of precipitation characteristics for the CPPs was proposed. This approach incorporated information about predictors ― large-scale atmospheric covariates from the National Center for Environmental Prediction (NCEP) Reanalysis-I, teleconnection indices and geographical site attributes that impact spatial patterns of precipitation in order to delineate homogeneous precipitation regions using a combination of multivariate approaches. This resulted in the delimitation of five homogeneous climatic regions which were validated independently for homogeneity using statistics computed from observations recorded at 120 stations across the CPPs. For multisite multivariate statistical downscaling, an approach based on the Generalized Linear Model (GLM) framework was developed to downscale daily observations of precipitation and minimum and maximum temperatures from 120 sites located across the CPPs. First, the aforementioned predictors and observed daily precipitation and temperature records were used to calibrate GLMs for the 1971–2000 period. Then the calibrated GLMs were used to generate daily sequences of precipitation and temperatures for the 1962–2005 historical (conditioned on NCEP predictors), and future period (2006–2100) using outputs from six CMIP5 (Coupled Model Intercomparison Project Phase-5) AOGCMs corresponding to Representative Concentration Pathway (RCP): RCP2.6, RCP4.5, and RCP8.5 scenarios. The results indicated that the fitted GLMs were able to capture spatiotemporal characteristics of observed climatic fields. According to the downscaled future climate, mean precipitation is projected to increase in summer and decrease in winter while minimum temperature is expected to warm faster than the maximum temperature. Climate extremes are projected to intensify with increased radiative forcing.
3

Experimental Designs for Generalized Linear Models and Functional Magnetic Resonance Imaging

January 2014 (has links)
abstract: In this era of fast computational machines and new optimization algorithms, there have been great advances in Experimental Designs. We focus our research on design issues in generalized linear models (GLMs) and functional magnetic resonance imaging(fMRI). The first part of our research is on tackling the challenging problem of constructing exact designs for GLMs, that are robust against parameter, link and model uncertainties by improving an existing algorithm and providing a new one, based on using a continuous particle swarm optimization (PSO) and spectral clustering. The proposed algorithm is sufficiently versatile to accomodate most popular design selection criteria, and we concentrate on providing robust designs for GLMs, using the D and A optimality criterion. The second part of our research is on providing an algorithm that is a faster alternative to a recently proposed genetic algorithm (GA) to construct optimal designs for fMRI studies. Our algorithm is built upon a discrete version of the PSO. / Dissertation/Thesis / Doctoral Dissertation Statistics 2014
4

Regulation of glucosamine-6-phosphate synthase synthesis by a hierarchical acting cascade composed of two small regulatory RNAs in <i>Escherichia coli</i>. / Regulation der Synthese der Glukosamin-6-Phosphat Synthase durch eine aus zwei kleinen regulatorischen RNAs bestehende hierarchische Kaskade in <i>Escherichia coli</i>.

Reichenbach, Birte 19 October 2009 (has links)
No description available.
5

廣義線性模式下處理比較之最適設計 / Optimal Designs for Treatment Comparisons under Generalized Linear Models

何漢葳, Ho, Han Wei Unknown Date (has links)
本研究旨在建立廣義線性模式下之D-與A-最適設計(optimal designs),並依不同處理結構(treatment structure)分成完全隨機設計(completely randomized design, CRD)與隨機集區設計(randomized block design, RBD)兩部分探討。 根據完全隨機設計所推導出之行列式的性質與理論結果,我們首先提出一個能快速大幅限縮尋找D-最適正合(exact)設計範圍的演算法。解析解的部分,則從將v個處理的變異數分為兩類出發,建立其D-最適近似(approximate)設計,並由此發現 (1) 各水準對應之樣本最適配置的上下界並非與水準間不同變異有關,而是與有多少處理之變異相同有關;(2) 即使是變異很大的處理,也必須分配觀察值,始能極大化行列式值。此意味著當v較大時,均分應不失為一有效率(efficient)的設計。至於正合設計,我們僅能得出某一處理特別大或特別小時的D-最適設計,並舉例說明求不出一般解的原因。 除此之外,我們亦求出當三個處理的變異數皆不同時之D-最適近似設計,以及v個處理皆不同時之A-最適近似設計。 至於最適隨機集區設計的建立,我們的重點放在v=2及v=3的情形,並假設集區樣本數(block size)為給定。當v=2時,各集區對應之行列式值不受其他集區的影響,故僅需依照完全隨機設計之所得,將各集區之行列式值分別最佳化,即可得出D-與A-最適設計。值得一提的是,若進一步假設各集區中兩處理變異的比例(>1)皆相同,且集區大小皆相同,則將各處理的「近似設計下最適總和」取最接近的整數,再均分給各集區,其結果未必為最適設計。當v=3時,即使只有2個集區,行列式也十分複雜,我們目前僅能證明當集區內各處理的變異相同時(不同集區之處理變異可不同),均分給定之集區樣本數為D-最適設計。當集區內各處理的變異不全相同時,我們僅能先以2個集區為例,類比完全隨機設計的性質,舉例猜想當兩集區中處理之變異大小順序相同時,各處理最適樣本配置的多寡亦與變異大小呈反比。由於本研究對處理與集區兩者之效應假設為可加,因此可合理假設集區中處理之變異大小順序相同。 / The problem of finding D- and A-optimal designs for the zero- and one-way elimination of heterogeneity under generalized linear models is considered. Since GLM designs rely on the values of parameters to be estimated, our strategy is to employ the locally optimal designs. For the zero-way elimination model, a theorem-based algorithm is proposed to search for the D-optimal exact designs. A formula for the construction of D-optimal approximate design when values of unknown parameters are split into two, with respective sizes m and v-m, are derived. Analytic solutions provided to the exact counterpart, however, are restricted to the cases when m=1 and m=v-1. An example is given to explain the problem involved. On the other hand, the upper bound and lower bound of the optimal number of replicates per treatment are proved dependent on m, rather than the unknown parameters. These bounds imply that designs having as equal number of replications for each treatment as possible are efficient in D-optimality. In addition, a D-optimal approximate design when values of unknown parameters are divided into three groups is also obtained. A closed-form expression for an A-optimal approximate design for comparing arbitrary v treatments is given. For the one-way elimination model, our focus is on studying the D-optimal designs for v=2 and v=3 with each block size given. The D- and A-optimality for v=2 can be achieved by assigning units proportional to square root of the ratio of two variances, which is larger than 1, to the treatment with smaller variance in each block separately. For v=3, the structure of determinant is much more complicated even for two blocks, and we can only show that, when treatment variances are the same within a block, design having equal number of replicates as possible in each block is a D-optimal block design. Some numerical evidences conjecture that a design satisfying the condition that the number of replicates are inversely proportional to the treatment variances per block is better in terms of D-optimality, as long as the ordering of treatment variances are the same across blocks, which is reasonable for an additive model as we assume.

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