Some combinatorial structures in experimental design: overview, statistical models and applications

Author(s):  
Petya  Valcheva
2020 ◽  
pp. 71-76
Author(s):  
M.A. Levantsevich ◽  
E.V. Pilipchuk ◽  
N.N Maksimchenko ◽  
L.S. Belevskiy ◽  
R.R. Dema

Experimental-statistical models of the process of forming composite chromium coatings by electrodeformation cladding with a flexible tool are developed, which allow to determine the parameters of the regimes for obtaining coatings of the required thickness and roughness. Keywords electrodeformation cladding, flexible tool, coating, composite material, experiment planning, noncompositional plan, thickness, roughness. [email protected]


2006 ◽  
Vol 3 (2) ◽  
pp. 77-89
Author(s):  
Y. E. Pittelkow ◽  
S. R. Wilson

Summary Various statistical models have been proposed for detecting differential gene expression in data from microarray experiments. Given such detection, we are usually interested in describing the differential expression patterns. Due to the large number of genes that are typically analysed in microarray experiments, possibly more than ten thousand, the tasks of interpretation and communication of all the corresponding statistical models pose a considerable challenge, except perhaps in the simplest experiment involving only two groups. A further challenge is to find methods to summarize the resulting models. These challenges increase with experimental complexity.Biologists often wish to sort genes into ‘classes’ with similar response profiles/patterns. So, in this paper we describe a likelihood approach for assigning genes to these different class patterns for data from a replicated experimental design.The number of potential patterns increases very quickly as the number of combinations in the experimental design increases. In a two group experimental design there are only three patterns required to describe the mean response: up, down and no difference. For a factorial design with three treatments there are 13 different patterns, and with four levels there are 75 potential patterns to be considered, and so on. The approach is applied to the identification of differential response patterns in gene expression from a microarray experiment using RNAextracted from the leaves of Arabidopsis thaliana plants. We compare patterns of response found using additive and multiplicative models. A multiplicative model is more commonly used in the statistical analysis of microarray data because of the variance stabilizing properties of the logarithmic function. Then the error structure of the model is taken to be log-Normal. On the other hand, for the additive model the gene expression value is modeled directly as being from a gamma distribution which successfully accounts for the constant coefficient of variation often observed. Appropriate visualization displays for microarray data are important as a way of communicating the patterns of response amongst the genes. Here we use graphical ‘icons’ to represent the patterns of up/down and no response and two alternative displays, the Gene-plot and a grid layout to provide rapid overall summaries of the gene expression patterns.


1998 ◽  
Vol 06 (04) ◽  
pp. 357-375
Author(s):  
Gabriela Ciuperca

In this paper we present a method for the estimation of the parameters of models described by a nonlinear system of differential equations: we study the maximum likelihood estimator and the jackknife estimator for parameters of the system and for the covariance matrix of the state variables and we seek possible linear relations between parameters. We take into account the difficulty due to the small number of observations. The optimal experimental design for this kind of problem is determined. We give an application of this method for the glucose metabolism of goats.


2010 ◽  
Vol 15 (8) ◽  
pp. 990-1000 ◽  
Author(s):  
Nathalie Malo ◽  
James A. Hanley ◽  
Graeme Carlile ◽  
Jing Liu ◽  
Jerry Pelletier ◽  
...  

Identification of active compounds in high-throughput screening (HTS) contexts can be substantially improved by applying classical experimental design and statistical inference principles to all phases of HTS studies. The authors present both experimental and simulated data to illustrate how true-positive rates can be maximized without increasing false-positive rates by the following analytical process. First, the use of robust data preprocessing methods reduces unwanted variation by removing row, column, and plate biases. Second, replicate measurements allow estimation of the magnitude of the remaining random error and the use of formal statistical models to benchmark putative hits relative to what is expected by chance. Receiver Operating Characteristic (ROC) analyses revealed superior power for data preprocessed by a trimmed-mean polish method combined with the RVM t-test, particularly for small- to moderate-sized biological hits.


2020 ◽  
Vol 17 (166) ◽  
pp. 20200156 ◽  
Author(s):  
Hayden Moffat ◽  
Markus Hainy ◽  
Nikos E. Papanikolaou ◽  
Christopher Drovandi

Understanding functional response within a predator–prey dynamic is a cornerstone for many quantitative ecological studies. Over the past 60 years, the methodology for modelling functional response has gradually transitioned from the classic mechanistic models to more statistically oriented models. To obtain inferences on these statistical models, a substantial number of experiments need to be conducted. The obvious disadvantages of collecting this volume of data include cost, time and the sacrificing of animals. Therefore, optimally designed experiments are useful as they may reduce the total number of experimental runs required to attain the same statistical results. In this paper, we develop the first sequential experimental design method for predator–prey functional response experiments. To make inferences on the parameters in each of the statistical models we consider, we use sequential Monte Carlo, which is computationally efficient and facilitates convenient estimation of important utility functions. It provides coverage of experimental goals including parameter estimation, model discrimination as well as a combination of these. The results of our simulation study illustrate that for predator–prey functional response experiments sequential design outperforms static design for our experimental goals. R code for implementing the methodology is available via https://github.com/haydenmoffat/sequential_design_for_predator_prey_experiments .


BioResources ◽  
2020 ◽  
Vol 15 (3) ◽  
pp. 5899-5912
Author(s):  
Bouchaib El Idrissi ◽  
Éric Loranger ◽  
Robert Lanouette ◽  
Jean Pierre Bousquet ◽  
Mark Martinez

Statistical modeling of a screw press was established by using an experimental design based on the screw rotational speed, the pulp feed consistency, the pulp feed suspension freeness, the inlet pressure, and the counter-pressure at the discharge end. The statistical models showed that the screw press outputs for each pulp could be predicted. When including all data in a global model to predict the outputs of the press for any pulp, a global statistical model was found not to be efficient by using just the five fixed parameters. The solution to this problem was to use a multivariate analysis to include more parameters, mainly about the fiber characteristics (crowding factor, fiber length, fiber width, and fines content). By including these fiber properties, the differences between each pulp were more properly analyzed. The multivariate analysis predicted the press outsets very well in a global model by using eight parameters instead of five. The R2 values of the multivariate prediction model were all higher than 0.70 and had the goodness of prediction (Q2¬¬¬) higher than 0.60.


2019 ◽  
Author(s):  
An Zheng ◽  
Michael Lamkin ◽  
Yutong Qiu ◽  
Kevin Ren ◽  
Alon Goren ◽  
...  

AbstractA major challenge in evaluating quantitative ChIP-seq analyses, such as peak calling and differential binding, is a lack of reliable ground truth data. We present Tulip, a toolkit for rapidly simulating ChIP-seq data using statistical models of the experimental steps. Tulip may be used for a range of applications, including power analysis for experimental design, benchmarking of analysis tools, and modeling effects of processes such as replication on ChIP-seq signals.


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