Estimator

About: Estimator is a research topic. Over the lifetime, 97381 publications have been published within this topic receiving 2606057 citations. The topic is also known as: statistical estimator.

Linear Models and Empirical Bayes Methods for Assessing Differential Expression in Microarray Experiments

Abstract: The problem of identifying differentially expressed genes in designed microarray experiments is considered. Lonnstedt and Speed (2002) derived an expression for the posterior odds of differential expression in a replicated two-color experiment using a simple hierarchical parametric model. The purpose of this paper is to develop the hierarchical model of Lonnstedt and Speed (2002) into a practical approach for general microarray experiments with arbitrary numbers of treatments and RNA samples. The model is reset in the context of general linear models with arbitrary coefficients and contrasts of interest. The approach applies equally well to both single channel and two color microarray experiments. Consistent, closed form estimators are derived for the hyperparameters in the model. The estimators proposed have robust behavior even for small numbers of arrays and allow for incomplete data arising from spot filtering or spot quality weights. The posterior odds statistic is reformulated in terms of a moderated t-statistic in which posterior residual standard deviations are used in place of ordinary standard deviations. The empirical Bayes approach is equivalent to shrinkage of the estimated sample variances towards a pooled estimate, resulting in far more stable inference when the number of arrays is small. The use of moderated t-statistics has the advantage over the posterior odds that the number of hyperparameters which need to estimated is reduced; in particular, knowledge of the non-null prior for the fold changes are not required. The moderated t-statistic is shown to follow a t-distribution with augmented degrees of freedom. The moderated t inferential approach extends to accommodate tests of composite null hypotheses through the use of moderated F-statistics. The performance of the methods is demonstrated in a simulation study. Results are presented for two publicly available data sets.

Mean shift: a robust approach toward feature space analysis

Abstract: A general non-parametric technique is proposed for the analysis of a complex multimodal feature space and to delineate arbitrarily shaped clusters in it. The basic computational module of the technique is an old pattern recognition procedure: the mean shift. For discrete data, we prove the convergence of a recursive mean shift procedure to the nearest stationary point of the underlying density function and, thus, its utility in detecting the modes of the density. The relation of the mean shift procedure to the Nadaraya-Watson estimator from kernel regression and the robust M-estimators; of location is also established. Algorithms for two low-level vision tasks discontinuity-preserving smoothing and image segmentation - are described as applications. In these algorithms, the only user-set parameter is the resolution of the analysis, and either gray-level or color images are accepted as input. Extensive experimental results illustrate their excellent performance.

Estimates of the Regression Coefficient Based on Kendall's Tau

Abstract: The least squares estimator of a regression coefficient β is vulnerable to gross errors and the associated confidence interval is, in addition, sensitive to non-normality of the parent distribution. In this paper, a simple and robust (point as well as interval) estimator of β based on Kendall's [6] rank correlation tau is studied. The point estimator is the median of the set of slopes (Yj - Yi )/(tj-ti ) joining pairs of points with ti ≠ ti , and is unbiased. The confidence interval is also determined by two order statistics of this set of slopes. Various properties of these estimators are studied and compared with those of the least squares and some other nonparametric estimators.

Ideal spatial adaptation by wavelet shrinkage

Abstract: SUMMARY With ideal spatial adaptation, an oracle furnishes information about how best to adapt a spatially variable estimator, whether piecewise constant, piecewise polynomial, variable knot spline, or variable bandwidth kernel, to the unknown function. Estimation with the aid of an oracle offers dramatic advantages over traditional linear estimation by nonadaptive kernels; however, it is a priori unclear whether such performance can be obtained by a procedure relying on the data alone. We describe a new principle for spatially-adaptive estimation: selective wavelet reconstruction. We show that variable-knot spline fits and piecewise-polynomial fits, when equipped with an oracle to select the knots, are not dramatically more powerful than selective wavelet reconstruction with an oracle. We develop a practical spatially adaptive method, RiskShrink, which works by shrinkage of empirical wavelet coefficients. RiskShrink mimics the performance of an oracle for selective wavelet reconstruction as well as it is possible to do so. A new inequality in multivariate normal decision theory which we call the oracle inequality shows that attained performance differs from ideal performance by at most a factor of approximately 2 log n, where n is the sample size. Moreover no estimator can give a better guarantee than this. Within the class of spatially adaptive procedures, RiskShrink is essentially optimal. Relying only on the data, it comes within a factor log 2 n of the performance of piecewise polynomial and variableknot spline methods equipped with an oracle. In contrast, it is unknown how or if piecewise polynomial methods could be made to function this well when denied access to an oracle and forced to rely on data alone.

Estimating the mean and variance from the median, range, and the size of a sample.

Abstract: Usually the researchers performing meta-analysis of continuous outcomes from clinical trials need their mean value and the variance (or standard deviation) in order to pool data. However, sometimes the published reports of clinical trials only report the median, range and the size of the trial. In this article we use simple and elementary inequalities and approximations in order to estimate the mean and the variance for such trials. Our estimation is distribution-free, i.e., it makes no assumption on the distribution of the underlying data. We found two simple formulas that estimate the mean using the values of the median (m), low and high end of the range (a and b, respectively), and n (the sample size). Using simulations, we show that median can be used to estimate mean when the sample size is larger than 25. For smaller samples our new formula, devised in this paper, should be used. We also estimated the variance of an unknown sample using the median, low and high end of the range, and the sample size. Our estimate is performing as the best estimate in our simulations for very small samples (n ≤ 15). For moderately sized samples (15 70), the formula range/6 gives the best estimator for the standard deviation (variance). We also include an illustrative example of the potential value of our method using reports from the Cochrane review on the role of erythropoietin in anemia due to malignancy. Using these formulas, we hope to help meta-analysts use clinical trials in their analysis even when not all of the information is available and/or reported.