Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Estimation of population mean in the presence of measurement error and non response under stratified random sampling.

ABSTRACT: In the present paper we propose an improved class of estimators in the presence of measurement error and non-response under stratified random sampling for estimating the finite population mean. The theoretical and numerical studies reveal that the proposed class of estimators performs better than other existing estimators.

SUBMITTER: Zahid E

PROVIDER: S-EPMC5798808 | biostudies-literature | 2018

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

Estimation of population mean in the presence of measurement error and non response under stratified random sampling.

Zahid Erum E Shabbir Javid J

PloS one 20180205 2

In the present paper we propose an improved class of estimators in the presence of measurement error and non-response under stratified random sampling for estimating the finite population mean. The theoretical and numerical studies reveal that the proposed class of estimators performs better than other existing estimators. ...[more]

PMID: 29401519

Similar Datasets

Semiparametric location estimation under non-random sampling.

Project description:We study a class of semiparametric skewed distributions arising when the sample selection process produces non-randomly sampled observations. Based on semiparametric theory and taking into account the symmetric nature of the population distribution, we propose both consistent estimators, i.e. robust to model mis-specification, and efficient estimators, i.e. reaching the minimum possible estimation variance, of the location of the symmetric population. We demonstrate the theoretical properties of our estimators through asymptotic analysis and assess their finite sample performance through simulations. We also implement our methodology on a real data example of ambulatory expenditures to illustrate the applicability of the estimators in practice.

| S-EPMC3922234 | biostudies-literature

Estimation of finite population mean for a sensitive variable using dual auxiliary information in the presence of measurement errors.

Project description:In this study, we propose a new improved estimator of population mean for the sensitive variable in the presence of measurement error under simple and stratified random sampling. This estimator accounts the auxiliary information as well as the ranks of the auxiliary variable. From theoretical and numerical studies it is shown that a new improved estimator performs better than the existing estimators under study.

| S-EPMC6370250 | biostudies-literature

COVID-19 prevalence estimation by random sampling in population - optimal sample pooling under varying assumptions about true prevalence.

Project description:BackgroundThe number of confirmed COVID-19 cases divided by population size is used as a coarse measurement for the burden of disease in a population. However, this fraction depends heavily on the sampling intensity and the various test criteria used in different jurisdictions, and many sources indicate that a large fraction of cases tend to go undetected.MethodsEstimates of the true prevalence of COVID-19 in a population can be made by random sampling and pooling of RT-PCR tests. Here I use simulations to explore how experiment sample size and degrees of sample pooling impact precision of prevalence estimates and potential for minimizing the total number of tests required to get individual-level diagnostic results.ResultsSample pooling can greatly reduce the total number of tests required for prevalence estimation. In low-prevalence populations, it is theoretically possible to pool hundreds of samples with only marginal loss of precision. Even when the true prevalence is as high as 10% it can be appropriate to pool up to 15 samples. Sample pooling can be particularly beneficial when the test has imperfect specificity by providing more accurate estimates of the prevalence than an equal number of individual-level tests.ConclusionSample pooling should be considered in COVID-19 prevalence estimation efforts.

| S-EPMC7376319 | biostudies-literature

Population Size Estimation using Zero-truncated Poisson Regression with Measurement Error.

Project description:Population size estimation is an important research field in biological sciences. In practice, covariates are often measured upon capture on individuals sampled from the population. However, some biological measurements, such as body weight may vary over time within a subject's capture history. This can be treated as a population size estimation problem in the presence of covariate measurement error. We show that if the unobserved true covariate and measurement error are both normally distributed, then a naïve estimator without taking into account measurement error will under-estimate the population size. We then develop new methods to correct for the effect of measurement errors. In particular, we present a conditional score and a nonparametric corrected score approach that are both consistent for population size estimation. Importantly, the proposed approaches do not require the distribution assumption on the true covariates, furthermore the latter does not require normality assumptions on the measurement errors. This is highly relevant in biological applications, as the distribution of covariates is often non-normal or unknown. We investigate finite sample performance of the new estimators via extensive simulated studies. The methods are applied to real data from a capture-recapture study.

| S-EPMC9269986 | biostudies-literature

An efficient class of estimators for finite population mean in the presence of non-response under ranked set sampling (RSS).

Project description:In this study, we address the problem of estimating the finite population mean when the non-response occurs on the characteristics under study. We propose a class of Rao-regression type estimators when ranked set sampling (RSS) procedure is used to collect the data from non-response group only and from both, the response and non-response groups. The information provided on the auxiliary variable is used at both stages i.e., at designing stage and the estimation stage. Expressions for bias and mean square error of the estimators are obtained up to first order of approximation. A comprehensive simulation study is carried out to observe the performances of the estimators under non-response.

| S-EPMC9757593 | biostudies-literature

Conditional Density Estimation in Measurement Error Problems.

Project description:This paper is motivated by a wide range of background correction problems in gene array data analysis, where the raw gene expression intensities are measured with error. Estimating a conditional density function from the contaminated expression data is a key aspect of statistical inference and visualization in these studies. We propose re-weighted deconvolution kernel methods to estimate the conditional density function in an additive error model, when the error distribution is known as well as when it is unknown. Theoretical properties of the proposed estimators are investigated with respect to the mean absolute error from a "double asymptotic" view. Practical rules are developed for the selection of smoothing-parameters. Simulated examples and an application to an Illumina bead microarray study are presented to illustrate the viability of the methods.

| S-EPMC4183069 | biostudies-literature

Corruption of the Pearson correlation coefficient by measurement error and its estimation, bias, and correction under different error models.

Project description:Correlation coefficients are abundantly used in the life sciences. Their use can be limited to simple exploratory analysis or to construct association networks for visualization but they are also basic ingredients for sophisticated multivariate data analysis methods. It is therefore important to have reliable estimates for correlation coefficients. In modern life sciences, comprehensive measurement techniques are used to measure metabolites, proteins, gene-expressions and other types of data. All these measurement techniques have errors. Whereas in the old days, with simple measurements, the errors were also simple, that is not the case anymore. Errors are heterogeneous, non-constant and not independent. This hampers the quality of the estimated correlation coefficients seriously. We will discuss the different types of errors as present in modern comprehensive life science data and show with theory, simulations and real-life data how these affect the correlation coefficients. We will briefly discuss ways to improve the estimation of such coefficients.

| S-EPMC6965177 | biostudies-literature

Stratified Sampling of Neighborhood Sections for Population Estimation: A Case Study of Bo City, Sierra Leone.

Project description:There is a need for better estimators of population size in places that have undergone rapid growth and where collection of census data is difficult. We explored simulated estimates of urban population based on survey data from Bo, Sierra Leone, using two approaches: (1) stratified sampling from across 20 neighborhoods and (2) stratified single-stage cluster sampling of only four randomly-sampled neighborhoods. The stratification variables evaluated were (a) occupants per individual residence, (b) occupants per neighborhood, and (c) residential structures per neighborhood. For method (1), stratification variable (a) yielded the most accurate re-estimate of the current total population. Stratification variable (c), which can be estimated from aerial photography and zoning type verification, and variable (b), which could be ascertained by surveying a limited number of households, increased the accuracy of method (2). Small household-level surveys with appropriate sampling methods can yield reasonably accurate estimations of urban populations.

| S-EPMC4503693 | biostudies-literature

Estimation of Heterogeneous Restricted Mean Survival Time Using Random Forest.

Project description:Estimation and prediction of heterogeneous restricted mean survival time (hRMST) is of great clinical importance, which can provide an easily interpretable and clinically meaningful summary of the survival function in the presence of censoring and individual covariates. The existing methods for the modeling of hRMST rely on proportional hazards or other parametric assumptions on the survival distribution. In this paper, we propose a random forest based estimation of hRMST for right-censored survival data with covariates and prove a central limit theorem for the resulting estimator. In addition, we present a computationally efficient construction for the confidence interval of hRMST. Our simulations show that the resulting confidence intervals have the correct coverage probability of the hRMST, and the random forest based estimate of hRMST has smaller prediction errors than the parametric models when the models are mis-specified. We apply the method to the ovarian cancer data set from The Cancer Genome Atlas (TCGA) project to predict hRMST and show an improved prediction performance over the existing methods. A software implementation, srf using R and C++, is available at https://github.com/lmy1019/SRF.

| S-EPMC7873855 | biostudies-literature

Measurement protocols, random-variable-valued measurements, and response process error: Estimation and inference when sample data are not deterministic.

Project description:Random-variable-valued measurements (RVVMs) are proposed as a new framework for treating measurement processes that generate non-deterministic sample data. They operate by assigning a probability measure to each observed sample instantiation of a global measurement process for some particular random quantity of interest, thus allowing for the explicit quantification of response process error. Common methodologies to date treat only measurement processes that generate fixed values for each sample unit, thus generating full (though possibly inaccurate) information on the random quantity of interest. However, many applied research situations in the non-experimental sciences naturally contain response process error, e.g. when psychologists assess patient agreement with various diagnostic survey items or when conservation biologists perform formal assessments to classify species-at-risk. Ignoring the sample-unit-level uncertainty of response process error in such measurement processes can greatly compromise the quality of resulting inferences. In this paper, a general theory of RVVMs is proposed to handle response process error, and several applications are considered.

| S-EPMC7529193 | biostudies-literature

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data