Piazza Chapter on "Fundamentals of Applied Sampling"
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Choosing the Sample
CHAPTER IV CHOOSING THE SAMPLE This chapter is written for survey coordinators and technical resource persons. It will enable you to: U Understand the basic concepts of sampling. U Calculate the required sample size for national and subnational estimates. U Determine the number of clusters to be used. U Choose a sampling scheme. UNDERSTANDING THE BASIC CONCEPTS OF SAMPLING In the context of multiple-indicator surveys, sampling is a process for selecting respondents from a population. In our case, the respondents will usually be the mothers, or caretakers, of children in each household visited,1 who will answer all of the questions in the Child Health modules. The Water and Sanitation and Salt Iodization modules refer to the whole household and may be answered by any adult. Questions in these modules are asked even where there are no children under the age of 15 years. In principle, our survey could cover all households in the population. If all mothers being interviewed could provide perfect answers, we could measure all indicators with complete accuracy. However, interviewing all mothers would be time-consuming, expensive and wasteful. It is therefore necessary to interview a sample of these women to obtain estimates of the actual indicators. The difference between the estimate and the actual indicator is called sampling error. Sampling errors are caused by the fact that a sample&and not the entire population&is surveyed. Sampling error can be minimized by taking certain precautions: 3 Choose your sample of respondents in an unbiased way. 3 Select a large enough sample for your estimates to be precise. -
Statistical Theory and Methodology for the Analysis of Microbial Compositions, with Applications
Statistical Theory and Methodology for the Analysis of Microbial Compositions, with Applications by Huang Lin BS, Xiamen University, China, 2015 Submitted to the Graduate Faculty of the Graduate School of Public Health in partial fulfillment of the requirements for the degree of Doctor of Philosophy University of Pittsburgh 2020 UNIVERSITY OF PITTSBURGH GRADUATE SCHOOL OF PUBLIC HEALTH This dissertation was presented by Huang Lin It was defended on April 2nd 2020 and approved by Shyamal Das Peddada, PhD, Professor and Chair, Department of Biostatistics, Graduate School of Public Health, University of Pittsburgh Jeanine Buchanich, PhD, Research Associate Professor, Department of Biostatistics, Graduate School of Public Health, University of Pittsburgh Ying Ding, PhD, Associate Professor, Department of Biostatistics, Graduate School of Public Health, University of Pittsburgh Matthew Rogers, PhD, Research Assistant Professor, Department of Surgery, UPMC Children's Hospital of Pittsburgh Hong Wang, PhD, Research Assistant Professor, Department of Biostatistics, Graduate School of Public Health, University of Pittsburgh Dissertation Director: Shyamal Das Peddada, PhD, Professor and Chair, Department of Biostatistics, Graduate School of Public Health, University of Pittsburgh ii Copyright c by Huang Lin 2020 iii Statistical Theory and Methodology for the Analysis of Microbial Compositions, with Applications Huang Lin, PhD University of Pittsburgh, 2020 Abstract Increasingly researchers are finding associations between the microbiome and human diseases such as obesity, inflammatory bowel diseases, HIV, and so on. Determining what microbes are significantly different between conditions, known as differential abundance (DA) analysis, and depicting the dependence structure among them, are two of the most challeng- ing and critical problems that have received considerable interest. -
Computing Effect Sizes for Clustered Randomized Trials
Computing Effect Sizes for Clustered Randomized Trials Terri Pigott, C2 Methods Editor & Co-Chair Professor, Loyola University Chicago [email protected] The Campbell Collaboration www.campbellcollaboration.org Computing effect sizes in clustered trials • In an experimental study, we are interested in the difference in performance between the treatment and control group • In this case, we use the standardized mean difference, given by YYTC− d = gg Control group sp mean Treatment group mean Pooled sample standard deviation Campbell Collaboration Colloquium – August 2011 www.campbellcollaboration.org 1 Variance of the standardized mean difference NNTC+ d2 Sd2 ()=+ NNTC2( N T+ N C ) where NT is the sample size for the treatment group, and NC is the sample size for the control group Campbell Collaboration Colloquium – August 2011 www.campbellcollaboration.org TREATMENT GROUP CONTROL GROUP TT T CC C YY,,..., Y YY12,,..., YC 12 NT N Overall Trt Mean Overall Cntl Mean T Y C Yg g S 2 2 Trt SCntl 2 S pooled Campbell Collaboration Colloquium – August 2011 www.campbellcollaboration.org 2 In cluster randomized trials, SMD more complex • In cluster randomized trials, we have clusters such as schools or clinics randomized to treatment and control • We have at least two means: mean performance for each cluster, and the overall group mean • We also have several components of variance – the within- cluster variance, the variance between cluster means, and the total variance • Next slide is an illustration Campbell Collaboration Colloquium – August 2011 www.campbellcollaboration.org TREATMENT GROUP CONTROL GROUP Cntl Cluster mC Trt Cluster 1 Trt Cluster mT Cntl Cluster 1 TT T T CC C C YY,...ggg Y ,..., Y YY11,.. -
Evaluating Probability Sampling Strategies for Estimating Redd Counts: an Example with Chinook Salmon (Oncorhynchus Tshawytscha)
1814 Evaluating probability sampling strategies for estimating redd counts: an example with Chinook salmon (Oncorhynchus tshawytscha) Jean-Yves Courbois, Stephen L. Katz, Daniel J. Isaak, E. Ashley Steel, Russell F. Thurow, A. Michelle Wargo Rub, Tony Olsen, and Chris E. Jordan Abstract: Precise, unbiased estimates of population size are an essential tool for fisheries management. For a wide variety of salmonid fishes, redd counts from a sample of reaches are commonly used to monitor annual trends in abundance. Using a 9-year time series of georeferenced censuses of Chinook salmon (Oncorhynchus tshawytscha) redds from central Idaho, USA, we evaluated a wide range of common sampling strategies for estimating the total abundance of redds. We evaluated two sampling-unit sizes (200 and 1000 m reaches), three sample proportions (0.05, 0.10, and 0.29), and six sampling strat- egies (index sampling, simple random sampling, systematic sampling, stratified sampling, adaptive cluster sampling, and a spatially balanced design). We evaluated the strategies based on their accuracy (confidence interval coverage), precision (relative standard error), and cost (based on travel time). Accuracy increased with increasing number of redds, increasing sample size, and smaller sampling units. The total number of redds in the watershed and budgetary constraints influenced which strategies were most precise and effective. For years with very few redds (<0.15 reddsÁkm–1), a stratified sampling strategy and inexpensive strategies were most efficient, whereas for years with more redds (0.15–2.9 reddsÁkm–1), either of two more expensive systematic strategies were most precise. Re´sume´ : La gestion des peˆches requiert comme outils essentiels des estimations pre´cises et non fausse´es de la taille des populations. -
Cluster Sampling
Day 5 sampling - clustering SAMPLE POPULATION SAMPLING: IS ESTIMATING THE CHARACTERISTICS OF THE WHOLE POPULATION USING INFORMATION COLLECTED FROM A SAMPLE GROUP. The sampling process comprises several stages: •Defining the population of concern •Specifying a sampling frame, a set of items or events possible to measure •Specifying a sampling method for selecting items or events from the frame •Determining the sample size •Implementing the sampling plan •Sampling and data collecting 2 Simple random sampling 3 In a simple random sample (SRS) of a given size, all such subsets of the frame are given an equal probability. In particular, the variance between individual results within the sample is a good indicator of variance in the overall population, which makes it relatively easy to estimate the accuracy of results. SRS can be vulnerable to sampling error because the randomness of the selection may result in a sample that doesn't reflect the makeup of the population. Systematic sampling 4 Systematic sampling (also known as interval sampling) relies on arranging the study population according to some ordering scheme and then selecting elements at regular intervals through that ordered list Systematic sampling involves a random start and then proceeds with the selection of every kth element from then onwards. In this case, k=(population size/sample size). It is important that the starting point is not automatically the first in the list, but is instead randomly chosen from within the first to the kth element in the list. STRATIFIED SAMPLING 5 WHEN THE POPULATION EMBRACES A NUMBER OF DISTINCT CATEGORIES, THE FRAME CAN BE ORGANIZED BY THESE CATEGORIES INTO SEPARATE "STRATA." EACH STRATUM IS THEN SAMPLED AS AN INDEPENDENT SUB-POPULATION, OUT OF WHICH INDIVIDUAL ELEMENTS CAN BE RANDOMLY SELECTED Cluster sampling Sometimes it is more cost-effective to select respondents in groups ('clusters') Quota sampling Minimax sampling Accidental sampling Voluntary Sampling …. -
Analytic Inference in Finite Population Framework Via Resampling Arxiv
Analytic inference in finite population framework via resampling Pier Luigi Conti Alberto Di Iorio Abstract The aim of this paper is to provide a resampling technique that allows us to make inference on superpopulation parameters in finite population setting. Under complex sampling designs, it is often difficult to obtain explicit results about su- perpopulation parameters of interest, especially in terms of confidence intervals and test-statistics. Computer intensive procedures, such as resampling, allow us to avoid this problem. To reach the above goal, asymptotic results about empirical processes in finite population framework are first obtained. Then, a resampling procedure is proposed, and justified via asymptotic considerations. Finally, the results obtained are applied to different inferential problems and a simulation study is performed to test the goodness of our proposal. Keywords: Resampling, finite populations, H´ajekestimator, empirical process, statistical functionals. arXiv:1809.08035v1 [stat.ME] 21 Sep 2018 1 Introduction The use of superpopulation models in survey sampling has a long history, going back (at least) to [8], where the limits of assuming the population characteristics as fixed, especially in economic and social studies, are stressed. As clearly appears, for instance, from [30] and [26], there are basically two types of inference in the finite populations setting. The first one is descriptive or enumerative inference, namely inference about finite population parameters. This kind of inference is a static \picture" on the current state of a population, and does not take into account the mechanism generating the characters of interest of the population itself. The second one is analytic inference, and consists in inference on superpopulation parameters. -
Sampling and Evaluation
Sampling and Evaluation A Guide to Sampling for Program Impact Evaluation Peter M. Lance Aiko Hattori Suggested citation: Lance, P. and A. Hattori. (2016). Sampling and evaluation: A guide to sampling for program impact evaluation. Chapel Hill, North Carolina: MEASURE Evaluation, University of North Carolina. Sampling and Evaluation A Guide to Sampling for Program Impact Evaluation Peter M. Lance, PhD, MEASURE Evaluation Aiko Hattori, PhD, MEASURE Evaluation ISBN: 978-1-943364-94-7 MEASURE Evaluation This publication was produced with the support of the United States University of North Carolina at Chapel Agency for International Development (USAID) under the terms of Hill MEASURE Evaluation cooperative agreement AID-OAA-L-14-00004. 400 Meadowmont Village Circle, 3rd MEASURE Evaluation is implemented by the Carolina Population Center, University of North Carolina at Chapel Hill in partnership with Floor ICF International; John Snow, Inc.; Management Sciences for Health; Chapel Hill, NC 27517 USA Palladium; and Tulane University. Views expressed are not necessarily Phone: +1 919-445-9350 those of USAID or the United States government. MS-16-112 [email protected] www.measureevaluation.org Dedicated to Anthony G. Turner iii Contents Acknowledgments v 1 Introduction 1 2 Basics of Sample Selection 3 2.1 Basic Selection and Sampling Weights . 5 2.2 Common Sample Selection Extensions and Complications . 58 2.2.1 Multistage Selection . 58 2.2.2 Stratification . 62 2.2.3 The Design Effect, Re-visited . 64 2.2.4 Hard to Find Subpopulations . 64 2.2.5 Large Clusters and Size Sampling . 67 2.3 Complications to Weights . 69 2.3.1 Non-Response Adjustment . -
Introduction to Survey Sampling and Analysis Procedures (Chapter)
SAS/STAT® 9.3 User’s Guide Introduction to Survey Sampling and Analysis Procedures (Chapter) SAS® Documentation This document is an individual chapter from SAS/STAT® 9.3 User’s Guide. The correct bibliographic citation for the complete manual is as follows: SAS Institute Inc. 2011. SAS/STAT® 9.3 User’s Guide. Cary, NC: SAS Institute Inc. Copyright © 2011, SAS Institute Inc., Cary, NC, USA All rights reserved. Produced in the United States of America. For a Web download or e-book: Your use of this publication shall be governed by the terms established by the vendor at the time you acquire this publication. The scanning, uploading, and distribution of this book via the Internet or any other means without the permission of the publisher is illegal and punishable by law. Please purchase only authorized electronic editions and do not participate in or encourage electronic piracy of copyrighted materials. Your support of others’ rights is appreciated. U.S. Government Restricted Rights Notice: Use, duplication, or disclosure of this software and related documentation by the U.S. government is subject to the Agreement with SAS Institute and the restrictions set forth in FAR 52.227-19, Commercial Computer Software-Restricted Rights (June 1987). SAS Institute Inc., SAS Campus Drive, Cary, North Carolina 27513. 1st electronic book, July 2011 SAS® Publishing provides a complete selection of books and electronic products to help customers use SAS software to its fullest potential. For more information about our e-books, e-learning products, CDs, and hard-copy books, visit the SAS Publishing Web site at support.sas.com/publishing or call 1-800-727-3228. -
Sampling and Household Listing Manual [DHSM4]
SAMPLING AND HOUSEHOLD LISTING MANuaL Demographic and Health Surveys Methodology This document is part of the Demographic and Health Survey’s DHS Toolkit of methodology for the MEASURE DHS Phase III project, implemented from 2008-2013. This publication was produced for review by the United States Agency for International Development (USAID). It was prepared by MEASURE DHS/ICF International. [THIS PAGE IS INTENTIONALLY BLANK] Demographic and Health Survey Sampling and Household Listing Manual ICF International Calverton, Maryland USA September 2012 MEASURE DHS is a five-year project to assist institutions in collecting and analyzing data needed to plan, monitor, and evaluate population, health, and nutrition programs. MEASURE DHS is funded by the U.S. Agency for International Development (USAID). The project is implemented by ICF International in Calverton, Maryland, in partnership with the Johns Hopkins Bloomberg School of Public Health/Center for Communication Programs, the Program for Appropriate Technology in Health (PATH), Futures Institute, Camris International, and Blue Raster. The main objectives of the MEASURE DHS program are to: 1) provide improved information through appropriate data collection, analysis, and evaluation; 2) improve coordination and partnerships in data collection at the international and country levels; 3) increase host-country institutionalization of data collection capacity; 4) improve data collection and analysis tools and methodologies; and 5) improve the dissemination and utilization of data. For information about the Demographic and Health Surveys (DHS) program, write to DHS, ICF International, 11785 Beltsville Drive, Suite 300, Calverton, MD 20705, U.S.A. (Telephone: 301-572- 0200; fax: 301-572-0999; e-mail: [email protected]; Internet: http://www.measuredhs.com). -
Taylor's Power Law and Fixed-Precision Sampling
87 ARTICLE Taylor’s power law and fixed-precision sampling: application to abundance of fish sampled by gillnets in an African lake Meng Xu, Jeppe Kolding, and Joel E. Cohen Abstract: Taylor’s power law (TPL) describes the variance of population abundance as a power-law function of the mean abundance for a single or a group of species. Using consistently sampled long-term (1958–2001) multimesh capture data of Lake Kariba in Africa, we showed that TPL robustly described the relationship between the temporal mean and the temporal variance of the captured fish assemblage abundance (regardless of species), separately when abundance was measured by numbers of individuals and by aggregate weight. The strong correlation between the mean of abundance and the variance of abundance was not altered after adding other abiotic or biotic variables into the TPL model. We analytically connected the parameters of TPL when abundance was measured separately by the aggregate weight and by the aggregate number, using a weight–number scaling relationship. We utilized TPL to find the number of samples required for fixed-precision sampling and compared the number of samples when sampling was performed with a single gillnet mesh size and with multiple mesh sizes. These results facilitate optimizing the sampling design to estimate fish assemblage abundance with specified precision, as needed in stock management and conservation. Résumé : La loi de puissance de Taylor (LPT) décrit la variance de l’abondance d’une population comme étant une fonction de puissance de l’abondance moyenne pour une espèce ou un groupe d’espèces. En utilisant des données de capture sur une longue période (1958–2001) obtenues de manière cohérente avec des filets de mailles variées dans le lac Kariba en Afrique, nous avons démontré que la LPT décrit de manière robuste la relation entre la moyenne temporelle et la variance temporelle de l’abondance de l’assemblage de poissons capturés (peu importe l’espèce), que l’abondance soit mesurée sur la base du nombre d’individus ou de la masse cumulative. -
Sampling Handout
SAMPLING SIMPLE RANDOM SAMPLING – A sample in which all population members have the same probability of being selected and the selection of each member is independent of the selection of all other members. SIMPLE RANDOM SAMPLING (RANDOM SAMPLING): Selecting a group of subjects (a sample) for study from a larger group (population) so that each individual (or other unit of analysis) is chosen entirely by chance. When used without qualifications (such as stratified random sampling), random sampling means “simple random sampling.” Also sometimes called “equal probability sample,” because every member of the population has an equal probability (chance) of being included in the sample. A random sample is not the same thing as a haphazard or accidental sample. Using random sampling reduces the likelihood of bias. SYSTEMATIC SAMPLING – A procedure for selecting a probability sample in which every kth member of the population is selected and in which 1/k is the sampling fraction. SYSTEMATIC SAMPLING: A sample obtained by taking every ”nth” subject or case from a list containing the total population (or sampling frame). The size of the n is calculated by dividing the desired sample size into the population size. For example, if you wanted to draw a systematic sample of 1,000 individuals from a telephone directory containing 100,000 names, you would divide 1,000 into 100,000 to get 100; hence, you would select every 100th name from the directory. You would start with a randomly selected number between 1 and 100, say 47, and then select the 47th name, the 147th, the 247th, the 347th, and so on. -
Target Population” – Do Not Use “Sample Population.”
NCES Glossary Analysis of Variance: Analysis of variance (ANOVA) is a collection of statistical models and their associated estimation procedures (such as the "variation" among and between groups) used to test or analyze the differences among group means in a sample. This technique is operated by modeling the value of the dependent variable Y as a function of an overall mean “µ”, related independent variables X1…Xn, and a residual “e” that is an independent normally distributed random variable. Bias (due to nonresponse): The difference that occurs when respondents differ as a group from non-respondents on a characteristic being studied. Bias (of an estimate): The difference between the expected value of a sample estimate and the corresponding true value for the population. Bootstrap: See Replication techniques. CAPI: Computer Assisted Personal Interviewing enables data collection staff to use portable microcomputers to administer a data collection form while viewing the form on the computer screen. As responses are entered directly into the computer, they are used to guide the interview and are automatically checked for specified range, format, and consistency edits. CATI: Computer Assisted Telephone Interviewing uses a computer system that allows a telephone interviewer to administer a data collection form over the phone while viewing the form on a computer screen. As the interviewer enters responses directly into the computer, the responses are used to guide the interview and are automatically checked for specified range, format, and consistency edits. Cluster: a group of similar people, things or objects positioned or occurring closely together. Cluster Design: Cluster Design refers to a type of sampling method in which the researcher divides the population into separate groups, of similarities - called clusters.