Descriptive Statistics Once an Experiment Is Carried out and The
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Introduction to Biostatistics
Introduction to Biostatistics Jie Yang, Ph.D. Associate Professor Department of Family, Population and Preventive Medicine Director Biostatistical Consulting Core Director Biostatistics and Bioinformatics Shared Resource, Stony Brook Cancer Center In collaboration with Clinical Translational Science Center (CTSC) and the Biostatistics and Bioinformatics Shared Resource (BB-SR), Stony Brook Cancer Center (SBCC). OUTLINE What is Biostatistics What does a biostatistician do • Experiment design, clinical trial design • Descriptive and Inferential analysis • Result interpretation What you should bring while consulting with a biostatistician WHAT IS BIOSTATISTICS • The science of (bio)statistics encompasses the design of biological/clinical experiments the collection, summarization, and analysis of data from those experiments the interpretation of, and inference from, the results How to Lie with Statistics (1954) by Darrell Huff. http://www.youtube.com/watch?v=PbODigCZqL8 GOAL OF STATISTICS Sampling POPULATION Probability SAMPLE Theory Descriptive Descriptive Statistics Statistics Inference Population Sample Parameters: Inferential Statistics Statistics: 흁, 흈, 흅… 푿ഥ , 풔, 풑ෝ,… PROPERTIES OF A “GOOD” SAMPLE • Adequate sample size (statistical power) • Random selection (representative) Sampling Techniques: 1.Simple random sampling 2.Stratified sampling 3.Systematic sampling 4.Cluster sampling 5.Convenience sampling STUDY DESIGN EXPERIEMENT DESIGN Completely Randomized Design (CRD) - Randomly assign the experiment units to the treatments -
Experimentation Science: a Process Approach for the Complete Design of an Experiment
Kansas State University Libraries New Prairie Press Conference on Applied Statistics in Agriculture 1996 - 8th Annual Conference Proceedings EXPERIMENTATION SCIENCE: A PROCESS APPROACH FOR THE COMPLETE DESIGN OF AN EXPERIMENT D. D. Kratzer K. A. Ash Follow this and additional works at: https://newprairiepress.org/agstatconference Part of the Agriculture Commons, and the Applied Statistics Commons This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 4.0 License. Recommended Citation Kratzer, D. D. and Ash, K. A. (1996). "EXPERIMENTATION SCIENCE: A PROCESS APPROACH FOR THE COMPLETE DESIGN OF AN EXPERIMENT," Conference on Applied Statistics in Agriculture. https://doi.org/ 10.4148/2475-7772.1322 This is brought to you for free and open access by the Conferences at New Prairie Press. It has been accepted for inclusion in Conference on Applied Statistics in Agriculture by an authorized administrator of New Prairie Press. For more information, please contact [email protected]. Conference on Applied Statistics in Agriculture Kansas State University Applied Statistics in Agriculture 109 EXPERIMENTATION SCIENCE: A PROCESS APPROACH FOR THE COMPLETE DESIGN OF AN EXPERIMENT. D. D. Kratzer Ph.D., Pharmacia and Upjohn Inc., Kalamazoo MI, and K. A. Ash D.V.M., Ph.D., Town and Country Animal Hospital, Charlotte MI ABSTRACT Experimentation Science is introduced as a process through which the necessary steps of experimental design are all sufficiently addressed. Experimentation Science is defined as a nearly linear process of objective formulation, selection of experimentation unit and decision variable(s), deciding treatment, design and error structure, defining the randomization, statistical analyses and decision procedures, outlining quality control procedures for data collection, and finally analysis, presentation and interpretation of results. -
Chapter 6: Random Errors in Chemical Analysis
Chapter 6: Random Errors in Chemical Analysis Source slideplayer.com/Fundamentals of Analytical Chemistry, F.J. Holler, S.R.Crouch Random errors are present in every measurement no matter how careful the experimenter. Random, or indeterminate, errors can never be totally eliminated and are often the major source of uncertainty in a determination. Random errors are caused by the many uncontrollable variables that accompany every measurement. The accumulated effect of the individual uncertainties causes replicate results to fluctuate randomly around the mean of the set. In this chapter, we consider the sources of random errors, the determination of their magnitude, and their effects on computed results of chemical analyses. We also introduce the significant figure convention and illustrate its use in reporting analytical results. 6A The nature of random errors - random error in the results of analysts 2 and 4 is much larger than that seen in the results of analysts 1 and 3. - The results of analyst 3 show outstanding precision but poor accuracy. The results of analyst 1 show excellent precision and good accuracy. Figure 6-1 A three-dimensional plot showing absolute error in Kjeldahl nitrogen determinations for four different analysts. Random Error Sources - Small undetectable uncertainties produce a detectable random error in the following way. - Imagine a situation in which just four small random errors combine to give an overall error. We will assume that each error has an equal probability of occurring and that each can cause the final result to be high or low by a fixed amount ±U. - Table 6.1 gives all the possible ways in which four errors can combine to give the indicated deviations from the mean value. -
Double Blind Trials Workshop
Double Blind Trials Workshop Introduction These activities demonstrate how double blind trials are run, explaining what a placebo is and how the placebo effect works, how bias is removed as far as possible and how participants and trial medicines are randomised. Curriculum Links KS3: Science SQA Access, Intermediate and KS4: Biology Higher: Biology Keywords Double-blind trials randomisation observer bias clinical trials placebo effect designing a fair trial placebo Contents Activities Materials Activity 1 Placebo Effect Activity Activity 2 Observer Bias Activity 3 Double Blind Trial Role Cards for the Double Blind Trial Activity Testing Layout Background Information Medicines undergo a number of trials before they are declared fit for use (see classroom activity on Clinical Research for details). In the trial in the second activity, pupils compare two potential new sunscreens. This type of trial is done with healthy volunteers to see if the there are any side effects and to provide data to suggest the dosage needed. If there were no current best treatment then this sort of trial would also be done with patients to test for the effectiveness of the new medicine. How do scientists make sure that medicines are tested fairly? One thing they need to do is to find out if their tests are free of bias. Are the medicines really working, or do they just appear to be working? One difficulty in designing fair tests for medicines is the placebo effect. When patients are prescribed a treatment, especially by a doctor or expert they trust, the patient’s own belief in the treatment can cause the patient to produce a response. -
Observational Studies and Bias in Epidemiology
The Young Epidemiology Scholars Program (YES) is supported by The Robert Wood Johnson Foundation and administered by the College Board. Observational Studies and Bias in Epidemiology Manuel Bayona Department of Epidemiology School of Public Health University of North Texas Fort Worth, Texas and Chris Olsen Mathematics Department George Washington High School Cedar Rapids, Iowa Observational Studies and Bias in Epidemiology Contents Lesson Plan . 3 The Logic of Inference in Science . 8 The Logic of Observational Studies and the Problem of Bias . 15 Characteristics of the Relative Risk When Random Sampling . and Not . 19 Types of Bias . 20 Selection Bias . 21 Information Bias . 23 Conclusion . 24 Take-Home, Open-Book Quiz (Student Version) . 25 Take-Home, Open-Book Quiz (Teacher’s Answer Key) . 27 In-Class Exercise (Student Version) . 30 In-Class Exercise (Teacher’s Answer Key) . 32 Bias in Epidemiologic Research (Examination) (Student Version) . 33 Bias in Epidemiologic Research (Examination with Answers) (Teacher’s Answer Key) . 35 Copyright © 2004 by College Entrance Examination Board. All rights reserved. College Board, SAT and the acorn logo are registered trademarks of the College Entrance Examination Board. Other products and services may be trademarks of their respective owners. Visit College Board on the Web: www.collegeboard.com. Copyright © 2004. All rights reserved. 2 Observational Studies and Bias in Epidemiology Lesson Plan TITLE: Observational Studies and Bias in Epidemiology SUBJECT AREA: Biology, mathematics, statistics, environmental and health sciences GOAL: To identify and appreciate the effects of bias in epidemiologic research OBJECTIVES: 1. Introduce students to the principles and methods for interpreting the results of epidemio- logic research and bias 2. -
An Approach for Appraising the Accuracy of Suspended-Sediment Data
An Approach for Appraising the Accuracy of Suspended-sediment Data U.S. GEOLOGICAL SURVEY PROFESSIONAL PAl>£R 1383 An Approach for Appraising the Accuracy of Suspended-sediment Data By D. E. BURKHAM U.S. GEOLOGICAL SURVEY PROFESSIONAL PAPER 1333 UNITED STATES GOVERNMENT PRINTING OFFICE, WASHINGTON, 1985 DEPARTMENT OF THE INTERIOR DONALD PAUL MODEL, Secretary U.S. GEOLOGICAL SURVEY Dallas L. Peck, Director First printing 1985 Second printing 1987 For sale by the Books and Open-File Reports Section, U.S. Geological Survey, Federal Center, Box 25425, Denver, CO 80225 CONTENTS Page Page Abstract ........... 1 Spatial error Continued Introduction ....... 1 Application of method ................................ 11 Problem ......... 1 Basic data ......................................... 11 Purpose and scope 2 Standard spatial error for multivertical procedure .... 11 Sampling error .......................................... 2 Standard spatial error for single-vertical procedure ... 13 Discussion of error .................................... 2 Temporal error ......................................... 13 Approach to solution .................................. 3 Discussion of error ................................... 13 Application of method ................................. 4 Approach to solution ................................. 14 Basic data .......................................... 4 Application of method ................................ 14 Standard sampling error ............................. 4 Basic data ........................................ -
Approximating the Distribution of the Product of Two Normally Distributed Random Variables
S S symmetry Article Approximating the Distribution of the Product of Two Normally Distributed Random Variables Antonio Seijas-Macías 1,2 , Amílcar Oliveira 2,3 , Teresa A. Oliveira 2,3 and Víctor Leiva 4,* 1 Departamento de Economía, Universidade da Coruña, 15071 A Coruña, Spain; [email protected] 2 CEAUL, Faculdade de Ciências, Universidade de Lisboa, 1649-014 Lisboa, Portugal; [email protected] (A.O.); [email protected] (T.A.O.) 3 Departamento de Ciências e Tecnologia, Universidade Aberta, 1269-001 Lisboa, Portugal 4 Escuela de Ingeniería Industrial, Pontificia Universidad Católica de Valparaíso, Valparaíso 2362807, Chile * Correspondence: [email protected] or [email protected] Received: 21 June 2020; Accepted: 18 July 2020; Published: 22 July 2020 Abstract: The distribution of the product of two normally distributed random variables has been an open problem from the early years in the XXth century. First approaches tried to determinate the mathematical and statistical properties of the distribution of such a product using different types of functions. Recently, an improvement in computational techniques has performed new approaches for calculating related integrals by using numerical integration. Another approach is to adopt any other distribution to approximate the probability density function of this product. The skew-normal distribution is a generalization of the normal distribution which considers skewness making it flexible. In this work, we approximate the distribution of the product of two normally distributed random variables using a type of skew-normal distribution. The influence of the parameters of the two normal distributions on the approximation is explored. When one of the normally distributed variables has an inverse coefficient of variation greater than one, our approximation performs better than when both normally distributed variables have inverse coefficients of variation less than one. -
Design of Experiments and Data Analysis,” 2012 Reliability and Maintainability Symposium, January, 2012
Copyright © 2012 IEEE. Reprinted, with permission, from Huairui Guo and Adamantios Mettas, “Design of Experiments and Data Analysis,” 2012 Reliability and Maintainability Symposium, January, 2012. This material is posted here with permission of the IEEE. Such permission of the IEEE does not in any way imply IEEE endorsement of any of ReliaSoft Corporation's products or services. Internal or personal use of this material is permitted. However, permission to reprint/republish this material for advertising or promotional purposes or for creating new collective works for resale or redistribution must be obtained from the IEEE by writing to [email protected]. By choosing to view this document, you agree to all provisions of the copyright laws protecting it. 2012 Annual RELIABILITY and MAINTAINABILITY Symposium Design of Experiments and Data Analysis Huairui Guo, Ph. D. & Adamantios Mettas Huairui Guo, Ph.D., CPR. Adamantios Mettas, CPR ReliaSoft Corporation ReliaSoft Corporation 1450 S. Eastside Loop 1450 S. Eastside Loop Tucson, AZ 85710 USA Tucson, AZ 85710 USA e-mail: [email protected] e-mail: [email protected] Tutorial Notes © 2012 AR&MS SUMMARY & PURPOSE Design of Experiments (DOE) is one of the most useful statistical tools in product design and testing. While many organizations benefit from designed experiments, others are getting data with little useful information and wasting resources because of experiments that have not been carefully designed. Design of Experiments can be applied in many areas including but not limited to: design comparisons, variable identification, design optimization, process control and product performance prediction. Different design types in DOE have been developed for different purposes. -
Analysis of the Coefficient of Variation in Shear and Tensile Bond Strength Tests
J Appl Oral Sci 2005; 13(3): 243-6 www.fob.usp.br/revista or www.scielo.br/jaos ANALYSIS OF THE COEFFICIENT OF VARIATION IN SHEAR AND TENSILE BOND STRENGTH TESTS ANÁLISE DO COEFICIENTE DE VARIAÇÃO EM TESTES DE RESISTÊNCIA DA UNIÃO AO CISALHAMENTO E TRAÇÃO Fábio Lourenço ROMANO1, Gláucia Maria Bovi AMBROSANO1, Maria Beatriz Borges de Araújo MAGNANI1, Darcy Flávio NOUER1 1- MSc, Assistant Professor, Department of Orthodontics, Alfenas Pharmacy and Dental School – Efoa/Ceufe, Minas Gerais, Brazil. 2- DDS, MSc, Associate Professor of Biostatistics, Department of Social Dentistry, Piracicaba Dental School – UNICAMP, São Paulo, Brazil; CNPq researcher. 3- DDS, MSc, Assistant Professor of Orthodontics, Department of Child Dentistry, Piracicaba Dental School – UNICAMP, São Paulo, Brazil. 4- DDS, MSc, Full Professor of Orthodontics, Department of Child Dentistry, Piracicada Dental School – UNICAMP, São Paulo, Brazil. Corresponding address: Fábio Lourenço Romano - Avenida do Café, 131 Bloco E, Apartamento 16 - Vila Amélia - Ribeirão Preto - SP Cep.: 14050-230 - Phone: (16) 636 6648 - e-mail: [email protected] Received: July 29, 2004 - Modification: September 09, 2004 - Accepted: June 07, 2005 ABSTRACT The coefficient of variation is a dispersion measurement that does not depend on the unit scales, thus allowing the comparison of experimental results involving different variables. Its calculation is crucial for the adhesive experiments performed in laboratories because both precision and reliability can be verified. The aim of this study was to evaluate and to suggest a classification of the coefficient variation (CV) for in vitro experiments on shear and tensile strengths. The experiments were performed in laboratory by fifty international and national studies on adhesion materials. -
A Randomized Control Trial Evaluating the Effects of Police Body-Worn
A randomized control trial evaluating the effects of police body-worn cameras David Yokuma,b,1,2, Anita Ravishankara,c,d,1, and Alexander Coppocke,1 aThe Lab @ DC, Office of the City Administrator, Executive Office of the Mayor, Washington, DC 20004; bThe Policy Lab, Brown University, Providence, RI 02912; cExecutive Office of the Chief of Police, Metropolitan Police Department, Washington, DC 20024; dPublic Policy and Political Science Joint PhD Program, University of Michigan, Ann Arbor, MI 48109; and eDepartment of Political Science, Yale University, New Haven, CT 06511 Edited by Susan A. Murphy, Harvard University, Cambridge, MA, and approved March 21, 2019 (received for review August 28, 2018) Police body-worn cameras (BWCs) have been widely promoted as The existing evidence on whether BWCs have the anticipated a technological mechanism to improve policing and the perceived effects on policing outcomes remains relatively limited (17–19). legitimacy of police and legal institutions, yet evidence of their Several observational studies have evaluated BWCs by compar- effectiveness is limited. To estimate the effects of BWCs, we con- ing the behavior of officers before and after the introduction of ducted a randomized controlled trial involving 2,224 Metropolitan BWCs into the police department (20, 21). Other studies com- Police Department officers in Washington, DC. Here we show pared officers who happened to wear BWCs to those without (15, that BWCs have very small and statistically insignificant effects 22, 23). The causal inferences drawn in those studies depend on on police use of force and civilian complaints, as well as other strong assumptions about whether, after statistical adjustments policing activities and judicial outcomes. -
Randomized Controlled Trials, Development Economics and Policy Making in Developing Countries
Randomized Controlled Trials, Development Economics and Policy Making in Developing Countries Esther Duflo Department of Economics, MIT Co-Director J-PAL [Joint work with Abhijit Banerjee and Michael Kremer] Randomized controlled trials have greatly expanded in the last two decades • Randomized controlled Trials were progressively accepted as a tool for policy evaluation in the US through many battles from the 1970s to the 1990s. • In development, the rapid growth starts after the mid 1990s – Kremer et al, studies on Kenya (1994) – PROGRESA experiment (1997) • Since 2000, the growth have been very rapid. J-PAL | THE ROLE OF RANDOMIZED EVALUATIONS IN INFORMING POLICY 2 Cameron et al (2016): RCT in development Figure 1: Number of Published RCTs 300 250 200 150 100 50 0 1975 1980 1985 1990 1995 2000 2005 2010 2015 Publication Year J-PAL | THE ROLE OF RANDOMIZED EVALUATIONS IN INFORMING POLICY 3 BREAD Affiliates doing RCT Figure 4. Fraction of BREAD Affiliates & Fellows with 1 or more RCTs 100% 90% 80% 70% 60% 50% 40% 30% 20% 10% 0% 1980 or earlier 1981-1990 1991-2000 2001-2005 2006-today * Total Number of Fellows and Affiliates is 166. PhD Year J-PAL | THE ROLE OF RANDOMIZED EVALUATIONS IN INFORMING POLICY 4 Top Journals J-PAL | THE ROLE OF RANDOMIZED EVALUATIONS IN INFORMING POLICY 5 Many sectors, many countries J-PAL | THE ROLE OF RANDOMIZED EVALUATIONS IN INFORMING POLICY 6 Why have RCT had so much impact? • Focus on identification of causal effects (across the board) • Assessing External Validity • Observing Unobservables • Data collection • Iterative Experimentation • Unpack impacts J-PAL | THE ROLE OF RANDOMIZED EVALUATIONS IN INFORMING POLICY 7 Focus on Identification… across the board! • The key advantage of RCT was perceived to be a clear identification advantage • With RCT, since those who received a treatment are randomly selected in a relevant sample, any difference between treatment and control must be due to the treatment • Most criticisms of experiment also focus on limits to identification (imperfect randomization, attrition, etc. -
"The Distribution of Mckay's Approximation for the Coefficient Of
ARTICLE IN PRESS Statistics & Probability Letters 78 (2008) 10–14 www.elsevier.com/locate/stapro The distribution of McKay’s approximation for the coefficient of variation Johannes Forkmana,Ã, Steve Verrillb aDepartment of Biometry and Engineering, Swedish University of Agricultural Sciences, P.O. Box 7032, SE-750 07 Uppsala, Sweden bU.S.D.A., Forest Products Laboratory, 1 Gifford Pinchot Drive, Madison, WI 53726, USA Received 12 July 2006; received in revised form 21 February 2007; accepted 10 April 2007 Available online 7 May 2007 Abstract McKay’s chi-square approximation for the coefficient of variation is type II noncentral beta distributed and asymptotically normal with mean n À 1 and variance smaller than 2ðn À 1Þ. r 2007 Elsevier B.V. All rights reserved. Keywords: Coefficient of variation; McKay’s approximation; Noncentral beta distribution 1. Introduction The coefficient of variation is defined as the standard deviation divided by the mean. This measure, which is commonly expressed as a percentage, is widely used since it is often necessary to relate the size of the variation to the level of the observations. McKay (1932) introduced a w2 approximation for the coefficient of variation calculated on normally distributed observations. It can be defined in the following way. Definition 1. Let yj, j ¼ 1; ...; n; be n independent observations from a normal distribution with expected value m and variance s2. Let g denote the population coefficient of variation, i.e. g ¼ s=m, and let c denote the sample coefficient of variation, i.e. vffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffi u 1 u 1 Xn 1 Xn c ¼ t ðy À mÞ2; m ¼ y .