The Arrangement of Field Experiments" by R.A
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APPLICATION of the TAGUCHI METHOD to SENSITIVITY ANALYSIS of a MIDDLE- EAR FINITE-ELEMENT MODEL Li Qi1, Chadia S
APPLICATION OF THE TAGUCHI METHOD TO SENSITIVITY ANALYSIS OF A MIDDLE- EAR FINITE-ELEMENT MODEL Li Qi1, Chadia S. Mikhael1 and W. Robert J. Funnell1, 2 1 Department of BioMedical Engineering 2 Department of Otolaryngology McGill University Montréal, QC, Canada H3A 2B4 ABSTRACT difference in the model output due to the change in the input variable is referred to as the sensitivity. The Sensitivity analysis of a model is the investigation relative importance of parameters is judged based on of how outputs vary with changes of input parameters, the magnitude of the calculated sensitivity. The OFAT in order to identify the relative importance of method does not, however, take into account the parameters and to help in optimization of the model. possibility of interactions among parameters. Such The one-factor-at-a-time (OFAT) method has been interactions mean that the model sensitivity to one widely used for sensitivity analysis of middle-ear parameter can change depending on the values of models. The results of OFAT, however, are unreliable other parameters. if there are significant interactions among parameters. Alternatively, the full-factorial method permits the This paper incorporates the Taguchi method into the analysis of parameter interactions, but generally sensitivity analysis of a middle-ear finite-element requires a very large number of simulations. This can model. Two outputs, tympanic-membrane volume be impractical when individual simulations are time- displacement and stapes footplate displacement, are consuming. A more practical approach is the Taguchi measured. Nine input parameters and four possible method, which is commonly used in industry. It interactions are investigated for two model outputs. -
How Differences Between Online and Offline Interaction Influence Social
Available online at www.sciencedirect.com ScienceDirect Two social lives: How differences between online and offline interaction influence social outcomes 1 2 Alicea Lieberman and Juliana Schroeder For hundreds of thousands of years, humans only Facebook users,75% ofwhom report checking the platform communicated in person, but in just the past fifty years they daily [2]. Among teenagers, 95% report using smartphones have started also communicating online. Today, people and 45%reportbeingonline‘constantly’[2].Thisshiftfrom communicate more online than offline. What does this shift offline to online socializing has meaningful and measurable mean for human social life? We identify four structural consequences for every aspect of human interaction, from differences between online (versus offline) interaction: (1) fewer how people form impressions of one another, to how they nonverbal cues, (2) greater anonymity, (3) more opportunity to treat each other, to the breadth and depth of their connec- form new social ties and bolster weak ties, and (4) wider tion. The current article proposes a new framework to dissemination of information. Each of these differences identify, understand, and study these consequences, underlies systematic psychological and behavioral highlighting promising avenues for future research. consequences. Online and offline lives often intersect; we thus further review how online engagement can (1) disrupt or (2) Structural differences between online and enhance offline interaction. This work provides a useful offline interaction -
ARIADNE (Axion Resonant Interaction Detection Experiment): an NMR-Based Axion Search, Snowmass LOI
ARIADNE (Axion Resonant InterAction Detection Experiment): an NMR-based Axion Search, Snowmass LOI Andrew A. Geraci,∗ Aharon Kapitulnik, William Snow, Joshua C. Long, Chen-Yu Liu, Yannis Semertzidis, Yun Shin, and Asimina Arvanitaki (Dated: August 31, 2020) The Axion Resonant InterAction Detection Experiment (ARIADNE) is a collaborative effort to search for the QCD axion using techniques based on nuclear magnetic resonance. In the experiment, axions or axion-like particles would mediate short-range spin-dependent interactions between a laser-polarized 3He gas and a rotating (unpolarized) tungsten source mass, acting as a tiny, fictitious magnetic field. The experiment has the potential to probe deep within the theoretically interesting regime for the QCD axion in the mass range of 0.1- 10 meV, independently of cosmological assumptions. In this SNOWMASS LOI, we briefly describe this technique which covers a wide range of axion masses as well as discuss future prospects for improvements. Taken together with other existing and planned axion experi- ments, ARIADNE has the potential to completely explore the allowed parameter space for the QCD axion. A well-motivated example of a light mass pseudoscalar boson that can mediate new interactions or a “fifth-force” is the axion. The axion is a hypothetical particle that arises as a consequence of the Peccei-Quinn (PQ) mechanism to solve the strong CP problem of quantum chromodynamics (QCD)[1]. Axions have also been well motivated as a dark matter candidatedue to their \invisible" nature[2]. Axions can couple to fundamental fermions through a scalar vertex and a pseudoscalar vertex with very weak coupling strength. -
Removing Hidden Confounding by Experimental Grounding
Removing Hidden Confounding by Experimental Grounding Nathan Kallus Aahlad Manas Puli Uri Shalit Cornell University and Cornell Tech New York University Technion New York, NY New York, NY Haifa, Israel [email protected] [email protected] [email protected] Abstract Observational data is increasingly used as a means for making individual-level causal predictions and intervention recommendations. The foremost challenge of causal inference from observational data is hidden confounding, whose presence cannot be tested in data and can invalidate any causal conclusion. Experimental data does not suffer from confounding but is usually limited in both scope and scale. We introduce a novel method of using limited experimental data to correct the hidden confounding in causal effect models trained on larger observational data, even if the observational data does not fully overlap with the experimental data. Our method makes strictly weaker assumptions than existing approaches, and we prove conditions under which it yields a consistent estimator. We demonstrate our method’s efficacy using real-world data from a large educational experiment. 1 Introduction In domains such as healthcare, education, and marketing there is growing interest in using observa- tional data to draw causal conclusions about individual-level effects; for example, using electronic healthcare records to determine which patients should get what treatments, using school records to optimize educational policy interventions, or using past advertising campaign data to refine targeting and maximize lift. Observational datasets, due to their often very large number of samples and exhaustive scope (many measured covariates) in comparison to experimental datasets, offer a unique opportunity to uncover fine-grained effects that may apply to many target populations. -
Survey Experiments
IU Workshop in Methods – 2019 Survey Experiments Testing Causality in Diverse Samples Trenton D. Mize Department of Sociology & Advanced Methodologies (AMAP) Purdue University Survey Experiments Page 1 Survey Experiments Page 2 Contents INTRODUCTION ............................................................................................................................................................................ 8 Overview .............................................................................................................................................................................. 8 What is a survey experiment? .................................................................................................................................... 9 What is an experiment?.............................................................................................................................................. 10 Independent and dependent variables ................................................................................................................. 11 Experimental Conditions ............................................................................................................................................. 12 WHY CONDUCT A SURVEY EXPERIMENT? ........................................................................................................................... 13 Internal, external, and construct validity .......................................................................................................... -
Rothamsted in the Making of Sir Ronald Fisher Scd FRS
Rothamsted in the Making of Sir Ronald Fisher ScD FRS John Aldrich University of Southampton RSS September 2019 1 Finish 1962 “the most famous statistician and mathematical biologist in the world” dies Start 1919 29 year-old Cambridge BA in maths with no prospects takes temporary job at Rothamsted Experimental Station In between 1919-33 at Rothamsted he makes a career for himself by creating a career 2 Rothamsted helped make Fisher by establishing and elevating the office of agricultural statistician—a position in which Fisher was unsurpassed by letting him do other things—including mathematical statistics, genetics and eugenics 3 Before Fisher … (9 slides) The problems were already there viz. o the relationship between harvest and weather o design of experimental trials and the analysis of their results Leading figures in agricultural science believed the problems could be treated statistically 4 Established in 1843 by Lawes and Gilbert to investigate the effective- ness of fertilisers Sir John Bennet Lawes Sir Joseph Henry Gilbert (1814-1900) land-owner, fertiliser (1817-1901) professional magnate and amateur scientist scientist (chemist) In 1902 tired Rothamsted gets make-over when Daniel Hall becomes Director— public money feeds growth 5 Crops and weather and experimental trials Crops & the weather o examined by agriculturalists—e.g. Lawes & Gilbert 1880 o subsequently treated more by meteorologists Experimental trials a hotter topic o treated in Journal of Agricultural Science o by leading figures Wood of Cambridge and Hall -
Confounding Bias, Part I
ERIC NOTEBOOK SERIES Second Edition Confounding Bias, Part I Confounding is one type of Second Edition Authors: Confounding is also a form a systematic error that can occur in bias. Confounding is a bias because it Lorraine K. Alexander, DrPH epidemiologic studies. Other types of can result in a distortion in the systematic error such as information measure of association between an Brettania Lopes, MPH bias or selection bias are discussed exposure and health outcome. in other ERIC notebook issues. Kristen Ricchetti-Masterson, MSPH Confounding may be present in any Confounding is an important concept Karin B. Yeatts, PhD, MS study design (i.e., cohort, case-control, in epidemiology, because, if present, observational, ecological), primarily it can cause an over- or under- because it's not a result of the study estimate of the observed association design. However, of all study designs, between exposure and health ecological studies are the most outcome. The distortion introduced susceptible to confounding, because it by a confounding factor can be large, is more difficult to control for and it can even change the apparent confounders at the aggregate level of direction of an effect. However, data. In all other cases, as long as unlike selection and information there are available data on potential bias, it can be adjusted for in the confounders, they can be adjusted for analysis. during analysis. What is confounding? Confounding should be of concern Confounding is the distortion of the under the following conditions: association between an exposure 1. Evaluating an exposure-health and health outcome by an outcome association. -
Analysis of Variance and Analysis of Variance and Design of Experiments of Experiments-I
Analysis of Variance and Design of Experimentseriments--II MODULE ––IVIV LECTURE - 19 EXPERIMENTAL DESIGNS AND THEIR ANALYSIS Dr. Shalabh Department of Mathematics and Statistics Indian Institute of Technology Kanpur 2 Design of experiment means how to design an experiment in the sense that how the observations or measurements should be obtained to answer a qqyuery inavalid, efficient and economical way. The desigggning of experiment and the analysis of obtained data are inseparable. If the experiment is designed properly keeping in mind the question, then the data generated is valid and proper analysis of data provides the valid statistical inferences. If the experiment is not well designed, the validity of the statistical inferences is questionable and may be invalid. It is important to understand first the basic terminologies used in the experimental design. Experimental unit For conducting an experiment, the experimental material is divided into smaller parts and each part is referred to as experimental unit. The experimental unit is randomly assigned to a treatment. The phrase “randomly assigned” is very important in this definition. Experiment A way of getting an answer to a question which the experimenter wants to know. Treatment Different objects or procedures which are to be compared in an experiment are called treatments. Sampling unit The object that is measured in an experiment is called the sampling unit. This may be different from the experimental unit. 3 Factor A factor is a variable defining a categorization. A factor can be fixed or random in nature. • A factor is termed as fixed factor if all the levels of interest are included in the experiment. -
The Politics of Random Assignment: Implementing Studies and Impacting Policy
The Politics of Random Assignment: Implementing Studies and Impacting Policy Judith M. Gueron Manpower Demonstration Research Corporation (MDRC) As the only nonacademic presenting a paper at this conference, I see it as my charge to focus on the challenge of implementing random assignment in the field. I will not spend time arguing for the methodological strengths of social experiments or advocating for more such field trials. Others have done so eloquently.1 But I will make my biases clear. For 25 years, I and many of my MDRC colleagues have fought to implement random assignment in diverse arenas and to show that this approach is feasible, ethical, uniquely convincing, and superior for answering certain questions. Our organization is widely credited with being one of the pioneers of this approach, and through its use producing results that are trusted across the political spectrum and that have made a powerful difference in social policy and research practice. So, I am a believer, but not, I hope, a blind one. I do not think that random assignment is a panacea or that it can address all the critical policy questions, or substitute for other types of analysis, or is always appropriate. But I do believe that it offers unique power in answering the “Does it make a difference?” question. With random assignment, you can know something with much greater certainty and, as a result, can more confidently separate fact from advocacy. This paper focuses on implementing experiments. In laying out the ingredients of success, I argue that creative and flexible research design skills are essential, but that just as important are operational and political skills, applied both to marketing the experiment in the first place and to helping interpret and promote its findings down the line. -
Beyond Controlling for Confounding: Design Strategies to Avoid Selection Bias and Improve Efficiency in Observational Studies
September 27, 2018 Beyond Controlling for Confounding: Design Strategies to Avoid Selection Bias and Improve Efficiency in Observational Studies A Case Study of Screening Colonoscopy Our Team Xabier Garcia de Albeniz Martinez +34 93.3624732 [email protected] Bradley Layton 919.541.8885 [email protected] 2 Poll Questions Poll question 1 Ice breaker: Which of the following study designs is best to evaluate the causal effect of a medical intervention? Cross-sectional study Case series Case-control study Prospective cohort study Randomized, controlled clinical trial 3 We All Trust RCTs… Why? • Obvious reasons – No confusion (i.e., exchangeability) • Not so obvious reasons – Exposure represented at all levels of potential confounders (i.e., positivity) – Therapeutic intervention is well defined (i.e., consistency) – … And, because of the alignment of eligibility, exposure assignment and the start of follow-up (we’ll soon see why is this important) ? RCT = randomized clinical trial. 4 Poll Questions We just used the C-word: “causal” effect Poll question 2 Which of the following is true? In pharmacoepidemiology, we work to ensure that drugs are effective and safe for the population In pharmacoepidemiology, we want to know if a drug causes an undesired toxicity Causal inference from observational data can be questionable, but being explicit about the causal goal and the validity conditions help inform a scientific discussion All of the above 5 In Pharmacoepidemiology, We Try to Infer Causes • These are good times to be an epidemiologist -
Key Items to Get Right When Conducting Randomized Controlled Trials of Social Programs
Key Items to Get Right When Conducting Randomized Controlled Trials of Social Programs February 2016 This publication was produced by the Evidence-Based Policy team of the Laura and John Arnold Foundation (now Arnold Ventures). This publication is in the public domain. Authorization to reproduce it in whole or in part for educational purposes is granted. We welcome comments and suggestions on this document ([email protected]). 1 Purpose This is a checklist of key items to get right when conducting a randomized controlled trial (RCT) to evaluate a social program or practice. The checklist is designed to be a practical resource for researchers and sponsors of research. It describes items that are critical to the success of an RCT in producing valid findings about a social program’s effectiveness. This document is limited to key items, and does not address all contingencies that may affect a study’s success.1 Items in this checklist are categorized according to the following phases of an RCT: 1. Planning the study; 2. Carrying out random assignment; 3. Measuring outcomes for the study sample; and 4. Analyzing the study results. 1. Key items to get right in planning the study Choose (i) the program to be evaluated, (ii) target population for the study, and (iii) key outcomes to be measured. These should include, wherever possible, ultimate outcomes of policy importance. As illustrative examples: . An RCT of a pregnancy prevention program preferably should measure outcomes such as pregnancies or births, and not just intermediate outcomes such as condom use. An RCT of a remedial reading program preferably should measure outcomes such as reading comprehension, and not just participants’ ability to sound out words. -
Study Designs in Biomedical Research
STUDY DESIGNS IN BIOMEDICAL RESEARCH INTRODUCTION TO CLINICAL TRIALS SOME TERMINOLOGIES Research Designs: Methods for data collection Clinical Studies: Class of all scientific approaches to evaluate Disease Prevention, Diagnostics, and Treatments. Clinical Trials: Subset of clinical studies that evaluates Investigational Drugs; they are in prospective/longitudinal form (the basic nature of trials is prospective). TYPICAL CLINICAL TRIAL Study Initiation Study Termination No subjects enrolled after π1 0 π1 π2 Enrollment Period, e.g. Follow-up Period, e.g. three (3) years two (2) years OPERATION: Patients come sequentially; each is enrolled & randomized to receive one of two or several treatments, and followed for varying amount of time- between π1 & π2 In clinical trials, investigators apply an “intervention” and observe the effect on outcomes. The major advantage is the ability to demonstrate causality; in particular: (1) random assigning subjects to intervention helps to reduce or eliminate the influence of confounders, and (2) blinding its administration helps to reduce or eliminate the effect of biases from ascertainment of the outcome. Clinical Trials form a subset of cohort studies but not all cohort studies are clinical trials because not every research question is amenable to the clinical trial design. For example: (1) By ethical reasons, we cannot assign subjects to smoking in a trial in order to learn about its harmful effects, or (2) It is not feasible to study whether drug treatment of high LDL-cholesterol in children will prevent heart attacks many decades later. In addition, clinical trials are generally expensive, time consuming, address narrow clinical questions, and sometimes expose participants to potential harm.