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Related Concept Videos

Sample Size Calculation01:19

Sample Size Calculation

Knowledge of the sample size is the first requirement to conduct random sampling or an experiment. The sample size is the total number of units, observations, or groups (in some cases) used to get the data to estimate a population parameter. As the name suggests, the sample size is that of the sample drawn from the population and differs from the population size.
The sample size for the given experiment or sampling effort is fundamental to any study design. Sample size decides the number of...
Types of Biopharmaceutical Studies: Controlled and Non-Controlled Approaches01:23

Types of Biopharmaceutical Studies: Controlled and Non-Controlled Approaches

Biopharmaceutical studies constitute a vital field aiming to enhance drug delivery methods and refine therapeutic approaches, drawing upon diverse interdisciplinary knowledge. In research methodologies, the choice between controlled and non-controlled studies significantly influences the study's reliability and accuracy.
Non-controlled studies, commonly employed for initial exploration, lack a control group, rendering them susceptible to biases and external influences. In contrast, controlled...
Strategies for Assessing and Addressing Confounding01:25

Strategies for Assessing and Addressing Confounding

Confounding is a critical issue in epidemiological studies, often leading to misleading conclusions about associations between exposures and outcomes. It occurs when the relationship between the exposure and the outcome is mixed with the effects of other factors that influence the outcome. Given that, addressing confounding is of high importance for drawing accurate inferences in research.
Confounding can be addressed at both the design phase of a study and through analytical methods after data...
Margin of Error01:27

Margin of Error

The margin of error is also called the maximum error of an estimate. The margin of error is the maximum possible or expected difference between the observed sample parameter value and the actual population parameter value. For proportion, it is the maximum difference between the value of sample proportion obtained from the data and the true value of population proportion. As the true value of the population parameter is not known, the margin of error is calculated using the sample statistic.
Contaminants and Errors01:16

Contaminants and Errors

Effective sample preparation is crucial for accurate and reliable laboratory analysis. During this process, two significant sources of error can arise: concentration bias from improper sample splitting and contamination caused by methods used to reduce particle size, such as grinding or homogenization. Identifying and minimizing these potential errors is crucial to ensuring the validity of the analysis.
Another key consideration is determining the appropriate number of samples required to...
Sampling Plans01:23

Sampling Plans

Sampling is a crucial step in analytical chemistry, allowing researchers to collect representative data from a large population. Common sampling methods include random, judgmental, systematic, stratified, and cluster sampling.
Random sampling is a method where each member of the population has an equal chance of being selected for the sample. It involves selecting individuals randomly, often using random number generators or lottery-type methods. For example, when analyzing the properties of a...

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Related Experiment Video

Updated: May 7, 2026

Determining the Likelihood of Variant Pathogenicity Using Amino Acid-level Signal-to-Noise Analysis of Genetic Variation
07:15

Determining the Likelihood of Variant Pathogenicity Using Amino Acid-level Signal-to-Noise Analysis of Genetic Variation

Published on: January 16, 2019

Bayesian sample size determination for case-control studies when exposure may be misclassified.

Lawrence Joseph, Patrick Bélisle

    American Journal of Epidemiology
    |September 17, 2013
    PubMed
    Summary
    This summary is machine-generated.

    Accurate sample size calculation for case-control studies is crucial, especially when exposure data may be misclassified. This study provides Bayesian methods to determine sample sizes, accounting for exposure misclassification to improve estimate precision.

    Keywords:
    Bayesian methodscase-control studymisclassification errorsample size determinationstudy design

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    Inverse Probability of Treatment Weighting (Propensity Score) using the Military Health System Data Repository and National Death Index

    Published on: January 8, 2020

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    Last Updated: May 7, 2026

    Determining the Likelihood of Variant Pathogenicity Using Amino Acid-level Signal-to-Noise Analysis of Genetic Variation
    07:15

    Determining the Likelihood of Variant Pathogenicity Using Amino Acid-level Signal-to-Noise Analysis of Genetic Variation

    Published on: January 16, 2019

    Inverse Probability of Treatment Weighting (Propensity Score) using the Military Health System Data Repository and National Death Index
    06:55

    Inverse Probability of Treatment Weighting (Propensity Score) using the Military Health System Data Repository and National Death Index

    Published on: January 8, 2020

    Area of Science:

    • Epidemiology
    • Biostatistics

    Background:

    • Odds ratios are key for estimating exposure effects on disease in case-control studies.
    • Exposure misclassification, due to recall bias or measurement error, can significantly impact study accuracy and precision.
    • Existing methods for sample size determination often overlook the impact of anticipated exposure misclassification.

    Purpose of the Study:

    • To develop and present methods for sample size determination in case-control studies that account for exposure misclassification.
    • To provide a framework for ensuring sufficient accuracy and precision of odds ratio estimation when exposure data is imperfect.

    Main Methods:

    • Utilizing interval-based Bayesian criteria for sample size calculations.
    • Developing methods to adjust sample size requirements for anticipated exposure misclassification.
    • Comparing sample size needs with and without adjustment for misclassification using prototypical examples.

    Main Results:

    • The study demonstrates that accounting for exposure misclassification leads to different sample size requirements compared to ignoring it.
    • The proposed Bayesian methods offer a way to determine adequate sample sizes under realistic data quality conditions.
    • Sample size adjustments are necessary to maintain desired precision in the presence of misclassification.

    Conclusions:

    • Accurate sample size determination in case-control studies must consider potential exposure misclassification.
    • The developed Bayesian approach provides a robust method for planning studies with imperfect exposure data.
    • Applying these methods can lead to more precise and reliable estimation of odds ratios in epidemiologic research.