Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Multistage sampling for latent variable models.

Duncan C Thomas1

  • 1Department of Preventive Medicine, University of Southern California, 1540 Alcazar St., CHP-220, Los Angeles, CA 90089-9011, USA. dthomas@usc.edu

Lifetime Data Analysis
|October 19, 2007
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Characterization of Additive Gene-environment Interactions For Colorectal Cancer Risk.

Epidemiology (Cambridge, Mass.)·2024
Same author

Two genome-wide interaction loci modify the association of nonsteroidal anti-inflammatory drugs with colorectal cancer.

Science advances·2024
Same author

Genome-wide interaction study of dietary intake of fibre, fruits, and vegetables with risk of colorectal cancer.

EBioMedicine·2024
Same author

Genetic risk impacts the association of menopausal hormone therapy with colorectal cancer risk.

British journal of cancer·2024
Same author

Genome-Wide Gene-Environment Interaction Analyses to Understand the Relationship between Red Meat and Processed Meat Intake and Colorectal Cancer Risk.

Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology·2023
Same author

Genome-wide interaction analysis of folate for colorectal cancer risk.

The American journal of clinical nutrition·2023
Same journal

Shared frailty sieve estimation for dependent left truncated and interval censored data.

Lifetime data analysis·2026
Same journal

Functional win-fractions regression models for composite outcomes.

Lifetime data analysis·2026
Same journal

Variable selection in causal semiparametric transformation models with all-or-nothing treatment compliance.

Lifetime data analysis·2026
Same journal

Correction to: A uniformisation-driven algorithm for inference-related estimation of a phase-type ageing model.

Lifetime data analysis·2026
Same journal

Unobserved heterogeneity in threshold regression based on the hitting times of a reflected Brownian motion for recurrent hypoglycemia.

Lifetime data analysis·2026
Same journal

Variable selection with broken adaptive ridge regression for interval-censored competing risks data.

Lifetime data analysis·2026
See all related articles

This study introduces efficient multistage sampling designs for epidemiological research using latent variable models. Optimized sampling fractions improve cost-efficiency in studies with surrogate measurements.

Area of Science:

  • Epidemiology
  • Biostatistics
  • Statistical Modeling

Background:

  • Multistage sampling is crucial for epidemiological studies with latent variables and surrogate measurements.
  • Latent variable models are used when detailed exposure data is combined with limited measurements, or for unobserved pathophysiologic processes.

Purpose of the Study:

  • To design cost-efficient multistage sampling schemes for epidemiological studies.
  • To optimize sampling fractions for latent variable models with surrogate measurements.

Main Methods:

  • Considered analytic calculations for optimal design in specific scenarios: all binary variables, all normally distributed variables, and mixed binary/normal distributions.
  • Explored spatial correlation for improved exposure assignment in spatially distributed data.

Related Experiment Videos

  • Investigated informative sample selection based on location and exposure predictor data.
  • Main Results:

    • Appropriate selection of sampling fractions can significantly enhance the cost-efficiency of study designs.
    • Spatial correlation can be leveraged to improve exposure assignment for unmeasured locations.
    • Stratification on available data (outcomes, predictors, locations) can optimize subsample selection.

    Conclusions:

    • Optimized multistage sampling designs can substantially improve cost-efficiency in epidemiological studies with latent variables.
    • Spatial data and informative sampling strategies offer further improvements in design efficiency.