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

Association studies for quantitative traits in structured populations.

Silviu-Alin Bacanu1, Bernie Devlin, Kathryn Roeder

  • 1Department of Psychiatry, University of Pittsburgh School of Medicine, 3811 O'Hara Street, Pittsburgh, PA 15213, USA. roeder@stat.cmu.edu

Genetic Epidemiology
|January 5, 2002
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

Suicidality phenotypes reflect both shared and distinct genetic factors.

medRxiv : the preprint server for health sciences·2026
Same author

Spatial transcriptomics implicates the thalamus and cortex in autism and schizophrenia.

bioRxiv : the preprint server for biology·2026
Same author

Spatiotemporal analysis of autism gene enrichment implicates cortex, thalamus, and hypothalamus.

bioRxiv : the preprint server for biology·2026
Same author

Modeling rare coding variation on chromosome X provides insight into the genetics and differential sex prevalence of autism spectrum disorder.

medRxiv : the preprint server for health sciences·2026
Same author

A framework to infer de novo exonic variants when parental genotypes are missing enhances association studies of autism.

Bioinformatics (Oxford, England)·2026
Same author

Estimating protein isoform abundances with PAQu.

bioRxiv : the preprint server for biology·2026
Same journal

Applying Bayesian Multivariable Mendelian Randomisation to Prioritise Candidate Causal Traits From High-Dimensional Data: Illustration From Estimation of the Effect of Maternal Metabolites on Offspring Birthweight.

Genetic epidemiology·2026
Same journal

Individualized Bayesian Inference Identifies Novel Genetic Variants for Parkinson's Disease.

Genetic epidemiology·2026
Same journal

DRIVE v3: Command Line Application for Identity-by-Descent Haplotype Clustering in Large Biobank Scale Data.

Genetic epidemiology·2026
Same journal

Deep Unsupervised Domain Adaptation for Translating Cancer Dependency Maps From Cell Lines to Breast Cancer Tumor Genomics.

Genetic epidemiology·2026
Same journal

Polygenic Risk Scores for Incident Dementia in the Multi-Ethnic Study of Atherosclerosis.

Genetic epidemiology·2026
Same journal

Outcome and Exposure Polygenic Risk Scores Can Help Reduce Information Bias and Selection Bias in Regression Estimates From Biobank Data.

Genetic epidemiology·2026
See all related articles

Genomic control (GC) now extends to quantitative traits and multiple genes, effectively managing spurious associations from population structure. This method demonstrates good power for genetic studies, even with complex models.

Area of Science:

  • Genetics
  • Statistical genetics
  • Population genetics

Background:

  • Genetic polymorphisms are crucial for understanding common diseases.
  • Genomic control (GC) was developed to address spurious associations in population-based genetic studies.
  • Existing GC methods are limited to binary traits and single-locus models.

Purpose of the Study:

  • To generalize genomic control (GC) for quantitative traits (QT) and multilocus models.
  • To evaluate the effectiveness of GC in controlling spurious associations due to population substructure in QT analyses.
  • To assess the statistical power of GC for QT association tests.

Main Methods:

  • Statistical analysis and simulations were employed.
  • Generalized GC to accommodate quantitative traits and multilocus genetic models.

Related Experiment Videos

  • Simulated data to test GC performance under various population structures and genetic models.
  • Main Results:

    • GC successfully controls spurious associations for quantitative traits, including gene-gene interactions, in the presence of population substructure.
    • GC demonstrates good statistical power for detecting causal quantitative trait loci with 2.5-5% heritability, using both random and selected samples.
    • More complex genetic models result in smaller GC corrections, suggesting increased power when models are accurate.

    Conclusions:

    • The generalized GC method is effective for quantitative trait association studies with population structure.
    • GC provides a robust framework for genetic association studies involving complex traits and multiple genes.
    • Accurate a priori specification of genetic models enhances the power of GC analysis.