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

Statistical tests for admixture mapping with case-control and cases-only data.

Giovanni Montana1, Jonathan K Pritchard

  • 1Department of Human Genetics, University of Chicago, Chicago, IL 60637, USA.

American Journal of Human Genetics
|September 24, 2004
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

Allele Frequencies at Recessive Disease Genes are Mainly Determined by Pleiotropic Effects in Heterozygotes.

Genetics·2026
Same author

Genetic variants affect diurnal glucose levels throughout the day.

Nature communications·2026
Same author

Buffering of gene dosage response curves for human complex traits.

Cell genomics·2026
Same author

Regulatory network topology and the genetic architecture of gene expression.

Cell genomics·2026
Same author

Genetic architectures of brain-related traits are shaped by strong selective constraints.

bioRxiv : the preprint server for biology·2026
Same author

Life event trajectories and suicidal ideation throughout adolescence: a prospective cohort study from Germany, France, Ireland, and the UK.

The lancet. Psychiatry·2026
Same journal

Comparison of methods for assessing effects of risk factors on disease progression in Mendelian randomization under index event bias.

American journal of human genetics·2026
Same journal

Deciding "what" to screen for and "when": The importance of natural history information.

American journal of human genetics·2026
Same journal

Homologous recombination deficiency-driven genomic instability in ovarian cancer as an indicator of BRCA1 and BRCA2 variant pathogenicity.

American journal of human genetics·2026
Same journal

Individuals who deviate from polygenic expectation are enriched for damaging variants in genes linked to rare disease.

American journal of human genetics·2026
Same journal

Integrating social determinants of health and genetic risk in disease risk models.

American journal of human genetics·2026
Same journal

De novo variants in LDB1 are linked to distinct neurodevelopmental phenotypes determined by variant location and differing pathomechanisms.

American journal of human genetics·2026
See all related articles

Admixture mapping is a novel method for identifying genes linked to complex traits. New statistical approaches enable accurate detection of genetic associations in admixed populations, even with random markers.

Area of Science:

  • Genetics
  • Population Genetics
  • Genomic Research

Background:

  • Complex traits are influenced by multiple genes, making genetic discovery challenging.
  • Admixture mapping leverages genetic differences in admixed populations to identify disease-associated loci.
  • Recent advancements in genomic tools make admixture mapping a feasible approach for complex trait analysis.

Purpose of the Study:

  • To introduce novel statistical methods for analyzing multipoint data in admixture mapping studies.
  • To detect "ancestry association" without assuming specific disease models.
  • To evaluate the power and efficiency of admixture mapping compared to traditional association mapping.

Main Methods:

  • Development of new statistical tests based on deviations in locus-specific ancestry proportions from the genome average.

Related Experiment Videos

  • Power calculations to assess the effectiveness of admixture mapping under varying risk allele frequencies.
  • Comparison of performance using "ancestry informative markers" (AIMs) versus random single-nucleotide polymorphisms (SNPs).
  • Main Results:

    • The new statistical methods effectively detect "ancestry association" in admixture mapping studies.
    • Admixture mapping demonstrates comparable power to association mapping with fewer markers when ancestral risk allele frequencies differ significantly.
    • Random SNPs can be effective for admixture mapping when AIMs are unavailable, requiring only a modest increase in marker density.

    Conclusions:

    • New statistical methods enhance the utility of admixture mapping for complex trait gene discovery.
    • Admixture mapping offers a powerful and efficient alternative to traditional methods, particularly in admixed populations.
    • Researchers can utilize readily available random SNPs for admixture mapping, broadening its applicability.