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

Multipoint linkage analysis.

N E Morton, C J MacLean, R Lew

    American Journal of Human Genetics
    |June 1, 1986
    PubMed
    Summary
    This summary is machine-generated.

    While n-point sampling offers theoretical advantages, 2- and 3-point analyses efficiently extract key genetic mapping information. Assuming null interference inflates genetic distances and reduces mapping efficiency.

    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

    A DEVELOPMENTAL BASIS FOR DIFFERENTIAL TOOTH REDUCTION DURING HOMINID EVOLUTION.

    Evolution; international journal of organic evolution·2017
    Same author

    Closely linked cis-acting modifier of expansion of the CGG repeat in high risk FMR1 haplotypes.

    Human mutation·2007
    Same author

    Refined association mapping for a quantitative trait: weight in the H19-IGF2-INS-TH region.

    Annals of human genetics·2006
    Same author

    An investigation of FRAXA intermediate allele phenotype in a longitudinal sample.

    Annals of human genetics·2006
    Same author

    A map of the human genome in linkage disequilibrium units.

    Proceedings of the National Academy of Sciences of the United States of America·2005
    Same author

    The optimal measure of linkage disequilibrium reduces error in association mapping of affection status.

    Human molecular genetics·2004
    Same journal

    Bi-allelic missense variants in human GPN2 result in Perrault syndrome.

    American journal of human genetics·2026
    Same journal

    Integrative analysis of gastric tissue transcriptomes and gastric cancer GWAS implicates candidate susceptibility genes.

    American journal of human genetics·2026
    Same journal

    A transparent and generalizable deep-learning framework for genomic ancestry prediction.

    American journal of human genetics·2026
    Same journal

    Data-driven RNA phenotyping captures genetically regulated dimensions of the transcriptome.

    American journal of human genetics·2026
    Same journal

    Linkage disequilibrium and allelic heterogeneity explain variation in coronary artery disease risk at 9p21 across populations and reduced effect in Africans.

    American journal of human genetics·2026
    Same journal

    Genome-wide association study and predictors of neonatal blood cell traits in Hispanic newborns.

    American journal of human genetics·2026
    See all related articles

    Area of Science:

    • Genetics
    • Bioinformatics
    • Statistical Modeling

    Background:

    • N-point sampling in genetic analysis offers theoretical information advantages as the number of points (n) increases.
    • Existing methods for analyzing genetic samples can be computationally intensive and may require complex reevaluation of likelihoods.
    • Understanding the efficiency and accuracy of different sampling and analysis strategies is crucial for genetic mapping.

    Purpose of the Study:

    • To evaluate the practical information yield of n-point sampling in genetic analysis.
    • To assess the efficiency and utility of 2-point and 3-point analyses for extracting genetic mapping data.
    • To investigate the impact of assuming null interference on genetic map distances and recombination frequencies.

    Main Methods:

    Related Experiment Videos

  • Formulation of an advantage formula for n-point sampling.
  • Analysis of information extraction using 2-point and 3-point sampling strategies.
  • Comparison of information communicated via logarithm of odds (lod) and chi-squared (χ²) statistics.
  • Evaluation of the effects of null interference assumption on genetic map parameters.
  • Main Results:

    • 2-point and 3-point analyses capture nearly all available information from samples.
    • Information is effectively communicated as lods and χ² values, allowing simple additive combination with other data.
    • Assuming null interference leads to inflated map distances and recombination frequencies.
    • Null interference assumption results in significant loss of efficiency and reduced support for correct ordering of genetic markers.

    Conclusions:

    • 2- and 3-point analyses are highly efficient for extracting essential genetic mapping information.
    • These methods provide data (lods, χ²) that can be readily integrated into larger analyses.
    • The assumption of null interference in genetic mapping introduces significant biases and reduces analytical power.