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 mapping under genetic interference

D E Weeks1, G M Lathrop, J Ott

  • 1Department of Human Genetics, University of Pittsburgh, Pa 15261.

Human Heredity
|March 1, 1993
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

A genome-wide association study of anti-Müllerian hormone (AMH) levels in Samoan women.

medRxiv : the preprint server for health sciences·2024
Same author

A missense variant in CREBRF, rs373863828, is associated with fat-free mass, not fat mass in Samoan infants.

International journal of obesity (2005)·2020
Same author

Effect of Ar(3p<sup>5</sup>4p; 2p)+M → Ar(3p<sup>5</sup>4s; 1s)+M branching ratio on optically pumped rare gas laser performance.

Optics express·2019
Same author

Enhanced B Cell Alloantigen Presentation and Its Epigenetic Dysregulation in Liver Transplant Rejection.

American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons·2015
Same author

Genome-wide association study of primary dentition pit-and-fissure and smooth surface caries.

Caries research·2014
Same author

Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition.

Journal of dental research·2013
Same journal

Comparative profiles of pediatric Mendeliome: A Single-Centre 572-Whole-Exome Sequencing Study in Xinjiang.

Human heredity·2026
Same journal

Erratum.

Human heredity·2026
Same journal

Exploratory Analysis of HMGB1 Genetic Variants and Their Potential Association with Lung Cancer Susceptibility and Chemotherapy Response in a Chinese Population.

Human heredity·2025
Same journal

Weighted Burden Analysis of Rare Genetic Variants Identifies Novel Genes with Effects on BMI.

Human heredity·2025
Same journal

Generalized Stable Population and Agent-Based Models of Phenotypic Transmission in Human Populations, with an Application to Body Size.

Human heredity·2025
Same journal

Proteinase-activated receptor 2 (PAR-2) expression and F2RL1 genetic variants are associated with asthma: a case-control study in the Chinese population.

Human heredity·2025
See all related articles

Chiasma interference in human genetic mapping is often ignored, impacting map accuracy. Our new program accounts for this interference, improving genetic map construction by analyzing multipoint likelihoods in nuclear families.

Area of Science:

  • Genetics
  • Bioinformatics
  • Computational Biology

Background:

  • Chiasma interference, where one crossover affects nearby crossovers, is known in humans but typically ignored in genetic mapping.
  • Ignoring interference simplifies multipoint likelihood calculations but reduces the accuracy and power of genetic map construction.

Purpose of the Study:

  • To develop a computational tool that incorporates chiasma interference into multipoint likelihood calculations for genetic mapping.
  • To improve the accuracy of genetic map construction by accounting for biological realities of crossover interference.

Main Methods:

  • Developed a computer program to calculate multipoint likelihoods in three-generation nuclear families, integrating interference.
  • Modeled interference using map functions to convert genetic distances to recombination fractions.

Related Experiment Videos

  • Employed a simulation approach to assess the statistical significance of results due to unknown likelihood difference distributions.
  • Main Results:

    • The developed program successfully calculates multipoint likelihoods while accounting for genetic chiasma interference.
    • Analysis of chromosome 10 loci (D10S34, D10S19, D10S16, D10S14, D10S4, D10S20) revealed significant evidence for positive interference.
    • The Sturt map function was identified as the best fit for modeling interference in the studied dataset.

    Conclusions:

    • Accounting for chiasma interference is crucial for accurate human genetic map construction.
    • The developed computational tool and identified map functions offer a more biologically sound approach to genetic mapping.
    • This work enhances the power and precision of genetic mapping by integrating interference phenomena.