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

ALOHOMORA: a tool for linkage analysis using 10K SNP array data.

Franz Rüschendorf1, Peter Nürnberg

  • 1Bioinformatics Department, Gene Mapping Center, Max Delbrück Center (MDC) for Molecular Medicine Berlin-Buch, Germany. fruesch@mdc-berlin.de

Bioinformatics (Oxford, England)
|January 14, 2005
PubMed
Summary

ALOHOMORA is a Perl-based software tool that simplifies genome-wide linkage studies using high-density SNP marker panels. It preprocesses data for common linkage programs, enabling advanced linkage scans for various family structures and genetic models.

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

Macrocephaly and Digital Anomalies Expand the Phenotypic Spectrum of <i>PGAP2</i> Variants in Hyperphosphatasia with Impaired Intellectual Development Syndrome 3 (HPMRS3).

Human mutation·2025
Same author

Biallelic variants in WARS1 cause a highly variable neurodevelopmental syndrome and implicate a critical exon for normal auditory function.

Human mutation·2022
Same author

Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4.

Nature communications·2021
Same author

A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans.

Human genetics·2021
Same author

Phosphatidylinositol 4-kinase β mutations cause nonsyndromic sensorineural deafness and inner ear malformation.

Journal of genetics and genomics = Yi chuan xue bao·2020
Same author

Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families.

Genes·2020

Area of Science:

  • Genetics
  • Bioinformatics
  • Computational Biology

Background:

  • Genome-wide linkage studies are crucial for identifying genes associated with diseases.
  • High-density single nucleotide polymorphism (SNP) panels generate large datasets requiring specialized tools.
  • Existing software may not efficiently handle diverse family structures or genetic models.

Purpose of the Study:

  • To introduce ALOHOMORA, a novel software tool for facilitating genome-wide linkage analysis.
  • To enable efficient processing of high-density SNP data for linkage studies.
  • To support state-of-the-art linkage scans across various genetic models and family sizes.

Main Methods:

  • ALOHOMORA converts genotype data into formats compatible with common linkage programs.

Related Experiment Videos

  • The software incorporates standard quality control routines before initiating linkage analysis.
  • It is written in Perl, ensuring broad accessibility and compatibility.
  • Main Results:

    • ALOHOMORA supports linkage scans for both small and large families.
    • The tool accommodates any genetic model, enhancing its versatility.
    • It offers options for utilizing diverse genetic maps and ethnicity-specific allele frequencies.

    Conclusions:

    • ALOHOMORA is a valuable, free software tool for non-commercial research institutions.
    • It streamlines genome-wide linkage studies with high-density SNP data.
    • The software provides graphical outputs of multipoint LOD scores for comprehensive analysis.