Related Experiment Video

Updated: Jan 12, 2026

Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry
05:53

Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry

Published on: June 21, 2018

10.6K

Optimal two-stage testing for family-based genome-wide association studies

Stuart Macgregor

    American Journal of Human Genetics
    |March 6, 2008
    PubMed
    Summary

    No abstract available in PubMed .

    More Related Videos

    Screening for Functional Non-coding Genetic Variants Using Electrophoretic Mobility Shift Assay EMSA and DNA-affinity Precipitation Assay DAPA
    11:35

    Screening for Functional Non-coding Genetic Variants Using Electrophoretic Mobility Shift Assay EMSA and DNA-affinity Precipitation Assay DAPA

    Published on: August 21, 2016

    13.4K
    A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
    05:51

    A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia

    Published on: June 15, 2011

    26.3K

    Related Experiment Videos

    Last Updated: Jan 12, 2026

    Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry
    05:53

    Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry

    Published on: June 21, 2018

    10.6K
    Screening for Functional Non-coding Genetic Variants Using Electrophoretic Mobility Shift Assay EMSA and DNA-affinity Precipitation Assay DAPA
    11:35

    Screening for Functional Non-coding Genetic Variants Using Electrophoretic Mobility Shift Assay EMSA and DNA-affinity Precipitation Assay DAPA

    Published on: August 21, 2016

    13.4K
    A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
    05:51

    A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia

    Published on: June 15, 2011

    26.3K

    Related Concept Videos

    Genome-wide Association Studies-GWAS01:11

    Genome-wide Association Studies-GWAS

    15.3K
    Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
    GWAS does not require the identification of the target gene involved in...
    15.3K

    Articles linked to this work by shared authors, journal, and citation graph.

    Can we identify people with Alzheimer's disease from examination of the eye? A bidirectional Mendelian randomization (MR) study.

    The journal of prevention of Alzheimer's disease·2026

    Genome-Wide Association Study of Nevus Count Reveals Opposing Effects of Genetic Loci Near IRF4 and MC1R on Flat Versus Raised Nevus Count in the Brisbane Twin Nevus Study: A Cross-Sectional Analysis.

    Pigment cell & melanoma research·2026

    GWAS meta-analysis provides new insights into uveal melanoma risk.

    British journal of cancer·2026

    Genome-wide discovery reveals 30 loci for choroidal thickness and uncovers potential causal links with angle-closure glaucoma.

    medRxiv : the preprint server for health sciences·2026

    Multi-Ancestry, Multitrait Polygenic Risk Scores for Myopia: Improved Accuracy and Clinical Potential.

    Twin research and human genetics : the official journal of the International Society for Twin Studies·2026

    Genetics versus clinical risk scores for melanoma prediction.

    The British journal of dermatology·2026

    Systematic and proactive evaluation of AIRE missense variant effects.

    American journal of human genetics·2026

    Variants leading to ELAVL2 haploinsufficiency cause a neurodevelopmental disorder with prominent cognitive, behavioral, and neurological features.

    American journal of human genetics·2026

    Cell villages and Dirichlet modeling map human cell fitness genetics.

    American journal of human genetics·2026

    Mismapping of sequencing reads from polymorphic duplications generates spurious trans-eQTLs.

    American journal of human genetics·2026

    Position effect at the SOX3 locus by an interchromosomal insertion causes hereditary spastic paraplegia.

    American journal of human genetics·2026

    Allele frequency trajectories across age groups reveal ongoing natural selection shaping disease susceptibility.

    American journal of human genetics·2026

    Lessons from a systematic review of family-based studies in ALS.

    Amyotrophic lateral sclerosis & frontotemporal degeneration·2026

    Spadmiss with basal ganglia calcification and multilocus genetic disease: a novel phenotypic expansion.

    Annals of medicine and surgery (2012)·2026

    Genome-wide meta-analysis with 1,590,596 individuals identifies 12 novel risk loci for systemic lupus erythematosus.

    Mammalian genome : official journal of the International Mammalian Genome Society·2026

    Biology-informed neural networks learn nonlinear representations from omics data to improve genomic prediction and biological discovery.

    The Plant journal : for cell and molecular biology·2026

    The causal role of plasma protein ratios in ulcerative colitis: insights from mendelian randomization and single-cell sequencing.

    Open medicine (Warsaw, Poland)·2026

    Molecular Characterization of TSC1 and TSC2 Variants in a Greek Cohort of Tuberous Sclerosis Complex Patients.

    Human mutation·2026
    See all related articles
    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
    Jove
    Visualize
    Contact Us