Related Experiment Video

Updated: Apr 28, 2026

An Automated System for Sound Localization Testing in Hearing-Impaired Listeners
07:56

An Automated System for Sound Localization Testing in Hearing-Impaired Listeners

Published on: March 13, 2026

177

New testing guidelines for hearing loss support next-generation sequencing: testing method may help determine genetic

Deborah Levenson

    American Journal of Medical Genetics. Part A
    |June 20, 2014
    PubMed
    Abstract

    No abstract available in PubMed .

    More Related Videos

    Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
    09:34

    Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease

    Published on: April 4, 2018

    36.1K
    Neuro-rehabilitation Approach for Sudden Sensorineural Hearing Loss
    09:44

    Neuro-rehabilitation Approach for Sudden Sensorineural Hearing Loss

    Published on: January 25, 2016

    20.5K

    Related Experiment Videos

    Last Updated: Apr 28, 2026

    An Automated System for Sound Localization Testing in Hearing-Impaired Listeners
    07:56

    An Automated System for Sound Localization Testing in Hearing-Impaired Listeners

    Published on: March 13, 2026

    177
    Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
    09:34

    Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease

    Published on: April 4, 2018

    36.1K
    Neuro-rehabilitation Approach for Sudden Sensorineural Hearing Loss
    09:44

    Neuro-rehabilitation Approach for Sudden Sensorineural Hearing Loss

    Published on: January 25, 2016

    20.5K

    Related Concept Videos

    Next-generation Sequencing03:00

    Next-generation Sequencing

    87.7K
    The first human genome sequencing project cost $2.7 billion and was declared complete in 2003, after 15 years of international cooperation and collaboration between several research teams and funding agencies. Today, with the advent of next-generation sequencing technologies, the cost and time of sequencing a human genome have dropped over 100 fold.
    Next-Generation Sequencing Methods
    Although all next-generation methods use different technologies, they all share a set of standard features....
    87.7K
    RNA-seq03:21

    RNA-seq

    9.3K
    RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases. 
    Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
    9.3K
    Hearing01:31

    Hearing

    47.9K
    When we hear a sound, our nervous system is detecting sound waves—pressure waves of mechanical energy traveling through a medium. The frequency of the wave is perceived as pitch, while the amplitude is perceived as loudness.
    47.9K

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

    The Importance of Familial Co-segregation in the Classification of a Novel PKD1 Variant Associated With Autosomal Dominant Polycystic Kidney Disease.

    American journal of medical genetics. Part A·2026

    Exome Sequencing Uncovers Phenotypic and Genotypic Heterogeneity in 196 Indian Families Evaluated for Autoinflammatory Disorders.

    American journal of medical genetics. Part A·2026

    The Evaluation of Molecular Genetics and Clinical Manifestations in Patients With LZTR1-Associated Noonan Syndrome: A Retrospective Chart Review and Review of Literature.

    American journal of medical genetics. Part A·2026

    Expanding the Genotypic and Phenotypic Spectrum of Vissers-Bodmer Syndrome.

    American journal of medical genetics. Part A·2026

    Clinical and Functional Characterization of Gain-of-Function ABL1 Variants Expands the Phenotypic Spectrum of CHDSKM.

    American journal of medical genetics. Part A·2026

    Expanding the Clinical and Genetic Spectrum of Schmid Metaphyseal Chondrodysplasia: A Seven-Patient Series Including a Rare Homozygous COL10A1 Case.

    American journal of medical genetics. Part A·2026

    Molecular genetics analysis of genes BCL11A, HBS1L-MYB, and HBG2 variants association in thalassemic children.

    Personalized medicine·2026

    A Novel Helicobacter pylori Test Based on 16S rRNA Isothermal Amplification Point-of-Care Testing of Throat Swab.

    Helicobacter·2026

    Spatial multiomics in biomedical research: advances beyond transcriptomics.

    JCI insight·2026

    Detection rate of pathogenic variants by postmortem genetic testing for sudden cardiac death among children and young adults: systematic review and meta-analysis.

    Genetics in medicine : official journal of the American College of Medical Genetics·2026

    An Updated Evidence Assessment of the Genetic Causes of Dilated Cardiomyopathy.

    Circulation·2026

    Dietary sugar intake and risk of depression: findings from the TwinsUK cohort.

    Nutritional psychiatry·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