Related Experiment Video

Updated: Mar 2, 2026

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

26.5K

CORRIGENDUM: ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing

Robert C Green, Jonathan S Berg, Wayne W Grody

    Genetics in Medicine : Official Journal of the American College of Medical Genetics
    |May 12, 2017
    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

    34.9K
    Detecting Somatic Genetic Alterations in Tumor Specimens by Exon Capture and Massively Parallel Sequencing
    11:02

    Detecting Somatic Genetic Alterations in Tumor Specimens by Exon Capture and Massively Parallel Sequencing

    Published on: October 18, 2013

    20.0K

    Related Experiment Videos

    Last Updated: Mar 2, 2026

    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

    26.5K
    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

    34.9K
    Detecting Somatic Genetic Alterations in Tumor Specimens by Exon Capture and Massively Parallel Sequencing
    11:02

    Detecting Somatic Genetic Alterations in Tumor Specimens by Exon Capture and Massively Parallel Sequencing

    Published on: October 18, 2013

    20.0K

    Related Concept Videos

    Genome-wide Association Studies-GWAS01:11

    Genome-wide Association Studies-GWAS

    16.0K
    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...
    16.0K
    Next-generation Sequencing03:00

    Next-generation Sequencing

    99.6K
    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....
    99.6K

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

    Sequencing for a Lifetime: Professional Perspectives on the Value and Feasibility of Lifelong Genomic Medicine.

    medRxiv : the preprint server for health sciences·2026

    When to return genomic newborn screening results: health care professional perspectives.

    medRxiv : the preprint server for health sciences·2026

    Biallelic Variants in MIMS1 Produce a Form of Spondyloepimetaphyseal Dysplasia With Tracheal Stenosis and Ectodermal Dysplasia (SEMDTSED).

    American journal of medical genetics. Part A·2026

    Toward a nuanced framework for the medical development of ibogaine and its analogues and derivatives: implications for psychopharmacology.

    Expert opinion on drug discovery·2026

    Elective genomic sequencing for adults in research, clinical and commercial contexts.

    BMC medical genomics·2026

    Elective genomic sequencing for adults in research, clinical and commercial contexts.

    medRxiv : the preprint server for health sciences·2026

    Integrative long-read sequencing, RNA-seq and machine learning framework characterizes and predicts autosomal silencing in unbalanced X-autosome translocations.

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

    Epigenomic correlates of co-morbid psychosis in 22q deletion syndrome.

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

    "TRACEBACK has probably saved my life": experiences of being notified about clinically significant cancer genetic information by the Australian TRACEBACK program.

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

    Birt-Hogg-Dubé syndrome, prevalence of identified cases according to clinical indication in a cohort of 1,084 patients with genetic analysis.

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

    A budget impact analysis for the addition of rare disease genes to secondary findings screening during genome-wide sequencing.

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

    Individuals heterozygous for LTBP2 loss-of-function variants have an increased risk of adult-onset primary open-angle glaucoma.

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

    Moxifloxacin-induced Abducens Nerve Palsy: A Rare Neurological Complication During Mycobacterium avium Complex Lung Disease Treatment.

    Open respiratory archives·2026

    Purpureocillium lilacinum Fungemia Masquerading as an Unidentified Yeast in a Heavily Immunosuppressed Patient With Relapsed Multiple Myeloma and Therapy-Related Mixed-Phenotype Acute Leukemia: A Case Report.

    Cureus·2026

    Cervical Scrofula Revealing Miliary Tuberculosis and Previously Undiagnosed Advanced HIV: A Case Report.

    Cureus·2026

    Chromoblastomycosis in Timor-Leste: Highlighting an underdiagnosed condition.

    Medical mycology case reports·2026

    Phase 2 study of fazpilodemab, a FGFR1/Klothoβ agonist, in metabolic dysfunction-associated steatohepatitis (MASH).

    JHEP reports : innovation in hepatology·2026

    Conjunctival involvement with corneal extension in pediatric mycosis fungoides. Surgical and immunomodulatory management.

    Archivos de la Sociedad Espanola de Oftalmologia·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