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trio-wes  (MyGenostics Inc)

 
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    MyGenostics Inc trio-wes
    Trio Wes, supplied by MyGenostics Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/trio-wes/wes/pm40048818-50-0-1
    Average 90 stars, based on 1 article reviews
    trio-wes - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    other:

    Article Title: Genotype-phenotype correlation of ODLURO syndrome comorbid epilepsy associated with KMT2E variations: Report on a novel case and systematic literature review.
    Article Snippet: Trio-WES (Mygenostics, Beijing) was conducted after obtaining informed consent from the family members.

    Article Title: Trio‐WES reveals a novel de novo missense mutation of KMT2A in a Chinese patient with Wiedemann‐Steiner syndrome: A case report
    Article Snippet: Trio‐WES was performed by MyGenostics (Beijing, China) using the Illumina HiSeq X ten system.

    Article Title: Genetic analysis of a pedigree with MECP2 duplication syndrome in China
    Article Snippet: For sequencing the exomes of the patient and her parents, trio-WES technology (Mygenostics, Beijing) was employed.

    Article Title: A Case Series of Pediatric Intestinal Ganglioneuromatosis With Novel Phenotypic and Genotypic Profile
    Article Snippet: Trio-WES was performed by MyGenostics (a commercial genetic testing company) using the Illumina HiSeq X ten platform.

    Article Title: Genetic analysis of a pedigree with MECP2 duplication syndrome in China.
    Article Snippet: For sequencing the exomes of the patient and her parents, trio-WES technology (Mygenostics, Beijing) was employed.



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    Image Search Results


    Earliest studies for clinical exome and genome sequencing.

    Journal: Children

    Article Title: Rapid Whole-Genome Sequencing in Critically Ill Infants and Children with Suspected, Undiagnosed Genetic Diseases: Evolution to a First-Tier Clinical Laboratory Test in the Era of Precision Medicine

    doi: 10.3390/children12040429

    Figure Lengend Snippet: Earliest studies for clinical exome and genome sequencing.

    Article Snippet: Vissers et al. [ ], November 2010, Nature Genetics , Radboud University Nijmegen Medical Centre, The Netherlands, trio WES on 10 individuals with moderate to severe intellectual disability with a negative family history, and unexplained cause , Whole exome , Identified de novo mutations in 9 genes, 6 of which in 6 individuals were considered to be likely pathogenic , Family-based WES identified the de novo nature of mutations in individuals with intellectual disability.

    Techniques: Sequencing, Biomarker Discovery, Mutagenesis, Variant Assay, Control, Diagnostic Assay

    Key cohort studies for clinical exome and whole-genome sequencing in children, 2013–2017.

    Journal: Children

    Article Title: Rapid Whole-Genome Sequencing in Critically Ill Infants and Children with Suspected, Undiagnosed Genetic Diseases: Evolution to a First-Tier Clinical Laboratory Test in the Era of Precision Medicine

    doi: 10.3390/children12040429

    Figure Lengend Snippet: Key cohort studies for clinical exome and whole-genome sequencing in children, 2013–2017.

    Article Snippet: Vissers et al. [ ], November 2010, Nature Genetics , Radboud University Nijmegen Medical Centre, The Netherlands, trio WES on 10 individuals with moderate to severe intellectual disability with a negative family history, and unexplained cause , Whole exome , Identified de novo mutations in 9 genes, 6 of which in 6 individuals were considered to be likely pathogenic , Family-based WES identified the de novo nature of mutations in individuals with intellectual disability.

    Techniques: Sequencing, Genomic Sequencing, DNA Sequencing, Diagnostic Assay, Biomarker Discovery, Mutagenesis, Control