{"id":6018,"date":"2026-03-21T15:58:49","date_gmt":"2026-03-21T15:58:49","guid":{"rendered":"https:\/\/ty-biosolution.com\/?post_type=product&p=6018"},"modified":"2026-03-21T15:58:50","modified_gmt":"2026-03-21T15:58:50","slug":"genetic-whole-exome-sequencing","status":"publish","type":"product","link":"https:\/\/ty-biosolution.com\/zh\/product\/genetic-whole-exome-sequencing\/","title":{"rendered":"Genetic whole exome sequencing"},"content":{"rendered":"

ore Product Advantages<\/h2>\n
<\/div>\n
    \n
  1. Highly Economical<\/strong>\n
    <\/div>\n

    Targets only the 1%~2% exon regions of the human genome that encode functional proteins, covering most functional variations linked to individual phenotypes. It avoids redundant whole-genome detection, greatly reducing detection costs while meeting the core needs of genetic disease etiology identification.<\/li>\n

  2. Authoritative and Up-to-Date<\/strong>\n
    <\/div>\n

    Equips with a regularly updated disease database that closely follows the latest clinical and scientific research progress, continuously optimizing variation interpretation standards and improving the detection rate of pathogenic genetic variations for more reliable test results.<\/li>\n

  3. Comprehensive and Customized<\/strong>\n
    <\/div>\n

    Provides in-depth genetic variation analysis and interpretation guidelines, with a complete case management system and powerful NGS annotation and interpretation capabilities supported by an exclusive database system. It also offers customized test reports tailored to clinical diagnosis, treatment and research needs of different users.<\/li>\n<\/ol>\n

    <\/div>\n

    Applicable Population<\/h2>\n
    <\/div>\n
      \n
    1. Suspected patients with monogenic genetic diseases<\/li>\n
    2. Patients with clinical critical illnesses and unclear prognosis who need a definitive diagnosis for precise treatment planning<\/li>\n
    3. Patients with complex diseases and syndromes of unknown etiology that cannot be diagnosed by routine methods<\/li>\n
    4. High-risk groups with a family history of genetic diseases<\/li>\n
    5. Couples with a genetic disease family history or a child with genetic diseases who require prenatal diagnosis or genetic counseling<\/li>\n<\/ol>\n
      <\/div>\n

      Clinical Significance<\/h2>\n
      <\/div>\n
        \n
      1. Precise Etiological Diagnosis<\/strong>\n
        <\/div>\n

        Accurately identifies the genetic causes of genetic diseases, differentiates disease types with similar clinical phenotypes, and solves the problem of unclear diagnosis in difficult and complicated genetic disease cases.<\/li>\n

      2. Guides Personalized Treatment and Prognosis<\/strong>\n
        <\/div>\n

        Formulates targeted personalized treatment plans based on the identified genetic etiology; conducts cascade screening to find pathogenic variant carriers, and provides early prevention and intervention strategies to help them avoid disease-triggering factors.<\/li>\n

      3. Scientific Fertility Guidance<\/strong>\n
        <\/div>\n

        Combined with genetic counseling, it designs personalized fertility plans for high-risk couples, effectively reducing the birth rate of children with genetic diseases and realizing scientific prevention of hereditary birth defects.<\/li>\n

      4. Assists Academic and Clinical Research<\/strong>\n
        <\/div>\n

        Provides high-quality genetic variation data for scientific research, promoting in-depth studies on the pathogenesis of genetic diseases and the exploration of novel therapeutic targets and methods.<\/li>\n<\/ol>\n

        <\/div>\n

        Standard Detection Process<\/h2>\n
        <\/div>\n
          \n
        1. Nucleic acid extraction from clinical samples<\/li>\n
        2. Exome-targeted gene library construction<\/li>\n
        3. Probe hybridization for target region capture<\/li>\n
        4. Magnetic bead capture to enrich exon sequences<\/li>\n
        5. High-throughput sequencing of captured target exome sequences<\/li>\n
        6. Professional bioinformatics analysis and genetic variation result interpretation<\/li>\n
        7. Compilation and release of a detailed customized test report<\/li>\n<\/ol>\n
          <\/div>\n

          Lead Time<\/h2>\n
          <\/div>\n
          The whole detection process is rigorous and systematic, with the professional whole exome sequencing test report completed and released within 15 working days<\/strong> after receiving qualified samples, ensuring the timeliness of clinical genetic disease diagnosis, treatment decision-making and genetic counseling.<\/div>","protected":false},"excerpt":{"rendered":"

          Genetic Whole Exome Sequencing is a high-efficiency genomic detection technology focusing on human exon region sequencing, targeting the core genetic variation regions associated with monogenic and complex genetic diseases. As 85% of genetic disease-causing variations occur in exon regions (only 1%~2% of the human genome), this technology achieves cost-effective and accurate identification of genetic disease causes under economic constraints, providing a scientific genomic basis for genetic disease precise diagnosis, personalized treatment, fertility guidance and scientific research exploration.<\/p>","protected":false},"featured_media":0,"comment_status":"open","ping_status":"closed","template":"","meta":{"_uag_custom_page_level_css":"","site-sidebar-layout":"default","site-content-layout":"","ast-site-content-layout":"default","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","ast-disable-related-posts":"","theme-transparent-header-meta":"default","adv-header-id-meta":"","stick-header-meta":"default","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"set","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"ast-content-background-meta":{"desktop":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}}},"product_cat":[48],"product_tag":[],"class_list":{"0":"post-6018","1":"product","2":"type-product","3":"status-publish","5":"product_cat-application-products","6":"desktop-align-center","7":"tablet-align-center","8":"mobile-align-center","9":"ast-product-gallery-layout-horizontal","10":"ast-product-tabs-layout-horizontal","11":"ast-qv-on-image","13":"first","14":"instock","15":"shipping-taxable","16":"product-type-simple"},"uagb_featured_image_src":{"full":false,"thumbnail":false,"medium":false,"medium_large":false,"large":false,"1536x1536":false,"2048x2048":false,"trp-custom-language-flag":false,"woocommerce_thumbnail":false,"woocommerce_single":false,"woocommerce_gallery_thumbnail":false},"uagb_author_info":{"display_name":"admin","author_link":"https:\/\/ty-biosolution.com\/zh\/author\/"},"uagb_comment_info":0,"uagb_excerpt":"Genetic Whole Exome Sequencing is a high-efficiency genomic detection technology focusing on human exon region sequencing, targeting the core genetic variation regions associated with monogenic and complex genetic diseases. As 85% of genetic disease-causing variations occur in exon regions (only 1%~2% of the human genome), this technology achieves cost-effective and accurate identification of genetic disease…","_links":{"self":[{"href":"https:\/\/ty-biosolution.com\/zh\/wp-json\/wp\/v2\/product\/6018","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/ty-biosolution.com\/zh\/wp-json\/wp\/v2\/product"}],"about":[{"href":"https:\/\/ty-biosolution.com\/zh\/wp-json\/wp\/v2\/types\/product"}],"replies":[{"embeddable":true,"href":"https:\/\/ty-biosolution.com\/zh\/wp-json\/wp\/v2\/comments?post=6018"}],"wp:attachment":[{"href":"https:\/\/ty-biosolution.com\/zh\/wp-json\/wp\/v2\/media?parent=6018"}],"wp:term":[{"taxonomy":"product_cat","embeddable":true,"href":"https:\/\/ty-biosolution.com\/zh\/wp-json\/wp\/v2\/product_cat?post=6018"},{"taxonomy":"product_tag","embeddable":true,"href":"https:\/\/ty-biosolution.com\/zh\/wp-json\/wp\/v2\/product_tag?post=6018"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}