{"id":30689,"date":"2021-12-09T03:58:45","date_gmt":"2021-12-09T11:58:45","guid":{"rendered":"https:\/\/www.novogene.com\/us-en\/?page_id=30689"},"modified":"2026-03-19T03:57:17","modified_gmt":"2026-03-19T10:57:17","slug":"clinical-whole-exome-sequencing-clia-cap-iso","status":"publish","type":"page","link":"https:\/\/www.novogene.com\/us-en\/services\/research-services\/genome-sequencing\/target-capture-sequencing\/clinical-whole-exome-sequencing-clia-cap-iso\/","title":{"rendered":"Clinical Whole Exome Sequencing (CLIA\/CAP)"},"content":{"rendered":"<p>Genetic testing, known as DNA testing, allows geneticists to determine bloodlines and diagnose genetic diseases. With the advent of next-generation sequencing (NGS) technologies, whole exome sequencing (WES) is widely used as a cost-effective and accurate method of genetic testing.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Genetic testing, known as DNA testing, allows geneticists to determine bloodlines and diagnose genetic diseases. With the advent of next-generation sequencing (NGS) technologies, whole exome sequencing (WES) is widely used as a cost-effective and accurate method of genetic testing.<\/p>\n","protected":false},"author":41,"featured_media":5241,"parent":1465,"menu_order":184,"comment_status":"closed","ping_status":"closed","template":"templates\/clinical-page-clia.php","meta":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v20.8 (Yoast SEO v20.8) - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Clinical Whole Exome Sequencing (CLIA\/CAP) - Novogene<\/title>\n<meta name=\"description\" content=\"Novogene is certified with CLIA and CAP to detect rare diseases and associated variants in an individual\u2019s DNA via whole exome sequencing.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.novogene.com\/us-en\/services\/research-services\/genome-sequencing\/target-capture-sequencing\/clinical-whole-exome-sequencing-clia-cap-iso\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Clinical Whole Exome Sequencing (CLIA\/CAP)\" \/>\n<meta property=\"og:description\" content=\"Novogene is certified with CLIA and CAP to detect rare diseases and associated variants in an individual\u2019s DNA via whole exome sequencing.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.novogene.com\/us-en\/services\/research-services\/genome-sequencing\/target-capture-sequencing\/clinical-whole-exome-sequencing-clia-cap-iso\/\" \/>\n<meta property=\"og:site_name\" content=\"Novogene\" \/>\n<meta property=\"article:publisher\" content=\"https:\/\/www.facebook.com\/NovogeneAmerica\/\" \/>\n<meta property=\"article:modified_time\" content=\"2026-03-19T10:57:17+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/www.novogene.com\/us-en\/wp-content\/uploads\/sites\/4\/2020\/04\/intro-cliacap-638x428-2.jpg\" \/>\n\t<meta property=\"og:image:width\" content=\"638\" \/>\n\t<meta property=\"og:image:height\" content=\"428\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/jpeg\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:site\" content=\"@Novogene_Global\" \/>\n<meta name=\"twitter:label1\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data1\" content=\"1 minute\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\/\/www.novogene.com\/us-en\/services\/research-services\/genome-sequencing\/target-capture-sequencing\/clinical-whole-exome-sequencing-clia-cap-iso\/\",\"url\":\"https:\/\/www.novogene.com\/us-en\/services\/research-services\/genome-sequencing\/target-capture-sequencing\/clinical-whole-exome-sequencing-clia-cap-iso\/\",\"name\":\"Clinical Whole Exome Sequencing (CLIA\/CAP) - 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