{"id":19981,"date":"2021-05-12T00:26:42","date_gmt":"2021-05-12T07:26:42","guid":{"rendered":"https:\/\/novogene.com\/eu-en\/?page_id=19981"},"modified":"2025-03-31T02:08:33","modified_gmt":"2025-03-31T09:08:33","slug":"human-whole-genome-sequencing","status":"publish","type":"page","link":"https:\/\/www.novogene.com\/eu-en\/services\/research-services\/genome-sequencing\/whole-genome-sequencing\/human-whole-genome-sequencing\/","title":{"rendered":"Human Whole Genome Sequencing"},"content":{"rendered":"<div class=\"clear_p\" style=\"float: right; margin: 0 0 20px 50px;\"><img decoding=\"async\" class=\"clear_img\" style=\"width: 286px; min-height: 200px;\" src=\"https:\/\/www.novogene.com\/eu-en\/wp-content\/uploads\/sites\/7\/2021\/05\/istockphoto-1140489499-540x360-2-1.jpg\" alt=\"\" \/><\/p>\n<div class=\"col-sm-12 m-auto text-center\" style=\"padding-top: 20px; padding-left: 0;\"><span style=\"float: left; background: #3f6992; height: 2.6875rem; width: 2.875rem;\"><img decoding=\"async\" style=\"margin-top: 0.25rem;\" src=\"https:\/\/www.novogene.com\/eu-en\/wp-content\/uploads\/sites\/7\/2021\/01\/Novogene-button-icon-20210129.png\" \/><\/span><\/p>\n<div id=\"top_btn\" class=\"blue btn\" style=\"margin-top: 0px; padding: 8px 1.1875rem; float: left; background: #3789C7; border: none; line-height: 1.6875rem;width:241px;\"><a class=\"\" href=\"https:\/\/www.novogene.com\/eu-en\/wp-content\/uploads\/sites\/7\/2025\/02\/2025-Human-WGS-flyer.pdf\">Service Flyer<\/a><\/div>\n<\/div>\n<\/div>\n<p class=\"blue-box\" style=\"width: 70%; background-color: #e2f2ff!important; padding: 20px; font-family: 'Montserrat-Regular', Arial; color: #032e53; font-size: 16px;\">Human Whole Genome Sequencing (hWGS) is a powerful tool that has revolutionized our understanding of human biology and diseases. It enables researchers to comprehensively analyse the genetic makeup of individuals, identify <strong>genetic variants<\/strong>, including single-nucleotide variants (<strong>SNVs<\/strong>), insertions and deletions (<strong>InDels<\/strong>), structural variations (<strong>SVs<\/strong>), and copy number variations (<strong>CNVs<\/strong>), and diagnose diseases.\u00a0<\/p>\n<p style=\"line-height: 24px;\">Novogene has extensive experience with hWGS\u00a0 and offers the option of carrying out hWGS projects using the <strong>latest short or long read sequencing strategies<\/strong>, to cater to projects with different research goals. <strong>Low pass WGS (lpWGS)<\/strong> or <strong>shallow whole genome sequencing<\/strong> is a cost-effective alternative for large cohorts and is useful for discovering new, rare variants. Our hWGS service is complete with <strong>high-quality data<\/strong>, <strong>bioinformatics analysis<\/strong> to assist with data interpretation and \u201cpublication-ready\u2019\u2019 figures accompanying the analysis.\u00a0<\/p>\n<p style=\"line-height: 24px;\">Human Whole Genome Sequencing has a broad range of applications, including genetic diseases, cancers, pathogenesis mechanisms, or population genetics research.\u00a0 Long read sequencing technologies available at Novogene, such as those from PacBio and ONT can help one to sequence the <strong>highly polymorphic and repetitive regions<\/strong> within the genome and perform <strong>haplotype phasing<\/strong>, thereby providing a complete and accurate human genome characterization.\u00a0<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Service Flyer Human Whole Genome Sequencing (hWGS) is a powerful tool that has revolutionized our understanding of human biology and diseases. It enables researchers to comprehensively analyse the genetic makeup of individuals, identify genetic variants, including single-nucleotide variants (SNVs), insertions and deletions (InDels), structural variations (SVs), and copy number variations (CNVs), and diagnose diseases.\u00a0 Novogene<\/p>\n","protected":false},"author":10,"featured_media":0,"parent":1460,"menu_order":194,"comment_status":"closed","ping_status":"closed","template":"templates\/page-technical2.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>Human Whole Genome Sequencing - Novogene<\/title>\n<meta name=\"description\" content=\"Human whole genome sequencing (hWGS) enables researchers to describe the full genetic composition of individuals and characterize entire human genomes.\" \/>\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\/eu-en\/services\/research-services\/genome-sequencing\/whole-genome-sequencing\/human-whole-genome-sequencing\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Human Whole Genome Sequencing\" \/>\n<meta property=\"og:description\" content=\"Human whole genome sequencing (hWGS) enables researchers to describe the full genetic composition of individuals and characterize entire human genomes.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.novogene.com\/eu-en\/services\/research-services\/genome-sequencing\/whole-genome-sequencing\/human-whole-genome-sequencing\/\" \/>\n<meta property=\"og:site_name\" content=\"Novogene\" \/>\n<meta property=\"article:modified_time\" content=\"2025-03-31T09:08:33+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/www.novogene.com\/eu-en\/wp-content\/uploads\/sites\/7\/2021\/05\/istockphoto-1140489499-540x360-2-1.jpg\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data1\" content=\"2 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\/\/www.novogene.com\/eu-en\/services\/research-services\/genome-sequencing\/whole-genome-sequencing\/human-whole-genome-sequencing\/\",\"url\":\"https:\/\/www.novogene.com\/eu-en\/services\/research-services\/genome-sequencing\/whole-genome-sequencing\/human-whole-genome-sequencing\/\",\"name\":\"Human Whole Genome Sequencing - 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