{"id":19981,"date":"2021-05-12T00:26:42","date_gmt":"2021-05-12T07:26:42","guid":{"rendered":"https:\/\/www.novogene.com\/us-en\/?page_id=19981"},"modified":"2025-08-28T23:09:45","modified_gmt":"2025-08-29T06:09:45","slug":"human-whole-genome-sequencing","status":"publish","type":"page","link":"https:\/\/www.novogene.com\/us-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\">\n<img decoding=\"async\" class=\"clear_img\" style=\"width: 286px;min-height: 200px\" src=\"https:\/\/www.novogene.com\/us-en\/wp-content\/uploads\/sites\/4\/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\">\n<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\/us-en\/wp-content\/uploads\/sites\/4\/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\"><a class=\"\" href=\"https:\/\/www.novogene.com\/us-en\/wp-content\/uploads\/sites\/4\/2024\/02\/4-Detailed-Materials-for-hWGS-1.pdf\">Service Specifications<\/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\"><strong>Human whole genome sequencing (hWGS)<\/strong> enables researchers to describe the full genetic composition of individuals and characterize entire human genomes. It allows the identification of genomic variation information, including <strong>single-nucleotide polymorphisms (SNPs)<\/strong>, <strong>insertions and deletions (InDels)<\/strong>, <strong>structural variations (SVs)<\/strong>, and <strong>copy number variations (CNVs)<\/strong> in a single and cost-efficient assay.<\/p>\n<p style=\"line-height: 24px\">With extensive experience and well-developed bioinformatics know-how, Novogene delivers high-quality data, publication-ready analysis figures, and personalized results to meet different research objectives and customer needs. Novogene offers ultra-fast turnaround time, even for large projects: equipped with numerous <a href=\"https:\/\/www.novogene.com\/us-en\/technology\/platforms\/\" target=\"_blank\" rel=\"noopener noreferrer\"><strong>Illumina NovaSeq X Plus \/NovaSeq6000 platforms<\/strong><\/a>, <a href=\"https:\/\/www.novogene.com\/us-en\/technology\/platforms\/\" target=\"_blank\" rel=\"noopener noreferrer\"><strong>Oxford Nanopore PromethION<\/strong><\/a> and <a href=\"https:\/\/www.novogene.com\/us-en\/technology\/platforms\/\" target=\"_blank\" rel=\"noopener noreferrer\"><strong>PacBio Revio\/Sequel II system<\/strong><\/a>.<\/p>\n<p style=\"line-height: 24px\">Novogene is capable of sequencing up to 200,000 human genomes per year at a competitive cost. Novogene hWGS service can provide data across a broad range of applications, including studies on genetic diseases, cancers, pathogenesis mechanisms, or population genetics. Multiple DNA sequencing technologies available at Novogene can identify the highly polymorphic and highly repetitive regions within the genome of interest, thereby providing a complete and accurate human genome characterization <a href=\"https:\/\/www.genome.gov\/about-genomics\/fact-sheets\/Sequencing-Human-Genome-cost\" target=\"_blank\" rel=\"noopener noreferrer\"><sup>[1]<\/sup><\/a>.<\/p>\n<div style=\"display:none;\">\n<li class=\"nav-item novo-li-temp\"><a class=\"nav-link\" data-toggle=\"tab\" href=\"#novo-resources\" id=\"novo-resources-tab\">Resources<\/a><\/li>\n<div class=\"novo-div-temp tab-pane fade\">\n<div class=\"container-fluid\">\n<div class=\"row\">\n<div class=\"col-sm-12 col-md-10 col-lg-9 auto-lft novo-add-content\">\n<h1 style=\"margin:20px 0 20px 0;\">Resources<\/h1>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<style>\n.novo-border-right{border-right:0 !important;}\n<\/style>\n<p><script type=\"text\/javascript\">\n$(document).ready(function(){\nvar novo_li_tab=$(\".novo-li-temp\");\n$(\".nav-tabs .nav-item:eq(2)\").addClass(\"novo-border-right\")\nnovo_li_tab.remove()\n$(\".nav.nav-tabs.px-3\").append(novo_li_tab)\nvar novo_div_tmp=$(\".novo-div-temp\").remove()\nnovo_div_tmp.attr(\"id\",\"novo-resources\")\nnovo_div_tmp.find(\".novo-add-content\").append($(\"#novo-resources-content\").html())\n$(\"#novo-resources-content\").remove()\n$(\"#top_btn\").append(novo_div_tmp)\n})\n<\/script><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Service Specifications Human whole genome sequencing (hWGS) enables researchers to describe the full genetic composition of individuals and characterize entire human genomes. It allows the identification of genomic variation information, including single-nucleotide polymorphisms (SNPs), insertions and deletions (InDels), structural variations (SVs), and copy number variations (CNVs) in a single and cost-efficient assay. With extensive experience<\/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\/us-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\/us-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:publisher\" content=\"https:\/\/www.facebook.com\/NovogeneAmerica\/\" \/>\n<meta property=\"article:modified_time\" content=\"2025-08-29T06:09:45+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/www.novogene.com\/us-en\/wp-content\/uploads\/sites\/4\/2021\/05\/istockphoto-1140489499-540x360-2-1.jpg\" \/>\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=\"2 minutes\" \/>\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\/whole-genome-sequencing\/human-whole-genome-sequencing\/\",\"url\":\"https:\/\/www.novogene.com\/us-en\/services\/research-services\/genome-sequencing\/whole-genome-sequencing\/human-whole-genome-sequencing\/\",\"name\":\"Human Whole Genome Sequencing - 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