{"id":4258,"date":"2025-02-13T11:23:53","date_gmt":"2025-02-13T16:23:53","guid":{"rendered":"https:\/\/www.med.unc.edu\/genomics\/?p=4258"},"modified":"2025-02-13T11:25:57","modified_gmt":"2025-02-13T16:25:57","slug":"introducing-the-dnbseq-t7-advancing-genomic-research-through-innovative-sequencing","status":"publish","type":"post","link":"https:\/\/www.med.unc.edu\/genomics\/introducing-the-dnbseq-t7-advancing-genomic-research-through-innovative-sequencing\/","title":{"rendered":"Introducing the DNBSEQ-T7: Advancing Genomic Research Through Innovative Sequencing"},"content":{"rendered":"<p><img loading=\"lazy\" decoding=\"async\" class=\"size-medium wp-image-4259 alignleft\" src=\"https:\/\/www.med.unc.edu\/genomics\/wp-content\/uploads\/sites\/708\/2025\/02\/T7-promo-300x170.jpg\" alt=\"\" width=\"300\" height=\"170\" srcset=\"https:\/\/www.med.unc.edu\/genomics\/wp-content\/uploads\/sites\/708\/2025\/02\/T7-promo-300x170.jpg 300w, https:\/\/www.med.unc.edu\/genomics\/wp-content\/uploads\/sites\/708\/2025\/02\/T7-promo-1024x581.jpg 1024w, https:\/\/www.med.unc.edu\/genomics\/wp-content\/uploads\/sites\/708\/2025\/02\/T7-promo-768x435.jpg 768w, https:\/\/www.med.unc.edu\/genomics\/wp-content\/uploads\/sites\/708\/2025\/02\/T7-promo-1536x871.jpg 1536w, https:\/\/www.med.unc.edu\/genomics\/wp-content\/uploads\/sites\/708\/2025\/02\/T7-promo-600x340.jpg 600w, https:\/\/www.med.unc.edu\/genomics\/wp-content\/uploads\/sites\/708\/2025\/02\/T7-promo.jpg 1940w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>Genomic research is constantly pushing the boundaries of our understanding, and breakthrough technologies are the key to unlocking new scientific insights. The DNBSEQ-T7 represents a significant leap forward in our ability to read and understand genetic information with unprecedented precision and efficiency.<\/p>\n<p><strong>What makes DNA Nanoball Technology Revolutionary?<\/strong><\/p>\n<p>Genetic sequencing is fundamentally about capturing the most accurate snapshot of DNA possible. The DNBSEQ-T7 represents a significant advancement in how we approach this critical scientific challenge through its innovative DNA Nanoball technology.<\/p>\n<p>In conventional bridge amplification, DNA fragments are copied by attaching them to a surface and creating multiple copies through repeated synthesis cycles. During this process, the genetic material is denatured multiple times with each copying cycle carrying potential for errors. This replication process also has limitations like some regions being difficult to copy uniformly, sections being over- or under-represented, and fragments from different DNA molecules can merge incorrectly.<\/p>\n<p>The rolling circle amplification (RCR) used in DNB technology works differently. \u00a0An enzyme makes a small cut in a strain of circular DNA, grabs onto the strain, and creates a repeating strand based on the original material turning into a compact nanoball of DNA aka DNB. This amplification process eliminates the potential for errors found in bridge amplification such as index hopping while also severely reducing the chances of indel or clonal errors.<\/p>\n<p><strong>What does the performance and capabilities of the DNBSEQ-T7 look like?<\/strong><\/p>\n<p>The platform&#8217;s performance is nothing short of remarkable with:<\/p>\n<ul>\n<li>The capacity to sequence 12 human genomes on a single 300-cycle flow cell within 24 hours<\/li>\n<li>The ability to operate four flow cells concurrently<\/li>\n<li>Flexible configuration options to meet diverse research needs<\/li>\n<\/ul>\n<p>The DNBSEQ-T7 also provides researchers with the ability to combine next-generation sequencing with spatial transcriptomics also referred to as Stereo-Seq.<\/p>\n<p><strong>What is Stereo-Seq?<\/strong><\/p>\n<p>Stereo-seq is spatial transcriptomics technology created by Complete Genomics. Stereo-seq combines next-generation sequencing with spatial transcriptomics that allows researchers to map the spatial distribution of RNA transcripts within tissues. Stereo-seq offers insights into gene expression patterns with subcellular resolution. This technology, which was highlighted on the front cover of Cell in 2022, provides researchers with a new microscopic window in which to study development of diseases like cancer and further our understanding of cellular communication.<\/p>\n<p><strong>Where does the HTSF come in?<\/strong><\/p>\n<p>As we expand our technological capabilities, we remain committed to supporting innovative research through collaborative partnerships. The integration of the DNBSEQ-T7 into our facility enhances our ability to serve diverse research objectives while maintaining competitive pricing and rapid turnaround times.<\/p>\n<p>Our current service configurations for the DNBSEQ-T7 include:<\/p>\n<ul>\n<li>200-cycle configuration: Approximately 1 TB of data (5 billion clusters) at $4,500 ($4.5\/Gb)<\/li>\n<li>300-cycle configuration: Approximately 1.7 TB of data (8.5 billion clusters) at $5,000 ($5\/Gb)<\/li>\n<\/ul>\n<p>We&#8217;re genuinely excited to explore how DNBSEQ-T7 could enhance your research initiatives. Our team of experienced genomics specialists is eager to discuss your specific research questions and help determine how this platform&#8217;s capabilities could accelerate your discoveries. Whether you&#8217;re planning to scale up existing protocols or venture into new experimental territories, we&#8217;re here to support your scientific journey with both technical expertise and collaborative spirit.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Genomic research is constantly pushing the boundaries of our understanding, and breakthrough technologies are the key to unlocking new scientific insights. The DNBSEQ-T7 represents a significant leap forward in our ability to read and understand genetic information with unprecedented precision and efficiency. What makes DNA Nanoball Technology Revolutionary? Genetic sequencing is fundamentally about capturing the &hellip; <a href=\"https:\/\/www.med.unc.edu\/genomics\/introducing-the-dnbseq-t7-advancing-genomic-research-through-innovative-sequencing\/\" aria-label=\"Read more about Introducing the DNBSEQ-T7: Advancing Genomic Research Through Innovative Sequencing\">Read more<\/a><\/p>\n","protected":false},"author":117519,"featured_media":4259,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":"","_links_to":"","_links_to_target":""},"categories":[10,2,11],"tags":[],"class_list":["post-4258","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-director-spotlight","category-news","category-whats-new","odd"],"acf":[],"featured_image":"https:\/\/www.med.unc.edu\/genomics\/wp-content\/uploads\/sites\/708\/2025\/02\/T7-promo.jpg","featured_image_medium":"https:\/\/www.med.unc.edu\/genomics\/wp-content\/uploads\/sites\/708\/2025\/02\/T7-promo-300x170.jpg","featured_image_medium_large":"https:\/\/www.med.unc.edu\/genomics\/wp-content\/uploads\/sites\/708\/2025\/02\/T7-promo-768x435.jpg","featured_image_large":"https:\/\/www.med.unc.edu\/genomics\/wp-content\/uploads\/sites\/708\/2025\/02\/T7-promo-1024x581.jpg","featured_image_thumbnail":"https:\/\/www.med.unc.edu\/genomics\/wp-content\/uploads\/sites\/708\/2025\/02\/T7-promo-150x150.jpg","featured_image_alt":"","category_details":[{"name":"Director Spotlight","link":"https:\/\/www.med.unc.edu\/genomics\/category\/director-spotlight\/"},{"name":"News","link":"https:\/\/www.med.unc.edu\/genomics\/category\/news\/"},{"name":"What's New","link":"https:\/\/www.med.unc.edu\/genomics\/category\/whats-new\/"}],"tag_details":[],"_links_to":[],"_links_to_target":[],"_links":{"self":[{"href":"https:\/\/www.med.unc.edu\/genomics\/wp-json\/wp\/v2\/posts\/4258","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.med.unc.edu\/genomics\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.med.unc.edu\/genomics\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.med.unc.edu\/genomics\/wp-json\/wp\/v2\/users\/117519"}],"replies":[{"embeddable":true,"href":"https:\/\/www.med.unc.edu\/genomics\/wp-json\/wp\/v2\/comments?post=4258"}],"version-history":[{"count":3,"href":"https:\/\/www.med.unc.edu\/genomics\/wp-json\/wp\/v2\/posts\/4258\/revisions"}],"predecessor-version":[{"id":4262,"href":"https:\/\/www.med.unc.edu\/genomics\/wp-json\/wp\/v2\/posts\/4258\/revisions\/4262"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.med.unc.edu\/genomics\/wp-json\/wp\/v2\/media\/4259"}],"wp:attachment":[{"href":"https:\/\/www.med.unc.edu\/genomics\/wp-json\/wp\/v2\/media?parent=4258"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.med.unc.edu\/genomics\/wp-json\/wp\/v2\/categories?post=4258"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.med.unc.edu\/genomics\/wp-json\/wp\/v2\/tags?post=4258"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}