{"id":31,"date":"2023-08-08T11:35:37","date_gmt":"2023-08-08T11:35:37","guid":{"rendered":"https:\/\/sites.exeter.ac.uk\/rarediseasegenomics\/?page_id=31"},"modified":"2023-09-28T16:22:00","modified_gmt":"2023-09-28T16:22:00","slug":"sequencingfacilities","status":"publish","type":"page","link":"https:\/\/sites.exeter.ac.uk\/rarediseasegenomics\/sequencingfacilities\/","title":{"rendered":"Sequencing Facilities"},"content":{"rendered":"\n<p>The <a rel=\"noreferrer noopener\" href=\"https:\/\/biosciences.exeter.ac.uk\/sequencing\/\" data-type=\"URL\" data-id=\"https:\/\/biosciences.exeter.ac.uk\/sequencing\/\" target=\"_blank\">University of Exeter Sequencing Facility<\/a> provides state-of-the-art genomics and bioinformatics analysis, specialising in providing a bespoke sequencing services to researchers in academia and industry. Equipment includes short-read (<em>Illumina<\/em>) and long-read (<em>Oxford Nanopore Technologies <\/em>and <em>PacBio<\/em>) sequencing platforms.<\/p>\n\n\n\n<p>The <a rel=\"noreferrer noopener\" href=\"https:\/\/www.exeterlaboratory.com\/genomics\/\" data-type=\"URL\" data-id=\"https:\/\/www.exeterlaboratory.com\/genomics\/\" target=\"_blank\">NHS Exeter Genomics Laboratory<\/a> delivers high quality genetic and genomic testing for both NHS and research patients by combining the innovation and academic expertise of research scientists with the rigorous quality approach required in a clinical diagnostic service. Part of the <a rel=\"noreferrer noopener\" href=\"https:\/\/www.nbt.nhs.uk\/south-west-genomic-laboratory-hub\" target=\"_blank\">South West Genomics Laboratory Hub<\/a>, we provide diagnostic sequencing in the South West region, as well as the national NHS rapid genome sequencing service for acutely unwell children with a likely monogenic disorder (<a rel=\"noreferrer noopener\" href=\"https:\/\/www.exeterlaboratory.com\/genetics\/genome-sequencing\/\" target=\"_blank\">R14 service).<\/a><\/p>\n\n\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-large is-resized\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/sites.exeter.ac.uk\/rarediseasegenomics\/wp-content\/uploads\/sites\/239\/2023\/09\/Screenshot-2023-09-25-at-10.21.38-1024x300.png\" alt=\"\" class=\"wp-image-687\" width=\"914\" height=\"268\" srcset=\"https:\/\/sites.exeter.ac.uk\/rarediseasegenomics\/wp-content\/uploads\/sites\/239\/2023\/09\/Screenshot-2023-09-25-at-10.21.38-1024x300.png 1024w, https:\/\/sites.exeter.ac.uk\/rarediseasegenomics\/wp-content\/uploads\/sites\/239\/2023\/09\/Screenshot-2023-09-25-at-10.21.38-300x88.png 300w, https:\/\/sites.exeter.ac.uk\/rarediseasegenomics\/wp-content\/uploads\/sites\/239\/2023\/09\/Screenshot-2023-09-25-at-10.21.38-768x225.png 768w, https:\/\/sites.exeter.ac.uk\/rarediseasegenomics\/wp-content\/uploads\/sites\/239\/2023\/09\/Screenshot-2023-09-25-at-10.21.38.png 1249w\" sizes=\"(max-width: 914px) 100vw, 914px\" \/><\/figure><\/div>\n\n\n<div class=\"wp-block-group\"><div class=\"wp-block-group__inner-container is-layout-constrained wp-block-group-is-layout-constrained\">\n<div class=\"wp-block-group\"><div class=\"wp-block-group__inner-container is-layout-constrained wp-block-group-is-layout-constrained\">\n<div class=\"wp-block-columns is-layout-flex wp-container-core-columns-is-layout-1 wp-block-columns-is-layout-flex\">\n<div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\"><div class=\"wp-block-image is-style-default\">\n<figure class=\"aligncenter size-large is-resized\"><a href=\"https:\/\/www.exeterlaboratory.com\/genomics\/\" target=\"_blank\" rel=\"https:\/\/www.exeterlaboratory.com\/genomics\/ noopener\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/sites.exeter.ac.uk\/rarediseasegenomics\/wp-content\/uploads\/sites\/239\/2023\/08\/nhs-lab-1024x463.png\" alt=\"\" class=\"wp-image-191\" width=\"447\" height=\"202\" srcset=\"https:\/\/sites.exeter.ac.uk\/rarediseasegenomics\/wp-content\/uploads\/sites\/239\/2023\/08\/nhs-lab-1024x463.png 1024w, https:\/\/sites.exeter.ac.uk\/rarediseasegenomics\/wp-content\/uploads\/sites\/239\/2023\/08\/nhs-lab-300x136.png 300w, https:\/\/sites.exeter.ac.uk\/rarediseasegenomics\/wp-content\/uploads\/sites\/239\/2023\/08\/nhs-lab-768x348.png 768w, https:\/\/sites.exeter.ac.uk\/rarediseasegenomics\/wp-content\/uploads\/sites\/239\/2023\/08\/nhs-lab.png 1189w\" sizes=\"(max-width: 447px) 100vw, 447px\" \/><\/a><\/figure><\/div><\/div>\n<\/div>\n<\/div><\/div>\n<\/div><\/div>\n\n\n\n<p><\/p>\n\n\n\n<p><\/p>\n","protected":false},"excerpt":{"rendered":"<p>The University of Exeter Sequencing Facility provides state-of-the-art genomics and bioinformatics analysis, specialising in providing a bespoke sequencing services to researchers in academia and industry. Equipment includes short-read (Illumina) and long-read (Oxford Nanopore Technologies and PacBio) sequencing platforms. The NHS Exeter Genomics Laboratory delivers high quality genetic and genomic testing for both NHS and research [&hellip;]<\/p>\n","protected":false},"author":937,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"page-boxed-feature-img.php","meta":{"_acf_changed":false,"footnotes":""},"categories":[],"tags":[],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v23.0 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Sequencing Facilities - Rare Disease Genomics<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/sites.exeter.ac.uk\/rarediseasegenomics\/sequencingfacilities\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Sequencing Facilities - Rare Disease Genomics\" \/>\n<meta property=\"og:description\" content=\"The University of Exeter Sequencing Facility provides state-of-the-art genomics and bioinformatics analysis, specialising in providing a bespoke sequencing services to researchers in academia and industry. 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