{"version":"1.0","provider_name":"High-Throughput Sequencing Facility (HTSF)","provider_url":"https:\/\/www.med.unc.edu\/genomics","author_name":"Ivy Ingle","author_url":"https:\/\/www.med.unc.edu\/genomics\/author\/mivy\/","title":"Long Read Sequencing - High-Throughput Sequencing Facility (HTSF)","type":"rich","width":600,"height":338,"html":"<blockquote class=\"wp-embedded-content\" data-secret=\"YIrBKizCQZ\"><a href=\"https:\/\/www.med.unc.edu\/genomics\/overview-of-services\/long-read-sequencing\/\">Long Read Sequencing<\/a><\/blockquote><iframe sandbox=\"allow-scripts\" security=\"restricted\" src=\"https:\/\/www.med.unc.edu\/genomics\/overview-of-services\/long-read-sequencing\/embed\/#?secret=YIrBKizCQZ\" width=\"600\" height=\"338\" title=\"&#8220;Long Read Sequencing&#8221; &#8212; High-Throughput Sequencing Facility (HTSF)\" data-secret=\"YIrBKizCQZ\" frameborder=\"0\" marginwidth=\"0\" marginheight=\"0\" scrolling=\"no\" class=\"wp-embedded-content\"><\/iframe><script type=\"text\/javascript\">\n\/* <![CDATA[ *\/\n\/*! This file is auto-generated *\/\n!function(d,l){\"use strict\";l.querySelector&&d.addEventListener&&\"undefined\"!=typeof URL&&(d.wp=d.wp||{},d.wp.receiveEmbedMessage||(d.wp.receiveEmbedMessage=function(e){var t=e.data;if((t||t.secret||t.message||t.value)&&!\/[^a-zA-Z0-9]\/.test(t.secret)){for(var s,r,n,a=l.querySelectorAll('iframe[data-secret=\"'+t.secret+'\"]'),o=l.querySelectorAll('blockquote[data-secret=\"'+t.secret+'\"]'),c=new RegExp(\"^https?:$\",\"i\"),i=0;i<o.length;i++)o[i].style.display=\"none\";for(i=0;i<a.length;i++)s=a[i],e.source===s.contentWindow&&(s.removeAttribute(\"style\"),\"height\"===t.message?(1e3<(r=parseInt(t.value,10))?r=1e3:~~r<200&&(r=200),s.height=r):\"link\"===t.message&&(r=new URL(s.getAttribute(\"src\")),n=new URL(t.value),c.test(n.protocol))&&n.host===r.host&&l.activeElement===s&&(d.top.location.href=t.value))}},d.addEventListener(\"message\",d.wp.receiveEmbedMessage,!1),l.addEventListener(\"DOMContentLoaded\",function(){for(var e,t,s=l.querySelectorAll(\"iframe.wp-embedded-content\"),r=0;r<s.length;r++)(t=(e=s[r]).getAttribute(\"data-secret\"))||(t=Math.random().toString(36).substring(2,12),e.src+=\"#?secret=\"+t,e.setAttribute(\"data-secret\",t)),e.contentWindow.postMessage({message:\"ready\",secret:t},\"*\")},!1)))}(window,document);\n\/* ]]> *\/\n<\/script>\n","description":"Currently, many existing genome assemblies were created using short-read sequencing technology. However, short-read sequencing is limited in its ability to capture large structural variation, which are vital for areas of medical research as they have been associated with several diseases such as schizophrenia and cancer. Projects that require long reads can turn to the Oxford &hellip; Read more","thumbnail_url":"https:\/\/www.med.unc.edu\/genomics\/wp-content\/uploads\/sites\/708\/2020\/08\/Lib_tara2.jpg"}