{"id":247895,"date":"2012-02-15T02:19:51","date_gmt":"2012-02-15T02:19:51","guid":{"rendered":"http:\/\/www.eugenesis.com\/trade-news-agilent-technologies-introduces-first-dna-methylation-target-enrichment-system-for-disease-research\/"},"modified":"2012-02-15T02:19:51","modified_gmt":"2012-02-15T02:19:51","slug":"trade-news-agilent-technologies-introduces-first-dna-methylation-target-enrichment-system-for-disease-research","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/dna\/trade-news-agilent-technologies-introduces-first-dna-methylation-target-enrichment-system-for-disease-research.php","title":{"rendered":"TRADE NEWS: Agilent Technologies Introduces First DNA Methylation Target-Enrichment System for Disease Research"},"content":{"rendered":"<p><p>    MARCO ISLAND, Fla.--(BUSINESS WIRE)--  <\/p>\n<p>    (AGBT) \u2013 Agilent    Technologies Inc. (NYSE:A) today expanded its    target-enrichment platform with the     SureSelect XT Human Methyl-Seq system for epigenetic    research into DNA methylation sites. It is the first    comprehensive DNA    methylation discovery system using target enrichment.    Agilent    will unveil the product at the Advances in Genome Biology and    Technology meeting here tomorrow.  <\/p>\n<p>    Agilent SureSelect XT Methyl-Seq is a unique in-solution tool    for analyzing under- and over-methylated cytosine sites on the    human genome. The assay combines SureSelect, the leading    target-enrichment platform, with bisulfite sequencing, the gold    standard for DNA methylation research and the first    comprehensive discovery system. This enables unprecedented    sequence coverage of only the most relevant regions for    epigenetic studies, including those associated with a wide    range of disorders such as cancer, imprinting disorders,    behavioral and mental disorders, and many others.  <\/p>\n<p>    \u201cDNA methylation is a key epigenetic feature,\u201d said John    Stamatoyannopoulos, director of the Northwest Reference    Epigenome Mapping Center at the University of Washington. \u201cThe    availability of a cost-effective platform that intelligently    targets millions of CpGs for bisulfite sequencing will greatly    reduce the cost and expand the scope and utility of    genome-scale DNA methylation analysis.\u201d  <\/p>\n<p>    \u201cThe kit covers all interesting methyl-cytosine sites for    cancer research in the genome at an excellent effort-to-output    ratio,\u201d said Michal-Ruth Schweider, MD, Ph.D., Max Planck    Institute for Molecular Genetics.  <\/p>\n<p>    \u201cWe\u2019re very pleased to offer this new tool to meet growing    interest from the medical research community,\u201d said Robert    Schueren, Agilent vice president and general manager, Genomics.    \u201cBecause abnormal methylation is reversible, this type of    analysis holds great promise for the discovery of therapies.\u201d  <\/p>\n<p>    Agilent SureSelect XT Methyl-Seq allows researchers to analyze    over 3.7 million individual CpG dinucleotide sequences for    their methylation state. The system targets promoters,    canonical CpG islands, and the more recently described \u201cshores\u201d    and \u201cshelves\u201d found up to 4 kilobase pairs on either side of    CpG islands. Studies have indicated that many methylation    alterations are not in promoters or CpG islands, but most are    within 2kb, the CpG island shore. The kit also targets known    differentially methylated regions.  <\/p>\n<p>    Agilent SureSelect XT Methyl-Seq delivers higher throughput and    lower costs than whole genome bisulfite sequencing. It    identifies regions that are not detected by restriction    enzyme-based or immunoprecipitation-based methods. Because this    product is a SureSelect XT offering, Agilent provides the    complete workflow solution. This includes all reagents needed    for library prep and target enrichment.  <\/p>\n<p>    For more information, visit     <a href=\"http:\/\/www.agilent.com\/genomics\/ngs\" rel=\"nofollow\">http:\/\/www.agilent.com\/genomics\/ngs<\/a>.  <\/p>\n<p>    About Agilent Technologies  <\/p>\n<p>    Agilent Technologies Inc. (NYSE:A    -     News) is the world\u2019s premier measurement company and a    technology leader in chemical analysis, life sciences,    electronics and communications. The company\u2019s 18,700 employees    serve customers in more than 100 countries. Agilent had net    revenues of $6.6 billion in fiscal 2011. Information about    Agilent is available at     <a href=\"http:\/\/www.agilent.com\" rel=\"nofollow\">http:\/\/www.agilent.com<\/a>.  <\/p>\n<p>    NOTE TO EDITORS: Further technology, corporate citizenship and    executive news is available at     <a href=\"http:\/\/www.agilent.com\/go\/news\" rel=\"nofollow\">http:\/\/www.agilent.com\/go\/news<\/a>.  <\/p>\n<\/p>\n<p>View original post here:<br \/>\n<a target=\"_blank\" href=\"http:\/\/finance.yahoo.com\/news\/trade-news-agilent-technologies-introduces-000000349.html\" title=\"TRADE NEWS: Agilent Technologies Introduces First DNA Methylation Target-Enrichment System for Disease Research\">TRADE NEWS: Agilent Technologies Introduces First DNA Methylation Target-Enrichment System for Disease Research<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> MARCO ISLAND, Fla.--(BUSINESS WIRE)-- (AGBT) \u2013 Agilent Technologies Inc. (NYSE:A) today expanded its target-enrichment platform with the SureSelect XT Human Methyl-Seq system for epigenetic research into DNA methylation sites <a href=\"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/dna\/trade-news-agilent-technologies-introduces-first-dna-methylation-target-enrichment-system-for-disease-research.php\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":57,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"limit_modified_date":"","last_modified_date":"","_lmt_disableupdate":"","_lmt_disable":"","footnotes":""},"categories":[577489],"tags":[],"class_list":["post-247895","post","type-post","status-publish","format-standard","hentry","category-dna"],"modified_by":null,"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/247895"}],"collection":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/users\/57"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/comments?post=247895"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/247895\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/media?parent=247895"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/categories?post=247895"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/tags?post=247895"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}