{"id":489,"date":"2024-04-25T20:26:15","date_gmt":"2024-04-25T20:26:15","guid":{"rendered":"https:\/\/winterdev.cc\/nwgc-dev\/?page_id=489"},"modified":"2024-04-25T20:26:15","modified_gmt":"2024-04-25T20:26:15","slug":"sample-requirements","status":"publish","type":"page","link":"https:\/\/nwgc.gs.washington.edu\/wordpress\/services\/genotyping\/sample-requirements\/","title":{"rendered":"Genotyping Arrays"},"content":{"rendered":"<h3 class=\"wp-block-heading\">Infinium:<\/h3>\n<p>Illumina microarray kits offer a variety of targeted content and genomic coverage to enable identification of a variety of disease-specific and population-specific targets. This allows for expanded genomic coverage for genome-wide association studies, identification of specific sets of targeted SNPs, and methylation profiling. Some of the more common array kits include:<\/p>\n<ul class=\"wp-block-list\">\n<li><a href=\"https:\/\/www.illumina.com\/content\/dam\/illumina-marketing\/documents\/products\/datasheets\/infinium-global-screening-array-data-sheet-370-2016-016.pdf\"><strong>Global Screening Array<\/strong><\/a><\/li>\n<li><a href=\"https:\/\/www.illumina.com\/content\/dam\/illumina-marketing\/documents\/products\/datasheets\/infinium-global-diversity-array-data-sheet-370-2019-003.pdf\"><strong>Global Diversity Array<\/strong><\/a><\/li>\n<li><a href=\"https:\/\/www.illumina.com\/documents\/products\/product_information_sheets\/product_info_humanomniexpress.pdf\"><strong>Human OmniExpress<\/strong><\/a><\/li>\n<li><a href=\"https:\/\/www.illumina.com\/content\/dam\/illumina-marketing\/documents\/products\/datasheets\/datasheet_human_omni2.5.pdf\"><strong>Human Omni 2.5<\/strong><\/a><\/li>\n<li><a href=\"https:\/\/www.illumina.com\/content\/dam\/illumina-marketing\/documents\/products\/datasheets\/datasheet-human-omni-express-exome.pdf\"><strong>Human OmniExpress + Exome<\/strong><\/a><\/li>\n<\/ul>\n<p>For a full list of available Infinium Microarrays, please visit the Illumina <a href=\"http:\/\/www.illumina.com\/techniques\/microarrays.html\">website<\/a>.<\/p>\n<h3 class=\"wp-block-heading\">Methylation:<\/h3>\n<p>The Illumina Infinium MethylationEPIC kit offers the ability to detect 850,000 methylation sites quantitatively across the genome at single-nucleotide resolution. This high throughput assay enables genome-wide coverage of CpG sites, differentially methylated sites, enhancers, promoters and genes, suitable for epigenome-wide association studies. We use the Illumina-recommended ZYMO Research EZ-96 DNA Methylation kit to perform bisulfite conversion prior to the Infinium assay.<\/p>\n<p>For more information on this array kit, please visit the Illumina <a href=\"https:\/\/www.illumina.com\/products\/by-type\/microarray-kits\/infinium-methylation-epic.html\">website<\/a>.<\/p>\n<h3 class=\"wp-block-heading\">OpenArray:<\/h3>\n<p>TaqMan OpenArray gene expression assays are performed using the Thermo Fisher QuantStudio 12k Flex rt-PCR with the AccuFill System. Thermo Fisher has 4.5 million pre-designed genotyping assays to choose from, with the flexibility to create custom OpenArray plates, designed to fit your project needs.<\/p>\n<p>For a full description of the Thermo Fisher OpenArray technologies, please visit the Thermo <a href=\"https:\/\/www.thermofisher.com\/us\/en\/home\/life-science\/pcr\/real-time-pcr\/real-time-openarray.html\">website<\/a>.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Infinium: Illumina microarray kits offer a variety of targeted content and genomic coverage to enable identification of a variety of disease-specific and population-specific targets. This allows for expanded genomic coverage for genome-wide association studies, identification of specific sets of targeted SNPs, and methylation profiling. Some of the more common array kits include: For a full list of available Infinium Microarrays, please visit the Illumina website. Methylation: The Illumina Infinium MethylationEPIC kit offers the ability to detect 850,000 methylation sites quantitatively&#8230;<\/p>\n<div><a class=\"more-link\" href=\"https:\/\/nwgc.gs.washington.edu\/wordpress\/services\/genotyping\/sample-requirements\/\">Continue reading <span class=\"screen-reader-text\">Genotyping Arrays<\/span><\/a><\/div>\n","protected":false},"author":2,"featured_media":0,"parent":483,"menu_order":2,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-489","page","type-page","status-publish","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/nwgc.gs.washington.edu\/wordpress\/wp-json\/wp\/v2\/pages\/489","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/nwgc.gs.washington.edu\/wordpress\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/nwgc.gs.washington.edu\/wordpress\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/nwgc.gs.washington.edu\/wordpress\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/nwgc.gs.washington.edu\/wordpress\/wp-json\/wp\/v2\/comments?post=489"}],"version-history":[{"count":0,"href":"https:\/\/nwgc.gs.washington.edu\/wordpress\/wp-json\/wp\/v2\/pages\/489\/revisions"}],"up":[{"embeddable":true,"href":"https:\/\/nwgc.gs.washington.edu\/wordpress\/wp-json\/wp\/v2\/pages\/483"}],"wp:attachment":[{"href":"https:\/\/nwgc.gs.washington.edu\/wordpress\/wp-json\/wp\/v2\/media?parent=489"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}