{"id":81,"date":"2022-06-27T11:34:56","date_gmt":"2022-06-27T09:34:56","guid":{"rendered":"https:\/\/neuropediatoolbox.wordpress.com\/?p=81"},"modified":"2022-09-23T12:47:29","modified_gmt":"2022-09-23T12:47:29","slug":"decipher-genome-browser","status":"publish","type":"post","link":"https:\/\/neuropediatoolkit.org\/de\/decipher-genome-browser\/","title":{"rendered":"Genom-Browser entschl\u00fcsseln"},"content":{"rendered":"<p>Verwendungsmethode: <\/p>\n\n\n\n<p>In Ihrem Vergleichsbericht zum genomischen Hybridisierungsarray finden Sie eine Tabelle mit den beim Patienten identifizierten CNVs. In jedem CNV wird das Chromosom, in dem es sich befindet, sowie die Position des Startnukleotids und des Endnukleotids identifiziert (normalerweise handelt es sich dabei um Zahlen in der Gr\u00f6\u00dfenordnung von einer Million Basenpaaren (Mb).<\/p>\n\n\n\n<p>Geben Sie die Chromosomennummer, das :-Zeichen, die Startposition, ein - und die Endposition ein. Eine Angabe, ob es sich um eine Vervielf\u00e4ltigung oder L\u00f6schung handelt, ist nicht erforderlich.<\/p>\n\n\n\n<p><a href=\"https:\/\/www.deciphergenomics.org\/browser\">https:\/\/www.deciphergenomics.org\/browser<\/a><\/p>","protected":false},"excerpt":{"rendered":"<p>M\u00e9todo de utilizaci\u00f3n: En tu informe de array de hibridaci\u00f3n gen\u00f3mica comparada, existir\u00e1 una tabla con las CNV identificadas en el paciente. En cada CNV, se identificar\u00e1 el cromosoma en el que se localiza, as\u00ed como la posici\u00f3n del nucle\u00f3tido de inicio y la del nucle\u00f3tido de fin (habitualmente son n\u00fameros del \u00f3rden del mill\u00f3n &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/neuropediatoolkit.org\/de\/decipher-genome-browser\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> \u00abDecipher Genome Browser\u00bb<\/span><\/a><\/p>","protected":false},"author":1,"featured_media":2359,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_themeisle_gutenberg_block_has_review":false,"footnotes":""},"categories":[10],"tags":[],"class_list":["post-81","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-neurogenetica","entry"],"_links":{"self":[{"href":"https:\/\/neuropediatoolkit.org\/de\/wp-json\/wp\/v2\/posts\/81","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/neuropediatoolkit.org\/de\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/neuropediatoolkit.org\/de\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/neuropediatoolkit.org\/de\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/neuropediatoolkit.org\/de\/wp-json\/wp\/v2\/comments?post=81"}],"version-history":[{"count":0,"href":"https:\/\/neuropediatoolkit.org\/de\/wp-json\/wp\/v2\/posts\/81\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/neuropediatoolkit.org\/de\/wp-json\/wp\/v2\/media\/2359"}],"wp:attachment":[{"href":"https:\/\/neuropediatoolkit.org\/de\/wp-json\/wp\/v2\/media?parent=81"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/neuropediatoolkit.org\/de\/wp-json\/wp\/v2\/categories?post=81"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/neuropediatoolkit.org\/de\/wp-json\/wp\/v2\/tags?post=81"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}