{"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\/fr\/decipher-genome-browser\/","title":{"rendered":"D\u00e9chiffrer le navigateur du g\u00e9nome"},"content":{"rendered":"<p>M\u00e9thode d'utilisation : <\/p>\n\n\n\n<p>Dans votre rapport comparatif de matrice d\u2019hybridation g\u00e9nomique, il y aura un tableau avec les CNV identifi\u00e9es chez le patient. Dans chaque CNV, le chromosome dans lequel il se trouve sera identifi\u00e9, ainsi que la position du nucl\u00e9otide de d\u00e9part et du nucl\u00e9otide de fin (il s'agit g\u00e9n\u00e9ralement de nombres de l'ordre d'un million de paires de bases (Mb).<\/p>\n\n\n\n<p>Entrez le num\u00e9ro du chromosome, le signe :, la position de d\u00e9part, un - et la position de fin. Il n'est pas n\u00e9cessaire d'indiquer s'il s'agit d'une duplication ou d'une suppression.<\/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\/fr\/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\/fr\/wp-json\/wp\/v2\/posts\/81","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/neuropediatoolkit.org\/fr\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/neuropediatoolkit.org\/fr\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/neuropediatoolkit.org\/fr\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/neuropediatoolkit.org\/fr\/wp-json\/wp\/v2\/comments?post=81"}],"version-history":[{"count":0,"href":"https:\/\/neuropediatoolkit.org\/fr\/wp-json\/wp\/v2\/posts\/81\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/neuropediatoolkit.org\/fr\/wp-json\/wp\/v2\/media\/2359"}],"wp:attachment":[{"href":"https:\/\/neuropediatoolkit.org\/fr\/wp-json\/wp\/v2\/media?parent=81"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/neuropediatoolkit.org\/fr\/wp-json\/wp\/v2\/categories?post=81"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/neuropediatoolkit.org\/fr\/wp-json\/wp\/v2\/tags?post=81"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}