{"id":5801,"date":"2019-01-11T07:25:54","date_gmt":"2019-01-11T06:25:54","guid":{"rendered":"https:\/\/kreftgenomikk.no\/?p=5801"},"modified":"2020-08-10T14:24:24","modified_gmt":"2020-08-10T13:24:24","slug":"vilkar-for-bruk-av-1000genomes-no","status":"publish","type":"post","link":"https:\/\/kreftgenomikk.w.uib.no\/no\/vilkar-for-bruk-av-1000genomes-no\/","title":{"rendered":"Vilk\u00e5r for bruk av 1000genomes.no"},"content":{"rendered":"<p>[et_pb_section admin_label=&raquo;Seksjon&raquo; fullwidth=&raquo;on&raquo; specialty=&raquo;off&raquo;][et_pb_fullwidth_post_title admin_label=&raquo;Fullbreddes innleggstittel&raquo; title=&raquo;on&raquo; meta=&raquo;off&raquo; author=&raquo;on&raquo; date=&raquo;on&raquo; categories=&raquo;on&raquo; comments=&raquo;on&raquo; featured_image=&raquo;on&raquo; featured_placement=&raquo;background&raquo; parallax_effect=&raquo;off&raquo; parallax_method=&raquo;on&raquo; text_orientation=&raquo;right&raquo; text_color=&raquo;light&raquo; text_background=&raquo;on&raquo; text_bg_color=&raquo;rgba(21,150,137,0.9)&raquo; module_bg_color=&raquo;rgba(255,255,255,0)&raquo; title_font=&raquo;|on|||&raquo; title_font_size=&raquo;35px&raquo; title_all_caps=&raquo;off&raquo; use_border_color=&raquo;off&raquo; border_color=&raquo;#ffffff&raquo; border_style=&raquo;solid&raquo; module_id=&raquo;header-image-and-text&raquo;]<\/p>\n<p>&nbsp;<\/p>\n<p>[\/et_pb_fullwidth_post_title][\/et_pb_section][et_pb_section admin_label=&raquo;Seksjon&raquo; fullwidth=&raquo;off&raquo; specialty=&raquo;off&raquo;][et_pb_row admin_label=&raquo;Rad&raquo;][et_pb_column type=&raquo;2_3&#8243;][et_pb_text admin_label=&raquo;Tekst&raquo; background_layout=&raquo;light&raquo; text_orientation=&raquo;left&raquo; use_border_color=&raquo;off&raquo; border_color=&raquo;#ffffff&raquo; border_style=&raquo;solid&raquo;]<\/p>\n<p>Ved \u00e5 trykke p\u00e5 OK-knappen aksepterer du v\u00e5re vilk\u00e5r for bruk av variantdatabasen.<\/p>\n<p>Databasen er laget for \u00e5 bidra til utredning av pasienter med mistenkt arvelig sykdom eller filtrering av antatt normale men uvanlige varianter fra forskningsdata.<\/p>\n<p>Det er ikke tillatt \u00e5 bruke dataene for \u00e5 identifisere pasienter i v\u00e5re forskningsstudier. &nbsp;&nbsp;<a href=\"https:\/\/invivo.hpc.uio.no\/vcf-miner\/\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-5823 alignright\" src=\"https:\/\/kreftgenomikk.no\/files\/2019\/01\/okknapp.gif\" alt=\"\" width=\"114\" height=\"46\"><\/a><\/p>\n<p>[\/et_pb_text][\/et_pb_column][et_pb_column type=&raquo;1_3&#8243;][et_pb_sidebar admin_label=&raquo;Nyhetsarkiv og konferanser&raquo; orientation=&raquo;left&raquo; area=&raquo;primary&raquo; background_layout=&raquo;light&raquo; remove_border=&raquo;off&raquo;]<\/p>\n<p>&nbsp;<\/p>\n<p>[\/et_pb_sidebar][\/et_pb_column][\/et_pb_row][\/et_pb_section]<\/p>","protected":false},"excerpt":{"rendered":"<p>[et_pb_section admin_label=&raquo;Seksjon&raquo; fullwidth=&raquo;on&raquo; specialty=&raquo;off&raquo;][et_pb_fullwidth_post_title admin_label=&raquo;Fullbreddes innleggstittel&raquo; title=&raquo;on&raquo; meta=&raquo;off&raquo; author=&raquo;on&raquo; date=&raquo;on&raquo;&#46;&#46;&#46;<\/p>\n","protected":false},"author":3681,"featured_media":5894,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[],"class_list":["post-5801","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-uncategorized"],"_links":{"self":[{"href":"https:\/\/kreftgenomikk.w.uib.no\/no\/wp-json\/wp\/v2\/posts\/5801","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/kreftgenomikk.w.uib.no\/no\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/kreftgenomikk.w.uib.no\/no\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/kreftgenomikk.w.uib.no\/no\/wp-json\/wp\/v2\/users\/3681"}],"replies":[{"embeddable":true,"href":"https:\/\/kreftgenomikk.w.uib.no\/no\/wp-json\/wp\/v2\/comments?post=5801"}],"version-history":[{"count":10,"href":"https:\/\/kreftgenomikk.w.uib.no\/no\/wp-json\/wp\/v2\/posts\/5801\/revisions"}],"predecessor-version":[{"id":5969,"href":"https:\/\/kreftgenomikk.w.uib.no\/no\/wp-json\/wp\/v2\/posts\/5801\/revisions\/5969"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/kreftgenomikk.w.uib.no\/no\/wp-json\/wp\/v2\/media\/5894"}],"wp:attachment":[{"href":"https:\/\/kreftgenomikk.w.uib.no\/no\/wp-json\/wp\/v2\/media?parent=5801"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/kreftgenomikk.w.uib.no\/no\/wp-json\/wp\/v2\/categories?post=5801"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/kreftgenomikk.w.uib.no\/no\/wp-json\/wp\/v2\/tags?post=5801"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}