{"id":19230,"date":"2021-03-23T16:41:09","date_gmt":"2021-03-23T15:41:09","guid":{"rendered":"https:\/\/www.hollandbio.nl\/?p=19230"},"modified":"2021-03-26T10:52:44","modified_gmt":"2021-03-26T09:52:44","slug":"whole-genome-sequencing-nog-niet-goedkoper-wel-minder-complex","status":"publish","type":"post","link":"https:\/\/www.hollandbio.nl\/en\/nieuws\/whole-genome-sequencing-nog-niet-goedkoper-wel-minder-complex\/","title":{"rendered":"Whole genome sequencing: nog niet goedkoper, wel minder complex"},"content":{"rendered":"\n<p class=\"wp-block-paragraph\">Wanneer je ziek bent wil je maar \u00e9\u00e9n ding, beter worden. Om de juiste diagnose te stellen, het verloop van de ziekte te voorspellen en een passende behandeling te kiezen zijn biomarkers van groot belang. Er zijn verschillende technieken en platforms beschikbaar voor het testen van biomarkers. En het test-arsenaal breidt zich uit door de komst van innovatieve technologie\u00ebn, zoals whole genome sequencing (WGS). Maar wanneer gebruik je nou welke moleculair diagnostische test? Een lastige vraag waar vele partijen zich momenteel over buigen, waaronder het <a href=\"https:\/\/www.zorginstituutnederland.nl\/werkagenda\/kanker\/advies-moleculaire-diagnostiek\"><strong>Zorginstituut<\/strong><\/a> en het <a href=\"https:\/\/www.utwente.nl\/nl\/techmed\/\"><strong>Technisch Medisch Centrum<\/strong><\/a> van de Universiteit Twente.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Aan de Universiteit van Twente brachten onderzoekers het diagnostisch testlandschap en de doorlooptijden hiervan bij pati\u00ebnten met stage IV niet-kleincellige longkanker in kaart. In <a href=\"https:\/\/www.elsevier.com\/about\/press-releases\/research-and-journals\/significant-variation-found-in-the-timing-and-selection-of-genetic-tests-for-nonsmall-cell-lung-cancer\"><strong>het onderzoek<\/strong><\/a> zijn ook de totale kosten per pati\u00ebnt voor individuele biomarker testen vergeleken met de kosten van WGS. Een voorzichtige conclusie: WGS is nog niet goedkoper, maar biedt wel kansen om de complexiteit van het testlandschap te verminderen.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">HollandBIO gelooft heilig dat brede genetische testen de toekomst zijn. We zitten midden in een biorevolutie en de kosten van DNA sequencing nemen sneller af dan de wet van Moore. Binnen \u00e9\u00e9n decennium zouden deze zelfs lager dan $100 kunnen liggen, <a href=\"ttps:\/\/www.mckinsey.com\/industries\/pharmaceuticals-and-medical-products\/our-insights\/the-bio-revolution-innovations-transforming-economies-societies-and-our-lives\"><strong>geeft McKinsey aan<\/strong><\/a>. Willen we dat een boost geven, dan is schaalgrootte d\u00e9 knop om nu aan te draaien. Nu investeren, zodat we daar straks de vruchten te plukken: bijvoorbeeld door bij de eerste diagnose gelijk het volledig tumorprofiel van pati\u00ebnten in kaart te brengen. Want waarom zouden we moeilijk doen als het ook (steeds) sneller, beter en goedkoper kan?<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Bronnen:<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><a href=\"https:\/\/www.elsevier.com\/about\/press-releases\/research-and-journals\/significant-variation-found-in-the-timing-and-selection-of-genetic-tests-for-nonsmall-cell-lung-cancer\">https:\/\/www.elsevier.com\/about\/press-releases\/research-and-journals\/significant-variation-found-in-the-timing-and-selection-of-genetic-tests-for-nonsmall-cell-lung-cancer<\/a><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><a href=\"https:\/\/www.jmdjournal.org\/article\/S1525-1578(21)00005-2\/fulltext#secsectitle0070\">https:\/\/www.jmdjournal.org\/article\/S1525-1578(21)00005-2\/fulltext#secsectitle0070<\/a><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><a href=\"https:\/\/www.mckinsey.com\/industries\/pharmaceuticals-and-medical-products\/our-insights\/the-bio-revolution-innovations-transforming-economies-societies-and-our-lives\">https:\/\/www.mckinsey.com\/industries\/pharmaceuticals-and-medical-products\/our-insights\/the-bio-revolution-innovations-transforming-economies-societies-and-our-lives<\/a><\/p>\n\n\n\n<figure class=\"wp-block-embed-wordpress wp-block-embed is-type-wp-embed is-provider-stichting-hartwig-medical-foundation\"><div class=\"wp-block-embed__wrapper\">\n<div class='avia-iframe-wrap'><blockquote class=\"wp-embedded-content\" data-secret=\"Dx1yQpuZHj\"><a href=\"https:\/\/www.hartwigmedicalfoundation.nl\/dna-test-geeft-kankerpatienten-aanvullend-perspectief\/\">DNA-test geeft kankerpati\u00ebnten aanvullend perspectief<\/a><\/blockquote><iframe loading=\"lazy\" class=\"wp-embedded-content\" sandbox=\"allow-scripts\" security=\"restricted\" style=\"position: absolute; visibility: hidden;\" title=\"\u201cDNA-test geeft kankerpati\u00ebnten aanvullend perspectief\u201d \u2014 Hartwig Medical Foundation\" src=\"https:\/\/www.hartwigmedicalfoundation.nl\/dna-test-geeft-kankerpatienten-aanvullend-perspectief\/embed\/#?secret=ls9l6zukq1#?secret=Dx1yQpuZHj\" data-secret=\"Dx1yQpuZHj\" width=\"600\" height=\"338\" frameborder=\"0\" marginwidth=\"0\" marginheight=\"0\" scrolling=\"no\"><\/iframe><\/div>\n<\/div><\/figure>\n","protected":false},"excerpt":{"rendered":"<p>Wanneer je ziek bent wil je maar \u00e9\u00e9n ding, beter worden. Om de juiste diagnose te stellen, het verloop van de ziekte te voorspellen en een passende behandeling te kiezen zijn biomarkers van groot belang. Er zijn verschillende technieken en platforms beschikbaar voor het testen van biomarkers. En het test-arsenaal breidt zich uit door de [&hellip;]<\/p>\n","protected":false},"author":16,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[59,39],"tags":[],"class_list":["post-19230","post","type-post","status-publish","format-standard","hentry","category-gezondheid-op-maat","category-gezondheid"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.0 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Whole genome sequencing: nog niet goedkoper, wel minder complex - hollandbio<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.hollandbio.nl\/en\/nieuws\/whole-genome-sequencing-nog-niet-goedkoper-wel-minder-complex\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Whole genome sequencing: nog niet goedkoper, wel minder complex - hollandbio\" \/>\n<meta property=\"og:description\" content=\"Wanneer je ziek bent wil je maar \u00e9\u00e9n ding, beter worden. Om de juiste diagnose te stellen, het verloop van de ziekte te voorspellen en een passende behandeling te kiezen zijn biomarkers van groot belang. Er zijn verschillende technieken en platforms beschikbaar voor het testen van biomarkers. 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