{"id":2268,"date":"2022-02-21T11:02:11","date_gmt":"2022-02-21T10:02:11","guid":{"rendered":"https:\/\/www.hartwigmedicalfoundation.nl\/?page_id=2268"},"modified":"2026-08-25T13:55:05","modified_gmt":"2026-08-25T11:55:05","slug":"services","status":"publish","type":"page","link":"https:\/\/www.hartwigmedicalfoundation.nl\/en\/services\/","title":{"rendered":"Services"},"content":{"rendered":"\n
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We provide three services: OncoAct, OncoAnalyserDx and Hartwig Sequencing Services.  <\/p>\n<\/div>\n<\/div>\n\n\n\n

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OncoAct<\/h2>\n\n\n\n

Cancer is caused by DNA mutations. To find these mutations, we developed OncoAct<\/a>. OncoAct is a complete DNA test that can provide physicians with additional information about clinically relevant characteristics of a tumor (biomarkers) that may also be predictive of the response to treatment.  <\/p>\n\n\n\n

Changes in the genetic profile (mutations) sometimes provide clues to a potential treatment that can directly target these mutations. This is known as targeted therapy.  <\/p>\n\n\n\n

In addition, the OncoAct report contains possible leads for trials or experimental drugs. <\/p>\n\n\n\n

We have an agreement with most hospitals to carry out OncoAct for them. Would you like to know which hospitals these are and who the contact person is within your hospital? Please email info@oncoact.nl.<\/a> <\/p>\n\n\n\n

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OncoAnalyserDx RUO<\/h2>\n\n\n\n

For Australia and Research Use Only<\/p>\n\n\n\n

Hartwig Medical Foundation has developed software tools to analyse Next Generation Sequencing (NGS) data to detect genomic events in tumors. After extensive validations and landmark publications, these open-source tools called WiGiTS have proven to deliver comprehensive molecular analyses. Collaborators at the University of Melbourne, assembled WiGiTS into a single pipeline called oncoanalyser and made it freely available to the community via nf-core<\/a>.<\/p>\n\n\n\n

Oncoanalyser is now being incorporated into a Software as a Service (SaaS) cloud-based platform called OncoAnalyserDx. OncoAnalyserDx is in development with early access testing partners and is currently Research Use Only.<\/p>\n\n\n\n

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Sequencing Services<\/h2>\n\n\n\n

We sequence and analyze DNA for research purposes.  <\/p>\n\n\n\n

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We provide three services: OncoAct, OncoAnalyserDx and Hartwig Sequencing Services.   OncoAct Cancer is caused by DNA mutations. To find these …<\/p>\n","protected":false},"author":3,"featured_media":10822,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-2268","page","type-page","status-publish","has-post-thumbnail","hentry"],"acf":[],"yoast_head":"\nServices - Hartwig Medical Foundation<\/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.hartwigmedicalfoundation.nl\/en\/services\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Services - Hartwig Medical Foundation\" \/>\n<meta property=\"og:description\" content=\"We provide three services: OncoAct, OncoAnalyserDx and Hartwig Sequencing Services.   OncoAct Cancer is caused by DNA mutations. 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