ThromboGenomics

The first comprehensive next generation sequencing
test for the diagnosis of inherited bleeding, thrombotic
and platelet disorders.

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faster & Better test

Faster, better and affordable test for the diagnosis of inherited bleeding, thrombotic and platelet disorders.

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Submit
Your samples

Screen your patient with a comprehensive DNA based test for inherited bleeding, thrombotic, coagulation and platelet disorders just by sending a blood sample and a simple form.

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Gene
Disorders list

Check here to see if your suspected gene or disorder is available.

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The test is currently supported by the Cambridge Biomedical Research Centre. Charges will be introduced during 2017.

People

Multi Disciplinary Team and Project Team

The team behind the project is composed of clinicians, clinical geneticists and bioinformaticians involved in ThromboGenomics.
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Events

July 8

ISTH 2017

8 July 2017

We will be at this event in Berlin, Germany, on July 8-13, 2017. More information here.

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ThromboGenomics in The Bulletin of The Royal College of Pathologists

The ThromboGenomics consortium describe the use of high throughput sequencing to identify rare variants in genes encoding proteins involved in disorders of haemostasis.

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June 21

ThromboGenomics in the Belgian News

21 June 2016

The Belgian newspaper De Morgen has published an article about the ThromboGenomics test (in Flamish).

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