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We make targeted investments in highly qualified people to maintain a strong focus on innovation and development.

We believe that molecular diagnostic kits are essential to providing everyone with access to effective, affordable and personalized medicine.

September 13th, 2016 - September 16th, 2016 | Belgium | Full - Clarigo workshop September


believes that molecular diagnostic kits are essential to providing everyone with access to effective, affordable and personalized medicine.



News & Press

August 22nd, 2016

European Journal of Human Genetics: New challenges for BRCA testing: a view from the diagnostic laboratory

Many diagnostic laboratories are adopting next-generation sequencing (NGS) technology to increase their screening capacity and reduce processing time and unit costs. However, migration to NGS introduces complexities arising from choice of components of the BRCA testing workflow, such as NGS platform, enrichment method and bioinformatics analysis process. An efficient, cost-effective accurate mutation detection strategy and a standardised, systematic approach to the reporting of BRCA test results is imperative for diagnostic laboratories.

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August 17th, 2016

Research article: Analysis of Founder Mutations in Rare Tumors Associated With Hereditary Breast/ Ovarian Cancer Reveals a Novel Association of BRCA2 Mutations with Ampulla of Vater Carcinomas

A total of 102 male breast, 68 pancreatic and 33 peritoneal/fallopian tube carcinoma cases were included in the study. The BRCA2 c.156_157insAlu mutation was observed with a frequency of 7.8% in male breast cancers, 3.0% in peritoneal/fallopian tube cancers, and 1.6% in pancreatic cancers, with estimated total contributions of germline BRCA2 mutations of 14.3%, 5.5%, and 2.8%, respectively. No carriers of the BRCA1 c.3331_3334del mutation were identified.

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August 15th, 2016

AACR Publications: Validation of a MEK/MET-specific NGS panel for early phase trial interrogation

After combining well-established quality metrics to cover pre-analytical aspects with suitable technologies such as the MiSeq platform (Illumina) and appropriate bioinformatics, we recognize that this MEK/MET-specific NGS panel is fit for purpose.

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August 11th, 2016

Biovox - How to invest in Biotech - Rudi Mariën

"The current biotech landscape is full of interesting companies with a lot of potential. A great example is Multiplicom. They are doing a really good job with their genetic testing kits; they developed a BRCA test for detecting breast cancer – 1 in 2 labs uses their kits – and they just launched their line of NIPT prenatal tests. There's a good team in charge and the company has products on the market. This is an excellent position for a company to be in!"(...)

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August 10th, 2016

New job vacancies online

Multiplicom is hiring! At the moment, we are actively seeking to fill the positions below. We are fast-growing biotech company, so check our careers page on a regulary basis for new job openings.

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August 8th, 2016

AACR Publications: Highly sensitive and cost-effective detection of somatic cancer variants using single-molecule, real-time sequencing

Single Molecule, Real-Time (SMRT®) Sequencing offers several advantages, including the ability to sequence single molecules with very high accuracy (>QV40) using the circular consensus sequencing (CCS) approach. The availability of genetically defined, human genomic reference standards provides an industry standard for the development and quality control of molecular assays for studying cancer variants.

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August 6th, 2016

Swiss Medical Weekly: Identification and molecular characterisation of Lausanne Institutional Biobank participants with familial hypercholesterolaemia – a proof-of-concept study

METHODS: Familial hypercholesterolaemia was used as a model of a relatively common yet often underdiagnosed and inadequately treated Mendelian disease. Clinical and laboratory information was extracted from electronic hospital records.

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August 4th, 2016

Multiplicom N.V. reinforces its sales team in Benelux & Switzerland

Peter Van Hauwe is our new Sales Manager Benelux and Switzerland. He will be responsible for developing and maintaining direct sales in Belgium, the Netherlands, Luxembourg and Switzerland. Peter has over nine years of experience in the molecular diagnostic field and will work closely with Mira Van de Velde. Meet our sales team in person!

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July 27th, 2016

Canadian Journal of Diabetes: Searching for Maturity-Onset Diabetes of the Young (MODY): When and What for?

Maturity-onset diabetes of the young (MODY) is a group of monogenic diseases that results in primary defects in insulin secretion and dominantly inherited forms of nonautoimmune diabetes. Although many genes may be associated with monogenic diabetes, heterozygous mutations in 6 of them are responsible for the majority of cases of MODY.

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September 13th, 2016 - September 16th, 2016 | Belgium

Full - Clarigo workshop September

The workshop will span 4 days (Tuesday 2PM - Friday 2PM). Participants are offered the opportunity to send 1 or 2 non-hazardous/non-infectious blood samples collected in STRECK tubes to be processed during the workshop.If you would like to participate in one of our Clarigo workshops please click here to subscribe and you will be contacted by one of our Customer Service team members.

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September 19th, 2016 - September 21st, 2016 | Montpellier, France

The 24th a symposium ATC (association des Techniciens en cytogénétique) and the 23rd Symposium ACLF (Association des Cytogénéticiens de langue francaise)

This biannual congress attracts up to 400 cytogeneticists. This year’s topic relates to the basic issues and practices regarding chromosomes and pathology.Click here to see the full programme.Don’t hesitate to contact our local representative Hanaa Aissaoui for an appointment.  

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September 22nd, 2016 - September 23rd, 2016 | London , UK

BSGM Annual meeting 2016

The BSGM, organized by the British Society for Genetic Medicine, focusses on UK Clinical Genomic strategy together with high quality chosen abstracts and invites speakers of international reputations.

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September 22nd, 2016 - September 24th, 2016 | Barcelona, Spain

The 2nd World Congress on Controversies in Preconception, Preimplantation and Prenatal Genetic Diagnosis

Multiplicom is happy to welcome you to the 2nd World Congress on Controversies in Preconception, Preimplantation and Prenatal Genetic Diagnosis from 22– 24 September 2016 in Barcelona, Spain. How will genetics technology drive the future? Find out at our booth n°2, or come to our abstract presentation on Saturday 24 September at 14:00.

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September 23rd, 2016 - September 24th, 2016 | London, UK

Molecular Analysis for Personalised Therapy (MAP)

This conference, a joint initiative of Cancer Research UK, UNICANCER and ESMO, will explore clinical interpretation of molecular tests for metastatic cancers. The development of new biotechnologies has revolutionized the applications of personalized therapy in metastatic cancer. It is now possible to perform multigene sequencing for cancer patients, either in clinical trials, or in routine use. For more information on MAP, click here. 

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September 25th, 2016 - September 29th, 2016 | Cologne, Germany

XXXI International Congress of the International Academy of Pathology and the 28th Congress of the European Society of Pathology

The XXXI International Congress of the International Academy of Pathology and the 28th Congress of the European Society of Pathology will for the first time be organized as a joint venture. The motto of the Congress – Predictive Pathology, Guiding and Monitoring Therapy – indicates the future role of pathology as a strong partner for the different clinical specialties. The scientific programme will include science, translational research and clinical application to provide delegates with information on recent research findings, new technologies and up to date education.

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October 7th, 2016 - October 9th, 2016 | Berlin, Germany

16. Bundeskongress Pathologie

This conference, organized by the Bundesverband Deutscher Pathologen (BVDP) and the DVTA brings German pathologists, biologists, technicians and analysts together. This year’s congress treats the future of pathology and gives practical examples.Visit the website for the full programme.    

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October 7th, 2016 - October 11th, 2016 | Copenhagen, Denmark

ESMO 2016 Congress – from disease treatment to patient care

Don’t hesitate to visit our poster number 1174P on NRAS, KRAS and BRAF mutations in FFPE derived DNA or to contact us for further questions or explanation.

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October 11th, 2016 - October 14th, 2016 | Belgium

Clarigo workshop October

Multiplicom organizes workshops to help diagnostic centers implement Clarigo efficiently in their own laboratory facilities. The Clarigo workshop is intended to provide hands-on lab training of the complete Clarigo workflow and is therefore of particular interest to the person in charge of practical implementation or lab technicians. The workshop will span 4 days (Tuesday 2PM - Friday 2PM).

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