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Quick introduction into the practice, straightforward involvement of laboratory technicians, easy tech transfer, easy translation  

Clinical Institute of Medical Genetics, Slovenia

We have more control of the results and more interaction with clinicians who follow the patients

Vall d'Hebron Hospital - Spain

Fast, accurate, easy to use… we succeed in having good results!

Laboratory of Human Genetics – E.O. Ospedali Galliera – Italy

May 27th, 2017 - May 30th, 2017 | Copenhagen, Denmark | European Society of Human Genetics conference 2017 (ESHG)

Guiding you towards better results. Every step of the way. 

Multiplicom has been a strong and reliable player in molecular diagnostics for many years. All our products and solutions incorporate the latest medical findings on human genetics, oncology and prenatal testing and are developed and manufactured in compliance with the most stringent international quality standards. 

Here at Multiplicom, we provide your laboratory with a broad range of molecular Next-Generation Sequencing (NGS) solutions, which guide your laboratory towards the most reliable results. Our ready-to-use kits analyze the genes that matter in a simple, efficient and reliable manner. Our Reporter software ensures correct analysis and enables quality control, from sample to final result. Our Facility lab and Expert customer support team help you to set up our tests and secure your results in every step of the way.

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OUR SOLUTIONS

Testkits & Reporters

News & Press

May 23rd, 2017

Journal of Cancer - Towards Prognostic Profiling of Non-Small Cell Lung Cancer: New Perspectives on the Relevance of Polo-Like Kinase 1 Expression, the TP53 Mutation Status and Hypoxia

Currently, prognosis of non-small cell lung cancer patients is based on clinicopathological factors, including TNM stage. However, there are considerable differences in patient outcome within a similar staging group, even when patients received identical treatments. In order to improve prognostic predictions and to guide treatment options, additional parameters influencing outcome are required.

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May 22nd, 2017

Updated Instructions For Use (IFU) for Illumina Sequencing

We’ve recently updated our Instructions For Use (IFU) for Illumina for both RUO and Dx products. DxThe Dx IFUs for CE-IVD labeled applications on Illumina Sequencers have also been updated for the use with drMID Dx for Illumina NGS System kits. For the BRCA Dx assays, also guidelines for the use of MASTR Reporter are included.

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May 18th, 2017

Our career site has moved!

Multiplicom is now part of Agilent Technologies. Therefore, we’ve moved our career page to the Agilent Careers Site. Check out our job openings! Our employees are part of a rich Agilent culture that is diverse and yet shares the same Agilent values of speed, focus and accountability. 

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May 16th, 2017

Multiplicom launches complete CE-IVD solution for all BRCA testing needs

The updated BRCA MASTR Plus Dx in combination with the new MASTR Reporter is a CE-IVD-labeled molecular diagnostic solution that identifies variants in the coding regions of BRCA1 and BRCA2 genes.

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May 15th, 2017

Poster Abstract: Genetic testing of Familial Hypercholesterolemia: monogenic form and polygenic contribution to cardiovascular risk

Cascade screening of Familial Hypercholesterolemia (FH) using genetic testing has been recommended (Nordestgaard et al.) but polygenic origin could reduce the efficiency of such approach. A polyGenic Score (GeneScore) has been described helping to identify polygenic form of FH (Talmud et al.). The authors have developed a genetic test combining detection of monogenic form as well as polygenic contribution in FH and cardiovascular risk.

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May 11th, 2017

The Journal of Molecular Diagnostics: Improving Mutation Screening in Patients with Colorectal Cancer Predisposition Using Next-Generation Sequencing

Jean-Marc Rey, Vincent Ducros, 

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May 8th, 2017

Update Sequencing Calculator

Multiplicom provides your laboratory with a complete range of molecular diagnostics solutions, which guide you towards better and more reliable results. One part of our solutions are customer and quality support tools. These tools help you to set up our tests and improve your results. In order to help you calculate the number of samples per sequencing run and improve your results, we have updated our Sequencing Calculator as of 8 May 2017.

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May 2nd, 2017

MASTR Reporter launch

Multiplicom has been a strong and reliable player in molecular diagnostics for many years. We provide your laboratory with a broad range of molecular Next-Generation Sequencing solutions, which guide you towards the most reliable results. Our ready-to-use kits analyze the genes that matter in a simple, efficient and reliable manner. Our Facility lab and expert customer support team help you to set up our tests and secure your results in every step of the way.

read more

April 24th, 2017

Diabetes Journals: Diabetes, Associated Clinical Spectrum, Long-term Prognosis and Genotype/Phenotype Correlations in 201 Adult Patients With Hepatocyte Nuclear Factor 1 B (HNF1B) Molecular Defects

Abstract OBJECTIVEMolecular defects of hepatocyte nuclear factor 1B (HNF1B) are associated with a multiorgan disease, including diabetes (maturity-onset diabetes of the young 5) and kidney abnormalities. The HNF1B-syndrome is related to HNF1B mutations or to a 17q12 deletion spanning 15 genes, including HNF1B.

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Events

May 27th, 2017 - May 30th, 2017 | Copenhagen, Denmark

European Society of Human Genetics conference 2017 (ESHG)

Multiplicom, now part of Agilent Technologies, will be present at the 50th Anniversary of the European Human Genetics Conference (ESHG) 2017 from May 27 – 30 in Copenhagen, Denmark. We would like to invite to our booth no. 662 and to our symposium on Sunday, 28 May from 3.00 - 4.30 PM in room Belgrade.

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June 7th, 2017 - June 9th, 2017 | Niel, Belgium

MASTR Workshop June

The MASTR workshop is intended to provide hands-on lab training of the complete MASTR and/or MASTR Plus workflow, and is therefore of particular interest to the person in charge of practical implementation or lab technicians.

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June 7th, 2017 - June 10th, 2017 | Seville, Spain

40th European Cystic Fibrosis Conference (ECFS 2017)

Come by our booth during the ECFS 2017 from 7-10 June 2017 in sunny Seville, Spain. We will be talking about our molecular diagnostic solutions to identify sequence variants covering the complete CFTR gene in individuals with increased risk. The conference is organized by ECFS, the European Cystic Fibrosis Society.

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June 13th, 2017 - June 16th, 2017 | Niel, Antwerp

Clarigo Workshop June

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.

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June 22nd, 2017 - July 24th, 2017 | Erlangen, Germany

101. Jahrestagung der Deutschen Gesellschaft für Pathologie e.V. 2017 (DGP)

Come and visit our local representatives during the DGP meeting from 22 – 24 June 2017 in Erlangen, Germany. Check out our newest pathology solutions at our booth. The theme of this year’s meeting is Pathology: ‘innovation and cooperation’. 

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June 29th, 2017 - July 1st, 2017 | Berlin, Germany

37. Jahrestagung der Deutschen Gesellschaft für Senologie (DGS)

Discover our total NGS solutions for pathology during the 37. Jahrestagung der Deutschen Gesellschaft für Senologie (DGS) from 29 June - 1st July 2017 in Berlin at our booth no. 52. We will be presenting a wide range of ready-to-use molecular kits and solutions for Pathology. Each of them is aimed at analyzing specific genes to reveal genetic predispositions.

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September 2nd, 2017 - September 6th, 2017 | Amsterdam, The Netherlands

29th European Congress of Pathology (ECP-ESP)

From 2 – 6 September 2017, you can find Multiplicom at the 29th European Congress of Pathology in Amsterdam, The Netherlands. Visit us at our booth to find out more on the newest pathology solutions.

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September 12th, 2017 - September 15th, 2017 | Niel, Belgium

Clarigo Workshop September

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.

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September 14th, 2017 - September 16th, 2017 | Wörthersee, Austria

Herbsttagung der Österreichischen Gesellschaft für Pathologie ÖGPath / Österreichische Abteilung der IAP

Multiplicom, now part of Agilent Technologies, is happy to welcome you during the Herbsttagung der Österreichischen Gesellschaft für Pathologie ÖGPath / Österreichische Abteilung der IAP from 14 – 16 September in Wörthersee, Austria. Discover our newest Next-Generation Sequencing solutions for Pathology or get a demo of our newest MASTR Reporter software.

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Frequently Asked Questions