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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.

March 29th, 2017 - March 31st, 2017 | Bochum, Germany | 28th Annual Meeting of the German Society for Human Genetics (GfH2017)

Multiplicom...

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

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OUR PRODUCTS

News & Press

March 21st, 2017

Opening New Customer Service Lab

Last week, we opened up our new Customer Service Lab at our Niel Office. This lab will be used for hosting our Clarigo & MASTR workshops but also for trainings and testing for customer libraries.This new lab complements both the current technical wet-lab support offered on-site by the Field Application Specialist and the proof-of-principle and servicing offered by our MASTR Facility.

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March 6th, 2017

Publication - Tumor Biology: Deep sequencing of the TP53 gene reveals a potential risk allele for non–small cell lung cancer and supports the negative prognostic value of TP53 variants

The TP53 gene remains the most frequently altered gene in human cancer, of which variants are associated with cancer risk, therapy resistance, and poor prognosis in several tumor types. To determine the true prognostic value of TP53 variants in non–small cell lung cancer, this study conducted further research, particularly focusing on subtype and tumor stage.

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February 27th, 2017

Breast Cancer solutions for Next-Generation Sequencing during Tri-Con 2017

We were happy to receive so many people at our booth during the Molecular Med Tri-Con from 20-24 February 2017 in San Francisco. During the Tri-con, we introduced our Breast Cancer solutions for Next-Generation Sequencing and gave visitors a preview of our new MASTR Reporter. As the European market leader in BRCA testing, we build on our expertise to develop other NGS amplicon-based, molecular assays for oncology in order to find all mutations.

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February 20th, 2017

Somatic Mosaicism in Genodermatoses at BeSHG 2017

On February 17, 2017, we welcomed many people at our booth during the annual BeSHG meeting in Louvain-La-Neuve, Belgium. This year’s theme was ‘Human Genetics goes Somatic’. During our sponsored presentation, Hilde Brems from the Center of Human Genetics at KU Leuven talked about ‘Somatic Mosaicism in Genodermatoses’.

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February 2nd, 2017

IOVS - Mutation Spectrum of the ABCA4 Gene in 335 Stargardt Disease Patients From a Multicenter German Cohort— Impact of Selected Deep Intronic Variants and Common SNPs

Heidi L.

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January 31st, 2017

Agilent Technologies completed its acquisition of Multiplicom

On January 20th, 2017, Agilent Technologies completed its acquisition of Multiplicom. As you are a valued Multiplicom customer, we want to take this opportunity to welcome you to Agilent and let you know that we are committed to your business. We look forward to continuing this important relationship.

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January 30th, 2017

European Urology - Comprehensive Profiling of the Androgen Receptor in Liquid Biopsies from Castration-resistant Prostate Cancer Reveals Novel Intra-AR Structural Variation and Splice Variant Expression Patterns

Bram De Laerea, 

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January 3rd, 2017

Discontinuation 454 MID kits RUO & CE-IVD

We would like to inform you that we are discontinuing the 454 MID Dx (product codes ML-2008.192, ML-2116.192 and ML-2124.192) as well as the 454 MID RUO (product codes ML-0008.192, ML-0116.192 and ML-0124.192), as Roche is no longer supporting the 454 sequencing platforms.We apologize for any inconvenience this may cause.Please contact your sales representative for further details.Click here to go to our product page.

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January 2nd, 2017

Publication: BMC Cancer - The effect of a germline mutation in the APC gene on β-catenin in human embryonic stem cells

Most cases of colorectal cancer (CRC) are initiated by inactivation mutations in the APC gene, which is a negative regulator of the Wnt-β-catenin pathway. Patients with familial adenomatous polyposis (FAP) inherit a germline mutation in one APC allele, and loss of the second allele leads to the development of polyps that will turn malignant if not removed. It is not fully understood which molecular mechanisms are activated by APC loss and when the loss of the second APC allele occurs.

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Events

March 29th, 2017 - March 31st, 2017 | Bochum, Germany

28th Annual Meeting of the German Society for Human Genetics (GfH2017)

Multiplicom is hoping to see you during the 28th Annual Meeting of the German Society for Human Genetics from 29-31 March 2017 in Bochum, Germany. Join our technical workshop or come and visit our local representatives at our booth. We will be sharing our latest solutions and services in the field of human genetics and Next-Generation Sequencing.

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March 31st, 2017 - April 2nd, 2017 | Melbourne, Australia

ASDG - Australasian Society of Diagnostic Genomics Conference

Multiplicom is a proud silver sponsor of the ASDG conference from 31 March until 2 April 2017 in Melbourne, Australia. The theme for the meeting is ‘Evolving problems, new solutions’. During this meeting, experts will look at how new technologies are being applied to existing genetic problems – which continue to evolve as people get more information from new technologies.Come to our booth n° 15 and discover our molecular diagnostic solutions for Next-generation sequencing!For more info on ASDG, click here.

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April 1st, 2017 - April 5th, 2017 | Washington, USA

AACR Annual Meeting 2017

Don’t hesitate to come by our booth n° 2949 during the AACR Annual meeting 2017 in Washington from 1-5 April 2017! The AACR Annual Meeting highlights the best cancer science and medicine from institutions all over the world. Attendees are invited to stretch their boundaries, form collaborations, attend sessions outside their own areas of expertise, and learn how to apply exciting new concepts, tools, and techniques to their own research.

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April 3rd, 2017 - April 5th, 2017 | Berlin, Germany

AMP 2017 Global Congress on Molecular Pathology

Interested in hearing more on diagnostic technologies and clinical applications in the field of molecular Pathology? Then please, don’t hesitate to visit us at our booth n° 7 during the AMP Global Congress on Molecular Pathology from 3-5 April 2017 in Berlin.

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April 19th, 2017 - April 21st, 2017 | Niel, Belgium

MASTR Workshop April

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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May 16th, 2017 - May 19th, 2017 | Niel, Belgium

Clarigo Workshop May

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

European Society of Human Genetics conference 2017 (ESHG)

Multiplicom welcomes you to the 50th Anniversary of the ESHG Conference. This year, you can find us at booth n° 662 from 27 – 30 May 2017. We will also be presenting our newest products and services during our satellite symposium on Sunday, 28 May from 15-16:30.

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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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