"Thanks to new Multiplicom test kits physicians are able to identify all the genetic mutations of a condition at once, and use this information to initiate the right - personalized - treatment.”
European Society of Human Genetics conference 2017 (ESHG)
Multiplicom, part of Agilent Technologies, provides your lab with a broad range of Next-Generation Sequencing solutions, which guide you towards the most reliable results. During our Symposium on Sunday, 28 May from 3.00-4.30 PM, we will be talking about how we make a difference in genetic diagnostics. One of our key speakers is Orlando Diez from Vall D’Hebron University Hospital. He will explain the diverse spectrum of causal mutations in hereditary cancer families and show some remarkable results. Furthermore, Katrien De Mulder from the Sint-Lucas will elaborate on how their lab has implemented NIPT via the Clarigo solutions in their workflow. Last but not least we will be talking about how our new Reporter software ensures the correct analysis and enables quality control from sample to results. Come to our booth no. 662 for a demonstration of our new software and discover how we guide your lab towards better results. Every step of the way.
- BRCA MASTR Dx and MASTR Reporter: a tester experience)
- Diverse spectrum of causal mutations in hereditary cancer families
Dr. Orland Diez – Val d’Hebron, Institute of Oncology, Barcelona, Spain
- Clarigo: a decentralized NIPT solution
Dr. Katrien De Mulder – General hospital Sint-Lucas, Ghent, Belgium
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.
Click here for more information on the ESHG 2017.