About European Society of Human Genetics: ESHG is a non-profit organization. Its aims are to promote research in basic and applied human and medical genetics, to ensure high standards in clinical practice and to facilitate contacts between all persons who share these aims, particularly those working in Europe. The Society will encourage and seek to integrate research and its translation into clinical benefits and professional and public education in all areas of human genetics.
May 27-30, 2017
Roche Booth #430
You are invited! Cell-free DNA Testing Symposium
Join us to hear experts in cell-free DNA testing present the latest data and describe real-world experience with NIPT in their laboratory. Seats available on a first come first serve basis.
Date: Sunday, May 28th 2017, 15:00 – 16:30, refreshments will be served
Room: BALLERUP, Bella Center Blvd 5, 2300 Copenhagen, Denmark
Live Stream: Watch the Cell-Free DNA Testing Symposium online
Francesca Grati, PhD, ErCLG,
Toma Advanced Biomedical Assays S.p.A., Busto Arsizio, Italy
Experiences with laboratory implementation of a microarray based cell-free DNA testing system
|Junaid Shabbeer, PhD, FACMG,
Roche Sequencing Solutions, San Jose, USA
Non-invasive prenatal testing (NIPT) with different cell-free DNA testing technologies
|Maria Del Mar Gil, MD, PhD,
Hospital Universitario de Torrejón, Madrid, Spain
Cell-free DNA screening for aneuploidy in clinical practice - results of an updated meta-analysis
Roche Booth #430
Come by and check out our product portfolio and help us support The Danish Cancer Society.
Learn more about our Sample Prep and NIPT products:
|SeqCap® EZ Inherited Disease Panel (IDP) design*– Roche is making it simple to access pre designed NGS panels from researchers around the world. An example is our new IDP design covering 4100 genes and regions associated with inherited diseases. It requires just 100 ng of gDNA and yields >98% coverage at 20x depth with only 15M reads|
|KAPA RNA HyperPrep Kits* – Roche is bringing more streamlined solutions that reduce hands-on and overall time for NGS library construction. Our new KAPA RNA HyperPrep Kit enables single-day library construction, inclusive of rRNA depletion and has high success rates with lower input and degraded samples, such as FFPE|
|NEW! KAPA Dual-Indexed Adapters*, with Illumina TruSeq HT design, are ready to use, automation friendly, QC tested and provide a complete library preparation solution
*For Research Use Only. Not for use in diagnostic procedures.
|Harmony® IVD Kit CE*– the global leading NIPT brand1 with over one million tests performed worldwide – for testing for trisomies 21, 18, 13, fetal sex, monosomy X and sex chromosome aneuploidies|
|Offerings for laboratories - AcfS system with Harmony IVD Kit CE*, CLIA Test Send Out and Send Out services provided by Roche partners|
*Available outside of the US
- More than 1,000,000 Harmony prenatal tests performed and available in more than 100 countries and territories worldwide. Data on file.
SEQCAP and KAPA are trademarks of Roche. HARMONY and HARMONY and Design are trademarks of Ariosa Diagnostics, Inc. in the US. HARMONY is a trademark of Roche in other countries. All other trademarks are the property of their respective owners.
Harmony Prental Test is a non-invasive prenatal test (NIPT) based on cell-free DNA analysis and is considered a prenatal screening test, not a diagnostic test. Harmony Prenatal Test does not screen for potential chromosomal or genetic conditions other than those expressly identified in this document. Before making any treatment decisions, all women should discuss their results with their healthcare provider, who can recommend confirmatory, diagnostic testing where appropriate. The Ariosa cell-free DNA System (AcfS) is only available outside of the US. AcfS is designed for use with DANSR, FORTE, and the Harmony Kit. The Harmony IVD Kit is CE Marked under the IVD Directive 98/79/EC. This material is intended for regions outside of the United States which recognize the CE Mark.