The European Society
of Human Genetics

Corporate Satellites

Corporate Satellites

If you would like to receive more information on organising a corporate satellite meetings at ESHG 2016, please contact:
Ms. Jantie de Roos (eshg(at)rose-international.com) at Rose INTERNATIONAL.

Saturday, May 21, 2016

Ambry Genetics

Saturday, May 21, 12.15 - 13.45 hrs, Room 129+130

A Journey into the Unknown: Exploring the Clinical Diagnostic Path from Targeted Panel to Whole Exome Sequencing

BGI

Saturday, May 21, 12.15 - 13.45 hrs, Room 120+121

Recent Advances in Next Generation Sequencing - with success stories in clinical and research applications

Personalis

Saturday, May 21, 12.15 - 13.45 hrs, Room 131

Advanced Genomic Sequencing and Analysis Platform for Cancer Research, Clinical Trials, and Immuno-oncology Applications

QIAGEN Bioinformatics

Saturday, May 21, 12.15 - 13.45 hrs, Room 132

Using next-generation sequencing bioinformatics solutions to compare exomes in rare and inherited diseases and identify the cause of the disease

Sunday, May 22, 2016

Affymetrix

Sunday, May 22, 11.15 - 12.45 hrs, Room 129+130

Find out how microarray technologies are having a profound impact on unravelling the cancer genome in both liquid and solid tumors

Cartagenia

Sunday, May 22, 11.15 - 12.45 hrs, Room 120+121

Practical experience with the OneSight platform for cfDNA analysis of aneuploidies in chromosomes 1-22
&
Whole-Exome Sequencing diagnostics for patients with intellectual disability at University Medical Center Utrecht. An efficient tiered analysis and interpretation pipeline on Cartagenia Bench Lab


QIAGEN

Sunday, May 22, 11.15 - 12.45 hrs, Room 131

Sample to Insight: the journey where information from biological samples is transformed into valuable molecular insights.Let us embark on this journey together and make improvements in life possible!  

Sophia Genetics

Sunday, May 22, 11.15 - 12.45 hrs, Room 132

 

Data Driven Medicine: Providing the best NGS-based diagnostics to your patients

Thermo Fisher Scientific

Sunday, May 22, 11.15 - 12.45 hrs, Room 212

Mutation discovery to functional understanding: genetic solutions for all

AstraZeneca

Sunday, May 22, 15.00 - 16.30 hrs, Room 212

Ovarian cancer testing: Translating molecular pathways to patient pathways

BioMarin Europe

Sunday, May 22, 15.00 - 16.30 hrs, Room 129+130

Advances in molecular diagnostics: the spotlight on Duchenne

Multiplicom

Sunday, May 22, 15.00 - 16.30 hrs, Room 131

Multiplicom MASTR™ technology: enabling NGS diagnostics for all

Thermo Fisher Scientific

Sunday, May 22, 15.00 - 16.30 hrs, Room 132

Rapid and highly efficient cell engineering via CRISPR-Cas9

Illumina

Sunday, May 22, 19.15 - 20.45 hrs, Room 212

Genomic Solutions, Transform Possibility into Progress

Monday, May 23, 2016

Agilent Technologies

Monday, May 23, 11.15 - 12.45 hrs, Room 212

Leading New Discoveries in Human Genetics

Centogene

Monday, May 23, 11.15 - 12.45 hrs, Room 129+130

CentoMD®, the largest mutation database for rare diseases  -  How to find the right answer in your patients in the era of whole exome sequencing

NanoString Technologies

Monday, May 23, 11.15 - 12.45 hrs, Room 132

3D BiologyTM:  Simultaneous Single-molecule Quantification of DNA (SNVs), mRNA, Fusion Genes and Proteins Using Molecular Barcodes

Roche Sequencing

Monday, May 23, 11.15 - 12.45 hrs, Room 120+121

Targeted gene enrichment and long-read SMRT® sequencing for clinically relevant loci

Sistemas Genomicos

Monday, May 23, 11.15 - 12.45 hrs, Room 131

New technological developments in genetic and genomic studies

Canon BioMedical

Monday, May 23, 15.00 - 16.30 hrs, Room 131

Revealing New Genotyping Solutions

Integrated DNA Technologies

Monday, May 23, 15.00 - 16.30 hrs, Room 132

Advances in genotyping and NGS target enrichment for diagnostics

NIPD Genetics

Monday, May 23, 15.00 - 16.30 hrs, Room 129+130

The new generation of non-invasive prenatal testing

Oxford Gene Technology

Monday, May 23, 15.00 - 16.30 hrs, Room 120+121

Exon–Focused Microarray Designs: Enhanced Detection of Important CNV in Genetic Syndrome Research