We can’t wait to meet you at booth #348, June 1-3. Meet our team to learn how SOPHiA GENETICS can help turn complex genetic data into life-changing insights.
We will also be hosting a talk on Monday, June 3 from 8:30-10:00 am. Don’t miss it!
Breaking Boundaries: Unveiling New SOPHiA DDM™ Capabilities for Genomic Advancement
The era of precision medicine has arrived. Let’s continue the momentum.
As our understanding of genomics evolves, personalized healthcare and treatment strategies are becoming a reality across the spectrum of hereditary disorders – from cancer, to psychiatric conditions, rare diseases, and everything in between.
Join our panel of experts to discover how our new and enhanced NGS applications are working in synergy with the expanded capabilities of our web-based SOPHiA DDM™ Platform to break boundaries for genomic advancement. From hereditary cancer to pharmacogenomics and WGS, we have a jam-packed agenda that showcases how SOPHiA DDM™ overcomes variant analysis challenges to resolve hard-to-capture variants of uncertain significance in clinical practice.
Join us to hear how our esteemed speakers are utilizing SOPHiA DDM™ to make precision medicine a reality:
SOPHiA DDM™ Hereditary Cancer Solution v2.0: The ultimate NGS application for characterizing genetic variants predisposing to cancer
Matteo Dal Molin, Medical Genetics Lab, European Institute of Oncology, Milan, Italy
Unlocking precision medicine through high-throughput sequencing in pharmacogenetics - RNPGx experience
Nicolas Picard, Professor of pharmacology, President of RNPGx, Limoges University, France
Accelerated Omics with NVIDIA
Harry Clifford, Genomics Product Lead, NVIDIA, Cambridge, UK
An introduction to the SOPHiA DDM™️ Whole Genome Sequencing Analytical Pipeline
Ximena Bonilla Bustillo, Head of Tertiary Analysis, SOPHiA GENETICS, Rolle, Switzerland
