Biomarker Discovery & Diagnostic Development Using Whole Genome Sequences Paired with Clinical Data
Time: 2:30 pm
day: Conference Day One - Track One - PM
Details:
- Recruiting participants from the NHS with rare diseases and cancer, to enable molecular diagnosis and best treatment opportunities, paving the way for the first national WGS standard of care offering in the world
- Deidentifying whole genome sequences linked with longitudinal clinical data, to accelerate genomic research and advance R&D into the clinical indications represented in this dataset
- Analysing data together (along with additional multiomic and multimodal data) gives context to the genome and supports researchers in characterising diagnostic variants, identifying biomarkers and elucidating novel drug targets/opportunities
