Patrick Short is experienced in genomics research with a focus on large-scale genome sequencing projects and rare disorders. Prior to Sano Genetics, Patrick was previously at the Wellcome Trust Sanger Institute and the University of Cambridge.
Clinical & Research Tools Showcase:
Sano connects people with research in personalised medicine We provide access to free genome sequencing and analysis for research participants. You own your data and have full control over how it is used.
Enabling Precision Medicine Trials in Movement Disorders
To be successful, precision medicine trials must recruit patients informed by the patient’s unique genetic information. We will present a real-world example of a program in the movement disorder setting that successfully identified and tested patients for precision medicine trials.
The PMWC 2022 Clinical & Research Tools Showcase will provide a 15-minute time slot for selected companies in this space. The Clinical & Research Tools is a showcase for innovative technologies that are used for the analysis of genetic variation and function, helping to advance breakthroughs in genetic health, rare disease conditions on individuals of all ages, complex diseases and cancer care. Next-generation sequencing (NGS) and microarray technologies empower rapidly evolving genomic revolution.