Genomics of Rare Disease 2018

Genomics of Rare Disease is organized by Wellcome Genome Campus and would be held during Mar 26 - 28, 2018 at Wellcome Genome Campus, Cambridgeshire, England, United Kingdom.

The target audience for this medical event for clinicians (consultants and trainees), research and clinical scientists, bioinformaticians and technology developers interested in understanding the impact of recent advances in genomics and technology on the care of patients with rare diseases.

Course Description:
This meeting will explore how cutting-edge genomic research translates into clinical care and informs our understanding of the biology of rare disease. The conference features the latest findings related to the genomic basis of rare diseases, providing powerful insights into human biology, disease mechanisms and therapeutic approaches. As genomic sequencing becomes more available in the hospital setting, we also examine the opportunities and challenges for clinical practice.

This year’s programme will focus on the lessons learned from large-scale whole genome sequencing studies and discuss the new multiomic and single cell technologies that are having an impact on our understanding of rare diseases. There will also be the opportunity for bioinformaticians working in this area to showcase the innovative tools that they have developed. We will also include sessions on the legal and ethical issues around sharing patient data and explore the new therapeutic approaches to rare diseases.

This conference provides an excellent multi-disciplinary forum for clinicians (consultants and trainees), research and clinical scientists, bioinformaticians and technology developers interested in understanding the impact of recent advances in genomics and technology on the care of patients with rare diseases.

Topics:
• What's new in rare disease?
• Lessons from large-scale whole genome studies
• Data sharing - legal and ethical issues
• Multiomic and single cell technologies
• Informatic tools
• Model organisms and systems
• Developmental genetics
• New therapeutic approaches to rare disease

Additional details will be posted as soon as they are available.