Conferences

21–24 March 2012, Cambridge, UK
Genomic Disorders 2012: The Genomics of Rare Diseases

This year’s meeting will discuss the latest findings relating to the genomic basis of rare disorders, and the role of rare variants in common disease, as these can provide such powerful insights into human biology. Genome wide analyses, including most recently Whole Exome Sequencing, are proving to be of great value in discovering the genetic basis of rare disorders and illustrate the power of humans as a model organism to study. As sequencing technology advances apace, other key aspects of genome science need to develop and grow in parallel.

https://registration.hinxton.wellcome.ac.uk/display_info.asp?id=273

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