| Literature DB >> 20725090 |
Abstract
The EMBO/EMBL symposium 'Human Variation: Cause and Consequence' highlighted advances in understanding the molecular basis of human genetic variation and its myriad implications for biology, human origins and disease. As high-throughput sequencing allows us to define genetic variation and its functional consequences at genome-wide resolution for a large number of people, important questions need to be asked about how to use new technologies to maximize the translational relevance of genetic research for society and the individual patient.Entities:
Mesh:
Year: 2010 PMID: 20725090 PMCID: PMC2933874 DOI: 10.1038/embor.2010.126
Source DB: PubMed Journal: EMBO Rep ISSN: 1469-221X Impact factor: 8.807