Abstract
Rare variation has a key role in the genetic etiology of complex traits. Genetically isolated populations have been established as a powerful resource for novel locus discovery and they combine advantageous characteristics that can be leveraged to expedite discovery. Genome-wide genotyping approaches coupled with sequencing efforts have transformed the landscape of disease genomics and highlight the potentially significant contribution of studies in founder populations.
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CITATION STYLE
Zeggini, E. (2014). Using genetically isolated populations to understand the genomic basis of disease. Genome Medicine, 6(10). https://doi.org/10.1186/s13073-014-0083-5
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