The Population Genetics Research Lab utilizes state-of-the-art genomic analyses and cutting-edge technologies to facilitate discovery of genes associated with disease risk. In collaboration with local, state, national and international researchers, the Lab studies the genetic basis of both common and rare diseases including colon cancer and auriculo-chondylar syndrome (ACS), respectively. The latest genomic resources such as the International HapMap in conjunction with numerous genotyping and liquid handling robotic technologies available in the laboratory are being used to test hypotheses related to SNP and haplotype variation. Furthermore, the latest gene expression technologies are being used to examine the genetic basis of disease at the messenger RNA level.
2. Rare human disease: For example, in collaboration with the University of Arizona College of Medicine, we are working to identify the gene mutation or genetic basis of disease for a rare and facial disfiguring congenital abnormality known as ACS.
Staff: David Duggan, Ph.D., Unit Head Kristine K. Friesen, Research Associate III Kathleen Kennedy, Senior Research Associate Jan Egan, Student, University of Arizona Jason Johnson, Student, University of Arizona College of Medicine
Copyright 2009, The Translational Genomics Research Institute (TGen)
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