A research team led by the University of California, Irvine has built the first genetic reference maps for short lengths of DNA repeated multiple times which are known to cause more than 50 lethal human diseases. The study introduces the UC Irvine TR-gnomAD, which addresses a critical gap in current biobank genome sequencing efforts.
A research team led by the University of California, Irvine has built the first genetic reference maps for short lengths of DNA repeated multiple times which are known to cause more than 50 lethal human diseases , including amyotrophic lateral sclerosis, Huntington's disease and multiple cancers.
The UC Irvine Tandem Genome Aggregation Database enables researchers to study how these mutations – called tandem repeat expansions – are connected to diseases, to better understand health disparities and to improve clinical diagnostics. The study, published online today in the journal Cell, introduces the UC Irvine TR-gnomAD, which addresses a critical gap in current biobank genome sequencing efforts. Although TR expansions constitute about 6 percent of our genome and substantially contribute to complex congenial conditions, scientific understanding of them remains limite
University Of California Irvine Genetic Reference Maps DNA Lethal Human Diseases Tandem Repeat Expansions Health Disparities Clinical Diagnostics Biobank Genome Sequencing
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Research team builds first tandem repeat expansions genetic reference mapsA research team led by the University of California, Irvine has built the first genetic reference maps for short lengths of DNA repeated multiple times which are known to cause more than 50 lethal human diseases, including amyotrophic lateral sclerosis, Huntington's disease and multiple cancers.
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