Not exact matches
Using
whole exome sequencing (a next generation test to
analyze the exons or coding regions of thousands of genes simultaneously) conducted at the Baylor College of Medicine
Human Genome Sequencing Center, the researchers identified CLP1 mutations in two unrelated families with the disorder.
We focus on developing computational methods and tools for (a)
analyzing large - scale gene expression data related to
human cancer in search for gene markers and disease sub-categories, (b) identifying regulatory elements such as miRNA precursors and their targets in
whole genomes of plants and mammals, (c) building theoretical models of gene regulatory networks.
Analyzes whole genome and detailed clinical data from nearly 300,000 Icelanders Finds several novel variations in the sequence of the
human genome modulating cholesterol levels Five variants are also causally linked to increased risk of coronary artery disease Shows...