Genome-wide high-throughput screens in functional genomics
27890 friedman.pdf (151.2Kb)
Access StatusFull text of the requested work is not available in DASH at this time ("dark deposit"). For more information on dark deposits, see our FAQ.
MetadataShow full item record
CitationFriedman, Adam, and Norbert Perrimon. 2004. “Genome-Wide High-Throughput Screens in Functional Genomics.” Current Opinion in Genetics & Development 14 (5): 470–76. https://doi.org/10.1016/j.gde.2004.07.010.
AbstractThe availability of complete genome sequences from many organisms has yielded the ability to perform high-throughput, genome-wide screens of gene function. Within the past year, rapid advances have been made towards this goal in many major model systems, including yeast, worms, flies, and mammals. Yeast genome-wide screens have taken advantage of libraries of deletion strains, but RNA-interference has been used in other organisms to knockdown gene function. Examples of recent large-scale functional genetic screens include drug-target identification in yeast, regulators of fat accumulation in worms, growth and viability in flies, and proteasome-mediated degradation in mammalian cells. Within the next five years, such screens are likely to lead to annotation of function of most genes across multiple organisms. Integration of such data with other genomic approaches will extend our understanding of cellular networks.
Citable link to this pagehttp://nrs.harvard.edu/urn-3:HUL.InstRepos:41384515
- HMS Scholarly Articles