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Tuyển tập các báo cáo nghiên cứu về y học được đăng trên tạp chí y học Critical Care giúp cho các bạn có thêm kiến thức về ngành y học đề tài: Shaken not stirred: a global research cocktail served in Hinxton. | Meeting report Shaken not stirred a global research cocktail served in Hinxton Samuel Marguerat Brian T Wilhelm t and Jurg Bahler Address Cancer Research UK Fission Yeast Functional Genomics Group Wellcome Trust Sanger Institute Hinxton Cambridge CB10 1HH UK. tPresent address Institut de Recherche en Immunologie et en Cancérologie IRIC Montreal H3C 3J7 Canada. Correspondence Jurg Bahler. Email jurg@sanger.ac.uk Published 22 November 2007 Genome Biology 2007 8 320 doi l0.ll86 gb-2007-8-ll-320 The electronic version of this article is the complete one and can be found online at http genomebiology.com 2007 8 ll 320 2007 BioMed Central Ltd A report of the 2007 Cold Spring Harbor Laboratory Wellcome Trust Conference on Functional Genomics and Systems Biology Hinxton UK 10-13 October 2007. The organizers of the 2007 Cold Spring Harbor Laboratory Wellcome Trust Conference on Functional Genomics and Systems Biology built on the tradition of past workshops by keeping the number of participants low and choosing presentations covering a wide range of topics on multiple aspects of global genomic and systems-biological approaches. Like in a good cocktail the varied talks blended into an interesting mix. Here we present a selection of talks with emphasis on unpublished work. Genome-wide cellular screens Several talks introduced global cellular screens covering data-intensive experiments and efforts to improve the design and readout of current approaches. Brenda Andrews University of Toronto Canada described an elegant system to screen for factors involved in the regulation of periodic gene expression during the budding yeast cell cycle. She and her colleagues developed a two-color reporter assay with cell-cycle-regulated promoters driving expression of green fluorescent protein GFP and a control promoter driving red fluorescent protein RFP expression. Using the synthetic genetic array SGA platform expression levels can be assayed in combination with 5 000 deletion mutants or .