Wellcome Trust Sanger Institute.The Cambridge, United Kingdom--based Wellcome Trust The Wellcome Trust is a United Kingdom-based charity established in 1936 to administer the fortune of the American-born pharmaceutical magnate Sir Henry Wellcome. Its income was derived from what was originally called Burroughs Wellcome & Co, later renamed in the UK as the Sanger institute The Wellcome Trust Sanger Institute (formerly the Sanger Centre) is a genome research centre in Cambridgeshire, England. It was set up in 1992 by the Wellcome Trust and the Medical Research Council, the purpose of which is stated on their website ([1] as "to further our (WTSI WTSI Wellcome Trust Sanger Institute (UK) WTSI Wordpress Theme Sparkling Index ) was founded in 1993 to provide a center for research on the genomes of humans and other organisms. The institute has been a leading contributor to the Human Genome Project and now focuses much of its work on studying human DNA sequence DNA sequence Genetics The precise order of bases–A,T,G,C–in a segment of DNA, gene, chromosome, or an entire genome. See Base pair, Base sequence analysis, Chromosome, Gene, Genome. variations and how these correlate with genetic diseases. The institute has developed a website located at http://www.sanger.ac.uk/to serve as a central repository for information on its varied areas of study. The densely packed website offers a wealth of scientific resources related to its research on human genetics Human genetics A discipline concerned with genetically determined resemblances and differences among human beings. Technological advances in the visualization of human chromosomes have shown that abnormalities of chromosome number or structure are surprisingly , model organisms, pathogens, bioinformatics, sequencing, and proteomics. Visitors also have several points of access to databases including Ensembl, COSMIC, Pfam, GeneDB, Wormbase, Vega, MEROP5, and DECIPHER. Clicking on any of the topic headers in the center of the homepage leads to an assemblage of resources, project information, and laboratory homepage links related to the WTSI's six main areas of study. Clicking on Human Genetics, for example, takes visitors to a lengthy menu of team links, each of which leads to information on what that team is working on, along with relevant references and illustrations. The Model Organisms link yields resources categorized by organism: mouse, zebrafish, Caenorhabditis elegans, Schizosaccharomyces pombe, and Xenopus tropicalis. The Pathogens link leads to organism-specific sequencing information for more than 100 bacteria, fungi, protozoa, helminths helminths (hel´minths), n.pl the parasitic worms that cause disease and illness in humans such as tapeworm, pinworm, and trichinosis. They are usually transmitted via contaminated food, water, soil, or other objects. , vectors, and plasmids, as well as a variety of computational toots toots n. Slang Babe; sweetie. [Perhaps short for tootsie.] . The Bioinformatics header leads to links for down loading a number of programs, including packages for product on sequencing, physical mapping, informatics analysis, and special data descriptions and specifications used at the WTSI. The Sequencing link pulls together in one area those resources specific to sequencing of various organisms. And the Proteomics link offers information on three groups at the institute that are working in this field of study. Visitors can also navigate through a bar down the left-hand side of the homepage, which offers quick links to biological resources, the database resources mentioned above, and news releases from the institute. Biological resources listed here include the Mutagenic mutagenic inducing genetic mutation. Insertion and Chromosome Engineering Resource and the Sanger Institute Gene Trap Resource (both of which aid in developing genetically modified animal models), the WTSI Microarray Facility (which produces arrays for a range of organisms largely for use by Sanger researchers), and Clone Ordering (which allows external scientists to order mouse and human clone cells free of charge). Delving deeper into the site through the Site Map, visitors will find a page on Functional Genomics projects including the Human Epigenome Project (HEP), a public-private consortium of the WTSI, Epigenomics AG, and France's Centre National de Genotypage. The goal of the HEP is to locate, identify, and catalog methylation methylation, n a phase-II detoxification pathway in the liver; methyl groups combine with toxins to rid the body of various substances. methylation (meth´ variable positions within the human genome, The partners have conducted a pilot study of the methylation patterns within the major histocompatibility complex major histocompatibility complex n. Abbr. MHC A chromosomal segment that codes for cell-surface histocompatibility antigens and is the principal determinant of tissue type and transplant compatibility. Also called HLA complex. , a region of chromosome 6 that is associated with more diseases than any other region of the human genome. An overview of this pilot study is available within the HEP section, along with a look at the data analysis process employed by this study, information on epigenotyping, and links to the HEP partners. |
|
||||||||||||||||||

Printer friendly
Cite/link
Email
Feedback
Reader Opinion