Monday, March 12, 2012
Database Curator@EBI for InterPro database
Tuesday, April 12, 2011
Cognizant & Eagle Genomics with Pistoia Alliance to Develop a Cloud-based Platform
Sunday, August 8, 2010
EBI–Sanger Postdoctoral (ESPOD) Programme
The EBI and Wellcome Trust Sanger Institute share the Wellcome Trust Genome Campus. This proximity fosters close collaborations and contributes to an international and vibrant campus environment. Researchers are supported by easy access to scientific expertise, well-equipped facilities and an active seminar programme.
The EBI–Sanger Postdoctoral (ESPOD) Programme builds on the strong collaborative relationship between the two institutes, offering projects which combine experimental (wet lab) and computational approaches. Projects may be selected from the areas defined below or proposed by the applicant. In the case of self-defined projects, the area of work must have been agreed with both the EBI- and Sanger-based group leaders. Two postdoctoral fellowships will be awarded in 2010, to start as soon as possible after October 2010 but within 12 months of the fellowship being awarded.
Available projects
| Birney/Semple: Integrated high resolution phenotyping and genetics in the zebrafish |
| Flicek/Hurles: Functional genomic analysis of structural variations in the human genome |
| Le Novere/Grant: Inference and representation of post-synaptic protein pathways using proteomic and phenotypic data |
| Luscombe/Bilker: Identification of regulatory networks that control development in a malaria parasite |
| Luscombe/Dougan: Genome-scale investigation of pathogenic regulatory networks in Salmonella |
| Overington/Rayner: Target discovery and validation for novel malaria drugs using an integrated chemical biology approach |
The full directory of EBI group leaders can be found here and the Wellcome Trust Sanger Institute Faculty page lists the academic faculty members.
Application and selection dates:
Application deadline: 15 August 2010.
Applications should consist of:
(a) cover letter specifying the project the candidate wished to apply for;
(b) CV with two references;
(c) project proposal if the candidate opts to propose a project themselves (please note that this is not required if a project is selected from the list of available projects). Self-proposed projects should be described in a maximum of 1000 words and must be pre-approved by the group and team leaders involved before the application is submitted.
Applications should be submitted via email to Tracey Andrew, by 15 August at the latest.
Benefits of working at EMBL-EBI
EMBL is an inclusive, equal opportunity employer offering attractive conditions and benefits appropriate to an international research organisation. In addition to a competitive salary, EMBL offers additional allowances dependent on family circumstances as well as an optional healthcare scheme for fellows and their families (spouse and children). Please see our leaflet about working at EMBL-EBI.Contact:
For questions on ESPOD projects, please contact the group leader in question (for individual projects) orTracey Andrew for general enquiries on how to apply.Share |
Sunday, May 30, 2010
GSK and Online Communities Create Unique Alliance to Stimulate Open Source Drug Discovery for Malaria
- GSK becomes first company to freely share chemical structures on 13,500 molecules from its compound library
- Alliances formed with leading scientific research communities from private industry and public-domain data provider
courtesy CDD Blog
GlaxoSmithKline (GSK) had teamed up with leading public-domain data providers European Bioinformatics Institute (EMBL-EBI), the U.S. National Library of Medicine (NLM) and the US-based informatics service provider Collaborative Drug Discovery (CDD) to make freely available key scientific information on more than 13,500 compounds that could ultimately lead to new treatments for malaria.
The release of this data marks the first time that a pharmaceutical company has made available the structures of so many compounds and is made possible through the collaboration of the web hosts and their specialist research tools, which will be available at no cost to researchers. The information, which is hosted on websites regularly used by researchers, includes high quality scientific data about the molecules from GSK’s own compound library which have demonstrated potency against the most deadly malaria parasite, P. falciparum.
“We are delighted that EMBL-EBI, NLM and CDD have joined us in this worthwhile endeavour to apply the principles of open source to drug discovery for malaria,” said Patrick Vallance, head of drug discovery at GSK. “Defeating this disease will require many scientific minds working together. We hope researchers from across the world will now use this information to drive further studies, and that other groups from pharmaceutical industry to academia will add their information to this on-line resource.”
This type of data is the first step on the road to developing new medicines. With the structure of the compounds and information about where they affect the malaria parasite, scientists could then carry out further research on these compounds for drug discovery or to understand how these might be used to inhibit the parasite’s life cycle and ultimately lead to new medicines. Opening up this information widely is essentially an example of ‘open source’ tactic being applied to drug discovery.
“Making life-science information openly available to the research community is at the heart of the EMBL-EBI’s mission,” added John Overington, leader of the EMBL-EBI’s ChEMBL team, which will act as the primary repository for the data through its ChEMBL resource. “We’re proud to be able to add value to the GSK data by incorporating it into ChEMBL and linking it with a vast array of information that could help researchers to find new treatments for malaria. This is the beginning of a new era of public–private collaboration in drug research.”
“NLM is excited to be involved in this groundbreaking release of information to the public,” said Steve Bryant, head of NLM’s PubChem database, which is housing the data. “By making these data available through public resources such as PubChem, GSK is greatly facilitating the research process, as the information is linked to related compounds, bioactivity results, published literature, and other resources that will assist researchers in making new discoveries to combat malaria.”
“CDD is delighted to be playing a role in this truly historic event,” commented Barry A. Bunin, CEO of Collaborative Drug Discovery. “In decades of medical breakthroughs from Big Pharmas, this is the first time a group is openly sharing all the chemical and biological data – not just the few hits. Furthermore, for phenotypic screens, the CDD tools allow researchers to begin to hypothesize and validate the targets from the whole cell screens.”
EMBL-EBI will act as the primary repository for the data on this compound set, and will index and format further information that is contributed. GSK will add more information as it is generated and external scientists researching these compounds and the data will be asked do the same.
About the data
The data contains the ‘hits’ or results from a screening of the 2 million compounds in GSK’s compound library to determine the effect of these compounds on the malaria parasite. The screening project identified ~13,500 compounds that showed strong inhibition on the parasite.
Kinase inhibitors constituted a large proportion of the molecules with previously known activity and now identified as antimalarial hits. The data includes the chemical families that GSK is currently researching for this indication and the ‘mechanisms of action’ for those compounds which the company has previously tested for other indications.
Most of the compound structures identified have been classified as capable of being converted into medicine.
The current microbiological information for the compounds and the structures have been put on online resources that are easily accessed by researchers. The EMBL-EBI site has been constructed so that scientists globally can add their data to the information there, with access free to all. The value of the release of information is enhanced by the collaboration of the web hosts and the specialist research tools on the site, that are being made available to researchers at no cost to them.
GSK gratefully recognises the support of Medicines for Malaria Venture, which contributed funding for this project.
Full information can be viewed online at:
Tuesday, May 11, 2010
EMBL Launches Genomics Data Resource
EMBL's European Bioinformatics Institute (EMBL-EBI) will host the ENA resource, which is made up of the EMBL Nucleotide Sequence Database, the European Trace Archive, and the Sequence Read Archive (SRA).
The European Trace Archive, formerly maintained at the Wellcome Trust Sanger Institute, contains raw data from electrophoresis-based sequencing machines, while the SRA is a new repository for raw data from next-generation, array-based sequencing platforms.
The ENA research team plans to launch new features for the resource over the coming year, including enhancements for the browser, improved interactive submissions tools and organism and project-centered portals into ENA data.
"ENA has been designed to provide our users with improved access both to annotated and to raw sequence data through the same user-friendly interface," Guy Cochrane, ENA's team leader, said in a statement.
"It provides graphical browsing, web services, text search, and a new rapid sequence similarity search. ENA also provides access to related information, with over 190 million cross references to external records, many of which are in other EMBL-EBI data resources," Cochrane added.
"As major generators of DNA sequence data, it is important to us that the research community has ready access not only to annotated sequence information, but also to raw data," Tim Hubbard, head of informatics at the Wellcome Trust Sanger Institute, added in the statement.
Funding for the ENA is provided by EMBL, the Wellcome Trust, and the European Commission's Framework Programme 7.