Showing posts with label NLM. Show all posts
Showing posts with label NLM. Show all posts

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
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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:

www.ebi.ac.uk/chembl/

http://pubchem.ncbi.nlm.nih.gov/

www.collaborativedrug.com/

Do you want to know more?

Thursday, May 6, 2010

Opportunity: Microarray & Next-generation Sequence Curator for Gene Expression Omnibus (GEO) curation team

Computercraft seeks a highly motivated Molecular Biologist to join the Gene Expression Omnibus (GEO) curation team onsite at the National Institutes of Health (NIH) in Bethesda, MD. GEO is the largest fully public repository for functional genomic data, primarily microarray and next-generation sequence datasets. More information on GEO can be found on the web site http://www.ncbi.nlm.nih.gov/geo.

RESPONSIBILITIES:
We are currently looking for someone with a background in molecular biology, genomics, or biomedicine that is capable of working with large datasets. This person will be a member of the GEO curation team, helping to review and process incoming data submissions. The successful candidate will work at NIH's National Center for Biotechnology Information (NCBI) in the National Library of Medicine (NLM).

The successful candidate will perform the following tasks:
- Review and evaluate data submissions for structural integrity and content.
- Communicate extensively with researchers, resolving issues relating to submission procedures, formats, content, and site navigation.
- Utilize UNIX C shell commands and scripts to assemble, edit, and upload large data files to the database.
- Perform advanced database curation and assembly of comparable datasets to reflect biological variables and experimental design
- Test
, develop, and troubleshoot new query, data display, and analysis features.

REQUIREMENTS:
- This challenging position requires a Ph.D. or M.Sc in molecular biology or related field.
- Excellent general computer skills, including familiarity with spreadsheets, are required.
- Excellent written/verbal communication skills are an absolute requirement.

PREFERENCES:
- Practical experience with microarrays or high-throughput sequencing is highly desirable but not required to apply.
- Experience with LINUX/UNIX is highly desired.

SALARY & BENEFITS:
Computercraft offers a competitive salary and an excellent benefits package including PPO health insurance with 100% company paid premiums, 401K program with matching, paid time off and holiday pay, life insurance, flexible spending and disability coverage. We offer an excellent work life balance with a standard 40 hour work week and the chance to work alongside accomplished scientists at NIH/NCBI.

HOW TO APPLY:
To apply for this position or learn about other Computercraft job opportunities, please visit the Careers section of our website: http://www.computercraft-usa.com/.

Computercraft is an equal opportunity employer.

Wednesday, August 20, 2008

Customize your Data Needs from PUBMED

Provision to change keywords with user’s changing research preferences in PUBMED data

Be a part of the XTractor community. XTractor is the first of its kind - Literature alert service, that provides manually curated and annotated sentences for the Keywords of user preference. XTractor maps the extracted entities (genes, processes, drugs, diseases etc) to multiple ontologies and enables customized report generation. With XTractor the sentences are categorized into biological significant relationships and it also provides the user with the ability to create his own database for a set of Key terms. Also the user could change the Keywords of preference from time to time, with changing research needs. The categorized sentences could then be tagged and shared across multiple users. Thus XTractor proves to be a platform for getting real-time highly accurate data along with the ability to Share and collaborate.

Sign up it's free, and takes less than a minute. Just click here:www.xtractor.in.












Tuesday, April 15, 2008

Position open dbSNP Curator

The Single Nucleotide Polymorphisms database (dbSNP) serves as a central repository for both single base nucleotide substitutions and short deletion and insertion polymorphisms. Computercraft seeks a biologist with significant knowledge in life sciences to help curate dbSNP records, process submission, and perform data analyst tasks. Candidates should also have the ability to rapidly develop applications to process data into database and to generate reports.

The individual will work onsite at the National Institutes of Health (NIH) in Bethesda, MD. Our scientists work with genomic experts at NIH's National Center for Biotechnology Information (NCBI) in the National Library of Medicine (NLM) to create and enhance a suite of databases and tools available to researchers worldwide.

Requirements:
• PhD or M.S. in molecular biology, bioinformatics, or highly related field
• Linux/UNIX experience
• Relational database and SQL experience
• Programming experience (Perl, Python, or C++)
• Excellent verbal and written communication skills as well as organizational skills are essential
• Ability to work with a team in a production environment and communicate well with NCBI biologists and programmers as well as external scientist
• Strong interest in contributing to the development of public database resources
• Ideal candidate will have experience with dbSNP, genotyping, and QC processing

Other Desirable Experience:
• XML/XSLT
• Javascript and AJAX
• Web development

Additional information about the Single Nucleotide Polymorphisms is available at: http://www.ncbi.nlm.nih.gov/projects/SNP/


To apply for this position or learn about other Computercraft job opportunities, please visit the Careers section of our website: http://www.computercraft-usa.com/

Monday, April 7, 2008

GenBank celebrates 25 years of service

Leading scientists discuss DNA database at April 7-8 Meeting

For a quarter century, GenBank has helped advance scientific discovery worldwide. Established by the National Institutes of Health (NIH) in 1982, the database of nucleic acid sequences is one of the key tools that scientists use to conduct biomedical and biologic research. Since its creation, GenBank has grown at an exponential rate, doubling in size every 18 months. In celebration of this vital resource and its contribution to science over the last 25 years, the National Center for Biotechnology Information, National Library of Medicine (NLM), NIH, is holding a two-day conference on GenBank.

The conference will take place April 7-8, 2008 at the Natcher Conference Center on the main NIH campus in Bethesda, Maryland. For details on the meeting, see the conference Web site, at http://www.tech-res.com/GenBank25. The conference is open to the public and also will be available via live and archived webcast; the April 7 proceedings can be viewed at http://www.videocast.nih.gov/summary.asp?live=6670 and the April 8 proceedings at http://www.videocast.nih.gov/summary.asp?live=6671.

The conference will bring together a slate of world-renowned scientists in molecular biology, genetics, bioinformatics and other areas to discuss GenBank's applications, the discoveries it has enabled, its history, and future directions. Speakers include Rich Roberts, Ph.D., a Nobel Prize winner for his discoveries of split genes, and currently Chief Scientific Officer at New England BioLabs; Sydney Brenner, Ph.D., a Nobel Prize winner for his work on genetic regulation of organ development and programmed cell death, and currently a professor at the Salk Institute; Francis Collins, M.D., Ph.D., who led the Human Genome Project and is Director of NIH's National Human Genome Research Institute; and Craig Venter, Ph.D., who led the private-sector effort to sequence the human genome and is President of the J. Craig Venter Institute. More than a dozen other eminent scientists will be speaking; the full list of presenters can be viewed at the GenBank conference Web site.

"Each day, researchers across the world submit tens of thousands of sequences to GenBank and collaborating databases in Europe and Japan," said Donald A. B. Lindberg, M.D., Director of the National Library of Medicine. "Because of these contributions, GenBank has become an essential tool for molecular biology. The National Library of Medicine is proud to partner with the research community in making this valuable resource available."

Rich Roberts, Ph।D., Chief Scientific Officer at New England BioLabs, commented, "GenBank has provided a foundation upon which much of contemporary biology is now based. It is becoming almost impossible to conceive of any serious biological study of a new organism that does not begin with the determination of its DNA sequence, which of course must be stored in GenBank." Roberts, one of the early proponents of the database, added, "the availability of this wealth of sequence information in a single repository is something we could only dream about in 1979 at the Rockefeller Conference that led to its creation and which we could not imagine being without today."

for more details