Bio Saga Headlines

Bio Saga

Thursday, December 30, 2010

Bioinformatics position

Courtesy Bioclues

Are you a skilled bioinformatician? Do you have experience with analysis and integration 
of large data sets? Would you like to work with leading experts and constantly improve 
your skills? Then you may be Intomics’ next bioinformatician.

We are expanding our bioinformatics team and are seeking a skilled bioinformatician to 
help the team provide innovative solutions for our clients in the pharmaceutical industry. 
You will play an important role in implementing data mining strategies for projects in 
areas such as target identification, biomarker identification, disease systems biology, and 
translation research.

Our preferred candidate has the following profile:
  • Bioinformatics or computational biology background
  • Experience with large-scale data mining
  • Strong experience with programming (e.g.  Perl,  Python,  Java),  databases (e.g. MySQL, PostgreSQL), and Unix
  • Excellent communication skills and the ability to work in a team
  • Strong reporting and documentation skills
  • A PhD in bioinformatics or systems biology is an advantage, but not a requirement
  • A solid understanding of basic molecular biology
  • Experience with several large scale data types is further an advantage
We are offering an  exciting and challenging job, where you get the opportunity to 
develop your skills and qualifications. You will get to work with interesting projects  in 
close collaboration with our clients.  Intomics A/S offers  a competitive salary  and  a 
friendly working environment. Some traveling must be expected.

Applications should be submitted electronically before 31st of January 2011 by email to marked with “application-1182” in the subject header.
Enquiries about the position can be made to CEO Thomas S. Jensen, tel: +45 88807979 
or All interested candidates irrespective of age, gender, race, or 
religion are encouraged to apply.

Wednesday, December 29, 2010

EMBO Courses, Workshops & Conference Series

Practical Course - European Molecular Biology Organization
Bioinformatics & Comparative Genome Analyses
27 June - 09 July, 2011 |Institute Pasteur | Paris | France

About the Practical Course

In the context of large-scale genome comparisons, the main objectives of this general purpose practical course are to strengthen capacities of students in Bioinformatics and data analyses skills by introducing reviews on advanced fundamental algorithms used in Bioinformatics and their applications in genome studies. 
Theoretical presentations will be followed by practical sessions, so that the same speaker will ensure links between theory and practice.
Reviews on each suggested topic will include their corresponding research perspectives, aiming at helping young scientists to gain insights into ongoing research in this domain. 
The course topics will include theoretical and practical aspects in: large-scale genome comparisons, evolutionary analyses, sequence and genome alignments, orthologs prediction and classification, Genome data visualization and statistical methods needed in Genome Wide Association Studies. 
Lectures related to recent hot topics in Bioinformatics and Genome studies will be programmed. 
Practical sessions in a Linux environment will involve Unix shell and Perl scripting. Students are expected to be familiar with this environment. 
Similar previous course programmes can be found here
Who can attend the course:
The course is aimed at motivated Phd students and young researchers in academic Institutions with background in Mathematics, Statistics, computing or Biology and who are involved in Bioinformatics and Genome Analyses. The course is intense and active participation of the students is expected.

Next generation sequencing establishes genetic link between two rare diseases

This one is not so recent article, nevertheless very interesting and path breaking,

Scientists have successfully used "next generation sequencing" to identify mutations that may cause a rare and mysterious genetic disorder. The research, published by Cell Press on July 29th in the American Journal of Human Genetics, demonstrates that sequencing an affected individual's entire "exome"; that is, all of the genes that carry instructions for producing proteins, can reveal critical genes that when mutant, cause inherited disorders.

Perrault syndrome is a recessive disorder that is associated with hearing loss in both boys and girls, and failure of ovarian function in girls. Some individuals with Perrault syndrome also have neurological symptoms. Prior to the current study, no genes for Perrault syndrome had been identified.
A research group led by Mary-Claire King, PhD, from the University of Washington in Seattle studied the genetics of Perrault syndrome in a small family, originally of Irish and Italian ancestry, that included two sisters with well-characterized Perrault syndrome.

"Because the family is small and not consanguineous (both parents descended from a common ancestor), standard genetic mapping techniques would not have been informative in identifying the responsible gene," explains Dr. King. "Instead, we attempted to identify the gene responsible for Perrault syndrome in this family through the use of whole exome sequencing." The exome can be thought of as a kind of genetic blueprint for the synthesis of proteins.

After sequencing the entire exome of one of the sisters, the researchers identified a single gene (HSD17B4) that exhibited two rare functional variants. This gene encodes D-bifunctional protein (DBP), a multifunctional enzyme involved in lipid metabolism. Underscoring the genetic diversity of the disease, the researchers went on to show that six other families with Perrault syndrome had normal HSD17B4.

"Other mutations in HSD17B4 are known to cause a very severe congenital syndrome called DBP deficiency that is generally fatal within the first two years of life," says Dr. King. "No girls with DBP deficiency have been reported to survive past puberty, so ovarian abnormalities have not previously been known to be associated with this illness. The few reported long term survivors of DBP deficiency exhibit hearing loss and neurological dysfunction."

Taken together, the findings indicate that Perrault syndrome and DBP deficiency share some clinical symptoms and that very mild cases of DBP deficiency may be under-diagnosed. "Our research also demonstrates that whole exome sequencing can reveal critical genes in small nonconsanguinous families," concludes Dr. King.

Tuesday, December 28, 2010

Extending pathways and processes using molecular interaction networks to analyse cancer genome data

This something really interesting to PPI, Systems biology  and molecular networks people, I just recently came across,
Cellular processes and pathways, whose deregulation may contribute to the development of cancers, are often represented as cascades of proteins transmitting a signal from the cell surface to the nucleus. However, recent functional genomic experiments have identified thousands of interactions for the signalling canonical proteins, challenging the traditional view of pathways as independent functional entities.
Combining information from pathway databases and interaction networks obtained from functional genomic experiments is therefore a promising strategy to obtain more robust pathway and process representations, facilitating the study of cancer-related pathways. 
Results: We present a methodology for extending pre-defined protein sets representing cellular pathways and processes by mapping them onto a protein-protein interaction network, and extending them to include densely interconnected interaction partners. The added proteins display distinctive network topological features and molecular function annotations, and can be proposed as putative new components, and/or as regulators of the communication between the different cellular processes.
Finally, these extended pathways and processes are used to analyse their enrichment in pancreatic mutated genes. Significant associations between mutated genes and certain processes are identified, enabling an analysis of the influence of previously non-annotated cancer mutated genes. 
Conclusions: The proposed method for extending cellular pathways helps to explain the functions of cancer mutated genes by exploiting the synergies of canonical knowledge and large-scale interaction data.
Author: Enrico GlaabAnais BaudotNatalio KrasnogorAlfonso Valencia
Credits/Source: BMC Bioinformatics 2010, 11:597

Monday, December 27, 2010

Largest Network Of Alzheimer’s Disease Protein Interactions

Through a complex analysis of protein interactions, researchers from IRB Barcelona and the Joint Programme IRB-BSC have discovered new molecular mechanisms that may be involved in the development of Alzheimer’s disease. The study, a collaboration between bioinformaticians and cell biologists, was led by IRB Barcelona group leader and ICREA researcher Patrick Aloy and appears today in the Genome Research, a reference journal in the field of genomics.

Alzheimer’s disease is an age-related neurodegenerative disease. Despite the considerable efforts made in recent years to understand the mechanisms that trigger this disease, an effective treatment is not yet available. This study reveals new molecular and functional data that could help researchers gain a better understanding of the disease and potentially to develop new therapies.

From the computer to the lab

Proteins are the molecular instruments that cells use to carry out their functions. Proteins don’t normally act alone, but interact with other proteins to form cellular networks. In this study, rather than looking at individual proteins as been done in many previous studies, the scientists analyzed the biology behind Alzheimer’s disease using a global approach. “We have combined computational and experimental methods to study the connections between proteins and put them in the context of their environment”, says Aloy.

To do so, the researchers used genetic methods to study the thousands of possible interactions between proteins known or thought likely to be involved in the disease, including proteins derived from the genes located on the chromosomes related to the Alzheimer’s disease. They obtained a total of 200 new interactions. This information, added to what is already known, brings the total number of Alzheimer’s-related interactions to 6000, and involves 1700 proteins, resulting in the largest network of interactions between proteins related to Alzheimer’s disease.

The computational analysis of these interactions, performed by the MareNostrum Supercomputer of the Barcelona Supercomputing Center (BSC), revealed that many of the groups of proteins are highly interconnected and have similar functions in cells. Some of these functions suggest new molecular mechanisms that could be linked to Alzheimer’s. A clear example is a protein called ECSIT, that relates oxidative stress to inflammation and changes in the mitochondria, indicating that these processes may play a role in the development of the disease.

The 94 terabyte MareNostrum is housed in the deconsecrated Chapel Torre Girona at the Polytechnic University of Catalonia, Barcelona, Spain:
Increased life expectancy and improvements in health care and diagnostics have led to the increased prevalence of the Alzheimer’s disease, which is a serious problem in both developed and developing countries. This study opens the door to new research aimed at finding a cure for the disease.

Sources: Institute for Research in Biomedicine-IRB, AlphaGalileo Foundation.

Friday, December 24, 2010

Reckitt Benckiser Buys India’s Paras Pharmaceuticals Ltd

Reckitt Benckiser emerged successful in race to buy Pars in spite of 4 global drugmakers submit bids for India's Paras Pharma buy

Reckitt Benckiser Group plc (RB) today announces that it has agreed to buy Paras Pharmaceuticals Limited (Paras) forINR 32.6 billion (Indian Rupees) (approximately GBP 460 million) from the current shareholders, including the Patel family and Actis, the emerging markets private equity investor. RB will finance the transaction from existing facilities. 
Paras is a privately-owned Indian company with a portfolio of leading Indian over the counter Health and Personal Care brands including: 
Moov, the No 2 topical analgesic pain ointment,
D’Cold, the No 2 cold & flu remedy,
Dermicool, the No 2 for prickly heat,
Krack, the No 1 medicated skin treatment for cracked heels and
Itch Guard and Ring Guard anti fungal creams.

In addition, Paras has a personal care business led by Set Wet, a leading hair gel and deodorant brand. In the fiscal year ending March 2010, Paras generated net sales of INR 4,014 million, representing a mid-teens average growth rate over the last four years, and operating EBITDA for the same year of INR 1,083 million (approximately GBP 56 million and GBP 15 million respectively). The company has a brand new state of the art and GMP compliant manufacturing plant located at Baddi in Northern India, which employs around 700 people.

Commenting on the acquisition, Reckitt Benckiser CEO, Bart Becht, says, “The acquisition of Paras is another step forward in RB’s growth strategy in consumer health care. It creates a material health care business in India, one of the most promising health care markets in the world with the addition of a number of strong and leading brands.”

“We believe the Paras business has not only extremely good growth potential, when supported by RB’s investment and innovation strength, we also expect to realize material synergies as a result of the integration of Paras into Reckitt Benckiser.”

“The growth potential of the business, the creation of a material health care business in India’s large and growing health care market and the global synergies available make Paras an exciting addition to our portfolio and attractive opportunity for our shareholders.”

RB was advised by JPMorgan. Actis and the other Paras shareholders were advised by Morgan Stanley.

New programming language will drive DNA

This is no Sci-Fi but reel to real! Yes we can in deed program the DNA for real Now! 

Bioinformatics scientists have built two logic gates for what they hope will become a new programming language for drug design as well as chemical and agricultural product engineering. The accomplishment seems hardly noteworthy except that these logic gates are made of E. coli. The two computational switches are based on two strains of the common bacterium. Researchers are now working to assemble them to perform computations.

This genetic programming software would resemble any other programming language, says Kevin Clancy, senior staff scientist for bioinformatics at Life Technologies Corp. The Carlsbad, CA, company is funding the work, which is being done by researchers at the UC San Francisco School of Pharmacy. Life Tech plans to commercialize the technology.

The software would convert instructions into a DNA sequence to be inserted into a bacterial, yeast or mammal cell. "It allows you to access and rewire biological systems on a scale that hasn't been possible in genetic engineering to date," says Christopher Voigt, UCSF associate professor.

Monday, December 20, 2010

ECCB 2010 Next-gen sequencing Tutorial

Check out this SlideShare Presentation:

Walk in interview - Project posts tenable at NCCS, Pune

Advertisement No. Admn P22/2010

Walk in interview program for the following Project posts tenable at NCCS, Pune.

Name of the Position & No. of PostReser- vationsName of the ProjectUpper Age LimitQualification and ExperienceMonthly Emoluments   TenureDate, Time and Place of Interview
Research Associate (One Post)
SC"Prognostic evaluation of the E-box binding transcription factors snail and slug in ovarian, breast, prostate and head and neck cancers"35 YearsPh.D / M.Tech / M.E / M.D / M.V.Sc (A.H) in Life Sciences / Bioinformatics / Biostatistics / Biotechnology / Microbiology / Biochemistry.Rs. 17250/- +15% HRA for 1st & 2nd year and Rs. 20830/- + 15% HRA for 3rd year.2.5 Years
Date: 30.12.10 Time: 9:30 am at NCCS Complex
Tenure: The Initial appointment will be for the period of one year likely to be extended for further one year and five months however, the salary for the extended period will be only made available after receipt of funds from the funding agencies.
Age: Age Relaxation of 5 years in case of SC/ST/Women/PH candidates will be given as per Government of India Rules.
Candidates fulfilling the above requirements may attend the Walk in Interview on the above date, time and address. No TA will be paid for attending the interview.
Candidates are required to report sharp at 9:30 am on the date of interview with the following documents:
1.       *Biodata form duly filled in.
2.       All relevant original documents with a set of attested copies thereof.

BioFocus Extends Contract with Amgen

Belgian biotech firm Galapagos today announced its BioFocus service division has extended a contract with Amgen through 2012 to include target discovery and validation work.
The extension will include the use of BioFocus' target discovery platform to deliver novel targets to support Amgen's therapeutic programs. Galapagos will receive €2 million ($2.6 million) in research fees in the first year, under the terms of the deal. It is also eligible for access fees and milestone payments.
Originally forged in 2002, the collaboration between BioFocus, which Galapagos acquired in 2005, and Amgen involves identifying new molecules against drug targets. The partnership was extended in 2006 and 2008.
BioFocus' discovery platform includes the use of in vitro and cell-based screening, structural biology, and chemogenomic and informatics tools.

Monday, December 6, 2010

Artificial neural networks-based approach to design ARIs using QSAR for diabetes mellitus

In this article, in the first part, we propose an artificial neural network-based intelligent technique to determine the quantitative structure-activity relationship (QSAR) among known aldose reductase inhibitors (ARIs) for diabetes mellitus using two molecular descriptors, i.e., the electronegativity and molar volume of functional groups present in the main ARI lead structure. We have shown that the multilayer perceptron-based model is capable of determining the QSAR quite satisfactorily, with high R-value. Usually, the design of potent ARIs requires the use of complex computer docking and quantum mechanical (QM) steps involving excessive time and human judgement. In the second part of this article, to reduce the design cycle of potent ARIs, we propose a novel ANN technique to eliminate the computer docking and QM steps, to predict the total score. The MLP-based QSAR models obtained in the first part are used to predict the potent ARIs, using the experimental data reported by Hu et al. (J Mol Graph Mod 2006, 24, 244). The proposed ANN-based model can predict the total score with an R-value of 0.88, which indicates that there exists a close match between the predicted and experimental total scores. Using the ANN model, we obtained 71 potent ARIs out of 6.25 million new ARI compounds created by substituting different functional groups at substituting sites of main lead structure of known ARI. Finally, using high bioactivity relationship and total score values, we determined four potential ARIs out of these 71 compounds. Interestingly, these four ARIs include the two potent ARIs reported by Hu et al. (J Mol Graph Mod 2006, 24, 244) who obtained these through the complex computer docking and QM steps. This fact indicates the effectiveness of our proposed ANN-based technique. We suggest these four compounds to be the most promising candidates for ARIs to prevent the diabetic complications and further recommend for wet bench experiments to find their potential against AR in vitro and in vivo. © 2009 Wiley Periodicals, Inc. J Comput Chem, 2009

Wednesday, December 1, 2010

Application/Resource Developer Position @ Linguamatics

Linguamatics is currently seeking a talented post graduate with experience of natural language processing to work on leading edge text mining products.

You will be responsible for developing and maintaining resources for domain specific adaptation of real-time semantic search software based on Natural Language Processing. Working closely with application scientists and the development team, you will ensure that the combination of software and resources satisfies customer requirements. This will include developing linguistic patterns, and programs to transform domain specific terminologies into common formats and keep them up-to-date. You will be working on life science applications, and some knowledge of the Pharmaceutical or Healthcare industry would be useful.In addition to resource and application development, you will be expected to contribute to ongoing UK or EU funded research projects as part of the research and resource development team.

You will have strong communication skills and be able to work with other staff to get across ideas and issues and to respond to requirements. You must also enjoy working in a fast-moving start-up environment, which requires multi-tasking, flexibility and the ability to work in a small, highly motivated team.


The ideal candidate will have the following skills and experience:
  • Post graduate qualification in computational linguistics or related discipline, including a good understanding of grammar.
  • Research experience, preferably in a commercial setting
  • Good interpersonal and communication skills
  • Attention to detail
  • Strong programming skills, ideally with experience of Java or C and a scripting language such as Perl
Additionally, the following attributes would be advantageous:
  • Research experience, preferably in a commercial setting
  • Background in or experience of the Life Science sector
  • Experience in using ontologies
Company Profile

Linguamatics is a leading provider of text mining solutions based on innovative use of semantic and natural language processing (NLP) technology. Our software is acknowledged as the leading solution in the pharmaceutical and biotech industry and has been adopted by most of the top pharmaceutical companies.
This is a challenging and exciting role in a young, growing company. If you think you have the right skills and experience, and are ready to make an outstanding contribution to the team and the success of our business, please send your CV with a covering letter by email to:

Sarah Mansfield
Linguamatics Ltd
St Johns Innovation Centre
Cowley Rd
Cambridge CB4 0WS, UK

Tuesday, November 30, 2010

23andMe has moved to a subscription-based pricing

Direct-to-consumer genetics testing firm 23andMe has moved to a subscription-based pricing plan that now includes a one year contract and an additional charge of $5 per month.
Along with the change in pricing, the company has done away with its separate Ancestry Edition and Health Edition products, which are now part of one service, called Complete Edition, that the firm offers. The base price for the testing service remains at $499.
The Ancestry and Health Edition products were launched a year ago by 23andMe.
The changes took effect on Nov. 22. After the initial year expires, the contract will go to a month-to-month model, and customers will be able to cancel their contract at any time, a spokeswoman for Mountain View, Calif.-based 23andMe said.
In an e-mail, she said the new monthly charge is based on the company's need to update its test and customers' test results as new genetic discoveries are made. The company's scientific team continually evaluates the latest scientific studies on genetic associations and on average incorporates two to five new genetic discoveries into 23andMe's service each month.
In a separate announcement today, 23andMe said that it has transitioned to the third version of its genotyping array, enabling it to test approximately one million SNPs. Customers who purchase the 23andMe Personal Genome Service today or after will have their DNA tested on the new version of the array, it said. The new chip nearly doubles the number of SNPs for which the firm previously tested.


Thomson Reuters today announced that it has acquired GeneGo, a leading provider of biology and disease information, analytics, and decision support solutions for pharmaceutical research and development.
Effective immediately, GeneGo will become part of the Healthcare & Science business of Thomson Reuters. Financial terms of the transaction were not disclosed.
The acquisition enables Thomson Reuters to provide the pharmaceutical, biotechnology, and academic research communities with solutions that provide better understanding of the underlying mechanism of disease and potential therapies. GeneGo’s scientific expertise and assets in biology-driven drug discovery complement the Thomson Reuters life sciences portfolio that covers drug pipeline competitive intelligence, patents, and chemistry.

Thursday, November 25, 2010

Position open for Genome Computational Specialist

Courtesy: Bioclues

Job Reference: G586-10LL

Genome Discovery Unit, The John Curtin School of Medical Research, ANU College of Medicine, Biology and Environment
We are seeking a Genome Computational Specialist to support the work of researchers engaged in cutting-edge projects involving analysis of high throughput sequencing data.
Term of ContractPermanent
GradeANU Senior Manager 1 (Information Technology)
Salary Package$88,417 - $92,781 pa plus 17% superannuation
Closing Date3 January 2011
Position OverviewThe ANU's genomic strategies and expertise has positioned it as a key partner in a number of national and international genomics / phenomics research consortia. The ANU is underpinning this excellence in genomic biology by establishing a Genome Discovery Unit (GDU) for the analysis of high throughput sequencing data. The facility will be staffed by highly skilled personnel who will provide the core expertise for constructing and operating a high performance computing cluster that will serve the needs of projects employing high throughput sequencing.
The ANU is seeking as the Genome Computational Specialist of the GDU a service-oriented individual with outstanding track record in high performance computing. The Genome Computational Specialist will have a successful track record in project management, of working collaboratively in a research environment and experience in biological data analysis and bioinformatics.
Enquiries: Stephanie Palmer, T: 02 6125 9637, E:
Additional InformationPEWER.pdf
Position description 
Responsible toManager, Genome Discovery Unit

The Genome Computational Specialist position has been identified as the crucial appointment for ensuring the successful creation and operation of the Genome Discovery Unit (GDU).

Position Dimension & Relationships:
The Genome Computation Specialist reports to the Manager of the GDU and oversees the work of other computational and bioinformatics service staff in the GDU. The Genome Computation Specialist plays a key liaison role with staff at the ANU Supercomputer Facility, The National Computational Infrastructure, The ANU Division of Information and the College of Medicine, Biology and Environment IT function to ensure the provision of effective and robust computing resources for the analysis and storage of high throughput sequencing (HTS) data.
The Genome Computational Specialist works in the Genome Discovery Unit (GDU) to:
1. Provide a centralised service for genome researchers including complete analysis pipelines for (HTS) projects encompassing sample preparation, sequencing, computational, data storage and bioinformatics needs. The service will also include other genomics services currently provided by the Biomolecular Resource Facility (BRF), including dideoxy sequencing & capillary electrophoresis, rtPCR and microarrays and genotyping.
2. Develop a critical mass of high level expertise in genomic analysis, particularly focussed on HTS and associated bioinformatics, with close integration of service provision with bioinformatic/genomics researchers and with education and outreach programs.
3. Develop and propagate genomics and bioinformatics capability and research strength at ANU and more generally in Canberra across a range of research areas, including through the joint development of major new research initiatives.
4. Develop and manage strategic relationships with key organisations including APF/APN, ANUSF/NCI, CSIRO, BPA, other genome/bioinformatics centres and facilities and major vendors and to leverage these relationships to enhance and grow areas of research strength at ANU and more generally in Canberra.
Role Statement:

Under the broad direction of the Manager, Genome Discovery Unit:
1. Develop and implement high performance computing strategies for the management, analysis and storage of HTS data.
2. Oversee the design, installation and ongoing maintenance of a computing environment that meets the needs of GDU researchers and facility users, including researchers throughout the Canberra region.
3. Oversee the development and execution of operating procedures that maximise the quality and robustness of GDU services including: provision of public data required for HTS analyses; design, implementation and routine testing of a backup and recovery plan for critical data; and mechanisms for end-user feedback.
4. Oversee the development of HTS analysis pipelines including assisting with choice and local installation of algorithms required to undertake these analyses.
5. Integration of the GDU computing facility with existing ANU IT infrastructure and the National Computational Infrastructure to maximise performance and availability of the computing capabilities to members and clients of the GDU.
6. Coordinate GDU bioinformaticians and instruct them on facility usage policy and the software engineering best-practices to ensure effective use of the facility and maximize the quality of results.
7. Prepare and deliver requested reports regarding service status.
8. Other duties as required consistent with the classification.
Selection criteria 
1. Progress towards a postgraduate qualification in computer science or equivalent combination of relevant experience and or education/training with several years subsequent relevant specialist/professional experience.
2. Project management skills with expertise in managing multi-contributor software engineering projects including the associated quality control and quality assurance processes.
3. Experience and a sophisticated understanding of high performance computing environments including a working knowledge of cluster computing, cluster maintenance and systems administration.
4. Experience in the management and analysis of complex data.
5. Demonstrated experience in effective staff management ensuring the on time delivery of a technically oriented service.
6. Prior exposure to genome biology with intellectual flexibility and a practical approach to completing projects.
7. Well developed written and oral communication skills including the ability to communicate and work cooperatively with colleagues and staff from diverse disciplines.
8. A demonstrated understanding of equal opportunity principles and policies and a commitment to their application in a university context.

Tuesday, November 23, 2010

Applications are invited for the post of Information Officer

Applications are invited for the post of Information Officer in Distributed Information Sub-Centre (DISC) established by Dept. of Biotechnology at Indian Institute of Advanced Research, Koba, Gandhinagar, Gujarat

Applications are invited for the post of information officer at Distributed Information Sub-Centre (DISC)

Position (scale), qualifications and experience:

1. Information Officer - one post

Qualifications and Experience: M. Tech in IT sciences, MSc Bioinformatics with 2-3 years experience in the bioinformatics domain with expertise in database management, software development, system administration, and work experience on linux environment.

Pay scale; Gross emoluments will be about Rs. 20.000/- pm in this post

Application process: Please submit your application with biodata to Dr. DD Singh Bioinformatics
Deptt. at You can call at 079-30514150 for any queries.

The application process is open till suitable candidate is found.

courtesy bioclues

GeneGo, Agilent Integrate Informatics Tools

GeneGo today said that Agilent's GeneSpring bioinformatics solution has been integrated with GeneGo's MetaCore.
The collaboration was announced in connection with the newest version of Agilent's GeneSpring. Agilent said today introduced GeneSpring GX 11.5, which can interpret microarray, proteomics, and metabolomics experiments together for the first time. The newest version includes a direct connection to the MetaCore pathway analysis engine, enabling users to seamlessly upload expression data analyzed in GeneSpring, said GeneGo.
"MetaCore can concurrently visualize multiple types of data and will be able to take advantage of this new functionality in GeneSpring which will be very helpful to our joint customers," Julie Bryant, VP of business development for St. Joseph, Mich.-based GeneGo, said in a statement.

Friday, November 19, 2010

Roche Restructuring Plan Includes 4,800 Job Cuts

Roche today announced a global restructuring plan, which includes reducing its global workforce by 4,800 jobs, most of which are in the firm's Pharmaceuticals Division.
The firm has dubbed the restructuring an "Operational Excellence Program" that is intended to result in annual cost savings of CHF2.4 billion ($2.4 billion). It expects to implement the changes, which also include the transfer of certain positions, consolidation at certain sites, and the closure of some facilities, during 2011 and 2012.
The 4,800 job cuts equates to 6 percent of Roche's global workforce. In addition to the reductions, it also expects to transfer around 800 jobs internally and approximately 700 positions to third parties.
The cost-cutting measure is not a surprise, as Roche had said in September that it would undertake such an initiative. However, the details of the effort were not announced until today.
Roche's Pharmaceuticals Division will bear the brunt of the cuts, with 5,400 jobs being affected. The firm said that it will reduce its pharma sales and marketing staff by a total of 2,650 positions. Another 1,350 jobs are expected to be affected by the reorganization of some technical operations within manufacturing at sites in California, Mannheim, Germany, and other places, which will cut around 750 positions, and includes Roche seeking buyers for its sites in Florence, SC, and Boulder, Col., which would affect 600 jobs.
Roche's cuts to R&D include discontinuing RNA interference research in Kulmbach, Germany, and in Nutley, NJ, and Madison, Wis.
Roche's Diagnostics Division, which includes its molecular tools and molecular diagnostics operations, will have 640 positions affected by the restructuring, though it appears the actions will affect the firm's blood gas diagnostics and diabetes care products. Its diagnostics chemical manufacturing and analytical services are expected to be discontinued in Mannheim and transferred to Penzberg, Germany.
"This is a comprehensive, focused initiative to reinforce Roche's long-term innovation capability in the face of increased price pressures and a more challenging market environment," Roche Group CEO Severin Schwan said in a statement.
Roche added that the restructuring effort "is a response to mounting cost pressures in healthcare — particularly in the US and Europe — and to increasing hurdles for the approval and pricing of new medicines."
The firm expects to incur one-time restructuring costs totaling CHF2.7 billion between 2010 and 2012, of which CHF1.5 billion are cash-related.
Roche re-affirmed its outlook for full-year 2010 of mid-single-digit sales growth in local currencies for the Roche Group and the Pharmaceuticals Division (excluding Tamiflu sales). It also said that sales for the Diagnostics Division are expected to grow significantly ahead of the market.

Tuesday, November 9, 2010

International PhD Program in the Biological Sciences

Under the auspices of the University of Tübingen, approximately 120 students from all over the world are working on their PhDs at the Max Planck Institute for Developmental Biology and the Friedrich Miescher Laboratory. Here, they profit from an interdisciplinary environment and first-rate scientific resources. Dedicated support and educational programs foster the scientific growth of doctoral students. The program offers cutting edge training in
  • Bioinformatics
  • Structural Biology
  • Plant & Animal Development 
  • Molecular & Cellular Biology/ Biochemistry
  • Developmental & Quantitative Genetics
  • Evolutionary Biology & Ecological Genetics
  • The application deadline is November 24, 2010.
Do you wish to know more?

Friday, October 29, 2010

OPENING - Manager or a Senior Bioinformatician

A manager or a senior bioinformatician is required.

Qualifications:- A Master degree in biology, bioinformatics

(or a related discipline), or equivalent experience in bioinformatics
in the pharmaceutical or biotech industry. 
An MS or Ph.D. is strongly preferred.

Required Skills:-Strong technical, analytical, and problem 

solving skills, Strong communication abilities, A dedication
to software development best practices and methodologies

Experience: - 2+ years experience developing software solutions

in the pharmaceutical R&D or biotech sector, Demonstrated
ability with several of the following: Java, Java/J2EE, 
.NET (VB, C#, ASP), Sharepoint, Oracle, JDBC, SQL, 
Unix/Linux, Windows, Mastery of at least one programming

Company:- MNC Bioinformatics.

Location:- Bangalore, Hyderabad and Pune.

Salary:- 15-20 lacks.

Further relevant information can be accessed from the given website:-

Life Science and Informatics

What is this?
is this a new industry?
or a old wine in a new bottle?

Well Life Sciences and Informatics can be anything form computational biology, all omes and omics, core bioinformatics to curation and literature mining, database creation, in the area of biology, chemistry , bio-chem space.

There are number of companies in India and bangalore is the forefront as a major bio-cluster with 20 to 30 companies in this sphere.

now how good are these companies doing?
how good are they in terms of the international markets and how profitable is their business?
what do they do?
their clients?

These are some interesting things that could be discussed in this blog page...

Tag It