similar to: Biostatistician position, Austria

We are looking for a MSc or PhD holder in Bioinformatics,Molecular/Computational Biology or Computer Science to support ourbiomarker team in the identification, validation and furtherdevelopment of biomarkers. The chosen candidate will be part of ourmultidisciplinary team conducting studies to discover and developdiagnostic biomarkers as well as biomarkers for the characterization ofdisease models

One Year Student in Bioinformatics (Biomarkers discovery)-1000435 See following URL for job application: http://www.merckserono.com/en/careers/job_center/job_center.html Description Background: Biomarker discovery is now an intricate part of the drug development process as it will allow for more accurate identification of patients who will benefit from those therapies. The blood tissue

*Vacancy: Scientific Collaborator in Statistical Bioinformatics* *Institute for Medical Informatics, Statistics and Documentation**, Medical University of Graz, Austria* predoc level with PhD opportunity, 30 hours per week available from May 1st, 2012 *Tasks:* * Working in the project "Biostatistical-genomical analysis of the clinical relevance of liver cancer models" which is

> Toxicogenomics Statistician > > The successful candidate will provide statistical support to nonclinical > areas of R&D, especially in the areas of investigative toxicology, safety > biomarkers, and toxicogenomics. The candidate will collaborate with > scientists to plan meaningful experimental studies, statistically analyze > the results of those and other studies,

Position: Statistician in a systems biology team focused on metabolic disorders such as diabetes and obesity. The position is part of a statistics group supporting Pfizer global research and development. Role and Responsibilities: The statistician will be an integral member of a systems biology team which develops and/or uses computational and statistical approaches to manage and derive

Dear all, The CRUK MI have multiple positions in and around bioinformatics, biostatistics and computational biology. These range from HPC and mathematical programming, through biostatistics and biomarkers, to computational biology and bioinformatics. Focuses include single cell genomics and personalised medicine in lung and prostate cancer. For full details, please visit our website at:

Job Title : Postdoctoral Position in Biostatistics/Bioinformatics Background The joint research unit between bioM?rieux, international leader in in vitro diagnostic, and Hospices Civils de Lyon, second-largest University Hospital Network in France, develops a research program dedicated to the study of injury induced immunosuppression. This program aims at (i) describing and understanding the

BioInformatics Scientist Job Code: 10-TR25 Location: Cambridge, MA Description We are seeking a highly motivated, independent bioinformatics scientist to join a group of scientists, analysts and programmers to develop tools and methodologies for large-scale gene expression data analysis. The group supports a variety of research projects in target and drug discovery as well as biomarker

I have 2 positions open with a top pharmaceutical company in New Jersey. This position is not requiring pharmaceutical experience as long as the candidate has strong SAS and R experience. In particular they are looking for strong graphics experience in S-Plus/R (lattice or Trellis?TM graphics). If you would like to learn more about this position please contact Christina Kinchen at ckinchen at

Hi, I want to be able to rename a folder using R, similar to file.rename. I want to paste " - done" onto the folder name. The reason for this is we run a loop on a large number of folders on a server and it would be nice for people to be able to log in and instantly see if their data has been processed so they can remove it. I have searched the help list but have not found anything and

Hi, I'm plotting PDFs and have a problem. If I have more than 8 sources of data the colours are repeated. These plots are used to remove poor data from the sets so it would be helpful if I could expand the colour range. Is there any way to do this? The plots are coloured by defining a vector colsVec<-1:(length(mzXMLfiles)) And defined in the loop for (file in 1:length(mzXMLfiles)) as

Hi As I can't find an example of my data structure I'd like some advice on which is the most appropriate test for significant effects. If I should be using either lme or anova, is the relevant example below the best/correct way to do the test? The Data... 2 groups of patients (5 in GroupA, 7 in GroupB) 3 short acting drugs, (I'm not concerned with residual effects from the previous

Hello, I'm trying to do some differential equation modeling in R using the package 'deSolve.' Briefly, I'm trying to use the law of mass action (the details of which aren't really important) to structure a vector of rate equation which will be passed into an ODE function and solved with associated functions from 'deSolve.' Roughly what this entails is scanning

Dear all, we seek a talented and motivated post-doc to develop computational methods for inferring the molecular basis of genetic diseases by integration of personal omics data. Research topics include: identifying causal mutations of rare disease patients by meta-analysis; inferring disease-causing molecular pathways from genotype, phenotypes, and omics profile of patient-derived cell lines

Dear R users,   I am new user for elastic net. I am trying to use elasticnet library. I have marker data with 359 markers and 168 samples, and response is metabolites. I am trying to do regression between a metabolite and markers.  But i am getting the following error:   > en<-enet(marker,as.numeric(vio),lambda=0.5,normalize=FALSE,intercept=TRUE) Error in one %*% x : requires numeric

Dear R-Helpers, I am a novice in survival analysis. I have the following code: for (i in 3:12) print(coxph(Surv(time, status)~a[,i], data=a)) I used it to fit the Cox Proportional Hazard models separately for every available parameter (columns 3:12) in my data set - with intention to compare the Hazard Ratios. However, some of my variables are in range 0.1 to 1.6, others in range 5000 to

Hi, Is there anyone know if BUGS language allows the combination of variables as response such as Y[i] <- a*X1[i]+b*X2[i] Y[i] ~ dnorm(c,d) It seems doesn't work in my model. The problem is between two ######. The error message is > modelCheck("BayesBioMarker.BUGS") model is syntactically correct > modelData(paste("BUGS_data.txt",sep="")) data

Dear mailing list, Genomics Medicine Ireland is opening new positions for our bioinformatics team. The team will analyse the ?omics data produced at GMI, which currently includes disease cohorts such as IBD, Multiple sclerosis, Alzheimer's, rare diseases, cancer and recently we have opened programs in diabetes and asthma. Our work will also focus on ancestry related topics, namely how

Hello, I have this data: Time AMP 0 0.2000000 10 0.1958350 20 0.2914560 40 0.6763628 60 0.8494534 90 0.9874526 120 1.0477692 where AMP is the concentration of this metabolite with time. If you plot the data, you can see that it could be fitted using a logistic regression. For this purpose, I used this code: AMP.nls <- nls(AMP~SSlogis(Time,Asym, xmid, scal), data

I currently have an opening with a Large Pharmaceutical Company for a Sr. SAS programmer with extensive R experience. This position is in New Jersey, but could possibly work out of Illinois or Massachusetts if necessary. Please email me at ckinchen@smithhanley.com, or contact me via my website link at http://www.smithhanleyconsulting.com/pharma/about/bios.asp?id=7 . I can be called at 800-684-9921