similar to: Postdoctoral researcher: genome informatics in psychiatry

Genome Institute of Singapore (GIS) Biostatistics Group The Genome Institute of Singapore ( http://www.gis.a-star.edu.sg <http://www.gis.a-star.edu.sg> ) is looking for statisticians who are interested in a wide range of biomedical probems. We are especially interested in hearing from senior researchers interested in leading their own group. The institute is well-funded and engaged

Dear R-help list, Apologies. I am trying to convert one table to another. It feels that it should be a very straightforward answer with a single (or two) commands with the right extensions, but I really can't figure this out right now. I have several hundred pheno factors actually, so manually doing this line by line is not an option. My original table is approximately like this : ID

Hello, I am using R to look at whole-genome gene expression data. This means about 27,000 genes, each with a vector of numbers reflecting expression at different tissues and times. I need to do an all against all co-expression calculation (basically, just calculate Pearson's r for every gene-gene pair). I try to store the result of such a thing in a 27000x27000 matrix, but r seems not to like

---------- Forwarded Message ---------- Subject: Re: [R] conditional coloring of image labels Date: Friday 11 November 2005 1:04 pm From: jim holtman <jholtman at gmail.com> To: Jake Michaelson <jjmichael at cc.usu.edu> Use 'mtext': genes=cbind(ABC1=c(3,4,4,5,6,3), ABC2=c(4,3,4,7,7,8), ABC3=c(8,7,8,6,3,2)) ###plot the image image(1:nrow(genes), 1:ncol(genes), genes, axes =

Hello, I have the following model: lm.7 <- lm(Y ~ F + C1 + C2 , data = EM4) F is a 4-level factor, the rest are covariates centered at their mean (Y is a two-column matrix). I have tried to find functions to give the model-adjusted means (adjusted at the covariates'means) and their standard deviations for each. (That is, what I believe is called in SAS "least square or LS-means,

Dear All, We are seeking a computational research scientist interested in studying the roles of non-coding RNAs in cancer. The successful applicant will join the Cancer Research UK RNA Biology Group at the Cancer Research UK Manchester Institute (www.cruk.manchester.ac.uk). Located in Manchester UK, the Cancer Research UK Manchester Institute is a centre for excellence in cancer research. We

On 04/05/2011 03:06 PM, asterisk-users-request at lists.digium.com wrote: > Message: 12 > Date: Tue, 5 Apr 2011 13:36:21 -0500 > From: Sherwood McGowan<sherwood.mcgowan at gmail.com> > Subject: Re: [asterisk-users] Iptables configuration to handle brute, > force registrations? > To: Asterisk Users Mailing List - Non-Commercial Discussion > <asterisk-users at

Dear all, we have an exciting PhD position applying HPC to the analysis of large scale cancer datasets. The post will suit an applicant from a strong computational background who wishes to apply their knowledge to help develop a better understanding of the processes that control how tumours develop. Details below:- High Performance Computing applied to cancer research: Computational analysis of

Hi, I was wondering I'm going about this in the correct way. I need to test if there are coding sequences or exons in hg19 which match a string of 100bp "D" i.e. [A,G or T]. However I'm getting a strange result. I get a hit on chr7, using the 100bp search however when I search with 60bp sequence of "D" I don't get any hits. library("BSgenome")

<URL: http://finzi.psych.upenn.edu/R/library/datasets/html/morley.html > "The classical data of Michaelson and Morley on the speed of light" Can you provide more information about the data? How were they obtained, etc.? I do not have the book "Genstat Primer" and the nearest location where it is available is University of York which is rather far from my location.

We are looking to add experts to our fast growing managed service practice that provides access to a research platform and selected commercial medical observational data bases. Preferred locations are Boston and Philadelphia Roles and Responsibilities: Assist clients in the use of the research platform and data, providing technical support to client researchers who want to use the research

On 01/05/16 13:23, Alice Wonder wrote: > On 05/01/2016 05:10 AM, Alice Wonder wrote: >> >> I think this is my autism coming in to play, I think what is very clear >> to me I just am not able to adequately communicate because clearly >> people are not even remotely grasping what I am trying to convey. >> > > Basically whether it is a white list or a black list

Dear All, We have two computational biology positions to advertise - details below: Crispin ---- The Paterson Institute for Cancer Research (www.paterson.man.ac.uk<http://www.paterson.man.ac.uk/>), an Institute of The University of Manchester, seeks two (one senior, one junior) computational biologists to join the Applied Computational Biology and Bioinformatics Group (ACBBG). The

Greetings. I hope my message finds you well. I know this question may be silly for some experts like you but it's a very important matter for me so, sorry for that. I was trying to make a network meta-analysis using R for the attached data set which shows the association between breast feeding and autism spectrum disorder (the event here is bad). I've searched a lot through the internet

Hello, I'm an MD working in an eye clinic. I'm learning by myself to use R for use in my research works and for implementation in a software project. There are some authors who recomends the use of Cox regression as a substitute for Logistic regression (<a href="http://www.biomedcentral.com/1471-2288/3/21.pdf"> Barros AJD, Hirakata VN. BMCMedical Research Methodology, 2003;

Dear all, I am currently analyzing a set of arrays hybe on the lattest affy Drosophila 2.0 GeneChip. I am trying to run simple annaffy analysis but can¹t find what is the name of the annotation file I need to use. Here is the output of the AffyBatch object I am using: > expData AffyBatch object size of arrays=732x732 features (16749 kb) cdf=Drosophila_2 (18952 affyids) number of samples=4

Hi, I have a set of genes and its chromosomal physical position in a text file. I want to view those genes in the chromosome using R package GenePlotter. Could any one please tell how to view this. Thanks in advance. Yours sincerely, S.Mahalakshmi [[alternative HTML version deleted]]

On 05/01/2016 01:57 AM, Leon Fauster wrote: > Am 01.05.2016 um 06:43 schrieb Alice Wonder <alice at domblogger.net>: >> On 04/30/2016 08:56 PM, Gordon Messmer wrote: >>> On Sat, Apr 30, 2016 at 12:44 PM, Alice Wonder <alice at domblogger.net> wrote: >>>> >>>> For e-mail sent to people, yes. >>>> >>>> But for what

Hi Sherief, First thing is your data set did not make it If it is not too large, perhaps you could send the output of "dput" in the body of the message or send a CSV file with the extension changed to ".txt". If the data set is very large, perhaps you could send a subset as described above. Jim On Wed, Sep 20, 2017 at 11:18 AM, Sherief Ghozy via R-help <r-help at

Dear All, A 1-year postdoctoral position in Computational Biology/Bioinformatics/Evol. Biology/Statistics is available in Madrid, Spain. Brief description: Simulation and analysis of evolutionary processes in cancer. Requirements: - Postdoc younger than 30 years. - Be registered as resident ("estar empadronado") in Madrid, Spain, since 08-August-2016. - Be registed in the