similar to: unable to compute MAD in aCGH package

Displaying 20 results from an estimated 600 matches similar to: "unable to compute MAD in aCGH package"

2012 Jul 27
2
R bioconductor agilent aCGH analysis
Hi, I would like to analyze some agilent aCGH copy number files. As a start, I would like to normalize this data. I don't know what is the standard way to do this. Which package is the standard one that people use for this purpose? The chips that I am looking at are the agilent sure print 1M (G4447a) array and a custom chip with similar format. My raw data is a text file with spot locations
2008 Oct 03
1
Problem with read.table in Windows and Linux
Hello everyone, I'm trying to open the same file under Linux and Windows. Under Windows everything is ok but when I try to do it under Linux I have a mistake and I don't know why. This is the mistake: Error in make.names(col.names,unique=TRUE): string multibyte 1 invalid why? I write this when I want to do it under Windows: zz.info<-read.table(file("C:/Documents and
2008 May 24
1
Problems with lme
Hello, I want to perform an lme on a database with this structure: ID Sequence Temperature Tumour Error 1 5 0 1 8.721872e-08 1 5 0 2 8.695348e-08 1 5 0 3 2.019604e-13 1 5 37 1
2011 Jan 13
1
question about svm(e1071)
Dear all, I executed svm calculation using e1071 library with a microarray data (http://www.iu.a.u-tokyo.ac.jp/~kadota/R/data_Singh_RMA_3274.txt). Then, I shuffled the data samples and executed svm calculation again. The results of 2 calculation were different (in SV, coefs and weights). I attached the script below. Could please tell me why this happens? If possible please tell me how to make
2009 Jul 13
0
adjusting survival using coxph
I have what I *think* should be a simple problem in R, and hope someone might be able to help me. I'm working with cancer survival data, and would like to calculate adjusted survival figures based on the age of the patient and the tumour classification. A friendly statistician told me I should use Cox proportional hazards to do this, and I've made some progress with using the
2010 Mar 17
1
question about multinom function (nnet)
Dear All. I have the following table that I want to analyze using multinom function freq segments sample 4271 Seg1 tumour 4311 Seg2 tumour 3515 Seg1 normal 3561 Seg2 normal I want to compare model with both factors to the one where only sample is present. model1=multinom(freq~segments+sample,data=table) model2=multinom(freq~ sample,data=table)
2013 Aug 23
1
A couple of questions regarding the survival:::cch function
Dear all, I have a couple of questions regarding the survival:::cch function. 1) I notice that Prentice and Self-Prentice functions are giving identical standard errors (not by chance but by programming design) while their estimates are different. My guess is they are both using the standard error form from Self and Prentice (1986). I see that standard errors for both methods are
2008 Oct 31
4
Help needed with Waterfall plot
Hi friends, I need suggestions/directions on how to producing a waterfall plot for present extend of change in tumour size for a set of respondents in a study.  Example of use of waterfall plot is in the following slides presented at ASCO 2007 by Axel Grothey. Link is
2014 Oct 01
2
JOB - PhD position: applying HPC in cancer research
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
2013 Nov 17
1
FactoMineR
Hola. Como te dijo Carlos, el problema está en los nombres de las columnas y en los nombres de las filas. Cuando hice la importación (con dd<-read.csv('mortality.csv'), tuve problemas con las filas de nombre: - Malignant tumour of the larynx trachea bronchus and lungs - Malignant tumour of the lip pharynx and mouth - Other endocrinological metabolic and nutritional conditions
2008 Jun 06
1
lsmeans
Hello, I have the next function call: lme(fixed=Error ~ Temperature * Tumour ,random = ~1|ID, data=error_DB) which returns an lme object. I am interested on carrying out some kind of lsmeans on the data returned, but I cannot find any function to do this in R. I'have seen the effect() function, but it does not work with lme objects. Any idea? Best, Dani -- Daniel Valverde Saub? Grup
2005 Nov 26
1
list.files(recursive=T) does not return directory names
list.files() (and dir()) don't appear to return names of directories when one uses the recursive=T argument. E.g., > dir(file.path(R.home(),"library"), pattern="^R$", recursive=T) [1] "Malmig/help/R" but the unix find commmand finds lots of R directories > z <- system(paste("find", file.path(R.home(),"library"), "-name
2019 Nov 15
2
S3 methods in packages. Change in R 4.0.0?
Hello, since Bioconductor devel branch 3.11 started, which is operating with R-devel 4.0.0 (for e.g. 2019-11-03 r77362 on OS X 10.11.6 El Capitan), my package CFAssay 1.21.0 is not built on none of all three Systems, Linux, Windos and Mac. The error message refers to xy.coords which is called by R function plot.default. I found out that it has to do with the S3 object system. In my package I
2019 Nov 16
0
S3 methods in packages. Change in R 4.0.0?
On 15/11/2019 8:42 a.m., Herbert Braselmann wrote: > Hello, > > since Bioconductor devel branch 3.11 started, which is operating with > R-devel 4.0.0 (for e.g. 2019-11-03 r77362 on OS X 10.11.6 El Capitan), > my package CFAssay 1.21.0 is not built on none of all three Systems, > Linux, Windos and Mac. The error message refers to xy.coords which is > called by R function
2014 Oct 03
0
JOBS: New positions in computational biology, bioinformatics, statistics, HPC and software engineering
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:
2004 May 17
0
Bioconductor 1.4 released
Greetings! The Bioconductor core group would like to announce the 5th release of Bioconductor, version 1.4. There are many new packages as well as several major upgrades and fixes in older packages, and users are encouraged to upgrade existing tools and check out the new packages. Release 1.4 is intended to be operated with R version 1.9.x, which can be obtained at CRAN
2006 Jul 06
0
pvclust Error:NA/NaN/Inf in foreign function call (arg 11)
Hi all, I'm new to R and I'm struggling to decipher an error message. Briefly, I am trying to use the pvclust package to do hierarchical clustering of some CGH data. The data is from the Progenetix CGH database. It is arranged as a table where each column is a single case and each row is a single chromosome band. The value in each cell is either 0, 1, 2, or -1. Corresponding to no change,
2008 Jan 26
0
Who can tell me how I adjust the R code for bootstrapping the Cox model?
Hi, The following code, from Angelo Canty article on line "Resampling Methods in R: the boot Package, 2002", works fine for Angelo Canty using R 2.6.0 on Windows XP. It also works for me using R 1.2.1 and S-PLUS 2000 on Windows XP after installing the S-PLUS bootstrap library, with slight differences in my outputs. > library(boot) > library(survival) >
2008 Jan 25
0
Please help me
Hi, The following code, from Angelo Canty article on line "Resampling Methods in R: the boot Package, 2002", works fine for Angelo Canty using R 2.6.0 on Windows XP. It also works for me using R 1.2.1 and S-PLUS 2000 on Windows XP after installing the S-PLUS bootstrap library, with slight differences in my outputs. > library(boot) > library(survival)
2006 Jul 10
2
pvclust missing values problem
Hello all, I posted a question to this list last week and received no response. I am unsure if this means no-one knows the answer or if I posed the question badly. I'm going to assume I posed the question badly and try again. I am new to R so it is quite likely it's a very naive question, however if there is something blindingly obvious that I am missing or if there is another resource I