search for: tumours

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

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

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 Noncoding RNA regulators of gene expression in individual tumour cells RNABiology/Computational Biology The goal of this project is to use computational tools to ask how patterns in gene exp...

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

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

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)

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

Hi, I am currently using the aCGH package in R version 2.1.0 Windows with some supporting packages (eg. cluster) built under R 2.1.1.Using aCGH package, I am able to identify regions of genomic aberrations in my cell lines using the HMM model. However, when I tried to use aCGH for my paraffin embeded tumour sample, I got the following warning. Warning: MAD could not ben computed for one of

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

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

...Biology Group - Crispin Miller ========================== Postdoctoral Scientist in Computational Biology: A position is now available for a highly motivated postdoctoral research scientist to develop computational models of gene expression across populations of cells, and to ask how they change in tumours. The goal is to identify novel regulatory noncoding RNA molecules that are disrupted in cancer. 4 Year PhD Studentship: This project will involve applying machine learning and pattern recognition techniques to high volumes of RNA-sequencing data representing a combination of single cells and bulk...

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) >

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

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,

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) >

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)

Estimados Queremos con el paquete FactoMineR hacer este tipo de tabla de mortalidad que lea los datos desde de una tabla csv Realizamos lo que viene en la ayuda y es muy interesante, sin embargo cuando mandamos a leer desde la tabla csv original de los autores no hace el análisis porque algo falta y no nos percatamos de que es. Adjunto tabla original Saludos cordiales #ESTO ES LO QUE

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) >

----- begin included message In case cohort study, we can fit proportional hazard regression model to case-cohort data. In R, the function is cch() in Survival package Now I am working on case cohort analysis with time dependent covariates using cch() of "Survival" R package. I wonder if cch() provide this utility or not? The cch() manual does not say if time dependent covariate is

I want to take the first row of each unique ID value from a data frame. For instance > ddTable <- data.frame(Id=c(1,1,2,2),name=c("Paul","Joe","Bob","Larry")) I want a dataset that is Id Name 1 Paul 2 Bob > unique(ddTable) Will give me all 4 rows, and > unique(ddTable$Id) Will give me c(1,2), but not accompanied by the name column.