similar to: Calculate R-Square for existing predictors

Hello, I have a cohort with approx 1,200 patients at the ages of 30-65 that had their first myocardial infarction during 1992: · They were in a follow up until 2005. · About 400 of them died during this period of time (right censored) · Each one of them had up to 4 mi recurrent events. I am using the semi-parametric model in order to assess the relationship of

Hi, I have two different imaging modalities (for the identification of areas of infarcted myocardium) that I need to compare regarding agreement and consistency. However, I don't think that methods like Cohen's Kappa, PCC, Bland-Altmann or ICC are sufficient here as there is not just a pairwise but also a spatial relationship between measured data points. For example if the results of the

Hello, I have few questions about recurring events. I would greatly appreciate it if anyone can assist me. I have data that consist of approx 1,100 Consecutive patients released from hospital after first Myocardial infarction (MI). They were followed for 13 years. Recurrent MI and unstable angina pectoris (UAP) leading to hospitalization were recorded (within-subject range: 0-4 for recurrent MI;

Hi , I have a data set with recurrence time (up to four) of myocardial infarction (MI). Part of the file is showing below: Num1 Trt Sex Time T1 T2 T3 T4 1011 1 1 9 1211 0 1 59 3020 1 2 14 3 1245 0 1 18 12 16 3069 1 2 26 6 12 13 2051 0 1 53 3 15 46 51 The data consist of the following eight variables: Num1 , patient number Trt, treatment group (1=placebo and 2=drug) Sex,

Hi everyone, I am doing 5 years mortality predictive index score with survival analysis using a Cox proportional hazard model where I have a continous predictive variable and a right censored response which is the mortality, and the individuals were followed a maximum of 7 years. I'd like to asses the discrimination ability of survival analysis Cox model by computing a ROC curve and area

Have the following problems: MBO USB-MultiCardREader 6-in-1 does not read 128MB CF-Card. Oct 3 13:49:23 katrin /kernel: da0 at umass-sim0 bus 0 target 0 lun 0 Oct 3 13:49:23 katrin /kernel: da0: <ICSI IC1100 CF 2.5B> Removable Direct Access SCSI-0 device Oct 3 13:49:23 katrin /kernel: da0: 650KB/s transfers Oct 3 13:49:23 katrin /kernel: da0: Attempt to query device size failed:

Dear All, I fear that this is a really easy question but I do seem to go around in circles.. I have 2 points on a plot and would like to calculate the slope of the line drawn through these 2 points. that cant be so hard?! Thank you in advance, Katrin -- Katrin Fleischer Vrije Universiteit Amsterdam Faculty of Earth and Life Sciences Subdepartment Hydrolgy and Geo-Environmental Sciences Room

I was hoping for some advice regarding possible explanations for the fitted probability values I obtained for a multinomial logistic regression. The analysis aims to predict whether Capgras delusions (present/absent) are associated with group (ABH, SV, homicide; values = 1,2,3,), controlling for previous violence. What has me puzzled is that for each combination the fitted probabilities are

Hello all, I am very new to R and i am facing two problems. First i didn't succeed changing the konsole language in english even after trying the line command set language='en'. I would like to plot ROC curves. I have a serie of 10 threshold tests that i do for 10 patients. The prediction for the patients is always the same but the status can change given to the considered threshold.

Hello, I am just a beginner of R 1.9.0. I try to construct a predictive score for the development of liver cancer in cirrhotic patients. So dependant variable is binanry (cancer yes or no). Independant variables are biological data. The aim is to find out a cut-off value which differentiate (theoratically) from normal to pathological state for each biological data. How can I step in procedue to

Hello I am new in R. I am trying to implement Biomod 2 package. However, I have a doubt. I want to calculate the mean and sd of "Testing.data" (ROC and TSS) > # let's print the ROC scores of all selected models > myBiomodModelEval_55["ROC","Testing.data",,,] RUN1 RUN2 RUN3 RUN4 RUN5 RUN6 RUN7 RUN8 RUN9 RUN10 0.938 0.938 0.926 0.931 0.939

Ol?, Please keep this in the list, I'm cc-ing r-help at r-project.org. And yes, I am Portuguese but R-Help is a mailing list in the English language. As for your new question, I believe that you should start a new thread. This is completely different from the question on computing mean and sd. Ask a new question. Font "arial" is a Microsoft font and as far as I know is not

Dear Experts, I am trying to do a time-stratified case-crossover analysis on air pollution data and number of myocardial infarctions. In order to avoid model selection bias, I started with a simple simulation. I'm still not sure if my simulation is right. But the results I get from the "ts-case-crossover" are much more variable than those from a glm. Is this: a. Due to

>>>>> Katrin Leinweber <katrin.leinweber at uni-konstanz.de> >>>>> on Sun, 25 Mar 2018 19:04:34 +0200 writes: > Dear Madams and Sirs, > because the DOI foundation recommends a new, secure resolver [1], I > wanted to suggest the attached patch. It > a) updates a static DOI link in the docu, > b) the code chunks that

Dear list, I am trying to build a cox model and then perform ROC analysis in order to retrieve some genes that are correlated with breast cancer. When I calculate the hazard score taking into account different numbers of genes and their coefficients ( I am trying to find the pest predictor number of genes), I retrieve from around 1 values (for few genes included ) to size of e+80 values (for many

Dear Experts, I am trying to do a time-stratified case-crossover analysis on air pollution data and number of myocardial infarctions. In order to avoid model selection bias, I started with a simple simulation. I'm still not sure if my simulation is right. But the results I get from the "ts-case-crossover" are much more variable than those from a glm. Is this: a. Due to the simple

Hi all, I am not sure how to handle interactions with categorical predictors in the GAM models. For example what is the different between these bellow two models. Tests are indicating that they are different but their predictions are essentially the same. Thanks a bunch, > gam.1 <- gam(mortality.under.2~ maternal_age_c+ I(maternal_age_c^2)+ + s(birth_year,by=wealth) + +

I am hoping for some advice regarding resolving error messages I have received when trying to use the expand.grid command. library(nnet) library(MASS) library(car) mod.multacute <-multinom(kc$group ~ kc$in.acute.danger * kc$violent.convictions, na.rm=T) summary(mod.multacute, cor=F, Wald=T) Anova (mod.multacute) confint (mod.multacute) > predictors <- expand.grid(group=1:3,

Hi all, I have this microarray large microarray data set (ALL) from which I would like to subset or extract a set of data based on a factor ($mol.biol). I looked up some example of subsetting in, picked up two commands and tried both but I got error messages as follows > testset <- subset(ALL, ALL$mol.biol %in% c("BCR/ABL","ALL1/AF4")) >> Error in

Dear All, I have data in HDF file format and would like to read it into R. I have tried the package hdf5 without success. Any ideas and suggestions?? Kind regards, Katrin -- Katrin Fleischer Vrije Universiteit Amsterdam Faculty of Earth and Life Sciences Subdepartment Hydrolgy and Geo-Environmental Sciences Room E-360 De Boelelaan 1085 1081 HV AMSTERDAM Tel: +31 20 59 87391