similar to: nlme Output

The file TENSILE.DAT from the Hand et al "Handbook of Small Data Sets" looks like this: 0.023 0.032 0.054 0.069 0.081 0.094 0.105 0.127 0.148 0.169 0.188 0.216 0.255 0.277 0.311 0.361 0.376 0.395 0.432 0.463 0.481 0.519 0.529 0.567 0.642 0.674 0.752 0.823 0.887 0.926 except that my mail client has replaced the tab separators by blanks. If I paste this data into R 2.2.1 what I get is

I am a total newbie at R but experienced with computers. If this is not the right forum for this question, please let me know one that is. I searched in the R manuals in the Help section, the Nabble help and Rseek but no luck. I am trying to install the package gcl on my recently installed R 2.8.1 I searched on cran for the windows version and found a zip file for the package In RGui, I ran

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

Full_Name: Sahotra Sarkar Version: 2.2.0 OS: Windows XP Professional Submission from: (NULL) (146.6.130.180) The following two commands should give the same results for the eigenvectors but do not (there is a sign reversal for the first one): > summary(princomp(bumpus),loading = TRUE) Importance of components: Comp.1 Comp.2 Comp.3 Comp.4 Comp.5

I've just found the lavaan package, and I really appreciate it, as it seems to succeed with models that were failing in sem::sem. I need some clarification, however, in the output, and I was hoping the list could help me. I'll go with the standard example from the help documentation, as my problem is much larger but no more complicated than that. My question is, why is there one latent

Hi, When I run the survfit function, I want to get the restricted mean value and the standard error also. I found out using the "print" function to do so, as shown below, print(km.fit,print.rmean=TRUE) Call: survfit(formula = Surv(diff, status) ~ 1, type = "kaplan-meier") records n.max n.start events *rmean *se(rmean) median 200.000

I am running 9 negative binomial regressions with count data. The nine models use 9 different dependent variables - items of a clinical screening instrument - and use the same set of 5 predictors. Goal is to find out whether these predictors have differential effects on the items. Due to various reasons, one being that I want to avoid overfitting models, I need to employ identical types of

Dear all,I am a new user of WinBUGS and need your help. After running the following code, I got parameters of beta0 through beta4 (stats, density), but I don't know how to get the prediction of the last value of h, the variable I set to NA and want to model it using the following code.Does anyone can given me a hint? Any advice would be greatly appreciated.Best

Dear useRs, I reran an analysis with bam (mgcv, version 1.7-17) originally conducted using an older version of bam (mgcv, version 1.7-11) and this resulted in the same estimates, but much lower standard errors (in some cases 20 times as low) and lower p-values. This obviously results in a larger set of significant predictors. Is this result expected given the improvements in the new version? Or

Hello, R-i-zens. I'm working on an data set with a factorial ANOVA that has a significant interaction. I'm interested in seeing whether the simple effects are different from 0, and I'm pondering how to do this. So, I have my.anova<-lm(response ~ trtA*trtB) The output for which gives me a number of coefficients and whether they are different from 0. However, I want the

Some help with how to re-label the vertical axis in a histogram would be appreciated. qplot(off.sc,weight=rel.freq,binwidth=.29,main="test Figure"+ylab("New from inside"))+ylab("New from outside")+ xlab("off.sc\nAggregated frequency plots for 17 equal intervals.") The code

Hi I compouted a multiple linear regression with repeated measures on one explanatory variable: BOLD peak (blood oxygenation) as dependent variable, and as independent variables I have: -age.group (binaray:young(0)/old(1)) -and task-difficulty measured by means of the reaction-time 'rt'. For 'rt' I have repeated measurements, since each subject did 12 different tasks. -> so

Hi R-users,   I would like to search for the values of seq that match my rand values.  In excel I will use =VLOOKUP(G2,$E$2:$F$32,2).  For example, for rand=.262 it will give me approximately seq=120 and rand=0.964293344, seq=460 and etc.   E           F     G cdf         seq   rand 0.00E+00    0     0.262123478 1.56E-03    20    0.964293344 1.55E-02    40    0.494827113 5.30E-02    60   

Hello, Apologies if this is the wrong list, I am a first-time poster here. I have an experiment in which an output is measured in response to 42 different categories. I am only interested which of the categories is significantly different from a reference category. Here is the summary of the results: summary(simple.fit) Call: lm(formula = as.numeric(as.vector(TNFa)) ~ Mutant.ID, data =

Dear Thomas, The head of my dataset > head(wsuv) parcel sp time censo treatment species 1 S8 Poecilanthe effusa ( Hub. ) Ducke. 1 1 1 1 2 S8 Poecilanthe effusa ( Hub. ) Ducke. 1 1 1 1 3 S8 Poecilanthe effusa ( Hub. ) Ducke. 1 1 1 1 4 S8 Poecilanthe effusa ( Hub. ) Ducke. 1 1 1

hello: my data looks like: time1  time2   event  catagoria 2004    2006        1            C 2004    2005        0            C 2005    2010        1            E 2007    2009        1            C 2006    2007        0            E 2008    2010        0            C 2008    2010        1            E ... and the census interval is 1 year I have tried  this

... and the mailing list is picky about attachments... whatever you attached did not conform to the stringent requirements mentioned in the Posting Guide. Pasting the code right into the email is usually safest, though you DO have to post using plain text (as the Posting Guide indicates) or your code may get mangled by the automatic html format removal. On May 15, 2018 7:04:31 AM PDT, Bert Gunter

OK, Let's try this again! Here is the reproducible script; it is long because I had to copy the panel dataset here. My question is related to systemfit; I don't know how to get the result for the entire panel. #Reproducible script Empdata<- read.csv("/Users/ngwinuiazenui/Documents/UPLOADemp.csv") View(Empdata) install.packages("systemfit")

Unless there is good reason not to, always cc the list -- there are lots of smarter folks than I on it who can help. I may or may not have time to look at this. Hopefully someone else will. -- Bert Bert Gunter "The trouble with having an open mind is that people keep coming along and sticking things into it." -- Opus (aka Berkeley Breathed in his "Bloom County" comic strip

Hi, There seems to be a problem with the timer resolution on x86_64. This is clear in ping results - I don't know if it's just a ping problem or if it manifests elsewhere as well. It does also affect mtr and traceroute times. I guess it's more a kernel issue than a CentOS problem, but is anyone else seeing the same? Ping results have a resolution of 10ms - so a ping <10ms