similar to: Normality tests on groups of rows in a data frame, grouped based on content in other columns

Hi everyone, I have a problem using rpart (R 2.0.1 under Unix) Indeed, I have a large matrix (9271x7), my response variable is numeric and all my predictor variables are categorical (from 3 to 8 levels). Here is an example : > mydata[1:5,] distance group3 group4 group5 group6 group7 group8 pos_1 0.141836040224967 a c e a g g pos_501

Hello, unfortunately, I don't know a better subject. I would like to be very flexible in how to process my data. Assume the following dataset: par1 <- seq(0,1,length.out = 100) par2 <- seq(1,100) fac1 <- factor(rep(c("group1", "group2"), each = 50)) fac2 <- factor(rep(c("group3", "group4", "group5", "group6"), each =

Hi I needed some help with ANOVA I have a problem with My ANOVA analysis. I have a dataset with a known ANOVA p-value, however I can not seem to re-create it in R. I have created a list (zzzanova) which contains 1)Intensity Values 2)Group Number (6 Different Groups) 3)Sample Number (54 different samples) this is created by the script in Appendix 1 I then conduct ANOVA with the command >

Sorry i had a misprint in the appendix code in the last email Hi I needed some help with ANOVA I have a problem with My ANOVA analysis. I have a dataset with a known ANOVA p-value, however I can not seem to re-create it in R. I have created a list (zzzanova) which contains 1)Intensity Values 2)Group Number (6 Different Groups) 3)Sample Number (54 different samples) this is created by the

I planned using ifmember.exe from Windows 2000 resource kit to map the right drive-mappings to the right shares with logon-scripts. Unfortunately it seems as ifmember simply doesnt report the right groups for the users. Even tho "id user1" shows the right groups; "uid=2082(user1) gid=1002(Group1)roups=1002(Group1),545(Users),1000(Group0)", User is a member of group

On 24.01.2020 14:01, Christian wrote: > On 23.01.2020 10:26, L.P.H. van Belle via samba wrote: >> Hai Christian, >> >>>>> Thism, this is just strange, Christian, did you already >>> run and if not, can you run it and post the ouputs. : >>>>> net cache flush >>>>> systemctl stop samba winbind >>>>> systemctl

Dear List, I am looking to perform exploratory analyses of two (relatively) large datasets of categorical data. The first one is a binary 80x100 matrix, in the form: matrix(sample(c(0,1),25,replace=TRUE), nrow = 5, ncol=5, dimnames = list(c( "group1", "group2","group3", "group4","group5"), c("V.1", "V.2", "V.3",

hi list can U help me caller id in USTM if now working -- Starting switch on '4211 at 4211-1' to 4203 -- Executing [4203 at office:1] DumpChan("USTM/4211 at 4211-0x7f7ba4228fd0", "") in new stack Dumping Info For Channel: USTM/4211 at 4211-0x7f7ba4228fd0: ================================================================================ Info: Name=

I'm creating a stacked bar chart using the likert command in the HH package. My data are in a data frame, with two numeric variables and a categorical variable, I can't get likert to use the column containing the categorical variable as a my y axis label. Here is a quick example: library(HH) #my data are:

Hi all, Running samba 3.5.5 in a Solaris non-global zone. I have created a folder (StudentJobApplications) on a share which I want to make accessible only to members of a Unix group (studempl). I have added myself to the group but when I or other group members try to access the folder via Windows Explorer I get the following: I:\StudentJobApplications is not accessible Access is denied Here

#I am trying to understand how R fits models for contrasts in a #simple one-way anova. This is an example, I am not stupid enough to want #to simultaneously apply all of these contrasts to real data. With a few #exceptions, the tests that I would compute by hand (or by other software) #will give the same t or F statistics. It is the contrast estimates that R produces #that I can't seem to

Good day. 1. We have configured two domain controllers on Windows 2003 R2. We named them TEST.LOCAL and CHILD.TEST.LOCAL respectively and made a trust relationships between them. 2. We have installed Samba 3.5.3 on Ubuntu 9.10, kernel 2.6.31-14 and configured it for using winbindd. We have encountered a problem with results that winbind returns upon a command GETGRENT. We

Hi, I am trying to execute the following SQL statement using two data frames: tab1, tab2 : Two Tables Select tab1.*, tab2.*, tab1.tobiiTime - tab2.ruiTime as timeDiff, IFNULL(n-m, -9999999) as alwaysIncrement FROM tab1 LEFT OUTER JOIN tab2 On tab1.data1 - tab2.mouseX = 0 And tab1.data2 - tab2.mouseY = 0 I am trying to do the following in R:- *#Getting error here:* data

Hi, Let s be a dataframe. > s A B C 0 0 1 1 0 1 1 0 1 0 0 1 1 0 1 0 1 1 0 1 1 0 1 1 0 0 1 > tab1=table(s[,c(1,2)]) > tab1 B A 0 1 0 3 3 1 3 0 > tab2=table(s[,c(1,3)]) > tab2 C A 1 0 6 1 3 The problem is I need to access frequency corresponding to (0,0). tab1[1] will give me the correct value

Hi, I am doing an analysis to see if these is tissue specific effects on the gene expression data . Our data were collected from 6 different labs (batch effects). lab 1 has tissue type 1 and tissue type 2, lab 2 has tissue 3, 4,5,6. The other labs has one tissue type each. The 'sample' data is as below:

Hello, I'm using aov() to analyse changes in brain volume between males and females. For every subject (there are 331 in total) I have 8 volume measurements (4 different brain lobes and 2 different tissues (grey/white matter)). The data looks like this: Subject Sex Lobe Tissue Volume subect1 1 F g 262374 subect1 1 F w 173758 subect1 1 O g 67155 subect1 1 O w 30067 subect1 1 P g 117981

HI Guy''s TAB1 and TAB2 have some radio button, checkbox and dropdown menu. When TAB1 is selected, I have to switch to TAB2 and then back to TAB1 to refresh the loaded content. How to make TAB1 refresh loaded content when click on its tab? *code is something like that* <ul class="tabs"> <li><a *href="#tab1"*>Gallery</a></li>

I'm working with a nested model (mixed). I have four factors: Patients, Tissue, sex, and tissue_stage. Totally I have 10 patients, for each patient, there are 2 tissues (Cancer vs. Normal). I think Tissue and sex are fixed. Patient is nested in sex,Tissue is nested in patient, and tissue_stage is nested in Tissue. I tried aov and lme as the following, > aov(gene ~ tissue + gender +

I'm having trouble with files being marked read-only in Windows because the Solaris file owner does not have write-permissions on the file; group-write is allowed: -r--rw---- 1 user group 32 Feb 13 14:19 testfile.txt I thought that setting "store dos attributes = yes" for this share would allow the "read only" setting to be stored in extended attributes, but it

My small brain is having trouble getting to grips with lme() I wonder if anyone can help me correctly set the random = argument to lme() for this kind of setup with (I think) 9 variance/covariance components ... Study.1 Study.2 ... Study.10 Treatment.A: subject: 1 2 3 4 5 6 etc. 28 29 30 Treatment.B: subject: 31