search for: sbpurohit

I would like to know if clogit function can be used as below clogit(group~., data=dataframe) When I try to use in above format it takes a long time, I would appreciate some pointers to get multiple combinations tested. set.seed(100) d=data.frame(x=rnorm(20)+5, x1=rnorm(20)+5, x2=rnorm(20)+5, x3=rnorm(20)+5, x4=rnorm(20)+5, x5=rnorm(20)+5, x6=rnorm(20)+5, x7=rnorm(20)+5, x8=rnorm(20)+5,

Hello list, I have a similar issue as this post http://tolstoy.newcastle.edu.au/R/e6/help/09/04/11438.html#options2 and I used the suggestion provided by Jorge with modifications to my data do.call(c,lapply(your_list_with_the_t_tests,function(x) x$p.value)) but I am getting the following error after excuting the code B<-by(eo,eo$PlateID, function(.sub) t.test(mcp1~Self_T1D,data=.sub,

so here is the code I need help to fix the line for 'st' when it reaches maximum, that's where i am getting stuck. thanks Sharad set.seed(100) d=data.frame(x=rnorm(20)+5, x1=rnorm(20)+5, x2=rnorm(20)+5, x3=rnorm(20)+5, x4=rnorm(20)+5, x5=rnorm(20)+5, x6=rnorm(20)+5, x7=rnorm(20)+5, x8=rnorm(20)+5) r2=c() cinit=0 for (col in 1:9) { cinit=cinit+1 st=cinit+1

Dear list, i am a biologist who needs to do some ttest between disease and non disease, sex, genotype and the serum levels of proteins on a large number of individuals. i have been using excel for a long time but it is very tedious and time consuming. i am posting the data below and ask your help in generating a code to get this analysis done in R. thanks gender disease genotype data M N CC

Hello gurus, I have a dataframe containing two groups viz., 'control' and 'case', each of these groups contains longitudinal data for 100 subjects. I have to plot all these subjects on a single chart and then put a regression line for each of the group for all the subjects. I have written a function to do the chart grpcharts<-function (dat, group,group2,molecule,cutoff){

Hello gurus, I have some variables, and i am creating combinations for analysis in the end i need these variables to be displayed like "LEPTIN+SAA+PTH". currently i am using loop to perform this. I would appreciate any pointers to do it without the loop. > mols=c("LEPTIN","SAA","PTH","sEGFR") > samples=mols[1:3] > samples [1]

Hello all, I am using 'plot' to create standard curves for elisa data. when I use 'plot' with type='b' i get the points connected with lines and one straigth line from the lowest datapoint to the highest data point. how can i avoid/remove it from the figure. i am using R2.9.1, below is the example of the data. od<-c(10, 8, 6,4,2,1, 10.5,7.8,6.4,3.8,2.1,0.95)

Hello all, I have arranged my data as per Dennis's suggestion in this post http://www.mail-archive.com/r-help at r-project.org/msg107156.html. the posted code works fine but when I try to apply it to my data, i get "> u2 <- ddply(xxm, .(plateid, cytokine), as.data.frame.function(f)) Error in t.test.formula(conc ~ Self_T1D, data = df, na.rm = T) : grouping factor must have

I have a data frame like this xx<-data.frame(cbind(Sample=c('Ctrl_6h','1+0_6h','1+200_6h','1+5k_6h','Ctrl_5K_6h','ConA_6h'), IFIT1=c(24,25,24.7,24.5,24.2,24.8))) grep('[[:digit:]]h',xx$Sample) yy<-xx$Sample strsplit(yy,"_") I have to extract the time information separated by '_' in the sample

Hello I have a data set like below: plate.id well.id Group HYB rlt1 1 P1 A1 Control SKOV3hyb 0.190 2 P1 A2 Control SKOV3hyb 0.210 3 P1 A3 Control SKOV3hyb 0.205 4 P1 A4 Control SKOV3hyb 0.206 5 P1 A5 Control SKOV3hyb 0.184 385 P1 A1 ovca SKOV3hyb 0.184 386 P1 A2 ovca SKOV3hyb 0.229 387

Dear All: I do see I have weeks of codes in my console when I check with my arrow up keys. I have been clearing them with Control L but it seems to clear it clear the screen temporally. I do see the previous codes again when I open R the next day, after quitting the session! Q: How do I clear this? Thanks; YA -- View this message in context:

hello gurus, i have a data frame like this HTN HTN_FDR Dyslipidemia CAD t1d_ptype[1:25] 1 Y Y Y T1D 2 T1D 3 Ctrl_FDR 4 T1D 5 Y Ctrl 6 Ctrl 7

...; 32 629.6 > 33 2250.1 > ... > -- View this message in context: http://www.nabble.com/ggplot2-Xlim-tp21161660p21170453.html Sent from the R help mailing list archive at Nabble.com. ------------------------------ Message: 15 Date: Thu, 25 Dec 2008 07:26:46 -0800 (PST) From: 1Rnwb <sbpurohit@gmail.com> Subject: Re: [R] creating standard curves for ELISA analysis To: r-help@r-project.org Message-ID: <21168216.post@talk.nabble.com> Content-Type: text/plain; charset=us-ascii Thank you for your suggestions, I am sorry that http://www.nabble.com/file/p21168216/ds2_panelA_p8_B3_...

I have 120 MS chromatograms containing two columns'Time' and 'Peak height'. how do in create a msSet file which is required by all the functions of 'msProcess' to process these files. I would appreciate help very much. Thanks Sharad -- View this message in context: http://r.789695.n4.nabble.com/msProcess-creating-msSet-file-s-tp3727959p3727959.html Sent from the R help

Hi I have a script which is designed to gather data from individual columns from a file, which is an output from an instrument. the file has multiple sections and each a section has data under each column (vars), I am using the name of the column as a variable to gather the column ID using vidx<-grep(vars[vi],gsub("[[:punct:]]","",strrl1[[datbeg-1]]),ignore.case=T) the

Hello, I have data in a dataframe with 139104 rows which is multiple of 96x1449. i have a phenotype file which contains the phenotype information for the 96 samples. the snp name is repeated 1449X96 samples. I haveto merge the two dataframes based on sid and sen. this is how my two dataframes look like dat<-data.frame(snpname=rep(letters[1:12],12),sid=rep(1:12,each=12),

I have question about log2 transformation and performing mean on log2 data. I am doing analysis for ELISA data. the OD values and the concentration values for the standards were log2 transformed before performing the lm. the OD values for samples were log2 transformed and coefficients of lm were applied to get the log2 concentration values. I then backtransformed these log2 concentrations and the

Hello R gurus, I have to create 12 plots, I have been using the following script, which leaves a large white space between two plot. I would appreciate if someone can suggest an alternative to reduce the white space. par(mar=c(3,3,.5,.5)) split.screen(c(6,2)) # split display into two screens for (i in 1:12) { if (i<11) { screen(i) plot(1:10,xaxt='n', xlab='',

how can i put the row labels on the left hand of the heatmap in heatmap.2? abnr<-structure(c(1, 0.678622097406395, 0.670294749652918, -0.0016314464654279, -0.000519068106572792, 0.199581999119988, -0.0106623494189115, 0.0840111691399559, -0.0461494399639137, 0.249279171677728, NA, 1, 0.757114062773504, 0.0352642759270137, -0.0255518450373996, 0.0943268190664674, -0.0536269679247722,

Hello R gurus, I have a data set from which i have to extract the gender and age matched rows from controls and disease group disease<-paste(rep(c('y','n'),11)) gender<-paste(rep(c('m','f'),11)) mcp<-rnorm(700,1400) age<-rnorm(32,34) dat<-data.frame(disease=disease,sex=gender,Dr_age=age[1:22],MCP=mcp[1:22]) I have other categorical variables also to