similar to: NA problem when use paste function

Hello,     Looking up a users group membership I'm showing different results on each DC. UID and GID mapping appears consistent but not all group membership is displayed. I've verified idmap.ldb is backup up and copied over to the other DC's. I do notice when taking a hot backup of idmap.ldb, the file size is dramatically smaller than the original. Using Microsoft RSAT to view

#Hello, #I have would like to paste a single column of a matrix # in pair wise fashion with other columns based upon # even and odd column numbers. # I can do it in a very clunky fashion and I know there # must be a better way. below is a sample matrix and my extremely # clunky code that gets the job done for a small matrix, but i plan to # do this on a much grander scale. any help would be very

After some more screwing around with leaving and rejoining the ADS domain I was finally able to access a share with "valid users =" set to a domain group I was a member of. The _only_ change I made after this was to add yet another group to the valid users on the share and restart samba...after that I could no longer access the share. I removed the additional group, restarted samba and

Dear all, I need to read an ASCII file with diffent length lines. This is what is contained in the file gene.txt: 1st line ID description snp_id genotype 2nd line 10003 Low rs152240 3rd line 10003 Moderate rs189011 TC 4th line 10004 Conservative rs152240 GC 5th line 10004 Bad rs154354 6th line 10013 Bad rs152240 7th line 10019 Conservative rs152240 AC etc... This is what I would like to obtain

#Hello, #I have a question about obtaining results from a loop I have written. #Below is a sample of individual genotypes from a genetic question I am working on called "P.genotype.sample ". P.genotype.sample<-matrix(10,10,10) P.genotype.sample[,1]<-c(2,2,1,5,1,1,5,6,1,3) P.genotype.sample[,2]<-c(6,3,3,6,8,1,6,7,2,3) P.genotype.sample[,3]<-c(2,2,2,3,3,2,2,2,3,3)

Hi. I was wondering if anyone might have some suggestions about how I can overcome a problem of "iteration limit reached without convergence" when fitting a mixed effects model. In this study: Outcome is a measure of heart action Age is continuous (in weeks) Gender is Male or Female (0 or 1) Genotype is Wild type or knockout (0 or 1) Animal is the Animal ID as a factor

Hi, I am conducting an association analysis of genotype and a phenotype such as cholesterol level as an outcome and the genotype as a regressor using multiple linear regression. There are 3 possibilities for the genotype AA, AG, GG. There are 5 people with the AA genotype, 100 with the AG genotype and 900 with the GG genotype. I coded GG genotype as 1, AG as 2 and AA as 3 and the p-value for the

Hello, My R skills are somewhere between novice and intermediary, and I am hoping that some of you very helpful forum members, whom I've seen work your magic on other peoples' problems/questions, can help me here. I have a matrix with the following format: (i) individual plants comprising many different genotype groups (i.e., a plant is genotype 1 or genotype 2 or genotype 3, etc). The

Dear R users, I have a problem with something called "NaNs" in a nested mixed model. The background is that I have studied the number of insect nymphs emerging from replicated Willow genotypes in the field. I have 15 replicates each of 4 Willow genotypes belonging two 2 Willow species. Now I want to elucidate the effect of Willow genotype on the number of emerging nymphs. Previously I

Hi, Could someone tell me if this is the correct model syntax for the following dataset: lme(height~treatment+genotype+treatment*genotype,drought,random=~genotyp e) The dataset has two factors: one fixed - treatment, and one random - genotype. I need to test the effect of both factors to identify their significance. There are multiple (but not equal) replicates at each level of genotype (the

-----Original Message----- From: Ghosh, Sandeep Sent: Thursday, June 30, 2005 5:43 PM To: 'Berton Gunter' Subject: plot legend outside the grid Thanks for the pointers... I managed to get everything to look and feel the way I want except for the legend to plot outside the grid... Thanks for the note on the par, but I'm not able to it to plot outside the plot grid.. dataFrame <-

Hello R Users, I am investigating the basic use of the LME function, using the following example; Response is Weight, covariate is Age, random factor is Genotype model.lme <- lme (Weight~Age, random=~ 1|Genotype) After summary(model.lme), I find that the estimate of Age is 0.098 with p=0.758. I am comparing the above model with the AOV function; model.aov <- aov (Weight~Age + Genotype)

I want to specify a two-factor model in lme, which should be easy? Here's what I have: factor 1 - treatment FIXED (two levels) factor 2 - genotype RANDOM (160 genotypes in total) I need a model that tells me whether the treatment, genotype and interaction terms are significant. I have been reading 'Mixed effects models in S' but in all examples the random factor is not in the main

Hi All, I've been working on updating the 'genetics' package. As a consequence of the upgrade, .First.lib() looks like: .First.lib <- function(libname, pkgname) { if (!require(combinat)) warning("Unable to load 'combinat' library. Function `diseq.ci' will fail.") require(gregmisc) genotype <-

Hi, (Please use ?dput() to share the example dataset. Avoid using images to show dataset. Also, please read the posting guide esp. regarding home work, assignments etc.) res <- sapply(Gene[,-1],function(x) tapply(x,list(Gene$Genotype),mean)) #or res2 <-? aggregate(.~Genotype, data=Gene,mean) #or library(plyr) ?res3 <- ddply(Gene,.(Genotype),numcolwise(mean)) identical(res2,res3)

Hello all, thanks for your time and help. Below are my commands, and it generates a really nice plot, however I am not happy with the reorder() function. I would like the order to be the same as they appear in the genotype variable "genotype <- c("CJ1450 NW 4/25/12","CJ1450 BAL 4/25/12","CJ1450 NW 4/27/12","CJ1450 BAL 4/27/12","CJ1721 NW

Dear all, Lattice provides automatic coloring for subgroups on each panel by the simple use of a groups statement. For an application I want to change these colors to a predifined set. This works well using a panel function in stead of the default as long as there are only points in the graphs. When I set type="b" things get messed up. Any idea why? I include sample code for

For the following code is there a way to make the jitter all line up horizontally, instead of them being just randomly spread around a value. So for ex if there are multiple values at 63 for genotype wt then all the values should be plotted on the same y value of 63 but spaced apart by a certain factor or noise.. library(lattice); dataFrame <- as.data.frame(t(structure(c( 64,'wt',

Hi friends, I have following data and would like to plot this with barchart() availble with lattice package. RsID Freqs Genotype AAA 63.636 1/1 AAA 32.727 1/2 AAA 3.636 2/2 BBB 85.965 2/2 BBB 14.035 2/1 CCC 63.158 1/1 CCC 21.053 1/2 CCC 15.789 2/2 DDD 26.786 2/2 DDD 46.429 2/1 DDD 26.786 1/1 EEE 32.759 2/2 EEE 43.103 2/1

I'm new to R (previously used SAS primarily) and I have a genetics data frame consisting of genotypes for each of 300+ subjects (ID1, ID2, ID3, ...) at 3000+ genetic locations (SNP1, SNP2, SNP3...). A small subset of the data is shown below: SNP_ID SNP1 SNP2 SNP3 SNP4 Maj_Allele C G C A Min_Allele T A T G ID1 CC GG CT AA ID2 CC GG CC AA ID3 CC GG nc AA