similar to: Density estimation graphs

Hello dear members of R-help and R-core mailing list, I am not sure if this request is a "ticket" that should be filled somewhere outside the mailing list. If so, I apologize for not doing and would like to know where I should have filled it. And to the subject matter: I would like to use a command like this: plot(c(1,8), 1:2, type="n") polygon(1:7, c(2,1,2,NA,2,1,2),

Hello dear members of R-help and R-core mailing list, I am not sure if this request is a "ticket" that should be filled somewhere outside the mailing list. If so, I apologize for not doing and would like to know where I should have filled it. And to the subject matter: I would like to use a command like this: plot(c(1,8), 1:2, type="n") polygon(1:7, c(2,1,2,NA,2,1,2),

Dear Listers, I am drawing a plot of two density curves, for male and female incomes. I would like to shade/hatch/color (whatever) the areas under the curves which are distinctive for each gender. This is the code I have tried so far: m <- density(topmal.d$y, bw = "sj") f <- density(topfem.d$y, bw = "sj") par(mfrow = c(1,1)) plot(x = c(0,400), y = c(0,0.02), type =

Hello R-help community, I have another question about filtering datasets. Please consider the following "toy" data matrix example, called "x" for simplicity. There are 20 different individuals ("ID"), with information about the alleles (A,T, G, C) at six different loci ("Locus1" - "Locus6") for each of these 20 individuals. At any single locus

Dear All, The following code extracts from NCBI very nice output for ONE allele of a SNP (often the allele with the second largest frequency - usually termed the minor allele). It gives an average minor allele frequency from all NCBI sources (which is what I want, except I'd like the addition of data for all the other alleles of one SNP) plus a table of minor allele frequencies from each

I have used polygon() to mark the confidence limits of a survival curve. In another project, I have used the col parameter to fill my boxplots. The poly() description refers to filling but actually produces hatching (i.e. lines ). boxplot() does truly fill the boxes with a colour or shades of grey (e.g. col="red"). My novices perception of R graphics is: If you can hatch it, you

I know that there are quite a few packages out that there for cluster analysis. The problem that I am facing is finding a package that will not incorporate all my samples into clusters but just the samples that fit a threshold (that I have not set yet and may need help finding the right level) for genotyping. It should be able to "no call" samples outside the clusters. It also needs to

Hi all, [this is a bit hard to describe, so if my initial description is confusing, please try running my code below] #WHAT I'M TRYING TO DO I'd appreciate any help in trying to speed up some code. I've written a script that converts a matrix of integers (usually between 1-10,000 - these represent allele names) into two new matrices of normally distributed values (representing

Dear all, I was wondering if anyone could help solve a problem of a missing interaction effect!! I carried out a 2 x 2 factorial experiment to see if eggs from 2 different locations (Origin = 1 or 2) had different hatching success under 2 different incubation schedules (Treat = 1 or 2). Six eggs were taken from 10 females (random = Female) at each location and split between the treatments,

Sorry that I was unclear. For an individual to qualify for my analysis I want both of the following two criteria to be fulfilled: First, I want to select measurement taken at a certain age: for the focal individual the year of measurement (year) should be the same as year.hatch Second, I want the focal individual to be born by a mother that reproduces for the first time. So the /parents /of

Dear list, i'm a new R user, so I apologize if the topic is already being addressed by some other user. I'm trying to determine if the reproductive success of a species of bird is related to a list of covariates. These are the covariates: ? elev: elevation of nest (meters) ? seadist: distance from the sea (meters) ? meanterranova: records of temperature ? minpengS1: records

Dear R listers, I have a data file looks like the following: Testing marker: s_1 --------------------------------------------- Allele df(0) -LnLk(0) df(T) -LnLk(T) ChiSq p 3 7995 29320.30 7994 29311.85 16.90 4e-05 (2229/8000 probands) Testing marker: s_2 --------------------------------------------- Allele df(0)

Hello All, Once again thanks for all of the help to date. I am climbing my R learning curve. I've got a few more questions that I hope I can get some guidance on though. I am not sure whether the etiquette is to break up multiple questions or not but I'll keep them together here for now as it may help put the questions in context despite the fact that the post may get a little long.

Dear all, I have received some data on birds that looks sth like this: # a unique id for each individual id <- c(1,1,1,2,2,2,3,3,3,4,4,5,6) # the year the bird was measured year <- c(1995, 1996, 1997, 1995, 1996, 1997, 1996, 1997, 1998, 1996, 1997, 1997, 1998) # the year the bird was hatched year.hatch <- c(1995, 1995, 1995, 1995, 1995, 1995, 1996, 1996, 1996, 1996, 1996, 1997, 1998)

I am involved in a study where, as in most of life, men demonstrate themselves to be recalcitrant. So while we have many probands and most of their mothers we only have about 50% of the trios being complete. I have been running tdt and trio.types. It appears as if it is ignoring the duos. Sometimes a duo can be informative. For instance Father ..missing Mother 1/2 Proband 1/1 This duo shows that

Dear All, Having now successfully started using Sweave, I have just noticed an odd side effect with fonts. Using plain LaTeX, I have had no problems using \usepackage{palatino} or \usepackage{times} and the font correctly changes. However, once I convert the tex document into Snw, and run it through R CMD SWEAVE, LaTeX seems to ignore this package directive. The LaTeX log suggests the font

I am about one step away from heaven on earth. I think only one step! I am using dgc.genetics to run a TDT test on thousands of genetic loci. I have learnt (through the help of others on this mailing list) to send the complex output to useful data frames which in turn allow me to look at the big picture and screen the thousands of loci. Resultdt<-lapply(PGWide[,240:290], tdt) the above

Hey, I am trying to create barplot of abundances over time (in days). The period is over 171 days, so I don't want to have all labels there but only the first day of the month. I couldn't find anything like this on the forum yet. Mostrly it's about year to year data. This is the relevant part of my table: datum month abundance 26/03/11 March 1 27/03/11 March 0 28/03/11 March 1

Dear R-experts, My problem is how to handle a 10GB data file containing genotype data. The file is in a particular format (Illumina final report) and needs to be altered and merged with phenotype data for further analysis. PERL seems to be an frequently used solution for this type of work, however I am inclined to think it should be doable with R. How do I open a text-file, line by line,

I'm sorry everyone for the inconvenience of spamming the R-help... Here's the complete post: Hi everyone, > > Since it's quite a while that I used the reshape package, I now feel kind > of rusty. > > I have a data.frame like this: > > > > id Sample.Name Marker Allele.1 > Allele.2 sample_id species