similar to: Allelic Differentiation, sampling, unique(), duplicated()

Displaying 20 results from an estimated 2000 matches similar to: "Allelic Differentiation, sampling, unique(), duplicated()"

2005 Jul 07
3
What method I should to use for these data?
Dear R user: I am studying the allele data of two populations. the following is the data: a1 a2 a3 a4 a5 a6 a7 a8 a9 a10 a11 a12 a13 a14 a15 a16 a17 pop1 0.0217 0.0000 0.0109 0.0435 0.0435 0.0000 0.0109 0.0543 0.1739 0.0761 0.1413 0.1522 0.1087 0.0870 0.0435 0.0217 0.0109 pop2 0.0213 0.0213 0.0000 0.0000 0.0000 0.0426 0.1702 0.2128 0.1596 0.1809 0.0957 0.0745 0.0106
2012 Oct 23
2
barplot
Hi, I want to make a barplot with the following datasets: I have a file as following: name chr position A1 A2 pop1 pop1 pop2 pop2 I have calculated a measure using all the values in columns "pops", the values are saved in a vector. Now I want to make a barplot using the values in this vector as the y axis and the values in the column "position" in the x-axis. thank you
2012 Jul 01
1
significant difference between Gompertz hazard parameters?
Hello, all. I have co-opted a number of functions that can be used to plot the hazard/survival functions and associated density distribution for a Gompertz mortality model, given known parameters. The Gompertz hazard model has been shown to fit relatively well to the human adult lifespan. For example, if I wanted to plot the hazard (i.e., mortality) functions: pop1 <- function (t) {
2012 Jan 04
3
[newbie] stack operations, or functions with side effects (or both)
summary: Specifically, how does one do stack/FIFO operations in R? Generally, how does one code functions with side effects in R? details: I have been a coder for years, mostly using C-like semantics (e.g., Java). I am now trying to become a scientist, and to use R, but I don't yet have the sense of "good R" and R idiom (i.e., expressions that are to R what (e.g.) the Schwartzian
2010 Jul 24
1
Doubt about a population competition function
Hi, I'm doing a function that describe two populations in competition. that's the function that i wrote: exclusao<-function(n10, n20, k1, k2, alfa, beta, t){ n1<-k1-(alfa*n20) n2<-k2-(beta*n10) if(t==0){plot(t, n10, type='b', xlim=range(c(1:t),c (1:t)), ylim=range(n10, n20), xlab='tempo', ylab='tamanho populacional') points(t, n20, type='b',
2010 May 14
2
multhist,labels and percentages
Hi All, I am in the annoying position of having to present some data to someone who seems to be somewhat less than numerate. I need to label the y-axes of a multhist with the y-axis labeled not as counts but as percentage of a population. Plotting the standard histogram is in a way fine, all I need is to: -- have a left-handside y-axis labels for pop 1 and a right-handside y-axis labels for pop2
2006 Feb 18
1
reshaping result of by()
Hello, I'm trying to build a frequency table for a vector, broken down by the combination of factors. For further analyses, I need to have the result arranged in a new data frame, with the upper limit of the histogram's breaks, the per bin count, and the factors identifying each record. My problem is including the latter: ---<---------------cut
2007 Mar 16
1
ideas to speed up code: converting a matrix of integers to a matrix of normally distributed values
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
2008 Apr 19
1
resampling from distributions
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.
2008 Aug 10
1
Scripting - query
I have a vector: alleles.present<-c("D3", "D16", ... ) The alleles present changes given the case I'm dealing with - i.e. either all of the alleles I use for my calculations are present, or some of them. Depending on what alleles are present, I need to make matrices and do calculations on those alleles present and completely disregard any formula or other use of the
2006 Feb 21
2
indexing within panels in xyplot
Dear R-helpers, I need to show a linear fit through a subset of the data within each combination of levels of two factors. So I prepared an xyplot with different panels for each level of one of the factors, and different symbols within each panel for the levels of the second factor. My problem is selecting the subset of each combination through which the line should be fit for subsequent
2009 Jan 19
1
Deleting columns where the frequency of values are too disparate
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
2007 Sep 21
1
Help create a loopto conduct multiple pairwise operations
#Hello, #I have three data frames, X,Y and Z with two columns each and different numbers of rows. # creation of data frame X X.alleles <- c(1,5,6,7,8) X.Freq <- c(0.35, 0.15, 0.05 , 0.10, 0.35) Loc1 <- cbind( X.alleles,X.Freq) X <- data.frame(Loc1) #creation of data frame Y Y.alleles <- c(1,4,6,8) Y.Freq <- c(0.35, 0.35, 0.10, 0.20 )
2010 Sep 01
2
Rd-file error: non-ASCII input and no declared encoding
Dear list, I came across the following error for three of my newly written Rd-files: non-ASCII input and no declared encoding I can't make sense of this. Below I copied in one of the three files. Can anybody please tell me what's wrong with it? Thank you, Christian \name{tetragonula} \alias{tetragonula} \alias{tetragonula.coord} \docType{data} % \non_function{} \title{Microsatellite
2007 Aug 30
2
How to multiply all dataframe rows by another dataframe's columns
Hello, I have two data frames, X and Y, with two columns each and different numbers of rows. # creation of data frame X Loc1.alleles <- c(1,5,6,7,8) Loc1.Freq <- c(0.35, 0.15, 0.05, 0.10, 0.35) Loc1 <- cbind( Loc1.alleles,Loc1.Freq) X <- data.frame(Loc1) #creation of data frame Y Loc2.alleles <- c(1,4,6,8) Loc2.Freq <- c(0.35, 0.35,
2012 Apr 22
10
Assignment problems
The text below is a part of, some work I have to do, which is due in 2 days and I am strung up with a lot of other stuff, so I was hoping someone would take 5 mins and help me ?? Here is a part of my data.frame: year country1 country2 contig comlang pop1 gdp1 pop2 gdp2 rta dist avgflow 1 1992 AUS AUT 0 0 17.4950008 321708.281
2013 Jul 02
2
Recoding variables based on reference values in data frame
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
2006 Dec 29
1
Genotypes are not all the same
I have been merrily using the genetics package and more specifically have been using the makeGenotypes and genotypes function. I check my accomplishments by going > class(g2) [1] "genotype" "factor" and likewise > class(g1) [1] "genotype" "factor" Yet when I execute a command such as allele count I get this > allele.count(g1) D I [1,]
2005 Apr 05
2
cat bailing out in a for loop
Dear All, I am trying to calculate the Hardy-Weinberg Equilibrium p-value for 42 SNPs. I am using the function HWE.exact from the package "genetics". In order not to do a lot of coding "by hand", I have a for loop that goes through each column (each column is one SNP) and gives me the p.value for HWE.exact. Unfortunately some SNP have reached fixation and HWE.exact requires a
2006 Apr 27
2
Incomplete Trio in TDT analysis
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