similar to: Problem with x labels of barplot

Displaying 20 results from an estimated 1000 matches similar to: "Problem with x labels of barplot"

2010 Jun 01
5
Help barplots
Dear All, I am newbie to R, and I wanted to plot a barplots with R and in such a way that It will also show me position which I can plot on the bar line. Here is my code that I am using to plot, > chromosome <- c(40.2, 35.6, 36.1, 29.6, 31, 29.6, 31, 29.4, 28.2, 23, 23, 28.2) >barplot (chromosome, col="purple", xlab="Oryza sativa Chromosomes", border = NA, space =
2009 Nov 20
1
how to specify the order of panels with xyplot
> chromosomes id refseq name length 1 0 NC_000001.9 Homo sapiens chromosome 1 247249719 2 1 NC_000002.10 Homo sapiens chromosome 2 242951149 3 2 NC_000003.10 Homo sapiens chromosome 3 199501827 4 3 NC_000004.10 Homo sapiens chromosome 4 191273063 5 4 NC_000005.8 Homo sapiens chromosome 5 180857866 6 5 NC_000006.10 Homo sapiens chromosome 6
2004 Aug 06
1
questions related to ploting in R
Dear all. I need to draw a scatter plot of 23 chromosome copy numbers (y axes) against chromosome and physical location within each chromosome in one plot. The data matrix looks as below: chr location copy_num 1 118345 1.320118 1 3776202 1.133879 1 4798845 0.989997 1 5350951 1.100967 . more data here . . 2 118345 2.459119 2 157739 1.915919 2 1530065 1.924372 2
2009 Dec 04
1
Lattice : Help with changing the labels of x-axis in respective panels
Dear R-Helpers, I am not very experienced in using lattice and I am still in the learning stage I have a data set which looks like this: (I have deleted a few lines in order to save space) Chromosome marker Marker.Name Distance 1 1 1 PeMm261 0.0000 2 1 2 Xtxp8 10.1013 .. 20 1 20 EbMi148 210.3099 21 1 21 Xtxp25
2008 Jul 09
2
replacing value in column of data frame
Dear all, Probably a very basic question but I need some help. I have a data frame (made by read.table from a text file) of microarray data, of which the first column is a factor and the rest of the columns are numeric. The factor column contains chromosome names, so values 1 through 22 plus X, Y and XY. The numeric columns contain positions or intensity measurements. What I need to do is
2007 Apr 02
3
Random number from density()
Hello, I'm writing some genetic simulations in R where I would like to place genes along a chromosome proportional to the density of markers in a given region. For example, a chromosome can be presented as a list of marker locations: Chr1<-c(0, 6.5, 17.5, 26.2, 30.5, 36.4, 44.8, 45.7, 47.8, 48.7, 49.2, 50.9, 52.9, 54.5, 56.5, 58.9, 61.2, 64.1) Where the numbers refer to the locations of
2012 Sep 10
3
plot: x and y chromosomes are missing
Hello, I have a list with gene names, fold changes (=expression level) and chromosomes. Names fold change chromosome hz 1.5 2 If I plot fold change versus chromosome (or vice versa): plot (ch, fc) I see only the chromosomes with numbers but not those with letter (x and y). What can I do? A second question: How can I add a single line in that plot at a certain
2011 Apr 20
2
'Record' row values every time the binary value in a collumn changes
My question is twofold. Part 1: My data looks like this: (example set, real data has 2*10^6 rows) binary<-c(1,1,1,0,0,0,1,1,1,0,0) Chromosome<-c(1,1,1,1,1,1,2,2,2,2,2) start<-c(12,17,18,20,25,36,12,15,16,17,19) Table<-cbind(Chromosome,start,binary) Chromosome start binary [1,] 1 12 1 [2,] 1 17 1 [3,] 1 18 1 [4,] 1
2011 Dec 09
1
minor allele frequency comparison
Hi all, We are using two methods to identify SNPs. One is based on resequencing the genome and aligning the reads to the sequenced genome to identify SNPs (data available for 44 individuals). Another is based on SNP array with selected loci (30000 loci, 870 individuals). I want to compare the results from the resequencing based minor allele frequency and Array based minor allele frequency.
2003 Jan 16
1
graphics
Dear R community, I need to plot the results of some simulations I did using QTL Cartographer. I am plotting LOD scores over three chromosomes. The three plot have to be one next to the other. The procedure I am using is: par(mfrow=c(1,3)) plot(x$x, x$y, ylim=c(0,35), type="l", col="blue", las=1, xaxs="i", yaxs="i", xlab="X Chromosome",
2017 Sep 04
1
Merge by Range in R
Hi,? I have two big data set.? data _1 :? > dim(data_1) [1] 15820 5 > head(data_1) ? ?Chromosome ?????Start????????End????????Feature GroupA_3 1: ? ? ? ????????chr1 521369 ?750000 ????chr1-0001 ? ?????0.170 2: ? ? ? ????????chr1 750001 ?800000 ????chr1-0002 ? ????-0.086 3: ? ? ? ????????chr1 800001 ?850000 ????chr1-0003 ? ?????0.006 4: ? ? ? ????????chr1 850001 ?900000 ????chr1-0004 ?
2012 Jul 13
2
alternate tick labels and tick marks with lattice xyplot
Hi, I would like to use xyplot to create a figure. Unfortunately, I cannot find documentation in xyplot to specify alternating the x-axis tick labels with the x-axis tick marks. I can do this with the regular R plot function as follows. #A small version of my data looks like this data<-data.frame(matrix(ncol=3,nrow=12)) data[,1]<-rep(c(1,2,3),c(4,4,4)) data[,2]<-rep(c(1,2,3,4),3)
2010 Nov 07
1
How do I order xyplot line points?
I have the following xyplot figure: http://img577.imageshack.us/img577/686/filesizeresults12000000.png The data are organized in a matrix file as follows: Type Elements Chromosome Time bedGz 12000000 chr1 14.240 bedGz 12000000 chr2 7.949 bedGz 12000000 chr3 5.103 bedGz 12000000 chr4 5.290 bedGz 12000000 chr5 5.161 ... The x-axis labels in the Chromosome column are ordered
2009 Mar 23
1
changing order of lattice plots
Hi, This is another question relating to my 2 factor figure. densityplot(~End-Begin | Type * Chromosome, data=Mon, layout=c(5,12), xlab="Element Length",type="percent", col="grey60", strip=strip.custom(style=3, bg="grey90", par.strip.text=list(cex=0.5))) I would like to flip the plot so those at the bottom are at the top and so on. I have tried using a
2007 Nov 18
1
how to sort a data.frame by ascending some columns
Dear list, I have a data frame (238304 rows and 6 columns). I want the data frame sorted by two columns in ascending order. I am showing the first 5 rows of the data frame > clones.info[1:5,1:6] USER_CLONE_ID CHROMOSOME Expr1002 KB_POSITION Allele_A WELL_ID 1 SNP_A-1855402 17 41419603 41419603 C rs17572851 2 SNP_A-4249904 17 41420045 41420045 A rs17572893 3 SNP_A-2174835 18 41407760
2009 Jan 15
3
How to create a chromosome location map by locus ID
Hi, I'm trying to make a chromosomal map in R by using the locus. I have a list of genes and their locus, and I want to visualise that so you can see if there are multiple genes on a specific place on a chromosome. A example of what I more or less want is below: http://www.nabble.com/file/p21474206/untitled.JPG untitled.JPG The genes and locus are here:
2007 Mar 01
1
object is not subsettable
Dear colleagues, I've just come across a problem with the following command which is a part of the "metaOverview.R" code file provided as an monography- accompanying file at http://www.bioconductor.org/docs/mogr/metadata: ################################## R> hasChr <- eapply(GOTERM, function(x) + x[grep("chromosome", Term(x))]) Error in
2011 Nov 06
2
Correlation analysis
Hi everyone, I am new to R-project. I did search through the list for my problem but i can't find it. I am sorry if this question has been asked. I would like to perform a correlation analysis between a hiv data and gene expression. Basically, i have a file that contains: hiv_name, start_position, end_position, chromosome. I would like to see if these data has anything to do with the
2019 Dec 19
1
ALTREP string methods for substr and nchar
A useful extension of ALTREP is having two new string methods which return the number of characters of a given string element and to return a substring of an element. Having these methods would allow retrieving these values without needing to create a CHARSXP for the full element data, which could potentially be costly for long elements. For example say you have an ALTREP altstring vector where
2010 May 14
1
finding the plot limits generated by default
I have two datasets that I would like to plot in a single figure. The first plot is generated by a function that then takes a subset of the data. (It is biological data so it is usually by chromosome e.g. function(data1,subset="chr8") ) Since not only are the chromosomes different sizes, but across different datasets there may be different numbers of points for a single chromosome, I