manhattanDMCs-method | R Documentation |
Creates a Manhattan plot based on the p-values obtained
from findDMCs
method
manhattanDMCs( object, col, chrlabs, suggestiveline, genomewideline, highlight, logp, annotatePval, annotateTop, ... ) ## S4 method for signature 'BSDMCs' manhattanDMCs( object, col, chrlabs, suggestiveline, genomewideline, highlight, logp, annotatePval, annotateTop, ... )
object |
A |
col |
A character vector indicating which colors to alternate. |
chrlabs |
A character vector equal to the number of chromosomes
specifying the chromosome labels (e.g., |
suggestiveline |
Where to draw a "suggestive" line. Default -log10(1e-5). Set to FALSE to disable. |
genomewideline |
Where to draw a "genome-wide sigificant" line. Default -log10(5e-8). Set to FALSE to disable. |
highlight |
A character vector of SNPs in your dataset to highlight. These SNPs should all be in your dataset. |
logp |
If TRUE, the -log10 of the p-value is plotted. It isn't very useful to plot raw p-values, but plotting the raw value could be useful for other genome-wide plots, for example, peak heights, bayes factors, test statistics, other "scores," etc. |
annotatePval |
If set, SNPs below this p-value will be annotated on the plot. |
annotateTop |
If TRUE, only annotates the top hit on each chromosome that is below the annotatePval threshold. |
... |
other possible parameters |
A Manhattan plot
Farhad Shokoohi <shokoohi@icloud.com>
set.seed(1980) nr <- 150; nc <- 8 metht <- matrix(as.integer(runif(nr * nc, 0, 100)), nr) methc <- matrix(rbinom(n=nr*nc,c(metht),prob = runif(nr*nc)),nr,nc) r1 <- GRanges(rep('chr1', nr), IRanges(1:nr, width=1), strand='*') names(r1) <- 1:nr cd1 <- DataFrame(Group=rep(c('G1','G2'),each=nc/2),row.names=LETTERS[1:nc]) OBJ1 <- cBSData(rowRanges=r1,methReads=methc,totalReads=metht,colData=cd1) OBJ2 <- methHMEM(OBJ1, MaxK=2, mc.cores=2) OBJ3 <- methHMMCMC(OBJ2, mc.cores=2) OBJ4 <- findDMCs(OBJ3, mc.cores=2) manhattanDMCs(OBJ4)
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