| plot.scanone {qtl} | R Documentation |
Plot the output from a single QTL scan. One may specify which chromosomes to plot
plot.scanone(x,output2,output3,chr,incl.markers=TRUE,ylim,
lty=c(1,2,3),col="black",lwd=2,add=FALSE,gap=25,...)
x |
A data.frame with at least three columns. The first three columns should be the following: |
output2 |
Data for another genome scan, like output (optional). |
output3 |
Data for another genome scan, like output (optional). |
chr |
Vector specifying which chromosomes to plot. |
incl.markers |
Indicate whether to plot line segments at the marker locations. |
ylim |
Limits for y-axis [optional]. |
lty |
Line type for output1, 2 and 3; this should be a vector of length 1 or 3. |
col |
Line color for output1, 2 and 3; this should be a vector of length 1 or 3. |
lwd |
Line width for output1, 2 and 3; this should be a vector of length 1 or 3. |
add |
If TRUE, add to a current plot. |
gap |
Gap separating chromosomes. |
... |
Ignored at this point. |
Plot of the lod score against marker position for the genome scan.
Karl W Broman,
kbroman@jhsph.edu
http://biosun01.biostat.jhsph.edu/~kbroman/software/qtl.html
scanone, vbscan,
summary.scanone
data(fake.f2) fake.f2 <- argmax.geno(fake.f2) output <- scanone(fake.f2,method="anova") output2 <- scanone(pull.chr(fake.f2,1),method="im") plot(output) plot(output,output2,chr=1)