effectplot {qtl}R Documentation

Plot phenotype means against genotypes at one or two markers.

Description

Plot the phenotype means for each group defined by the genotypes at one or two markers (or the values at a discrete covariate).

Usage

effectplot(cross, pheno.col=1, mname1, mark1, geno1, mname2, mark2,
           geno2, main, ylim, xlab, ylab, col, add.legend=TRUE,
           legend.lab, draw=TRUE, var.flag=c("pooled","group"))

Arguments

cross An object of class cross.
pheno.col Column number in the phenotype matrix to be drawn in the plot. One may also give a character string matching a phenotype name. Finally, one may give a numeric vector of phenotypes, in which case it must have the length equal to the number of individuals in the cross, and there must be either non-integers or values < 1 or > no. phenotypes; this last case may be useful for studying transformations.
mname1 Name for the first marker or pseudomarker. Pseudomarkers (that is, non-marker positions on the imputation grid) may be referred to in a form like "5@30.3", for position 30.3 on chromosome 5.
mark1 Genotype data for the first marker. If unspecified, genotypes will be taken from the data in the input cross object, using the name specified in mname1.
geno1 Optional labels for the genotypes (or classes in a covariate).
mname2 Name for the second marker or pseudomarker (optional).
mark2 Like mark1 (optional).
geno2 Optional labels for the genotypes (or classes in a covariate).
main Optional figure title.
ylim Optional y-axis limits.
xlab Optional x-axis label.
ylab Optional y-axis label.
col Optional vector of colors for the different line segments.
add.legend A logical value to indicate whether to add a legend.
legend.lab Optional title for the legend.
draw A logical value to indicate generate the plot or not. If FALSE, no figure will be plotted and this function can be used to calculate the group means and standard errors.
var.flag The method to calculate the group variance. "pooled" means to use the pooled variance and "group" means to calculate from individual group.

Details

In the plot, the y-axis is the phenotype. In the case of one marker, the x-axis is the genotype for that marker. In the case of two markers, the x-axis is for different genotypes of the second marker, and the genotypes of first marker are represented by lines in different colors. Error bars are plotted at +/- 1 SE.

The results of sim.geno are used; if they are not available, sim.geno is run with n.draws=16. The average phenotype for each genotype group takes account of missing genotype data by averaging across the imputations. The SEs take account of both the residual phenotype variation and the imputation error.

Value

A data.frame containing the phenotype means and standard errors for each group.

Author(s)

Hao Wu; Karl W Broman, kbroman@biostat.wisc.edu

See Also

plot.pxg, find.marker, effectscan, find.pseudomarker

Examples

data(fake.f2)


# impute genotype data
## Not run: 
fake.f2 <- sim.geno(fake.f2, step=5, n.draws=64)
## End(Not run)

########################################
# one marker plots
########################################
### plot of genotype-specific phenotype means for 1 marker
mname <- find.marker(fake.f2, 1, 37) # marker D1M437
effectplot(fake.f2, pheno.col=1, mname1=mname)

### plot a phenotype
# Plot of sex-specific phenotype means,
# note that "sex" must be a phenotype name here
effectplot(fake.f2, mname1="sex", geno1=c("F","M"))
# alternatively:
sex <- pull.pheno(fake.f2, "sex")
effectplot(fake.f2, mname1="Sex", mark1=sex, geno1=c("F","M"))

########################################
# two markers plots
########################################

### plot two markers
# plot of genotype-specific phenotype means for 2 markers
mname1 <- find.marker(fake.f2, 1, 37) # marker D1M437
mname2 <- find.marker(fake.f2, 13, 24) # marker D13M254
effectplot(fake.f2, mname1=mname1, mname2=mname2)

### plot two pseudomarkers
#####  refer to pseudomarkers by their positions
effectplot(fake.f2, mname1="1@35", mname2="13@25")

#####  alternatively, find their names via find.pseudomarker
pmnames <- find.pseudomarker(fake.f2, chr=c(1, 13), c(35, 25))
effectplot(fake.f2, mname1=pmnames[1], mname2=pmnames[2])

### Plot of sex- and genotype-specific phenotype means 
mname <- find.marker(fake.f2, 13, 24) # marker D13M254
# sex and a marker
effectplot(fake.f2, mname1=mname, mname2="Sex",
           mark2=sex, geno2=c("F","M"))

# Same as above, switch role of sex and the marker
# sex and marker
effectplot(fake.f2, mname1="Sex", mark1=sex,
           geno1=c("F","M"), mname2=mname)

# X chromosome marker
mname <- find.marker(fake.f2, "X", 14) # marker DXM66
effectplot(fake.f2, mname1=mname)

# Two markers, including one on the X
mnames <- find.marker(fake.f2, c(13, "X"), c(24, 14))
effectplot(fake.f2, mname1=mnames[1], mname2=mnames[2])

[Package qtl version 1.11-12 Index]