View source: R/genome_plotter.R
genome.plotter.whole | R Documentation |
This function takes the genome scan output from scan.h2lmm() and flexibly plots out the genome scan.
genome.plotter.whole(
scan.list,
use.lod = FALSE,
just.these.chr = NULL,
scale = "Mb",
main.colors = c("black", "cyan", "darkgreen"),
distinguish.chr.type = c("color", "box"),
distinguish.box.col = "gray88",
distinguish.chr.col = c("gray60", "#008080", "greenyellow"),
override.col = NULL,
use.legend = TRUE,
main = "",
my.legend.cex = 0.6,
my.legend.lwd = NULL,
my.legend.lty = 1,
my.legend.pos = "topright",
my.legend.bty = "n",
y.max.manual = NULL,
my.y.line = 2,
my.y.axis.cex = 1,
my.y.lab.cex = 0.7,
my.x.lab.cex = 0.7,
my.x.labels = TRUE,
my.x.lab.padj = -1.5,
no.title = FALSE,
override.title = NULL,
my.title.line = NA,
title.cex = 1,
hard.thresholds = NULL,
thresholds.col = "red",
thresholds.legend = NULL,
thresholds.lwd = NULL,
thresholds.legend.pos = "topleft",
thresholds.lty = NULL,
add.chr.to.label = FALSE,
axis.cram = TRUE,
include.x.axis.line = TRUE,
mark.locus = NULL,
mark.locus.col = "red",
which.mark = 1,
mark.lwd = 4,
mark.manual = list(chr = NULL, pos = NULL),
add.polygon = FALSE,
which.polygon = 1,
my.type = "l",
my.pch = 20,
my.cex = 0.5,
use_bold_axis = FALSE,
axis_lwd = 1,
include_y_axis = TRUE
)
scan.list |
A list of scan.h2lmm() objects that are to be plotted within the same genome scan plot. |
use.lod |
DEFAULT: FALSE. Plots either the LOD score or the -log10 p-value. |
just.these.chr |
DEFAULT: NULL. Specifies a subset of the chromosomes to be plotted. NULL results in all chromosomes being plotted. |
scale |
DEFAULT: "Mb". Specifies the scale of genomic position to be plotted. Either Mb or cM are expected. |
main.colors |
DEFAULT: "black". The color of the main association score to be plotted. |
distinguish.chr.type |
DEFAULT: "color". The default specifies rectangular block backgrounds to distinguish adjacent chromosomes. The "color" option specifies alternating colors. |
distinguish.box.col |
DEFAULT: "gray88". If distinguish.chr.type="box" is specified, this argument provides the color of the background rectangle. |
distinguish.chr.col |
DEFAULT: "gray60". If distinguish.chr.type="color" is specified, this argument provides the alternating color. Multiple colors should be specified if multiple scans are included in the plot. |
use.legend |
DEFAULT: TRUE. Include a legend for the different associations. If TRUE, the labels are the names of the non.mi.scan.list object. |
main |
DEFAULT: NULL. Adds a title above the model. |
my.legend.cex |
DEFAULT: 0.6. Specifies the size of the text in the legend. |
my.legend.lwd |
DEFAULT: NULL. If NULL, all lines have lwd=1.5. If not, option specifies the lwds. |
my.legend.pos |
DEFAULT: "topright". Specifies where to put the legend, if specified in use.legend. |
y.max.manual |
DEFAULT: NULL. Manually adds a max y-value. Allows multiple genome scans to easily be on the same scale. |
no.title |
DEFAULT: FALSE. If TRUE, no title is printed. |
override.title |
DEFAULT: NULL. If a string is specified, it is included on plot without any of the default automated title. |
hard.thresholds |
DEFAULT: NULL. Specify one or more horizontal threshold lines. |
thresholds.col |
DEFAULT: "red". Set the colors of the specified thresholds. |
thresholds.legend |
DEFAULT: NULL. If non-NULL, string arguments used as labels in thresholds legend. If NULL, no threshols legend is used. |
add.chr.to.label |
DEFAULT: FALSE. If TRUE, adds "Chr" before every chromosome label. If FALSE, "Chr" is added as an axis label under the y-axis. |
axis.cram |
DEFAULT: TRUE. This makes the plot much more likely to include all chromosome labels. With small plots, this could lead to overlapping labels. |
include.x.axis.line |
DEFAULT: TRUE. IF TRUE, this option adds an x-axis line with ticks between chromosomes. |
genome.plotter.whole()
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