Introduction to ‘gggenes’

Drawing gene arrows with geom_gene_arrow()

geom_gene_arrow() is a ‘ggplot2’ geom that represents genes with arrows. The start and end locations of the genes within their molecule(s) are mapped to the xmin and xmax aesthetics respectively. These start and end locations are used to determine the directions in which the arrows point. The y aesthetic must be mapped to the molecule(s). If you are drawing more than one molecule, and the numerical locations of the genes are not similar across molecules, you almost certainly want to facet the plot with scales = "free" to avoid drawing ridiculously large molecules with ridiculously tiny genes.

library(ggplot2)
library(gggenes)
ggplot(example_genes, aes(xmin = start, xmax = end, y = molecule, fill = gene)) +
  geom_gene_arrow() +
  facet_wrap(~ molecule, scales = "free", ncol = 1) +
  scale_fill_brewer(palette = "Set3")

Beautifying the plot with theme_genes()

Because the resulting plot can look cluttered, a ‘ggplot2’ theme theme_genes() is provided with some sensible defaults.

ggplot(example_genes, aes(xmin = start, xmax = end, y = molecule, fill = gene)) +
  geom_gene_arrow() +
  facet_wrap(~ molecule, scales = "free", ncol = 1) +
  scale_fill_brewer(palette = "Set3") +
  theme_genes()

Aligning genes across facets with make_alignment_dummies()

Often you will want a certain gene to be vertically aligned across the faceted molecules. make_alignment_dummies() generates a set of ‘dummy’ genes that if added to the plot with ggplot2::geom_blank() will extend the range of each facet to visually align the selected gene across facets.

dummies <- make_alignment_dummies(
  example_genes,
  aes(xmin = start, xmax = end, y = molecule, id = gene),
  on = "genE"
)

ggplot(example_genes, aes(xmin = start, xmax = end, y = molecule, fill = gene)) +
  geom_gene_arrow() +
  geom_blank(data = dummies) +
  facet_wrap(~ molecule, scales = "free", ncol = 1) +
  scale_fill_brewer(palette = "Set3") +
  theme_genes()

Labelling genes with geom_gene_label()

To label individual genes, provide a label aesthetic and use geom_gene_label(). geom_gene_label() uses the ‘ggfittext’ package to fit the label text inside the gene arrows; see the ‘ggfittext’ documentation for more details on how it resizes and reflows text to make it fit.

ggplot(example_genes, aes(xmin = start, xmax = end, y =
                                            molecule, fill = gene, label = gene)) +
  geom_gene_arrow(arrowhead_height = unit(3, "mm"), arrowhead_width = unit(1, "mm")) +
  geom_gene_label(align = "left") +
  geom_blank(data = dummies) +
  facet_wrap(~ molecule, scales = "free", ncol = 1) +
  scale_fill_brewer(palette = "Set3") +
  theme_genes()

Reversing gene direction with the optional forward aesthetic

By default, genes arrows are drawn pointing in the direction implied by xmin and xmax. You can override this with the optional forward aesthetic, which can be useful when the gene coordinates and orientation are encoded as separate variables.

If forward is TRUE (the default), or any value that coerces to TRUE such as 1, the gene will be drawn pointing in the implied direction, i.e. from xmin to xmax. If forward is FALSE, or any value that coerces to FALSE such as -1, the gene will be drawn in the reverse of this implied direction:

ggplot(example_genes, aes(xmin = start, xmax = end, y = molecule, fill = gene, 
                          forward = orientation)) +
  geom_gene_arrow() +
  facet_wrap(~ molecule, scales = "free", ncol = 1) +
  scale_fill_brewer(palette = "Set3") +
  theme_genes()

Viewing subgene segments

We can highlight subgene segments, such as protein domains or local alignments, using geom_subgene_arrow().

This works similarly to geom_gene_arrow(), but in addition to xmin and xmax (which determine the gene boundaries), we need the aesthetics xsubmin and xsubmax to determine the subgene boundaries. geom_gene_arrow() will produce pretty arrowheads, as long as xmin >= xsubmin and xmax >= xsubmax for all subgenes (subgenes that break gene boundaries will be skipped with a warning).

The suggested usage is to use geom_gene_arrow() with no fill, and then add a subgene layer over this:

ggplot(example_genes, aes(xmin = start, xmax = end, y = molecule)) +
  facet_wrap(~ molecule, scales = "free", ncol = 1) +
  geom_gene_arrow(fill = "white") +
  geom_subgene_arrow(data = example_subgenes,
    aes(xmin = start, xmax = end, y = molecule, fill = gene,
        xsubmin = from, xsubmax = to), color="black", alpha=.7) +
  theme_genes()

To label subgenes, we can use geom_subgene_label(), which works similarly to geom_gene_label() with the major difference that it requires xsubmin and xsubmax aesthetics (not xmin and xmax).

ggplot(subset(example_genes, molecule == "Genome4" & gene == "genA"),
       aes(xmin = start, xmax = end, y = strand)
  ) +
  geom_gene_arrow() +
  geom_gene_label(aes(label = gene)) +
  geom_subgene_arrow(
    data = subset(example_subgenes, molecule == "Genome4" & gene == "genA"),
    aes(xsubmin = from, xsubmax = to, fill = subgene)
  ) +
  geom_subgene_label(
    data = subset(example_subgenes, molecule == "Genome4" & gene == "genA"),
    aes(xsubmin = from, xsubmax = to, label = subgene),
    min.size = 0
  )