Get started with biopalette

Find a palette

Load biopalette and inspect the bundled collection:

library(biopalette)

list_palettes()[c("name", "type", "n_color")]
#>                  name        type n_color
#> 1        bcell_atlas2   diverging       5
#> 2        walter_white   diverging       5
#> 3       walter_white3   diverging       5
#> 4            gene_red qualitative       2
#> 5          heat_light qualitative       2
#> 6          three_body qualitative       3
#> 7       lactate_steps qualitative       5
#> 8       walter_white2 qualitative       5
#> 9          tam_pastel qualitative       6
#> 10        bcell_atlas qualitative       7
#> 11      cancer_mosaic qualitative      15
#> 12     bcell_clusters qualitative      20
#> 13              babel qualitative      21
#> 14   mitonuclear_blue  sequential       6
#> 15 mitonuclear_orange  sequential       6

Filter by type when the visual role is already known:

list_palettes(type = "sequential")[c("name", "n_color")]
#>                 name n_color
#> 1   mitonuclear_blue       6
#> 2 mitonuclear_orange       6

palette_info() returns the complete metadata for one palette without drawing it:

palette_info("mitonuclear_blue")
#>               name       type n_color       colors
#> 1 mitonuclear_blue sequential       6 #EEF4FB,....

For visual browsing, call palette_gallery() in an interactive R session. It builds one gallery page per palette type and reports each page as it is ready.

palette_gallery()

Retrieve colors

get_palette() returns a character vector of HEX colors. Palette names are unique across the bundled collection, so type is normally unnecessary:

get_palette("three_body")
#> [1] "#6495ED" "#339933" "#FF4500"
get_palette("mitonuclear_blue")
#> [1] "#EEF4FB" "#DDF1F5" "#B9DBF4" "#95AAD3" "#3A68AE" "#155289"

The meaning of n follows the palette type. For a qualitative palette, it selects the first n category colors and cannot exceed the palette size:

get_palette("babel", n = 5)
#> [1] "#1688A7" "#7673AE" "#B3DE69" "#D195F6" "#7E285E"

For sequential and diverging palettes, the stored colors are stops along a ramp. Asking for n colors samples the whole ramp in Lab color space rather than taking colors from only one end:

get_palette("mitonuclear_blue", n = 3)
#> [1] "#EEF4FB" "#A7C2E3" "#155289"
get_palette("walter_white", n = 7)
#> [1] "#1991A9" "#80B3BB" "#BAD1CF" "#E7E9E4" "#BEC7A6" "#889669" "#495A2E"

Use reverse = TRUE when the direction of a palette should be flipped:

get_palette("mitonuclear_blue", n = 3, reverse = TRUE)
#> [1] "#155289" "#A7C2E3" "#EEF4FB"

The returned vector can be used anywhere that accepts R color values. For ggplot2, the scale functions provide a shorter and safer route.

Use a discrete scale

Map a qualitative palette to unordered groups with scale_color_biopalette():

library(ggplot2)
#> Warning: package 'ggplot2' was built under R version 4.5.3

ggplot(iris, aes(Sepal.Length, Sepal.Width, color = Species)) +
  geom_point(size = 2.5) +
  scale_color_biopalette("three_body") +
  theme_minimal()

Use a color scale when the mapped aesthetic is color (or colour), and a fill scale when the mapped aesthetic is fill. This distinction belongs to the geometry, not to the palette itself:

ggplot(iris, aes(Species, Sepal.Length, fill = Species)) +
  geom_boxplot() +
  scale_fill_biopalette("three_body", guide = "none") +
  theme_minimal()

Discrete scales request exactly as many colors as the trained data has levels. Qualitative palettes use their first n colors; sequential and diverging palettes sample n colors across the complete ramp. A qualitative palette raises an informative error when it does not contain enough colors.

Use a continuous gradient

Continuous data requires a sequential or diverging palette and one of the gradient functions. A sequential fill gradient is appropriate for density:

ggplot(faithfuld, aes(waiting, eruptions, fill = density)) +
  geom_raster() +
  scale_fill_biopalette_gradient("mitonuclear_blue") +
  theme_minimal()

For values interpreted relative to a reference point, use a diverging palette and set midpoint. Here zero means no deviation from the mean:

plot_data <- transform(
  mtcars,
  cylinders = factor(cyl),
  gears = factor(gear),
  mpg_difference = mpg - mean(mpg)
)

ggplot(plot_data, aes(cylinders, gears, fill = mpg_difference)) +
  geom_tile(color = "white", linewidth = 0.5) +
  scale_fill_biopalette_gradient("walter_white", midpoint = 0) +
  labs(x = "Cylinders", y = "Gears", fill = "MPG difference") +
  theme_minimal()

Qualitative palettes cannot define continuous gradients because interpolating unordered category colors has no stable meaning.

Preview one palette

preview_palette() draws directly to the active graphics device. Its five styles are "bar", "pie", "point", "rect", and "circle":

preview_palette("walter_white", plot_type = "rect")

The same n and reverse rules used by get_palette() also apply to previews:

preview_palette(
  "mitonuclear_orange",
  n = 4,
  reverse = TRUE,
  plot_type = "circle"
)

Convert color formats

hex2rgb() and rgb2hex() convert between HEX and RGB or RGBA values. Alpha is preserved when present:

rgba <- hex2rgb(c("#1688A7", "#FF450080"))
rgba
#>         hex   r   g   b alpha
#> 1   #1688A7  22 136 167    NA
#> 2 #FF450080 255  69   0   128
rgb2hex(rgba)
#> [1] "#1688A7"   "#FF450080"

Next steps

• Read vignette("palette", package = "biopalette") for the sources, intended uses, and limitations of every bundled palette.
• Open ?scale_color_biopalette for discrete scale options.
• Open ?scale_color_biopalette_gradient for continuous gradients, transformations, custom stop positions, and diverging midpoints.
• Read vignette("tessera", package = "biopalette") to explore palettes, example datasets, Palette Lab, and complete R figure recipes.
• Report reproducible problems in GitHub Issues.