📦 microViz
is an R package for analysis and visualization of
microbiome sequencing data.
🔨 microViz
functions are intended to be beginner-friendly but
flexible.
🔬 microViz
extends or complements popular microbial ecology
packages, including phyloseq
, vegan
, & microbiome
.
📎 This website is the best place for documentation and examples: https://david-barnett.github.io/microViz/
-
This ReadMe shows a few example analyses
-
The Getting Started guide shows more example analyses and gives advice on using microViz with your own data
-
The Reference page lists all functions and links to help pages and examples
-
The News page describes important changes in new microViz package versions
-
The Articles pages give tutorials and further examples
-
Post on GitHub discussions if you have questions/requests
microViz is not (yet) available from CRAN. You can install microViz from R Universe, or from GitHub.
I recommend you first install the Bioconductor dependencies using the code below.
if (!requireNamespace("BiocManager", quietly = TRUE)) install.packages("BiocManager")
BiocManager::install(c("phyloseq", "microbiome", "ComplexHeatmap"), update = FALSE)
install.packages(
"microViz",
repos = c(davidbarnett = "https://david-barnett.r-universe.dev", getOption("repos"))
)
I also recommend you install the following suggested CRAN packages.
install.packages("ggtext") # for rotated labels on ord_plot()
install.packages("ggraph") # for taxatree_plots()
install.packages("DT") # for tax_fix_interactive()
install.packages("corncob") # for beta binomial models in tax_model()
# Installing from GitHub requires the remotes package
install.packages("remotes")
# Windows users will also need to have RTools installed! http://jtleek.com/modules/01_DataScientistToolbox/02_10_rtools/
# To install the latest version:
remotes::install_github("david-barnett/microViz")
# To install a specific "release" version of this package, e.g. an old version
remotes::install_github("david-barnett/[email protected]")
🍎 macOS users - might need to install
xquartz to make the heatmaps work (to do
this with homebrew, run the following command in your mac’s Terminal:
brew install --cask xquartz
📦 I highly recommend using renv for managing your R package installations across multiple projects.
🐳 For Docker users an image with the main branch installed is available at: https://hub.docker.com/r/barnettdavid/microviz-rocker-verse
📅 microViz is tested to work with R version 4.* on Windows, MacOS, and Ubuntu 20. R version 3.6.* should probably work, but I don’t fully test this.
library(microViz)
#> microViz version 0.12.3.9000 - Copyright (C) 2021-2024 David Barnett
#> ! Website: https://david-barnett.github.io/microViz
#> ✔ Useful? For citation details, run: `citation("microViz")`
#> ✖ Silence? `suppressPackageStartupMessages(library(microViz))`
microViz provides a Shiny app for an easy way to start exploring your microbiome data: all you need is a phyloseq object.
# example data from corncob package
pseq <- microViz::ibd %>%
tax_fix() %>%
phyloseq_validate()
ord_explore(pseq) # gif generated with microViz version 0.7.4 (plays at 1.75x speed)
library(phyloseq)
library(dplyr)
library(ggplot2)
# get some example data
data("dietswap", package = "microbiome")
# create a couple of numerical variables to use as constraints or conditions
dietswap <- dietswap %>%
ps_mutate(
weight = recode(bmi_group, obese = 3, overweight = 2, lean = 1),
female = if_else(sex == "female", true = 1, false = 0),
african = if_else(nationality == "AFR", true = 1, false = 0)
)
# add a couple of missing values to show how microViz handles missing data
sample_data(dietswap)$african[c(3, 4)] <- NA
You have quite a few samples in your phyloseq object, and would like to visualize their compositions. Perhaps these example data differ by participant nationality?
dietswap %>%
comp_barplot(
tax_level = "Genus", n_taxa = 15, other_name = "Other",
taxon_renamer = function(x) stringr::str_remove(x, " [ae]t rel."),
palette = distinct_palette(n = 15, add = "grey90"),
merge_other = FALSE, bar_outline_colour = "darkgrey"
) +
coord_flip() +
facet_wrap("nationality", nrow = 1, scales = "free") +
labs(x = NULL, y = NULL) +
theme(axis.text.y = element_blank(), axis.ticks.y = element_blank())
#> Registered S3 method overwritten by 'seriation':
#> method from
#> reorder.hclust vegan
htmp <- dietswap %>%
ps_mutate(nationality = as.character(nationality)) %>%
tax_transform("log2", add = 1, chain = TRUE) %>%
comp_heatmap(
taxa = tax_top(dietswap, n = 30), grid_col = NA, name = "Log2p",
taxon_renamer = function(x) stringr::str_remove(x, " [ae]t rel."),
colors = heat_palette(palette = viridis::turbo(11)),
row_names_side = "left", row_dend_side = "right", sample_side = "bottom",
sample_anno = sampleAnnotation(
Nationality = anno_sample_cat(
var = "nationality", col = c(AAM = "grey35", AFR = "grey85"),
box_col = NA, legend_title = "Nationality", size = grid::unit(4, "mm")
)
)
)
ComplexHeatmap::draw(
object = htmp, annotation_legend_list = attr(htmp, "AnnoLegends"),
merge_legends = TRUE
)
Ordination methods can also help you to visualize if overall microbial ecosystem composition differs markedly between groups, e.g. BMI.
Here is one option as an example:
- Aggregate the taxa into bacterial families (for example) - use
tax_agg()
- Transform the microbial data with the centered-log-ratio
transformation - use
tax_transform()
- Perform PCA with the clr-transformed features (equivalent to
Aitchison distance PCoA) - use
ord_calc()
- Plot the first 2 axes of this PCA ordination, colouring samples by
group and adding taxon loading arrows to visualize which taxa
generally differ across your samples - use
ord_plot()
- Customise the theme of the ggplot as you like and/or add features like ellipses or annotations
# perform ordination
unconstrained_aitchison_pca <- dietswap %>%
tax_agg("Family") %>%
tax_transform("clr") %>%
ord_calc()
# ord_calc will automatically infer you want a "PCA" here
# specify explicitly with method = "PCA", or you can pick another method
# create plot
pca_plot <- unconstrained_aitchison_pca %>%
ord_plot(
plot_taxa = 1:6, colour = "bmi_group", size = 1.5,
tax_vec_length = 0.325,
tax_lab_style = tax_lab_style(max_angle = 90, aspect_ratio = 1),
auto_caption = 8
)
# customise plot
customised_plot <- pca_plot +
stat_ellipse(aes(linetype = bmi_group, colour = bmi_group), linewidth = 0.3) + # linewidth not size, since ggplot 3.4.0
scale_colour_brewer(palette = "Set1") +
theme(legend.position = "bottom") +
coord_fixed(ratio = 1, clip = "off") # makes rotated labels align correctly
# show plot
customised_plot
You visualised your ordinated data in the plot above. Below you can see how to perform a PERMANOVA to test the significance of BMI’s association with overall microbial composition. This example uses the Family-level Aitchison distance to correspond with the plot above.
# calculate distances
aitchison_dists <- dietswap %>%
tax_transform("identity", rank = "Family") %>%
dist_calc("aitchison")
# the more permutations you request, the longer it takes
# but also the more stable and precise your p-values become
aitchison_perm <- aitchison_dists %>%
dist_permanova(
seed = 1234, # for set.seed to ensure reproducibility of random process
n_processes = 1, n_perms = 99, # you should use at least 999!
variables = "bmi_group"
)
#> 2024-06-30 10:55:51.862638 - Starting PERMANOVA with 99 perms with 1 processes
#> 2024-06-30 10:55:51.919099 - Finished PERMANOVA
# view the permanova results
perm_get(aitchison_perm) %>% as.data.frame()
#> Df SumOfSqs R2 F Pr(>F)
#> bmi_group 2 109.170 0.04104336 4.686602 0.01
#> Residual 219 2550.700 0.95895664 NA NA
#> Total 221 2659.869 1.00000000 NA NA
# view the info stored about the distance calculation
info_get(aitchison_perm)
#> psExtra info:
#> tax_agg = "Family" tax_trans = "identity" dist_method = "aitchison"
You could visualise the effect of the (numeric/logical) variables in
your permanova directly using the ord_plot
function with constraints
(and conditions).
perm2 <- aitchison_dists %>%
dist_permanova(variables = c("weight", "african", "sex"), seed = 321)
#> Dropping samples with missings: 2
#> 2024-06-30 10:55:51.930319 - Starting PERMANOVA with 999 perms with 1 processes
#> 2024-06-30 10:55:53.574252 - Finished PERMANOVA
We’ll visualise the effect of nationality and bodyweight on sample composition, after first removing the effect of sex.
perm2 %>%
ord_calc(constraints = c("weight", "african"), conditions = "female") %>%
ord_plot(
colour = "nationality", size = 2.5, alpha = 0.35,
auto_caption = 7,
constraint_vec_length = 1,
constraint_vec_style = vec_constraint(1.5, colour = "grey15"),
constraint_lab_style = constraint_lab_style(
max_angle = 90, size = 3, aspect_ratio = 0.8, colour = "black"
)
) +
stat_ellipse(aes(colour = nationality), linewidth = 0.2) +
scale_color_brewer(palette = "Set1", guide = guide_legend(position = "inside")) +
coord_fixed(ratio = 0.8, clip = "off", xlim = c(-4, 4)) +
theme(legend.position.inside = c(0.9, 0.1), legend.background = element_rect())
#>
#> Centering (mean) and scaling (sd) the constraints and/or conditions:
#> weight
#> african
#> female
microViz heatmaps are powered by ComplexHeatmap
and annotated with
taxa prevalence and/or abundance.
# set up the data with numerical variables and filter to top taxa
psq <- dietswap %>%
ps_mutate(
weight = recode(bmi_group, obese = 3, overweight = 2, lean = 1),
female = if_else(sex == "female", true = 1, false = 0),
african = if_else(nationality == "AFR", true = 1, false = 0)
) %>%
tax_filter(
tax_level = "Genus", min_prevalence = 1 / 10, min_sample_abundance = 1 / 10
) %>%
tax_transform("identity", rank = "Genus")
#> Proportional min_prevalence given: 0.1 --> min 23/222 samples.
# randomly select 30 taxa from the 50 most abundant taxa (just for an example)
set.seed(123)
taxa <- sample(tax_top(psq, n = 50), size = 30)
# actually draw the heatmap
cor_heatmap(
data = psq, taxa = taxa,
taxon_renamer = function(x) stringr::str_remove(x, " [ae]t rel."),
tax_anno = taxAnnotation(
Prev. = anno_tax_prev(undetected = 50),
Log2 = anno_tax_box(undetected = 50, trans = "log2", zero_replace = 1)
)
)
😇 If you find any part of microViz useful to your work, please consider citing the JOSS article:
Barnett et al., (2021). microViz: an R package for microbiome data visualization and statistics. Journal of Open Source Software, 6(63), 3201, https://doi.org/10.21105/joss.03201
Bug reports, questions, suggestions for new features, and other contributions are all welcome. Feel free to create a GitHub Issue or write on the Discussions page.
This project is released with a Contributor Code of Conduct and by participating in this project you agree to abide by its terms.
sessionInfo()
#> R version 4.4.0 (2024-04-24)
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#> attached base packages:
#> [1] stats graphics grDevices utils datasets methods base
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#> other attached packages:
#> [1] ggplot2_3.5.1 dplyr_1.1.4 phyloseq_1.48.0
#> [4] microViz_0.12.3.9000 testthat_3.2.1.1 devtools_2.4.5
#> [7] usethis_2.2.3
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#> [4] shape_1.4.6.1 magrittr_2.0.3 farver_2.1.2
#> [7] rmarkdown_2.27 GlobalOptions_0.1.2 fs_1.6.4
#> [10] zlibbioc_1.50.0 vctrs_0.6.5 multtest_2.60.0
#> [13] memoise_2.0.1 Cairo_1.6-2 htmltools_0.5.8.1
#> [16] curl_5.2.1 Rhdf5lib_1.26.0 rhdf5_2.48.0
#> [19] htmlwidgets_1.6.4 plyr_1.8.9 cachem_1.1.0
#> [22] commonmark_1.9.1 igraph_2.0.3 mime_0.12
#> [25] lifecycle_1.0.4 iterators_1.0.14 pkgconfig_2.0.3
#> [28] Matrix_1.7-0 R6_2.5.1 fastmap_1.2.0
#> [31] clue_0.3-65 GenomeInfoDbData_1.2.12 shiny_1.8.1.1
#> [34] digest_0.6.36 selectr_0.4-2 colorspace_2.1-0
#> [37] S4Vectors_0.42.0 ps_1.7.6 pkgload_1.3.4
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#> [52] highr_0.11 MASS_7.3-60.2 sessioninfo_1.2.2
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#> [79] xml2_1.3.6 utf8_1.2.4 XVector_0.44.0
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