In YuLab-SMU/MicrobiotaProcess: A comprehensive R package for managing and analyzing microbiome and other ecological data within the tidy framework
library(knitr)
knit_hooks$set(crop = hook_pdfcrop)
knitr::opts_chunk$set(crop = TRUE, tidy=FALSE, warning=FALSE,message=FALSE, fig.align="center")
Biocpkg <- function (pkg){
sprintf("[%s](http://bioconductor.org/packages/%s)", pkg, pkg)
}
CRANpkg <- function(pkg){
cran <- "https://CRAN.R-project.org/package"
fmt <- "[%s](%s=%s)"
sprintf(fmt, pkg, cran, pkg)
}
library(ggplot2)
library(phyloseq)
library(shadowtext)
library(ggtree)
library(ggtreeExtra)
library(treeio)
library(tidytree)
library(MicrobiotaProcess)
1. Anatomy of a MPSE
MicrobiotaProcess introduces MPSE S4 class. This class inherits the SummarizedExperiment[@SE] class. Here, the assays slot is used to store the rectangular abundance matrices of features for a microbiome experimental results. The colData slot is used to store the meta-data of sample and some results about samples in the downstream analysis. The rowData is used to store the meta-data of features and some results about the features in the downstream analysis. Compared to the SummarizedExperiment object, MPSE introduces the following additional slots:
- taxatree: is a
treedata[@treeio; @tidytree] class contained phylo class (hierarchical structure) and tibble class (associated data) to store the taxonomy information, the tip labels of taxonomy tree are the rows of the assays, but the internal node labels contain the differences level taxonomy of the rows of the assays. The tibble class contains the taxonomy classification of node labels.
- otutree: is also a
treedata class to store the phylogenetic tree (based with reference sequences) and the associated data, which its tip labels are also the rows of the assays.
- refseq: is a
XStringSet[@Biostrings] class contained reference sequences, which its names are also identical with the rows of the assays.
knitr::include_graphics("./mpse.png")
2. Overview of the design of MicrobiotaProcess package
With this data structure, MicrobiotaProcess will be more interoperable with the existing computing ecosystem. For example, the slots inherited SummarizedExperiment can be extracted via the methods provided by SummarizedExperiment. The taxatree and otutree can also be extracted via mp_extract_tree, and they are compatible with ggtree[@yu2017ggtree], ggtreeExtra[@ggtreeExtra], treeio[@treeio] and tidytree[@tidytree] ecosystem since they are all treedata class, which is a data structure used directly by these packages.
Moreover, the results of upstream analysis of microbiome based some tools, such as qiime2[@qiime2], dada2[@dada2] and MetaPhlAn[@metaphlan] or other classes (SummarizedExperiment[@SE], phyloseq[@ps] and TreeSummarizedExperiment[@TSE]) used to store the result of microbiome can be loaded or transformed to the MPSE class.
In addition, MicrobiotaProcess also introduces a tidy microbiome data structure paradigm and analysis grammar. It provides a wide variety of microbiome analysis procedures under a unified and common framework (tidy-like framework). We believe MicrobiotaProcess can improve the efficiency of related researches, and it also bridges microbiome data analysis with the tidyverse[@tidyverse].
knitr::include_graphics("./mp-design.png")
3. MicrobiotaProcess profiling
3.1 bridges other tools
MicrobiotaProcess provides several functions to parsing the output of upstream analysis tools of microbiome, such as qiime2[@qiime2], dada2[@dada2] and MetaPhlAn[@metaphlan], and return MPSE object. Some bioconductor class, such as phyloseq[@ps], TreeSummarizedExperiment[@TSE] and SummarizedExperiment[@SE] can also be converted to MPSE via as.MPSE().
library(MicrobiotaProcess)
#parsing the output of dada2
seqtabfile <- system.file("extdata", "seqtab.nochim.rds", package="MicrobiotaProcess")
seqtab <- readRDS(seqtabfile)
taxafile <- system.file("extdata", "taxa_tab.rds", package="MicrobiotaProcess")
taxa <- readRDS(taxafile)
# the seqtab and taxa are output of dada2
sampleda <- system.file("extdata", "mouse.time.dada2.txt", package="MicrobiotaProcess")
mpse1 <- mp_import_dada2(seqtab=seqtab, taxatab=taxa, sampleda=sampleda)
mpse1
# parsing the output of qiime2
otuqzafile <- system.file("extdata", "table.qza", package="MicrobiotaProcess")
taxaqzafile <- system.file("extdata", "taxa.qza", package="MicrobiotaProcess")
mapfile <- system.file("extdata", "metadata_qza.txt", package="MicrobiotaProcess")
mpse2 <- mp_import_qiime2(otuqza=otuqzafile, taxaqza=taxaqzafile, mapfilename=mapfile)
mpse2
# parsing the output of MetaPhlAn
file1 <- system.file("extdata/MetaPhlAn", "metaphlan_test.txt", package="MicrobiotaProcess")
sample.file <- system.file("extdata/MetaPhlAn", "sample_test.txt", package="MicrobiotaProcess")
mpse3 <- mp_import_metaphlan(profile=file1, mapfilename=sample.file)
mpse3
# convert phyloseq object to mpse
#library(phyloseq)
#data(esophagus)
#esophagus
#mpse4 <- esophagus %>% as.MPSE()
#mpse4
# convert TreeSummarizedExperiment object to mpse
# library(curatedMetagenomicData)
# tse <- curatedMetagenomicData::curatedMetagenomicData("ZhuF_2020.relative_abundance", dryrun=F)
# tse[[1]] %>% as.MPSE() -> mpse5
# mpse5
3.2 alpha diversity analysis
Rarefaction, based on sampling technique, was used to compensate for the effect of sample size on the number of units observed in a sample[@siegel2004rarefaction]. MicrobiotaProcess provided mp_cal_rarecurve and mp_plot_rarecurve to calculate and plot the curves based on rrarefy of r CRANpkg("vegan")[@Jari2019vegan].
library(ggplot2)
library(MicrobiotaProcess)
data(mouse.time.mpse)
mouse.time.mpse
# Rarefied species richness
mouse.time.mpse %<>% mp_rrarefy()
# 'chunks' represent the split number of each sample to calculate alpha
# diversity, default is 400. e.g. If a sample has total 40000
# reads, if chunks is 400, it will be split to 100 sub-samples
# (100, 200, 300,..., 40000), then alpha diversity index was
# calculated based on the sub-samples.
# '.abundance' the column name of abundance, if the '.abundance' is not be
# rarefied calculate rarecurve, user can specific 'force=TRUE'.
mouse.time.mpse %<>%
mp_cal_rarecurve(
.abundance = RareAbundance,
chunks = 400
)
# The RareAbundanceRarecurve column will be added the colData slot
# automatically (default action="add")
mouse.time.mpse %>% print(width=180)
# default will display the confidence interval around smooth.
# se=TRUE
p1 <- mouse.time.mpse %>%
mp_plot_rarecurve(
.rare = RareAbundanceRarecurve,
.alpha = Observe,
)
p2 <- mouse.time.mpse %>%
mp_plot_rarecurve(
.rare = RareAbundanceRarecurve,
.alpha = Observe,
.group = time
) +
scale_color_manual(values=c("#00A087FF", "#3C5488FF")) +
scale_fill_manual(values=c("#00A087FF", "#3C5488FF"), guide="none")
# combine the samples belong to the same groups if
# plot.group=TRUE
p3 <- mouse.time.mpse %>%
mp_plot_rarecurve(
.rare = RareAbundanceRarecurve,
.alpha = "Observe",
.group = time,
plot.group = TRUE
) +
scale_color_manual(values=c("#00A087FF", "#3C5488FF")) +
scale_fill_manual(values=c("#00A087FF", "#3C5488FF"),guide="none")
p1 + p2 + p3
# Users can extract the result with mp_extract_rarecurve to extract the result of mp_cal_rarecurve
# and visualized the result manually.
3.3 calculate alpha index and visualization
Alpha diversity can be estimated the species richness and evenness of some species communities. MicrobiotaProcess provides mp_cal_alpha to calculate alpha index (Observe, Chao1, ACE, Shannon, Simpson and J (Pielou's evenness)) and the mp_plot_alpha to visualize the result.
library(ggplot2)
library(MicrobiotaProcess)
mouse.time.mpse %<>%
mp_cal_alpha(.abundance=RareAbundance)
mouse.time.mpse
f1 <- mouse.time.mpse %>%
mp_plot_alpha(
.group=time,
.alpha=c(Observe, Chao1, ACE, Shannon, Simpson, Pielou)
) +
scale_fill_manual(values=c("#00A087FF", "#3C5488FF"), guide="none") +
scale_color_manual(values=c("#00A087FF", "#3C5488FF"), guide="none")
f2 <- mouse.time.mpse %>%
mp_plot_alpha(
.alpha=c(Observe, Chao1, ACE, Shannon, Simpson, Pielou)
)
f1 / f2
Users can extract the result with mp_extract_sample() to extract the result of mp_cal_alpha and visualized the result manually, see the example of mp_cal_alpha.
3.4 The visualization of taxonomy abundance
MicrobiotaProcess provides the mp_cal_abundance, mp_plot_abundance to calculate and plot the composition of species communities. And the mp_extract_abundance can extract the abundance of specific taxonomy level. User can also extract the abundance table to perform external analysis such as visualize manually (see the example of mp_cal_abundance).
mouse.time.mpse
mouse.time.mpse %<>%
mp_cal_abundance( # for each samples
.abundance = RareAbundance
) %>%
mp_cal_abundance( # for each groups
.abundance=RareAbundance,
.group=time
)
mouse.time.mpse
# visualize the relative abundance of top 20 phyla for each sample.
p1 <- mouse.time.mpse %>%
mp_plot_abundance(
.abundance=RareAbundance,
.group=time,
taxa.class = Phylum,
topn = 20,
relative = TRUE
)
# visualize the abundance (rarefied) of top 20 phyla for each sample.
p2 <- mouse.time.mpse %>%
mp_plot_abundance(
.abundance=RareAbundance,
.group=time,
taxa.class = Phylum,
topn = 20,
relative = FALSE
)
p1 / p2
The abundance of features also can be visualized by mp_plot_abundance with heatmap plot by setting geom='heatmap'.
h1 <- mouse.time.mpse %>%
mp_plot_abundance(
.abundance = RareAbundance,
.group = time,
taxa.class = Phylum,
relative = TRUE,
topn = 20,
geom = 'heatmap',
features.dist = 'euclidean',
features.hclust = 'average',
sample.dist = 'bray',
sample.hclust = 'average'
)
h2 <- mouse.time.mpse %>%
mp_plot_abundance(
.abundance = RareAbundance,
.group = time,
taxa.class = Phylum,
relative = FALSE,
topn = 20,
geom = 'heatmap',
features.dist = 'euclidean',
features.hclust = 'average',
sample.dist = 'bray',
sample.hclust = 'average'
)
# the character (scale or theme) of figure can be adjusted by set_scale_theme
# refer to the mp_plot_dist
aplot::plot_list(gglist=list(h1, h2), tag_levels="A")
# visualize the relative abundance of top 20 phyla for each .group (time)
p3 <- mouse.time.mpse %>%
mp_plot_abundance(
.abundance=RareAbundance,
.group=time,
taxa.class = Phylum,
topn = 20,
plot.group = TRUE
)
# visualize the abundance of top 20 phyla for each .group (time)
p4 <- mouse.time.mpse %>%
mp_plot_abundance(
.abundance=RareAbundance,
.group= time,
taxa.class = Phylum,
topn = 20,
relative = FALSE,
plot.group = TRUE
)
p3 / p4
3.5 Beta diversity analysis
Beta diversity is used to quantify the dissimilarities between the communities (samples). Some distance indexes, such as Bray-Curtis index, Jaccard index, UniFrac (weighted or unweighted) index, are useful for or popular with the community ecologists. Many ordination methods are used to estimated the dissimilarities in community ecology. MicrobiotaProcess implements mp_cal_dist to calculate the common distance, and provided mp_plot_dist to visualize the result. It also provides several commonly-used ordination methods, such as PCA (mp_cal_pca), PCoA (mp_cal_pcoa), NMDS (mp_cal_nmds), DCA (mp_cal_dca), RDA (mp_cal_rda), CCA (mp_cal_cca), and a function (mp_envfit) fits environmental vectors or factors onto an ordination. Moreover, it also wraps several statistical analysis for the distance matrices, such as adonis (mp_adonis), anosim (mp_anosim), mrpp (mp_mrpp) and mantel (mp_mantel). All these functions are developed based on tidy-like framework, and provided unified grammar, we believe these functions will help users to do the ordination analysis more conveniently.
3.5.1 The distance between samples or groups
# standardization
# mp_decostand wraps the decostand of vegan, which provides
# many standardization methods for community ecology.
# default is hellinger, then the abundance processed will
# be stored to the assays slot.
mouse.time.mpse %<>%
mp_decostand(.abundance=Abundance)
mouse.time.mpse
# calculate the distance between the samples.
# the distance will be generated a nested tibble and added to the
# colData slot.
mouse.time.mpse %<>% mp_cal_dist(.abundance=hellinger, distmethod="bray")
mouse.time.mpse
# mp_plot_dist provides there methods to visualize the distance between the samples or groups
# when .group is not provided, the dot heatmap plot will be return
p1 <- mouse.time.mpse %>% mp_plot_dist(.distmethod = bray)
p1
# when .group is provided, the dot heatmap plot with group information will be return.
p2 <- mouse.time.mpse %>% mp_plot_dist(.distmethod = bray, .group = time)
# The scale or theme of dot heatmap plot can be adjusted using set_scale_theme function.
p2 %>% set_scale_theme(
x = scale_fill_manual(
values=c("orange", "deepskyblue"),
guide = guide_legend(
keywidth = 1,
keyheight = 0.5,
title.theme = element_text(size=8),
label.theme = element_text(size=6)
)
),
aes_var = time # specific the name of variable
) %>%
set_scale_theme(
x = scale_color_gradient(
guide = guide_legend(keywidth = 0.5, keyheight = 0.5)
),
aes_var = bray
) %>%
set_scale_theme(
x = scale_size_continuous(
range = c(0.1, 3),
guide = guide_legend(keywidth = 0.5, keyheight = 0.5)
),
aes_var = bray
)
# when .group is provided and group.test is TRUE, the comparison of different groups will be returned
p3 <- mouse.time.mpse %>% mp_plot_dist(.distmethod = bray, .group = time, group.test=TRUE, textsize=2)
p3
3.5.2 The PCoA analysis
The distance can be used to do the ordination analysis, such as PCoA, NMDS, etc. Here, we only show the example of PCoA analysis, other ordinations can refer to the examples and the usages of the corresponding functions.
mouse.time.mpse %<>%
mp_cal_pcoa(.abundance=hellinger, distmethod="bray")
# The dimensions of ordination analysis will be added the colData slot (default).
mouse.time.mpse
# We also can perform adonis or anosim to check whether it is significant to the dissimilarities of groups.
mouse.time.mpse %<>%
mp_adonis(.abundance=hellinger, .formula=~time, distmethod="bray", permutations=9999, action="add")
mouse.time.mpse %>% mp_extract_internal_attr(name=adonis)
library(ggplot2)
p1 <- mouse.time.mpse %>%
mp_plot_ord(
.ord = pcoa,
.group = time,
.color = time,
.size = 1.2,
.alpha = 1,
ellipse = TRUE,
show.legend = FALSE # don't display the legend of stat_ellipse
) +
scale_fill_manual(values=c("#00A087FF", "#3C5488FF")) +
scale_color_manual(values=c("#00A087FF", "#3C5488FF"))
# The size of point also can be mapped to other variables such as Observe, or Shannon
# Then the alpha diversity and beta diversity will be displayed simultaneously.
p2 <- mouse.time.mpse %>%
mp_plot_ord(
.ord = pcoa,
.group = time,
.color = time,
.size = Observe,
.alpha = Shannon,
ellipse = TRUE,
show.legend = FALSE # don't display the legend of stat_ellipse
) +
scale_fill_manual(
values = c("#00A087FF", "#3C5488FF"),
guide = guide_legend(keywidth=0.6, keyheight=0.6, label.theme=element_text(size=6.5))
) +
scale_color_manual(
values=c("#00A087FF", "#3C5488FF"),
guide = guide_legend(keywidth=0.6, keyheight=0.6, label.theme=element_text(size=6.5))
) +
scale_size_continuous(
range=c(0.5, 3),
guide = guide_legend(keywidth=0.6, keyheight=0.6, label.theme=element_text(size=6.5))
)
p1 + p2
3.5.3 Hierarchical cluster analysis
The distance of samples can also be used to perform the hierarchical cluster analysis to estimated the dissimilarities of samples. MicrobiotaProcess presents mp_cal_clust to perform this analysis. It also is implemented with the tidy-like framework.
mouse.time.mpse %<>%
mp_cal_clust(
.abundance = hellinger,
distmethod = "bray",
hclustmethod = "average", # (UPGAE)
action = "add" # action is used to control which result will be returned
)
mouse.time.mpse
# if action = 'add', the result of hierarchical cluster will be added to the MPSE object
# mp_extract_internal_attr can extract it. It is a treedata object, so it can be visualized
# by ggtree.
sample.clust <- mouse.time.mpse %>% mp_extract_internal_attr(name='SampleClust')
sample.clust
library(ggtree)
p <- ggtree(sample.clust) +
geom_tippoint(aes(color=time)) +
geom_tiplab(as_ylab = TRUE) +
ggplot2::scale_x_continuous(expand=c(0, 0.01))
p
Since the result of hierarchical cluster is treedata object, so it is very easy to display the result with associated data. For example, we can display the result of hierarchical cluster and the abundance of specific taxonomy level to check whether some biological pattern can be found.
library(ggtreeExtra)
library(ggplot2)
phyla.tb <- mouse.time.mpse %>%
mp_extract_abundance(taxa.class=Phylum, topn=30)
# The abundance of each samples is nested, it can be flatted using the unnest of tidyr.
phyla.tb %<>% tidyr::unnest(cols=RareAbundanceBySample) %>% dplyr::rename(Phyla="label")
phyla.tb
p1 <- p +
geom_fruit(
data=phyla.tb,
geom=geom_col,
mapping = aes(x = RelRareAbundanceBySample,
y = Sample,
fill = Phyla
),
orientation = "y",
#offset = 0.4,
pwidth = 3,
axis.params = list(axis = "x",
title = "The relative abundance of phyla (%)",
title.size = 4,
text.size = 2,
vjust = 1),
grid.params = list()
)
p1
3.6 Biomarker discovery
The MicrobiotaProcess presents mp_diff_analysis for the biomarker discovery based on tidy-like framework. The rule of mp_diff_analysis is similar with the LEfSe[@Nicola2011LEfSe]. First, all features are tested whether values in different classes are differentially distributed. Second, the significantly different features are tested whether all pairwise comparisons between subclass in different classes distinctly consistent with the class trend. Finally, the significantly discriminative features are assessed by LDA (linear discriminant analysis) or rf(randomForest). However, mp_diff_analysis is more flexible. The test method of two step can be set by user, and we used the general fold change[@wirbel2019meta] and wilcox.test(default) to test whether all pairwise comparisons between subclass in different classes distinctly consistent with the class trend. And the result is stored to the treedata object, which can be processed and displayed via treeio[@treeio], tidytree[@tidytree], ggtree[@yu2017ggtree] and ggtreeExtra[@ggtreeExtra].
library(ggtree)
library(ggtreeExtra)
library(ggplot2)
library(MicrobiotaProcess)
library(tidytree)
library(ggstar)
library(forcats)
mouse.time.mpse %>% print(width=150)
mouse.time.mpse %<>%
mp_diff_analysis(
.abundance = RelRareAbundanceBySample,
.group = time,
first.test.alpha = 0.01
)
# The result is stored to the taxatree or otutree slot, you can use mp_extract_tree to extract the specific slot.
taxa.tree <- mouse.time.mpse %>%
mp_extract_tree(type="taxatree")
taxa.tree
# And the result tibble of different analysis can also be extracted
# with tidytree (>=0.3.5)
taxa.tree %>% select(label, nodeClass, LDAupper, LDAmean, LDAlower, Sign_time, pvalue, fdr) %>% dplyr::filter(!is.na(fdr))
# Since taxa.tree is treedata object, it can be visualized by ggtree and ggtreeExtra
p1 <- ggtree(
taxa.tree,
layout="radial",
size = 0.3
) +
geom_point(
data = td_filter(!isTip),
fill="white",
size=1,
shape=21
)
# display the high light of phylum clade.
p2 <- p1 +
geom_hilight(
data = td_filter(nodeClass == "Phylum"),
mapping = aes(node = node, fill = label)
)
# display the relative abundance of features(OTU)
p3 <- p2 +
ggnewscale::new_scale("fill") +
geom_fruit(
data = td_unnest(RareAbundanceBySample),
geom = geom_star,
mapping = aes(
x = fct_reorder(Sample, time, .fun=min),
size = RelRareAbundanceBySample,
fill = time,
subset = RelRareAbundanceBySample > 0
),
starshape = 13,
starstroke = 0.25,
offset = 0.04,
pwidth = 0.8,
grid.params = list(linetype=2)
) +
scale_size_continuous(
name="Relative Abundance (%)",
range = c(.5, 3)
) +
scale_fill_manual(values=c("#1B9E77", "#D95F02"))
# display the tip labels of taxa tree
p4 <- p3 + geom_tiplab(size=2, offset=7.2)
# display the LDA of significant OTU.
p5 <- p4 +
ggnewscale::new_scale("fill") +
geom_fruit(
geom = geom_col,
mapping = aes(
x = LDAmean,
fill = Sign_time,
subset = !is.na(LDAmean)
),
orientation = "y",
offset = 0.3,
pwidth = 0.5,
axis.params = list(axis = "x",
title = "Log10(LDA)",
title.height = 0.01,
title.size = 2,
text.size = 1.8,
vjust = 1),
grid.params = list(linetype = 2)
)
# display the significant (FDR) taxonomy after kruskal.test (default)
p6 <- p5 +
ggnewscale::new_scale("size") +
geom_point(
data=td_filter(!is.na(Sign_time)),
mapping = aes(size = -log10(fdr),
fill = Sign_time,
),
shape = 21,
) +
scale_size_continuous(range=c(1, 3)) +
scale_fill_manual(values=c("#1B9E77", "#D95F02"))
p6 + theme(
legend.key.height = unit(0.3, "cm"),
legend.key.width = unit(0.3, "cm"),
legend.spacing.y = unit(0.02, "cm"),
legend.text = element_text(size = 7),
legend.title = element_text(size = 9),
)
The visualization methods of result can be various, you can refer to the article or book of ggtree[@yu2017ggtree; @yu2018two] and the article of ggtreeExtra[@ggtreeExtra]. In addition, we also developed mp_plot_diff_res to display the result of mp_diff_analysis, it can decreases coding burden.
# this object has contained the result of mp_diff_analysis
mouse.time.mpse
# Because the released `ggnewscale` modified the internal new aesthetics name,
# The following code is to obtain the new aesthetics name according to version of
# `ggnewscale`
flag <- packageVersion("ggnewscale") >= "0.5.0"
new.fill <- ifelse(flag, "fill_ggnewscale_1", "fill_new_new")
new.fill2 <- ifelse(flag , "fill_ggnewscale_2", "fill_new")
p <- mouse.time.mpse %>%
mp_plot_diff_res(
group.abun = TRUE,
pwidth.abun=0.1
)
# if version of `ggnewscale` is >= 0.5.0, you can also use p$ggnewscale to view the renamed scales.
p <- p +
scale_fill_manual(values=c("deepskyblue", "orange")) +
scale_fill_manual(
aesthetics = new.fill2, # The fill aes was renamed to `new.fill` for the abundance dotplot layer
values = c("deepskyblue", "orange")
) +
scale_fill_manual(
aesthetics = new.fill, # The fill aes for hight light layer of tree was renamed to `new.fill2`
values = c("#E41A1C", "#377EB8", "#4DAF4A",
"#984EA3", "#FF7F00", "#FFFF33",
"#A65628", "#F781BF", "#999999"
)
)
p
We also developed mp_plot_diff_cladogram to visualize the result.
f <- mouse.time.mpse %>%
mp_plot_diff_cladogram(
label.size = 2.5,
hilight.alpha = .3,
bg.tree.size = .5,
bg.point.size = 2,
bg.point.stroke = .25
) +
scale_fill_diff_cladogram( # set the color of different group.
values = c('deepskyblue', 'orange')
) +
scale_size_continuous(range = c(1, 4))
f
The result also can be visualized with mp_plot_diff_boxplot.
f.box <- mouse.time.mpse %>%
mp_plot_diff_boxplot(
.group = time,
) %>%
set_diff_boxplot_color(
values = c("deepskyblue", "orange"),
guide = guide_legend(title=NULL)
)
f.bar <- mouse.time.mpse %>%
mp_plot_diff_boxplot(
taxa.class = c(Genus, OTU), # select the taxonomy level to display
group.abun = TRUE, # display the mean abundance of each group
removeUnknown = TRUE, # whether mask the unknown taxa.
) %>%
set_diff_boxplot_color(
values = c("deepskyblue", "orange"),
guide = guide_legend(title=NULL)
)
aplot::plot_list(f.box, f.bar)
Or visualizing the results with mp_plot_diff_manhattan
f.mahattan <- mouse.time.mpse %>%
mp_plot_diff_manhattan(
.group = Sign_time,
.y = fdr,
.size = 2.4,
taxa.class = c('OTU', 'Genus'),
anno.taxa.class = Phylum
)
f.mahattan
4. Need helps?
If you have questions/issues, please visit github issue tracker.
5. Session information
Here is the output of sessionInfo() on the system on which this document was compiled:
sessionInfo()
6. References
YuLab-SMU/MicrobiotaProcess documentation built on July 26, 2024, 4:21 a.m.
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library(knitr) knit_hooks$set(crop = hook_pdfcrop) knitr::opts_chunk$set(crop = TRUE, tidy=FALSE, warning=FALSE,message=FALSE, fig.align="center") Biocpkg <- function (pkg){ sprintf("[%s](http://bioconductor.org/packages/%s)", pkg, pkg) } CRANpkg <- function(pkg){ cran <- "https://CRAN.R-project.org/package" fmt <- "[%s](%s=%s)" sprintf(fmt, pkg, cran, pkg) }
library(ggplot2) library(phyloseq) library(shadowtext) library(ggtree) library(ggtreeExtra) library(treeio) library(tidytree) library(MicrobiotaProcess)
1. Anatomy of a MPSE
MicrobiotaProcess introduces MPSE S4 class. This class inherits the SummarizedExperiment[@SE] class. Here, the assays slot is used to store the rectangular abundance matrices of features for a microbiome experimental results. The colData slot is used to store the meta-data of sample and some results about samples in the downstream analysis. The rowData is used to store the meta-data of features and some results about the features in the downstream analysis. Compared to the SummarizedExperiment object, MPSE introduces the following additional slots:
- taxatree: is a
treedata[@treeio; @tidytree] class contained phylo class (hierarchical structure) and tibble class (associated data) to store the taxonomy information, the tip labels of taxonomy tree are the rows of theassays, but the internal node labels contain the differences level taxonomy of the rows of theassays. The tibble class contains the taxonomy classification of node labels. - otutree: is also a
treedataclass to store the phylogenetic tree (based with reference sequences) and the associated data, which its tip labels are also the rows of the assays. - refseq: is a
XStringSet[@Biostrings] class contained reference sequences, which its names are also identical with the rows of the assays.
knitr::include_graphics("./mpse.png")
2. Overview of the design of MicrobiotaProcess package
With this data structure, MicrobiotaProcess will be more interoperable with the existing computing ecosystem. For example, the slots inherited SummarizedExperiment can be extracted via the methods provided by SummarizedExperiment. The taxatree and otutree can also be extracted via mp_extract_tree, and they are compatible with ggtree[@yu2017ggtree], ggtreeExtra[@ggtreeExtra], treeio[@treeio] and tidytree[@tidytree] ecosystem since they are all treedata class, which is a data structure used directly by these packages.
Moreover, the results of upstream analysis of microbiome based some tools, such as qiime2[@qiime2], dada2[@dada2] and MetaPhlAn[@metaphlan] or other classes (SummarizedExperiment[@SE], phyloseq[@ps] and TreeSummarizedExperiment[@TSE]) used to store the result of microbiome can be loaded or transformed to the MPSE class.
In addition, MicrobiotaProcess also introduces a tidy microbiome data structure paradigm and analysis grammar. It provides a wide variety of microbiome analysis procedures under a unified and common framework (tidy-like framework). We believe MicrobiotaProcess can improve the efficiency of related researches, and it also bridges microbiome data analysis with the tidyverse[@tidyverse].
knitr::include_graphics("./mp-design.png")
3. MicrobiotaProcess profiling
3.1 bridges other tools
MicrobiotaProcess provides several functions to parsing the output of upstream analysis tools of microbiome, such as qiime2[@qiime2], dada2[@dada2] and MetaPhlAn[@metaphlan], and return MPSE object. Some bioconductor class, such as phyloseq[@ps], TreeSummarizedExperiment[@TSE] and SummarizedExperiment[@SE] can also be converted to MPSE via as.MPSE().
library(MicrobiotaProcess) #parsing the output of dada2 seqtabfile <- system.file("extdata", "seqtab.nochim.rds", package="MicrobiotaProcess") seqtab <- readRDS(seqtabfile) taxafile <- system.file("extdata", "taxa_tab.rds", package="MicrobiotaProcess") taxa <- readRDS(taxafile) # the seqtab and taxa are output of dada2 sampleda <- system.file("extdata", "mouse.time.dada2.txt", package="MicrobiotaProcess") mpse1 <- mp_import_dada2(seqtab=seqtab, taxatab=taxa, sampleda=sampleda) mpse1 # parsing the output of qiime2 otuqzafile <- system.file("extdata", "table.qza", package="MicrobiotaProcess") taxaqzafile <- system.file("extdata", "taxa.qza", package="MicrobiotaProcess") mapfile <- system.file("extdata", "metadata_qza.txt", package="MicrobiotaProcess") mpse2 <- mp_import_qiime2(otuqza=otuqzafile, taxaqza=taxaqzafile, mapfilename=mapfile) mpse2 # parsing the output of MetaPhlAn file1 <- system.file("extdata/MetaPhlAn", "metaphlan_test.txt", package="MicrobiotaProcess") sample.file <- system.file("extdata/MetaPhlAn", "sample_test.txt", package="MicrobiotaProcess") mpse3 <- mp_import_metaphlan(profile=file1, mapfilename=sample.file) mpse3 # convert phyloseq object to mpse #library(phyloseq) #data(esophagus) #esophagus #mpse4 <- esophagus %>% as.MPSE() #mpse4 # convert TreeSummarizedExperiment object to mpse # library(curatedMetagenomicData) # tse <- curatedMetagenomicData::curatedMetagenomicData("ZhuF_2020.relative_abundance", dryrun=F) # tse[[1]] %>% as.MPSE() -> mpse5 # mpse5
3.2 alpha diversity analysis
Rarefaction, based on sampling technique, was used to compensate for the effect of sample size on the number of units observed in a sample[@siegel2004rarefaction]. MicrobiotaProcess provided mp_cal_rarecurve and mp_plot_rarecurve to calculate and plot the curves based on rrarefy of r CRANpkg("vegan")[@Jari2019vegan].
library(ggplot2) library(MicrobiotaProcess) data(mouse.time.mpse) mouse.time.mpse # Rarefied species richness mouse.time.mpse %<>% mp_rrarefy() # 'chunks' represent the split number of each sample to calculate alpha # diversity, default is 400. e.g. If a sample has total 40000 # reads, if chunks is 400, it will be split to 100 sub-samples # (100, 200, 300,..., 40000), then alpha diversity index was # calculated based on the sub-samples. # '.abundance' the column name of abundance, if the '.abundance' is not be # rarefied calculate rarecurve, user can specific 'force=TRUE'. mouse.time.mpse %<>% mp_cal_rarecurve( .abundance = RareAbundance, chunks = 400 ) # The RareAbundanceRarecurve column will be added the colData slot # automatically (default action="add") mouse.time.mpse %>% print(width=180) # default will display the confidence interval around smooth. # se=TRUE p1 <- mouse.time.mpse %>% mp_plot_rarecurve( .rare = RareAbundanceRarecurve, .alpha = Observe, ) p2 <- mouse.time.mpse %>% mp_plot_rarecurve( .rare = RareAbundanceRarecurve, .alpha = Observe, .group = time ) + scale_color_manual(values=c("#00A087FF", "#3C5488FF")) + scale_fill_manual(values=c("#00A087FF", "#3C5488FF"), guide="none") # combine the samples belong to the same groups if # plot.group=TRUE p3 <- mouse.time.mpse %>% mp_plot_rarecurve( .rare = RareAbundanceRarecurve, .alpha = "Observe", .group = time, plot.group = TRUE ) + scale_color_manual(values=c("#00A087FF", "#3C5488FF")) + scale_fill_manual(values=c("#00A087FF", "#3C5488FF"),guide="none") p1 + p2 + p3 # Users can extract the result with mp_extract_rarecurve to extract the result of mp_cal_rarecurve # and visualized the result manually.
3.3 calculate alpha index and visualization
Alpha diversity can be estimated the species richness and evenness of some species communities. MicrobiotaProcess provides mp_cal_alpha to calculate alpha index (Observe, Chao1, ACE, Shannon, Simpson and J (Pielou's evenness)) and the mp_plot_alpha to visualize the result.
library(ggplot2) library(MicrobiotaProcess) mouse.time.mpse %<>% mp_cal_alpha(.abundance=RareAbundance) mouse.time.mpse f1 <- mouse.time.mpse %>% mp_plot_alpha( .group=time, .alpha=c(Observe, Chao1, ACE, Shannon, Simpson, Pielou) ) + scale_fill_manual(values=c("#00A087FF", "#3C5488FF"), guide="none") + scale_color_manual(values=c("#00A087FF", "#3C5488FF"), guide="none") f2 <- mouse.time.mpse %>% mp_plot_alpha( .alpha=c(Observe, Chao1, ACE, Shannon, Simpson, Pielou) ) f1 / f2
Users can extract the result with mp_extract_sample() to extract the result of mp_cal_alpha and visualized the result manually, see the example of mp_cal_alpha.
3.4 The visualization of taxonomy abundance
MicrobiotaProcess provides the mp_cal_abundance, mp_plot_abundance to calculate and plot the composition of species communities. And the mp_extract_abundance can extract the abundance of specific taxonomy level. User can also extract the abundance table to perform external analysis such as visualize manually (see the example of mp_cal_abundance).
mouse.time.mpse mouse.time.mpse %<>% mp_cal_abundance( # for each samples .abundance = RareAbundance ) %>% mp_cal_abundance( # for each groups .abundance=RareAbundance, .group=time ) mouse.time.mpse # visualize the relative abundance of top 20 phyla for each sample. p1 <- mouse.time.mpse %>% mp_plot_abundance( .abundance=RareAbundance, .group=time, taxa.class = Phylum, topn = 20, relative = TRUE ) # visualize the abundance (rarefied) of top 20 phyla for each sample. p2 <- mouse.time.mpse %>% mp_plot_abundance( .abundance=RareAbundance, .group=time, taxa.class = Phylum, topn = 20, relative = FALSE ) p1 / p2
The abundance of features also can be visualized by mp_plot_abundance with heatmap plot by setting geom='heatmap'.
h1 <- mouse.time.mpse %>% mp_plot_abundance( .abundance = RareAbundance, .group = time, taxa.class = Phylum, relative = TRUE, topn = 20, geom = 'heatmap', features.dist = 'euclidean', features.hclust = 'average', sample.dist = 'bray', sample.hclust = 'average' ) h2 <- mouse.time.mpse %>% mp_plot_abundance( .abundance = RareAbundance, .group = time, taxa.class = Phylum, relative = FALSE, topn = 20, geom = 'heatmap', features.dist = 'euclidean', features.hclust = 'average', sample.dist = 'bray', sample.hclust = 'average' ) # the character (scale or theme) of figure can be adjusted by set_scale_theme # refer to the mp_plot_dist aplot::plot_list(gglist=list(h1, h2), tag_levels="A")
# visualize the relative abundance of top 20 phyla for each .group (time) p3 <- mouse.time.mpse %>% mp_plot_abundance( .abundance=RareAbundance, .group=time, taxa.class = Phylum, topn = 20, plot.group = TRUE ) # visualize the abundance of top 20 phyla for each .group (time) p4 <- mouse.time.mpse %>% mp_plot_abundance( .abundance=RareAbundance, .group= time, taxa.class = Phylum, topn = 20, relative = FALSE, plot.group = TRUE ) p3 / p4
3.5 Beta diversity analysis
Beta diversity is used to quantify the dissimilarities between the communities (samples). Some distance indexes, such as Bray-Curtis index, Jaccard index, UniFrac (weighted or unweighted) index, are useful for or popular with the community ecologists. Many ordination methods are used to estimated the dissimilarities in community ecology. MicrobiotaProcess implements mp_cal_dist to calculate the common distance, and provided mp_plot_dist to visualize the result. It also provides several commonly-used ordination methods, such as PCA (mp_cal_pca), PCoA (mp_cal_pcoa), NMDS (mp_cal_nmds), DCA (mp_cal_dca), RDA (mp_cal_rda), CCA (mp_cal_cca), and a function (mp_envfit) fits environmental vectors or factors onto an ordination. Moreover, it also wraps several statistical analysis for the distance matrices, such as adonis (mp_adonis), anosim (mp_anosim), mrpp (mp_mrpp) and mantel (mp_mantel). All these functions are developed based on tidy-like framework, and provided unified grammar, we believe these functions will help users to do the ordination analysis more conveniently.
3.5.1 The distance between samples or groups
# standardization # mp_decostand wraps the decostand of vegan, which provides # many standardization methods for community ecology. # default is hellinger, then the abundance processed will # be stored to the assays slot. mouse.time.mpse %<>% mp_decostand(.abundance=Abundance) mouse.time.mpse # calculate the distance between the samples. # the distance will be generated a nested tibble and added to the # colData slot. mouse.time.mpse %<>% mp_cal_dist(.abundance=hellinger, distmethod="bray") mouse.time.mpse # mp_plot_dist provides there methods to visualize the distance between the samples or groups # when .group is not provided, the dot heatmap plot will be return p1 <- mouse.time.mpse %>% mp_plot_dist(.distmethod = bray) p1
# when .group is provided, the dot heatmap plot with group information will be return. p2 <- mouse.time.mpse %>% mp_plot_dist(.distmethod = bray, .group = time) # The scale or theme of dot heatmap plot can be adjusted using set_scale_theme function. p2 %>% set_scale_theme( x = scale_fill_manual( values=c("orange", "deepskyblue"), guide = guide_legend( keywidth = 1, keyheight = 0.5, title.theme = element_text(size=8), label.theme = element_text(size=6) ) ), aes_var = time # specific the name of variable ) %>% set_scale_theme( x = scale_color_gradient( guide = guide_legend(keywidth = 0.5, keyheight = 0.5) ), aes_var = bray ) %>% set_scale_theme( x = scale_size_continuous( range = c(0.1, 3), guide = guide_legend(keywidth = 0.5, keyheight = 0.5) ), aes_var = bray )
# when .group is provided and group.test is TRUE, the comparison of different groups will be returned p3 <- mouse.time.mpse %>% mp_plot_dist(.distmethod = bray, .group = time, group.test=TRUE, textsize=2) p3
3.5.2 The PCoA analysis
The distance can be used to do the ordination analysis, such as PCoA, NMDS, etc. Here, we only show the example of PCoA analysis, other ordinations can refer to the examples and the usages of the corresponding functions.
mouse.time.mpse %<>% mp_cal_pcoa(.abundance=hellinger, distmethod="bray") # The dimensions of ordination analysis will be added the colData slot (default). mouse.time.mpse # We also can perform adonis or anosim to check whether it is significant to the dissimilarities of groups. mouse.time.mpse %<>% mp_adonis(.abundance=hellinger, .formula=~time, distmethod="bray", permutations=9999, action="add") mouse.time.mpse %>% mp_extract_internal_attr(name=adonis) library(ggplot2) p1 <- mouse.time.mpse %>% mp_plot_ord( .ord = pcoa, .group = time, .color = time, .size = 1.2, .alpha = 1, ellipse = TRUE, show.legend = FALSE # don't display the legend of stat_ellipse ) + scale_fill_manual(values=c("#00A087FF", "#3C5488FF")) + scale_color_manual(values=c("#00A087FF", "#3C5488FF")) # The size of point also can be mapped to other variables such as Observe, or Shannon # Then the alpha diversity and beta diversity will be displayed simultaneously. p2 <- mouse.time.mpse %>% mp_plot_ord( .ord = pcoa, .group = time, .color = time, .size = Observe, .alpha = Shannon, ellipse = TRUE, show.legend = FALSE # don't display the legend of stat_ellipse ) + scale_fill_manual( values = c("#00A087FF", "#3C5488FF"), guide = guide_legend(keywidth=0.6, keyheight=0.6, label.theme=element_text(size=6.5)) ) + scale_color_manual( values=c("#00A087FF", "#3C5488FF"), guide = guide_legend(keywidth=0.6, keyheight=0.6, label.theme=element_text(size=6.5)) ) + scale_size_continuous( range=c(0.5, 3), guide = guide_legend(keywidth=0.6, keyheight=0.6, label.theme=element_text(size=6.5)) ) p1 + p2
3.5.3 Hierarchical cluster analysis
The distance of samples can also be used to perform the hierarchical cluster analysis to estimated the dissimilarities of samples. MicrobiotaProcess presents mp_cal_clust to perform this analysis. It also is implemented with the tidy-like framework.
mouse.time.mpse %<>% mp_cal_clust( .abundance = hellinger, distmethod = "bray", hclustmethod = "average", # (UPGAE) action = "add" # action is used to control which result will be returned ) mouse.time.mpse # if action = 'add', the result of hierarchical cluster will be added to the MPSE object # mp_extract_internal_attr can extract it. It is a treedata object, so it can be visualized # by ggtree. sample.clust <- mouse.time.mpse %>% mp_extract_internal_attr(name='SampleClust') sample.clust library(ggtree) p <- ggtree(sample.clust) + geom_tippoint(aes(color=time)) + geom_tiplab(as_ylab = TRUE) + ggplot2::scale_x_continuous(expand=c(0, 0.01)) p
Since the result of hierarchical cluster is treedata object, so it is very easy to display the result with associated data. For example, we can display the result of hierarchical cluster and the abundance of specific taxonomy level to check whether some biological pattern can be found.
library(ggtreeExtra) library(ggplot2) phyla.tb <- mouse.time.mpse %>% mp_extract_abundance(taxa.class=Phylum, topn=30) # The abundance of each samples is nested, it can be flatted using the unnest of tidyr. phyla.tb %<>% tidyr::unnest(cols=RareAbundanceBySample) %>% dplyr::rename(Phyla="label") phyla.tb p1 <- p + geom_fruit( data=phyla.tb, geom=geom_col, mapping = aes(x = RelRareAbundanceBySample, y = Sample, fill = Phyla ), orientation = "y", #offset = 0.4, pwidth = 3, axis.params = list(axis = "x", title = "The relative abundance of phyla (%)", title.size = 4, text.size = 2, vjust = 1), grid.params = list() ) p1
3.6 Biomarker discovery
The MicrobiotaProcess presents mp_diff_analysis for the biomarker discovery based on tidy-like framework. The rule of mp_diff_analysis is similar with the LEfSe[@Nicola2011LEfSe]. First, all features are tested whether values in different classes are differentially distributed. Second, the significantly different features are tested whether all pairwise comparisons between subclass in different classes distinctly consistent with the class trend. Finally, the significantly discriminative features are assessed by LDA (linear discriminant analysis) or rf(randomForest). However, mp_diff_analysis is more flexible. The test method of two step can be set by user, and we used the general fold change[@wirbel2019meta] and wilcox.test(default) to test whether all pairwise comparisons between subclass in different classes distinctly consistent with the class trend. And the result is stored to the treedata object, which can be processed and displayed via treeio[@treeio], tidytree[@tidytree], ggtree[@yu2017ggtree] and ggtreeExtra[@ggtreeExtra].
library(ggtree) library(ggtreeExtra) library(ggplot2) library(MicrobiotaProcess) library(tidytree) library(ggstar) library(forcats) mouse.time.mpse %>% print(width=150) mouse.time.mpse %<>% mp_diff_analysis( .abundance = RelRareAbundanceBySample, .group = time, first.test.alpha = 0.01 ) # The result is stored to the taxatree or otutree slot, you can use mp_extract_tree to extract the specific slot. taxa.tree <- mouse.time.mpse %>% mp_extract_tree(type="taxatree") taxa.tree # And the result tibble of different analysis can also be extracted # with tidytree (>=0.3.5) taxa.tree %>% select(label, nodeClass, LDAupper, LDAmean, LDAlower, Sign_time, pvalue, fdr) %>% dplyr::filter(!is.na(fdr)) # Since taxa.tree is treedata object, it can be visualized by ggtree and ggtreeExtra p1 <- ggtree( taxa.tree, layout="radial", size = 0.3 ) + geom_point( data = td_filter(!isTip), fill="white", size=1, shape=21 ) # display the high light of phylum clade. p2 <- p1 + geom_hilight( data = td_filter(nodeClass == "Phylum"), mapping = aes(node = node, fill = label) ) # display the relative abundance of features(OTU) p3 <- p2 + ggnewscale::new_scale("fill") + geom_fruit( data = td_unnest(RareAbundanceBySample), geom = geom_star, mapping = aes( x = fct_reorder(Sample, time, .fun=min), size = RelRareAbundanceBySample, fill = time, subset = RelRareAbundanceBySample > 0 ), starshape = 13, starstroke = 0.25, offset = 0.04, pwidth = 0.8, grid.params = list(linetype=2) ) + scale_size_continuous( name="Relative Abundance (%)", range = c(.5, 3) ) + scale_fill_manual(values=c("#1B9E77", "#D95F02")) # display the tip labels of taxa tree p4 <- p3 + geom_tiplab(size=2, offset=7.2) # display the LDA of significant OTU. p5 <- p4 + ggnewscale::new_scale("fill") + geom_fruit( geom = geom_col, mapping = aes( x = LDAmean, fill = Sign_time, subset = !is.na(LDAmean) ), orientation = "y", offset = 0.3, pwidth = 0.5, axis.params = list(axis = "x", title = "Log10(LDA)", title.height = 0.01, title.size = 2, text.size = 1.8, vjust = 1), grid.params = list(linetype = 2) ) # display the significant (FDR) taxonomy after kruskal.test (default) p6 <- p5 + ggnewscale::new_scale("size") + geom_point( data=td_filter(!is.na(Sign_time)), mapping = aes(size = -log10(fdr), fill = Sign_time, ), shape = 21, ) + scale_size_continuous(range=c(1, 3)) + scale_fill_manual(values=c("#1B9E77", "#D95F02")) p6 + theme( legend.key.height = unit(0.3, "cm"), legend.key.width = unit(0.3, "cm"), legend.spacing.y = unit(0.02, "cm"), legend.text = element_text(size = 7), legend.title = element_text(size = 9), )
The visualization methods of result can be various, you can refer to the article or book of ggtree[@yu2017ggtree; @yu2018two] and the article of ggtreeExtra[@ggtreeExtra]. In addition, we also developed mp_plot_diff_res to display the result of mp_diff_analysis, it can decreases coding burden.
# this object has contained the result of mp_diff_analysis mouse.time.mpse # Because the released `ggnewscale` modified the internal new aesthetics name, # The following code is to obtain the new aesthetics name according to version of # `ggnewscale` flag <- packageVersion("ggnewscale") >= "0.5.0" new.fill <- ifelse(flag, "fill_ggnewscale_1", "fill_new_new") new.fill2 <- ifelse(flag , "fill_ggnewscale_2", "fill_new") p <- mouse.time.mpse %>% mp_plot_diff_res( group.abun = TRUE, pwidth.abun=0.1 ) # if version of `ggnewscale` is >= 0.5.0, you can also use p$ggnewscale to view the renamed scales. p <- p + scale_fill_manual(values=c("deepskyblue", "orange")) + scale_fill_manual( aesthetics = new.fill2, # The fill aes was renamed to `new.fill` for the abundance dotplot layer values = c("deepskyblue", "orange") ) + scale_fill_manual( aesthetics = new.fill, # The fill aes for hight light layer of tree was renamed to `new.fill2` values = c("#E41A1C", "#377EB8", "#4DAF4A", "#984EA3", "#FF7F00", "#FFFF33", "#A65628", "#F781BF", "#999999" ) ) p
We also developed mp_plot_diff_cladogram to visualize the result.
f <- mouse.time.mpse %>% mp_plot_diff_cladogram( label.size = 2.5, hilight.alpha = .3, bg.tree.size = .5, bg.point.size = 2, bg.point.stroke = .25 ) + scale_fill_diff_cladogram( # set the color of different group. values = c('deepskyblue', 'orange') ) + scale_size_continuous(range = c(1, 4)) f
The result also can be visualized with mp_plot_diff_boxplot.
f.box <- mouse.time.mpse %>% mp_plot_diff_boxplot( .group = time, ) %>% set_diff_boxplot_color( values = c("deepskyblue", "orange"), guide = guide_legend(title=NULL) ) f.bar <- mouse.time.mpse %>% mp_plot_diff_boxplot( taxa.class = c(Genus, OTU), # select the taxonomy level to display group.abun = TRUE, # display the mean abundance of each group removeUnknown = TRUE, # whether mask the unknown taxa. ) %>% set_diff_boxplot_color( values = c("deepskyblue", "orange"), guide = guide_legend(title=NULL) ) aplot::plot_list(f.box, f.bar)
Or visualizing the results with mp_plot_diff_manhattan
f.mahattan <- mouse.time.mpse %>% mp_plot_diff_manhattan( .group = Sign_time, .y = fdr, .size = 2.4, taxa.class = c('OTU', 'Genus'), anno.taxa.class = Phylum ) f.mahattan
4. Need helps?
If you have questions/issues, please visit github issue tracker.
5. Session information
Here is the output of sessionInfo() on the system on which this document was compiled:
sessionInfo()
6. References
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