---
title: "miaViz"
output: 
  BiocStyle::html_document:
    fig_height: 7
    fig_width: 10
    toc: yes
    toc_depth: 2
    number_sections: true
vignette: >
  %\VignetteIndexEntry{miaViz}
  %\VignetteEngine{knitr::rmarkdown}
  %\VignetteEncoding{UTF-8}
bibliography: references.bib
---

```{r, include = FALSE}
knitr::opts_chunk$set(
  collapse = TRUE,
  comment = "#>"
)
```

`miaViz` implements plotting function to work with `TreeSummarizedExperiment`
and related objects in a context of microbiome analysis. For more general
plotting function on `SummarizedExperiment` objects the `scater` package offers
several options, such as `plotColData`, `plotExpression` and `plotRowData`.

# Installation

To install `miaViz`, install `BiocManager` first, if it is not installed.
Afterwards use the `install` function from `BiocManager` and load `miaViz`.

```{r, eval=FALSE}
if (!requireNamespace("BiocManager", quietly = TRUE))
    install.packages("BiocManager")
BiocManager::install("miaViz")
```

```{r setup, message=FALSE}
library(miaViz)
data(GlobalPatterns, package = "mia")
```

# Abundance plotting

in contrast to other fields of sequencing based fields of research for which
expression of genes is usually studied, microbiome research uses the more 
term ~Abundance~ to described the numeric data measured and analyzed.
Technically, especially in context of `SummarizedExperiment` objects, there is
no difference. Therefore `plotExpression` can be used to plot `Abundance` data.

`plotAbundance` can be used as well and as long as `rank` is set `NULL`, it
behaves as `plotExpression`.

```{r}
plotAbundance(GlobalPatterns, rank = NULL, 
              features = "549322", abund_values = "counts")
```

However, if the `rank` is set not `NULL` a bar plot is returned. At the same
time the `features` argument can be set to `NULL` (default).

```{r}
GlobalPatterns <- transformCounts(GlobalPatterns, method = "relabundance")
```

```{r}
plotAbundance(GlobalPatterns, rank = "Kingdom", abund_values = "relabundance")
```

With subsetting to selected features the plot can be fine tuned.

```{r}
prev_phylum <- getPrevalentTaxa(GlobalPatterns, rank = "Phylum",
                                detection = 0.01)
```

```{r}
plotAbundance(GlobalPatterns[rowData(GlobalPatterns)$Phylum %in% prev_phylum],
              rank = "Phylum",
              abund_values = "relabundance")
```

The `features` argument is reused for plotting data along the different samples.
In the next example the ~SampleType~ is plotted along the samples. In this case 
the result is a list, which can combined using external tools, for example
`patchwork`. 

```{r}
library(patchwork)
plots <- plotAbundance(GlobalPatterns[rowData(GlobalPatterns)$Phylum %in% prev_phylum],
                       features = "SampleType",
                       rank = "Phylum",
                       abund_values = "relabundance")
plots$abundance / plots$SampleType +
     plot_layout(heights = c(9, 1))
```

Further example about composition barplot can be found at Orchestrating Microbiome Analysis [@OMA].

# Prevalence plotting

To visualize prevalence within the dataset, two functions are available,
`plotTaxaPrevalence`, `plotPrevalenceAbundance` and `plotPrevalence`.


`plotTaxaPrevalence` produces a so-called landscape plot, which
visualizes the prevalence of samples across abundance thresholds.

```{r}
plotTaxaPrevalence(GlobalPatterns, rank = "Phylum",
                   detections = c(0, 0.001, 0.01, 0.1, 0.2))
```

`plotPrevalenceAbundance` plot the prevalence depending on the mean relative 
abundance on the chosen taxonomic level.

```{r}
plotPrevalentAbundance(GlobalPatterns, rank = "Family",
                       colour_by = "Phylum") +
    scale_x_log10()
```

`plotPrevalence` plot the number of samples and their prevalence across 
different abundance thresholds. Abundance steps can be adjusted using the 
`detections` argument, whereas the analyzed prevalence steps is set using the
`prevalences` argument.

```{r}
plotPrevalence(GlobalPatterns,
               rank = "Phylum",
               detections = c(0.01, 0.1, 1, 2, 5, 10, 20)/100,
               prevalences = seq(0.1, 1, 0.1))
```

# Tree plotting

The information stored in the `rowTree` can be directly plotted. However,
sizes of stored trees have to be kept in mind and plotting of large trees
rarely makes sense.

For this example we limit the information plotted to the top 100 taxa as judged
by mean abundance on the genus level.

```{r, message=FALSE}
library(scater)
library(mia)
```
```{r}
altExp(GlobalPatterns,"Genus") <- agglomerateByRank(GlobalPatterns,"Genus")
altExp(GlobalPatterns,"Genus") <- addPerFeatureQC(altExp(GlobalPatterns,"Genus"))
rowData(altExp(GlobalPatterns,"Genus"))$log_mean <-
    log(rowData(altExp(GlobalPatterns,"Genus"))$mean)
rowData(altExp(GlobalPatterns,"Genus"))$detected <- 
    rowData(altExp(GlobalPatterns,"Genus"))$detected / 100
top_taxa <- getTopTaxa(altExp(GlobalPatterns,"Genus"),
                       method="mean",
                       top=100L,
                       abund_values="counts")
```

Colour, size and shape of tree tips and nodes can be decorated based on data
present in the `SE` object or by providing additional information via the 
`other_fields` argument. Note that currently information for nodes have to be
provided via the `other_fields` arguments.

Data will be matched via the `node` or `label` argument depending on which was
provided. `label` takes precedent.

```{r plot1, fig.cap="Tree plot using ggtree with tip labels decorated by mean abundance (colour) and prevalence (size)"}
plotRowTree(altExp(GlobalPatterns,"Genus")[top_taxa,],
            tip_colour_by = "log_mean",
            tip_size_by = "detected")
```

Tip and node labels can be shown as well. Setting `show_label = TRUE` shows the
tip labels only ...

```{r plot2, fig.cap="Tree plot using ggtree with tip labels decorated by mean abundance (colour) and prevalence (size). Tip labels of the tree are shown as well."}
plotRowTree(altExp(GlobalPatterns,"Genus")[top_taxa,],
            tip_colour_by = "log_mean",
            tip_size_by = "detected",
            show_label = TRUE)
```

... whereas node labels can be selectively shown by providing a named logical
vector to `show_label`.

Please not that currently `ggtree` only can plot node labels in a rectangular
layout.

```{r plot3, fig.cap="Tree plot using ggtree with tip labels decorated by mean abundance (colour) and prevalence (size). Selected node and tip labels are shown."}
labels <- c("Genus:Providencia", "Genus:Morganella", "0.961.60")
plotRowTree(altExp(GlobalPatterns,"Genus")[top_taxa,],
            tip_colour_by = "log_mean",
            tip_size_by = "detected",
            show_label = labels,
            layout="rectangular")
```

Information can also be visualized on the edges of the tree plot.

```{r plot4, fig.cap="Tree plot using ggtree with tip labels decorated by mean abundance (colour) and edges labeled Kingdom (colour) and prevalence (size)"}
plotRowTree(altExp(GlobalPatterns,"Genus")[top_taxa,],
            edge_colour_by = "Phylum",
            tip_colour_by = "log_mean")
```

# Graph plotting

Similar to tree data, graph data can also be plotted in conjunction with
`SummarizedExperiment` objects. Since the graph data in itself cannot be stored
in a specialized slot, a graph object can be provided separately or as an 
element from the `metedata`.

Here we load an example graph. As graph data, all objects types accepted by
`as_tbl_graph` from the `tidygraph` package are supported. 

```{r}
data(col_graph)
```

In the following examples, the `weight` data is automatically generated from the
graph data. The `SummarizedExperiment` provided is required to have overlapping
rownames with the node names of the graph. Using this link the graph plot
can incorporated data from the `SummarizedExperiment`.

```{r}
plotColGraph(col_graph,
             altExp(GlobalPatterns,"Genus"),
             colour_by = "SampleType",
             edge_colour_by = "weight",
             edge_width_by = "weight",
             show_label = TRUE)
```

As mentioned the graph data can be provided from the `metadata` of the 
`SummarizedExperiment`.

```{r}
metadata(altExp(GlobalPatterns,"Genus"))$graph <- col_graph
```

This produces the same plot as shown above.

```{r include=FALSE}
plotColGraph(altExp(GlobalPatterns,"Genus"),
             name = "graph",
             colour_by = "SampleType",
             edge_colour_by = "weight",
             edge_width_by = "weight",
             show_label = TRUE)
```

# Plotting of serial data

```{r}
library(microbiomeDataSets)
silverman <- SilvermanAGutData()
silverman <- transformCounts(silverman, method = "relabundance")
taxa <- getTopTaxa(silverman, 2)
```

Data from samples collected along time can be visualized using `plotSeries`.
The `x` argument is used to reference data from the `colData` to use as 
descriptor for ordering the data. The `y` argument selects the feature to show.
Since plotting a lot of features is not advised a maximum of 20 features can 
plotted at the same time.
 
```{r}
plotSeries(silverman,
           x = "DAY_ORDER",
           y = taxa,
           colour_by = "Family")
```
If replicated data is present, data is automatically used for calculation of the
`mean` and `sd` and plotted as a range. Data from different assays can be used
for plotting via the `abund_values`.

```{r}
plotSeries(silverman[taxa,],
           x = "DAY_ORDER",
           colour_by = "Family",
           linetype_by = "Phylum",
           abund_values = "relabundance")
```

Additional variables can be used to modify line type aesthetics.

```{r}
plotSeries(silverman,
           x = "DAY_ORDER",
           y = getTopTaxa(silverman, 5),
           colour_by = "Family",
           linetype_by = "Phylum",
           abund_values = "counts")
```

# Plotting factor data

To visualize the relative relations between two groupings among the factor data,
two functions are available for the purpose; `plotColTile` and `plotRowTile`.

```{r}
data(GlobalPatterns)
se <- GlobalPatterns
plotColTile(se,"SampleType","Primer") +
  theme(axis.text.x.top = element_text(angle = 45, hjust = 0))
```

# DMN fit plotting

Searching for groups that are similar to each other among the samples, could be
approached with the Dirichlet Multinomial Mixtures [@DMM].
After using `runDMN` from the `mia` package, several k values as a number of clusters 
are used to observe the best fit (see also `getDMN` and `getBestDMNFit`).
To visualize the fit using e.g. "laplace" as a measure of goodness of fit:

```{r}
data(dmn_se, package = "mia")
names(metadata(dmn_se))
# plot the fit
plotDMNFit(dmn_se, type = "laplace")
```

More examples and materials are available at Orchestrating Microbiome Analysis [@OMA].

# Session info

```{r}
sessionInfo()
```


# References
