---
title: "Quantitative features for mass spectrometry data"
author:
- name: Laurent Gatto
package: QFeatures
abstract: >
 This vignette describes the functionality implemented in the QFeatures
 package. QFeatures provides infrastructure to manage and process
 quantitative features for high-throughput mass spectrometry assays,
 including proteomics and metabolomics. This vignette is distributed under
 a CC BY-SA license.
output:
  BiocStyle::html_document:
    toc_float: true
bibliography: QFeatures.bib
vignette: >
  %\VignetteIndexEntry{Quantitative features for mass spectrometry data}
  %\VignetteEngine{knitr::rmarkdown}
  %%\VignetteKeywords{Mass Spectrometry, MS, MSMS, Proteomics, Metabolomics, Infrastructure, Quantitative }
  %\VignetteEncoding{UTF-8}
---

```{r style, echo = FALSE, results = 'asis'}
BiocStyle::markdown()
```

```{r env, message = FALSE, warning = FALSE, echo = FALSE}
library("QFeatures")
```


# Introduction

The `QFeatures` package provides infrastructure (that is classes to
store data and the methods to process and manipulate them) to manage
and analyse quantitative features from mass spectrometry
experiments. It is based on the `SummarizedExperiment` and
`MultiAssayExperiment` classes. Assays in a QFeatures object have a
hierarchical relation: proteins are composed of peptides, themselves
produced by spectra, as depicted in figure
\@ref(fig:featuresplot). Throughout the aggregation and processing of
these data, the relations between assays are tracked and recorded,
thus allowing users to easily navigate across spectra, peptide and
protein quantitative data.


```{r featuresplot, fig.cap = "Conceptual representation of a `QFeatures` object and the aggregative relation between different assays.", echo = FALSE}
par(mar = c(0, 0, 0, 0))
plot(NA, xlim = c(0, 12), ylim = c(0, 20),
     xaxt = "n", yaxt = "n",
     xlab = "", ylab = "", bty = "n")

for (i in 0:7)
    rect(0, i, 3, i+1, col = "lightgrey", border = "white")


for (i in 8:12)
    rect(0, i, 3, i+1, col = "steelblue", border = "white")

for (i in 13:18)
    rect(0, i, 3, i+1, col = "orange", border = "white")

for (i in 19)
    rect(0, i, 3, i+1, col = "darkgrey", border = "white")


for (i in 5:7)
    rect(5, i, 8, i+1, col = "lightgrey", border = "white")

for (i in 8:10)
    rect(5, i, 8, i+1, col = "steelblue", border = "white")

for (i in 11:13)
    rect(5, i, 8, i+1, col = "orange", border = "white")

for (i in 14)
    rect(5, i, 8, i+1, col = "darkgrey", border = "white")

rect(9, 8, 12, 8+1, col = "lightgrey", border = "white")
rect(9, 9, 12, 9+1, col = "steelblue", border = "white")
rect(9, 10, 12, 10+1, col = "orange", border = "white")
rect(9, 11, 12, 11+1, col = "darkgrey", border = "white")

segments(3, 8, 5, 8, lty = "dashed")
segments(3, 6, 5, 7, lty = "dashed")
segments(3, 4, 5, 6, lty = "dashed")
segments(3, 0, 5, 5, lty = "dashed")

segments(3, 10, 5, 9, lty = "dashed")
segments(3, 11, 5, 10, lty = "dashed")
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segments(3, 14, 5, 12, lty = "dashed")
segments(3, 16, 5, 13, lty = "dashed")
segments(3, 19, 5, 14, lty = "dashed")

segments(3, 20, 5, 15, lty = "dashed")


segments(8, 5, 9, 8, lty = "dashed")
segments(8, 8, 9, 9, lty = "dashed")
segments(8, 11, 9, 10, lty = "dashed")
segments(8, 14, 9, 11, lty = "dashed")
segments(8, 15, 9, 12, lty = "dashed")
```

In the following sections, we are going to demonstrate how to create a
single-assay `QFeatures` objects starting from a spreadsheet, how to
compute the next assays (peptides and proteins), and how these can be
manipulated and explored.

```{r loadpkg}
library("QFeatures")
```

# Creating `QFeatures` object

```{r loaddfr, echo = FALSE}
data(hlpsms)
```

While `QFeatures` objects can be created manually (see `?QFeatures`
for details), most users will probably possess quantitative data in a
spreadsheet or a dataframe. In such cases, the easiest is to use the
`readQFeatures` function to extract the quantitative data and metadata
columns. Below, we load the `hlpsms` dataframe that contains data for
`r nrow(hlpsms)` PSMs from the TMT-10plex hyperLOPIT spatial
proteomics experiment from [@Christoforou:2016]. The `quantCols`
argument specifies that columns 1 to 10 contain quantitation data, and
that the assay should be named `psms` in the returned `QFeatures`
object, to reflect the nature of the data.


```{r readQFeatures}
data(hlpsms)
hl <- readQFeatures(hlpsms, quantCols = 1:10, name = "psms")
hl
```

Below, we see that we can extract an assay using its index or its
name. The individual assays are stored as *SummarizedExperiment*
object and further access its quantitative data and metadata using the
`assay` and `rowData` functions

```{r subsetassay}
hl[[1]]
hl[["psms"]]
head(assay(hl[["psms"]]))
head(rowData(hl[["psms"]]))
```

For further details on how to manipulate such objects, refer to the
`r BiocStyle::Biocpkg("MultiAssayExperiment")` [@Ramos:2017] and
`r BiocStyle::Biocpkg("SummerizedExperiment")` [@SE] packages.

As illustrated in figure \@ref(fig:featuresplot), an central
characteristic of `QFeatures` objects is the aggregative relation
between their assays. This can be obtained with the
`aggregateFeatures` function that will aggregate quantitative features
from one assay into a new one. In the next code chunk, we aggregate
PSM-level data into peptide by grouping all PSMs that were matched the
same peptide sequence. Below, the aggregation function is set, as an
example, to the mean. The new assay is named *peptides*.

```{r aggregateFeatures1}
hl <- aggregateFeatures(hl, "psms", "Sequence",
                        name = "peptides", fun = colMeans)
hl
hl[["peptides"]]
```

Below, we repeat the aggregation operation by grouping peptides into
proteins as defined by the *ProteinGroupAccessions* variable.

```{r aggregateFeatures2}
hl <- aggregateFeatures(hl, "peptides", "ProteinGroupAccessions",
                        name = "proteins", fun = colMeans)
hl
hl[["proteins"]]
```

The sample assayed in a `QFeatures` object can be documented in the
`colData` slot. The `hl` data doens't currently possess any sample
metadata. These can be addedd as a new `DataFrame` with matching names
(i.e. the `DataFrame` rownames must be identical assay's colnames) or
can be added one variable at at time, as shown below.

```{r}
colData(hl)
hl$tag <- c("126", "127N", "127C", "128N", "128C", "129N", "129C",
            "130N", "130C", "131")
colData(hl)
```

# Manipulating feature metadata

The `QFeatures` package provides some utility functions that streamline
the accession and manipulation of the feature metadata.

The feature metadata, more generally referred to as `rowData` in the
Bioconductor ecosystem, is specific to each assay in a `QFeatures`
object. Therefore there are as many `rowData` tables as there are
assays. `rowDataNames` provides a list where each element contains the
name of the `rowData` columns available in the corresponding assay.

```{r rowDataNames}
rowDataNames(hl)
```

We saw above how to get the `rowData` from an assay, but we can also
extract the `rowData` for all assays by calling the function on the
`QFeautures` object directly. Similarly to `rowDataNames`, a list is
returned where each element contains the `rowData` available in the
corresponding assay.

```{r rowData}
rowData(hl)
```

In some cases, we are interested in extracting the `rowData` as a
single data table. This is easily performed using the `rbindRowData`
function. The function will automatically select the columns that are
common to all selected assays.

```{r rbindRowData}
rbindRowData(hl, i = c("peptides", "proteins"))
```

We can also replace and add columns in the `rowData`.  This requires
to provide a `List` where the names of the `List` point to the assay
to be updated and the elements of the `List` contain `DataFrame`s with
the replacement values. If the `DataFrame` contains a column that is
not present in the `rowData`, that column will get added to the
`rowData`. For instance, let's add a `rowData` variables with the mean
protein expression as well as the associated standard deviation.
First, we need to create the `DataFrame` with the mean expression.

```{r}
dF <- DataFrame(mean = rowSums(assay(hl[["proteins"]])),
                sd = rowSds(assay(hl[["proteins"]])))
```

Then, we create the list and name the element `proteins` so that the
new data is added to the `rowData` of the `proteins` assay. To add
the list, we insert it back into the `rowData`.

```{r}
rowData(hl) <- List(proteins = dF)
```

As shown below, the new `mean` and `sd` variables have been added to the
`rowData` of the `proteins` assay.

```{r}
rowData(hl)[["proteins"]]
```

Note that you can also replace an existing column in the `rowData` by
naming the column name in the `DataFrame` after the column to replace.

# Subsetting

One particularity of the `QFeatures` infrastructure is that the
features of the constitutive assays are linked through an aggregative
relation. This relation is recorded when creating new assays with
`aggregateFeatures` and is exploited when subsetting `QFeature` by their
feature names.

In the example below, we are interested in the Stat3B isoform of the
Signal transducer and activator of transcription 3 (STAT3) with
accession number P42227-2. This accession number corresponds to a
feature name in the *proteins* assay. But this protein row was
computed from 8 peptide rows in the *peptides* assay, themselves
resulting from the aggregation of 8 rows in the *psms* assay.

```{r stat3}
stat3 <- hl["P42227-2", , ]
stat3
```

We can easily visualise this new *QFeatures* object using `ggplot2`
once converted into a `data.frame`. See the visualization vignette for
more details about data exploration from a `QFeatures` object.

```{r plotstat3}
stat3_df <- data.frame(longFormat(stat3))
stat3_df$assay <- factor(stat3_df$assay,
                        levels = c("psms", "peptides", "proteins"))
library("ggplot2")
ggplot(data = stat3_df,
       aes(x = colname,
           y = value,
           group = rowname)) +
    geom_line() + geom_point() +
    facet_grid(~ assay)
```

Below we repeat the same operation for the Signal transducer and
activator of transcription 1 (STAT1) and 3 (STAT3) accession numbers,
namely P42227-2 and P42225. We obtain a new `QFeatures` instance
containing 2 proteins, 9 peptides and 10 PSMS. From this, we can
readily conclude that STAT1 was identified by a single PSM/peptide.

```{r stat}
stat <- hl[c("P42227-2", "P42225"), , ]
stat
```

Below, we visualise the expression profiles for the two proteins.

```{r plotstat}
stat_df <- data.frame(longFormat(stat))
stat_df$stat3 <- ifelse(stat_df$rowname %in% stat3_df$rowname,
                        "STAT3", "STAT1")
stat_df$assay <- factor(stat_df$assay,
                        levels = c("psms", "peptides", "proteins"))

ggplot(data = stat_df,
       aes(x = colname,
           y = value,
           group = rowname)) +
    geom_line() + geom_point() +
    facet_grid(stat3 ~ assay)
```

The subsetting by feature names is also available as a call to the
`subsetByFeature` function, for use with the pipe operator.

```{r subsetByFeature}
hl |>
    subsetByFeature("P42227-2")

hl |>
    subsetByFeature(c("P42227-2", "P42225"))
```

and possibly

```{r subsetpipe, eval = FALSE}
hl |>
    subsetByFeature("P42227-2") |>
    longFormat() |>
    as.data.frame() |>
    ggplot(aes(x = colname,
               y = value,
               group = rowname)) +
    geom_line() +
    facet_grid(~ assay)
```

to reproduce the line plot.

# Filtering

QFeatures is assays can also be filtered based on variables in their
respective row data slots using the `filterFeatures` function. The
filters can be defined using the formula interface or using
`AnnotationFilter` objects from the `r
BiocStyle::Biocpkg("AnnotationFilter")` package
[@AnnotationFilter]. In addition to the pre-defined filters (such as
`SymbolFilter`, `ProteinIdFilter`, ... that filter on gene symbol,
protein identifier, ...), this package allows users to define
arbitrary character or numeric filters using the `VariableFilter`.

```{r varfilter}
mito_filter <- VariableFilter(field = "markers",
                              value = "Mitochondrion",
                              condition = "==")
mito_filter

qval_filter <- VariableFilter(field = "qValue",
                              value = 0.001,
                              condition = "<=")
qval_filter
```

These filter can then readily be applied to all assays' row data
slots. The `mito_filter` will return all PSMs, peptides and proteins
that were annotated as localising to the mitochondrion.

```{r mito_filter}
filterFeatures(hl, mito_filter)
```

The `qval_filter`, on the other hand, will only return a subset of
PSMs, because the `qValue` variable is only present in the `psms`
assays. The q-values are only relevant to PSMs and that variable was
dropped from the other assays.

```{r qval_filter}
filterFeatures(hl, qval_filter)
```

The same filters can be created using the forumla interface:

```{r formula_filter}
filterFeatures(hl, ~ markers == "Mitochondrion")
filterFeatures(hl, ~ qValue <= 0.001)
```


# Session information {-}

```{r sessioninfo, echo=FALSE}
sessionInfo()
```


# References {-}
