# The `SingleCellExperiment` class 

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## Overview

One of the main strengths of the Bioconductor project lies in the use of a common data infrastructure that powers interoperability across packages.
Users should be able to analyze their data using functions from different Bioconductor packages without the need to convert between formats. 
To this end, the `SingleCellExperiment` class (from the *[SingleCellExperiment](https://bioconductor.org/packages/3.20/SingleCellExperiment)* package) serves as the common currency for data exchange across 70+ single-cell-related Bioconductor packages.
This class implements a data structure that stores all aspects of our single-cell data - gene-by-cell expression data, per-cell metadata and per-gene annotation (Figure \@ref(fig:sce-structure)) - and manipulate them in a synchronized manner.

<div class="figure">
<img src="images/SingleCellExperiment.png" alt="Overview of the structure of the `SingleCellExperiment` class. Each row of the assays corresponds to a row of the `rowData` (pink shading), while each column of the assays corresponds to a column of the `colData` and `reducedDims` (yellow shading)." width="530" />
<p class="caption">(\#fig:sce-structure)Overview of the structure of the `SingleCellExperiment` class. Each row of the assays corresponds to a row of the `rowData` (pink shading), while each column of the assays corresponds to a column of the `colData` and `reducedDims` (yellow shading).</p>
</div>

Each piece of (meta)data in the `SingleCellExperiment` is represented by a separate "slot".
(This terminology comes from the [S4 class system](https://adv-r.hadley.nz/s4.html), but that's not important right now.)
If we imagine the `SingleCellExperiment` object to be a cargo ship, the slots can be thought of as individual cargo boxes with different contents, e.g., certain slots expect numeric matrices whereas others may expect data frames.
In the rest of this chapter, we will discuss the available slots, their expected formats, and how we can interact with them.
More experienced readers may note the similarity with the `SummarizedExperiment` class, and if you are such a reader, you may wish to jump directly to the end of this chapter for the single-cell-specific aspects of this class.

## Installing required packages

The *[SingleCellExperiment](https://bioconductor.org/packages/3.20/SingleCellExperiment)* package is automatically installed when using any package that depends on the `SingleCellExperiment` class, but it can also be explicitly installed:


``` r
BiocManager::install('SingleCellExperiment')
```

We then load the *[SingleCellExperiment](https://bioconductor.org/packages/3.20/SingleCellExperiment)* package into our R session.
This avoids the need to prefix our function calls with `::`, especially for packages that are heavily used throughout a workflow.


``` r
library(SingleCellExperiment)
```

For the demonstrations in this chapter, we will use some functions from a variety of other packages, installed as shown below.
These functions will be accessed through the `<package>::<function>` convention as needed.


``` r
BiocManager::install(c('scuttle', 'scran', 'scater', 'uwot', 'rtracklayer'))
```

## Storing primary experimental data 

### Filling the `assays` slot

To construct a rudimentary `SingleCellExperiment` object, we only need to fill the `assays` slot.
This contains primary data such as a matrix of sequencing counts where rows correspond to features (genes) and columns correspond to samples (cells) (Figure \@ref(fig:sce-structure), blue box).
To demonstrate, we will use a small scRNA-seq count matrix downloaded from the ArrayExpress servers [@lun2017assessing]:

<button class="rebook-collapse">Code to download file</button>
<div class="rebook-content">


``` r
library(BiocFileCache)
bfc <- BiocFileCache("raw_data", ask = FALSE)
calero.counts <- bfcrpath(bfc, file.path("https://www.ebi.ac.uk/biostudies", 
    "files/E-MTAB-5522/counts_Calero_20160113.tsv"))
```


</div>


``` r
mat <- read.delim(calero.counts, header=TRUE, row.names=1, check.names=FALSE)

# Only considering endogenous genes for now.
spike.mat <- mat[grepl("^ERCC-", rownames(mat)),] 
mat <- mat[grepl("^ENSMUSG", rownames(mat)),] 

# Splitting off the gene length column.
gene.length <- mat[,1]
mat <- as.matrix(mat[,-1]) 

dim(mat)
```

```
## [1] 46603    96
```

From this, we can now construct our first `SingleCellExperiment` object using the `SingleCellExperiment()` function.
Note that we provide our data as a named list where each entry of the list is a matrix - in this case, named `"counts"`. 


``` r
sce <- SingleCellExperiment(assays = list(counts = mat))
```

To inspect the object, we can simply type `sce` into the console to see some pertinent information.
This will print an overview of the various slots available to us, which may or may not have any data.


``` r
sce
```

```
## class: SingleCellExperiment 
## dim: 46603 96 
## metadata(0):
## assays(1): counts
## rownames(46603): ENSMUSG00000102693 ENSMUSG00000064842 ...
##   ENSMUSG00000096730 ENSMUSG00000095742
## rowData names(0):
## colnames(96): SLX-9555.N701_S502.C89V9ANXX.s_1.r_1
##   SLX-9555.N701_S503.C89V9ANXX.s_1.r_1 ...
##   SLX-9555.N712_S508.C89V9ANXX.s_1.r_1
##   SLX-9555.N712_S517.C89V9ANXX.s_1.r_1
## colData names(0):
## reducedDimNames(0):
## mainExpName: NULL
## altExpNames(0):
```

To access the count data we just supplied, we can do any one of the following:

* `assay(sce, "counts")` - this is the most general method, where we can supply the name of the assay as the second argument.
* `counts(sce)` - this is a short-cut for the above, but *only* works for assays with the special name `"counts"`.


``` r
mat2 <- counts(sce)
```

**NOTE:** For exported S4 classes, it is rarely a good idea to directly access the slots with the `@` oeprator.
This is considered bad practice as the class developers are free to alter the internal structure of the class, at which point any code using `@` may no longer work.
Rather, it is best to use the provided getter functions like `assay()` and `counts()` to extract data from the object.
Similarly, setting slots should be done via the provided setter functions, which are discussed in the next section.

### Adding more `assays`

One of the strengths of the `assays` slot is that it can hold multiple representations of the primary data. 
This is particularly useful for storing the raw count matrix as well as a normalized version of the data. 
For example, the `logNormCounts()` function from *[scuttle](https://bioconductor.org/packages/3.20/scuttle)* will compute a log-transformed normalized expression matrix and store it as another assay.


``` r
sce <- scuttle::logNormCounts(sce)
sce
```

```
## class: SingleCellExperiment 
## dim: 46603 96 
## metadata(0):
## assays(2): counts logcounts
## rownames(46603): ENSMUSG00000102693 ENSMUSG00000064842 ...
##   ENSMUSG00000096730 ENSMUSG00000095742
## rowData names(0):
## colnames(96): SLX-9555.N701_S502.C89V9ANXX.s_1.r_1
##   SLX-9555.N701_S503.C89V9ANXX.s_1.r_1 ...
##   SLX-9555.N712_S508.C89V9ANXX.s_1.r_1
##   SLX-9555.N712_S517.C89V9ANXX.s_1.r_1
## colData names(1): sizeFactor
## reducedDimNames(0):
## mainExpName: NULL
## altExpNames(0):
```

We overwrite our previous `sce` by reassigning the result of `logNormCounts()` back to `sce`.
This is possible because these particular functions return a `SingleCellExperiment` object that contains the results in addition to original data.
Indeed, viewing the object again, we see that this function added a new assay entry `"logcounts"`.


``` r
sce
```

```
## class: SingleCellExperiment 
## dim: 46603 96 
## metadata(0):
## assays(2): counts logcounts
## rownames(46603): ENSMUSG00000102693 ENSMUSG00000064842 ...
##   ENSMUSG00000096730 ENSMUSG00000095742
## rowData names(0):
## colnames(96): SLX-9555.N701_S502.C89V9ANXX.s_1.r_1
##   SLX-9555.N701_S503.C89V9ANXX.s_1.r_1 ...
##   SLX-9555.N712_S508.C89V9ANXX.s_1.r_1
##   SLX-9555.N712_S517.C89V9ANXX.s_1.r_1
## colData names(1): sizeFactor
## reducedDimNames(0):
## mainExpName: NULL
## altExpNames(0):
```

Similar to `"counts"`, the `"logcounts"` name can be conveniently accessed using `logcounts(sce)`.


``` r
dim(logcounts(sce))
```

```
## [1] 46603    96
```

While `logNormCounts()` will automatically add assays to our `sce` object and return the modified object, other functions may return a matrix directly.
In such cases, we need to manually insert the matrix into the `assays`, which we can do with the corresponding setter function.
To illustrate, we can create a new assay where we add 100 to all the counts:


``` r
counts_100 <- counts(sce) + 100
assay(sce, "counts_100") <- counts_100 # assign a new entry to assays slot
assays(sce) # new assay has now been added.
```

```
## List of length 3
## names(3): counts logcounts counts_100
```

### Further comments

To retrieve all the available assays within `sce`, we can use the `assays()` getter.
By comparison, `assay()` only returns a single assay of interest.


``` r
assays(sce)
```

```
## List of length 3
## names(3): counts logcounts counts_100
```

The setter of the same name can be used to modify the set of available assays:


``` r
# Only keeping the first two assays
assays(sce) <- assays(sce)[1:2]
sce
```

```
## class: SingleCellExperiment 
## dim: 46603 96 
## metadata(0):
## assays(2): counts logcounts
## rownames(46603): ENSMUSG00000102693 ENSMUSG00000064842 ...
##   ENSMUSG00000096730 ENSMUSG00000095742
## rowData names(0):
## colnames(96): SLX-9555.N701_S502.C89V9ANXX.s_1.r_1
##   SLX-9555.N701_S503.C89V9ANXX.s_1.r_1 ...
##   SLX-9555.N712_S508.C89V9ANXX.s_1.r_1
##   SLX-9555.N712_S517.C89V9ANXX.s_1.r_1
## colData names(1): sizeFactor
## reducedDimNames(0):
## mainExpName: NULL
## altExpNames(0):
```

Alternatively, if we just want the names of the assays, we can get or set them with `assayNames()`:


``` r
assayNames(sce)
```

```
## [1] "counts"    "logcounts"
```

``` r
names(assays(sce)) # same result, but slightly less efficient.
```

```
## [1] "counts"    "logcounts"
```

## Handling metadata

### On the columns

To further annotate our `SingleCellExperiment` object, we can add metadata to describe the columns of our primary data, e.g., the samples or cells of our experiment. 
This is stored in the `colData` slot, a `DataFrame` object where rows correspond to cells and columns correspond to metadata fields, e.g., batch of origin, treatment condition (Figure \@ref(fig:sce-structure), orange box).
We demonstrate using some of the metadata accompanying the counts from @lun2017assessing.

<button class="rebook-collapse">Code to download file</button>
<div class="rebook-content">


``` r
# Downloading the SDRF file containing the metadata.
lun.sdrf <- bfcrpath(bfc, file.path("https://www.ebi.ac.uk/arrayexpress/files",
    "E-MTAB-5522/E-MTAB-5522.sdrf.txt"))
```


</div>


``` r
coldata <- read.delim(lun.sdrf, check.names=FALSE)

# Only keeping the cells involved in the count matrix in 'mat'.
coldata <- coldata[coldata[,"Derived Array Data File"]=="counts_Calero_20160113.tsv",]

# Only keeping interesting columns, and setting the library names as the row names.
coldata <- DataFrame(
    genotype=coldata[,"Characteristics[genotype]"],
    phenotype=coldata[,"Characteristics[phenotype]"],
    spike_in=coldata[,"Factor Value[spike-in addition]"],
    row.names=coldata[,"Source Name"]
)

coldata
```

```
## DataFrame with 96 rows and 3 columns
##                                                    genotype
##                                                 <character>
## SLX-9555.N701_S502.C89V9ANXX.s_1.r_1 Doxycycline-inducibl..
## SLX-9555.N701_S503.C89V9ANXX.s_1.r_1 Doxycycline-inducibl..
## SLX-9555.N701_S504.C89V9ANXX.s_1.r_1 Doxycycline-inducibl..
## SLX-9555.N701_S505.C89V9ANXX.s_1.r_1 Doxycycline-inducibl..
## SLX-9555.N701_S506.C89V9ANXX.s_1.r_1 Doxycycline-inducibl..
## ...                                                     ...
## SLX-9555.N712_S505.C89V9ANXX.s_1.r_1 Doxycycline-inducibl..
## SLX-9555.N712_S506.C89V9ANXX.s_1.r_1 Doxycycline-inducibl..
## SLX-9555.N712_S507.C89V9ANXX.s_1.r_1 Doxycycline-inducibl..
## SLX-9555.N712_S508.C89V9ANXX.s_1.r_1 Doxycycline-inducibl..
## SLX-9555.N712_S517.C89V9ANXX.s_1.r_1 Doxycycline-inducibl..
##                                                   phenotype    spike_in
##                                                 <character> <character>
## SLX-9555.N701_S502.C89V9ANXX.s_1.r_1    wild type phenotype   ERCC+SIRV
## SLX-9555.N701_S503.C89V9ANXX.s_1.r_1    wild type phenotype   ERCC+SIRV
## SLX-9555.N701_S504.C89V9ANXX.s_1.r_1    wild type phenotype   ERCC+SIRV
## SLX-9555.N701_S505.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..   ERCC+SIRV
## SLX-9555.N701_S506.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..   ERCC+SIRV
## ...                                                     ...         ...
## SLX-9555.N712_S505.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..    Premixed
## SLX-9555.N712_S506.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..    Premixed
## SLX-9555.N712_S507.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..    Premixed
## SLX-9555.N712_S508.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..    Premixed
## SLX-9555.N712_S517.C89V9ANXX.s_1.r_1    wild type phenotype    Premixed
```

Now, we can take two approaches - either add the `coldata` to our existing `sce`, or start from scratch via the `SingleCellExperiment()` constructor.
If we start from scratch:


``` r
sce <- SingleCellExperiment(assays = list(counts=mat), colData=coldata)
```

Similar to `assays`, we can see our `colData` is now populated:


``` r
sce
```

```
## class: SingleCellExperiment 
## dim: 46603 96 
## metadata(0):
## assays(1): counts
## rownames(46603): ENSMUSG00000102693 ENSMUSG00000064842 ...
##   ENSMUSG00000096730 ENSMUSG00000095742
## rowData names(0):
## colnames(96): SLX-9555.N701_S502.C89V9ANXX.s_1.r_1
##   SLX-9555.N701_S503.C89V9ANXX.s_1.r_1 ...
##   SLX-9555.N712_S508.C89V9ANXX.s_1.r_1
##   SLX-9555.N712_S517.C89V9ANXX.s_1.r_1
## colData names(3): genotype phenotype spike_in
## reducedDimNames(0):
## mainExpName: NULL
## altExpNames(0):
```

We can access our column data with the `colData()` function:


``` r
colData(sce)
```

```
## DataFrame with 96 rows and 3 columns
##                                                    genotype
##                                                 <character>
## SLX-9555.N701_S502.C89V9ANXX.s_1.r_1 Doxycycline-inducibl..
## SLX-9555.N701_S503.C89V9ANXX.s_1.r_1 Doxycycline-inducibl..
## SLX-9555.N701_S504.C89V9ANXX.s_1.r_1 Doxycycline-inducibl..
## SLX-9555.N701_S505.C89V9ANXX.s_1.r_1 Doxycycline-inducibl..
## SLX-9555.N701_S506.C89V9ANXX.s_1.r_1 Doxycycline-inducibl..
## ...                                                     ...
## SLX-9555.N712_S505.C89V9ANXX.s_1.r_1 Doxycycline-inducibl..
## SLX-9555.N712_S506.C89V9ANXX.s_1.r_1 Doxycycline-inducibl..
## SLX-9555.N712_S507.C89V9ANXX.s_1.r_1 Doxycycline-inducibl..
## SLX-9555.N712_S508.C89V9ANXX.s_1.r_1 Doxycycline-inducibl..
## SLX-9555.N712_S517.C89V9ANXX.s_1.r_1 Doxycycline-inducibl..
##                                                   phenotype    spike_in
##                                                 <character> <character>
## SLX-9555.N701_S502.C89V9ANXX.s_1.r_1    wild type phenotype   ERCC+SIRV
## SLX-9555.N701_S503.C89V9ANXX.s_1.r_1    wild type phenotype   ERCC+SIRV
## SLX-9555.N701_S504.C89V9ANXX.s_1.r_1    wild type phenotype   ERCC+SIRV
## SLX-9555.N701_S505.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..   ERCC+SIRV
## SLX-9555.N701_S506.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..   ERCC+SIRV
## ...                                                     ...         ...
## SLX-9555.N712_S505.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..    Premixed
## SLX-9555.N712_S506.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..    Premixed
## SLX-9555.N712_S507.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..    Premixed
## SLX-9555.N712_S508.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..    Premixed
## SLX-9555.N712_S517.C89V9ANXX.s_1.r_1    wild type phenotype    Premixed
```

Or more simply, we can extract a single field using the `$` shortcut:


``` r
head(sce$Factor.Value.phenotype.)
```

```
## NULL
```

Alternatively, we can add `colData` to an existing object, either _en masse_:


``` r
sce <- SingleCellExperiment(list(counts=mat))
colData(sce) <- coldata
sce
```

```
## class: SingleCellExperiment 
## dim: 46603 96 
## metadata(0):
## assays(1): counts
## rownames(46603): ENSMUSG00000102693 ENSMUSG00000064842 ...
##   ENSMUSG00000096730 ENSMUSG00000095742
## rowData names(0):
## colnames(96): SLX-9555.N701_S502.C89V9ANXX.s_1.r_1
##   SLX-9555.N701_S503.C89V9ANXX.s_1.r_1 ...
##   SLX-9555.N712_S508.C89V9ANXX.s_1.r_1
##   SLX-9555.N712_S517.C89V9ANXX.s_1.r_1
## colData names(3): genotype phenotype spike_in
## reducedDimNames(0):
## mainExpName: NULL
## altExpNames(0):
```

Or piece by piece:


``` r
sce <- SingleCellExperiment(list(counts=mat))
sce$phenotype <- coldata$phenotype
colData(sce)
```

```
## DataFrame with 96 rows and 1 column
##                                                   phenotype
##                                                 <character>
## SLX-9555.N701_S502.C89V9ANXX.s_1.r_1    wild type phenotype
## SLX-9555.N701_S503.C89V9ANXX.s_1.r_1    wild type phenotype
## SLX-9555.N701_S504.C89V9ANXX.s_1.r_1    wild type phenotype
## SLX-9555.N701_S505.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..
## SLX-9555.N701_S506.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..
## ...                                                     ...
## SLX-9555.N712_S505.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..
## SLX-9555.N712_S506.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..
## SLX-9555.N712_S507.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..
## SLX-9555.N712_S508.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..
## SLX-9555.N712_S517.C89V9ANXX.s_1.r_1    wild type phenotype
```

Regardless of which strategy you pick, it is very important to make sure that the rows of your `colData` actually refer to the same cells as the columns of your count matrix.
It is usually a good idea to check that the names are consistent before constructing the `SingleCellExperiment`:


``` r
stopifnot(identical(rownames(coldata), colnames(mat)))
```

Some functions automatically add column metadata by returning a `SingleCellExperiment` with extra fields in the `colData` slot.
For example, the *[scuttle](https://bioconductor.org/packages/3.20/scuttle)* package contains the `addPerCellQC()` function that appends a number of quality control metrics to the `colData`:


``` r
sce <- scuttle::addPerCellQC(sce)
colData(sce)
```

```
## DataFrame with 96 rows and 4 columns
##                                                   phenotype       sum  detected
##                                                 <character> <numeric> <numeric>
## SLX-9555.N701_S502.C89V9ANXX.s_1.r_1    wild type phenotype    854171      7617
## SLX-9555.N701_S503.C89V9ANXX.s_1.r_1    wild type phenotype   1044243      7520
## SLX-9555.N701_S504.C89V9ANXX.s_1.r_1    wild type phenotype   1152450      8305
## SLX-9555.N701_S505.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..   1193876      8142
## SLX-9555.N701_S506.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..   1521472      7153
## ...                                                     ...       ...       ...
## SLX-9555.N712_S505.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..    203221      5608
## SLX-9555.N712_S506.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..   1059853      6948
## SLX-9555.N712_S507.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..   1672343      6879
## SLX-9555.N712_S508.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..   1939537      7213
## SLX-9555.N712_S517.C89V9ANXX.s_1.r_1    wild type phenotype   1436899      8469
##                                          total
##                                      <numeric>
## SLX-9555.N701_S502.C89V9ANXX.s_1.r_1    854171
## SLX-9555.N701_S503.C89V9ANXX.s_1.r_1   1044243
## SLX-9555.N701_S504.C89V9ANXX.s_1.r_1   1152450
## SLX-9555.N701_S505.C89V9ANXX.s_1.r_1   1193876
## SLX-9555.N701_S506.C89V9ANXX.s_1.r_1   1521472
## ...                                        ...
## SLX-9555.N712_S505.C89V9ANXX.s_1.r_1    203221
## SLX-9555.N712_S506.C89V9ANXX.s_1.r_1   1059853
## SLX-9555.N712_S507.C89V9ANXX.s_1.r_1   1672343
## SLX-9555.N712_S508.C89V9ANXX.s_1.r_1   1939537
## SLX-9555.N712_S517.C89V9ANXX.s_1.r_1   1436899
```

### On the rows

We store feature-level annotation in the `rowData` slot, a `DataFrame` where each row corresponds to a gene and contains annotations like the transcript length or gene symbol.
We can manually get and set this with the `rowData()` function, as shown below:


``` r
rowData(sce)$Length <- gene.length
rowData(sce)
```

```
## DataFrame with 46603 rows and 1 column
##                       Length
##                    <integer>
## ENSMUSG00000102693      1070
## ENSMUSG00000064842       110
## ENSMUSG00000051951      6094
## ENSMUSG00000102851       480
## ENSMUSG00000103377      2819
## ...                      ...
## ENSMUSG00000094431       100
## ENSMUSG00000094621       121
## ENSMUSG00000098647        99
## ENSMUSG00000096730      3077
## ENSMUSG00000095742       243
```

Some functions will return a `SingleCellExperiment` with the `rowData` populated with relevant bits of information, such as the `addPerFeatureQC()` function:


``` r
sce <- scuttle::addPerFeatureQC(sce)
rowData(sce)
```

```
## DataFrame with 46603 rows and 3 columns
##                       Length      mean  detected
##                    <integer> <numeric> <numeric>
## ENSMUSG00000102693      1070 0.0000000   0.00000
## ENSMUSG00000064842       110 0.0000000   0.00000
## ENSMUSG00000051951      6094 0.0000000   0.00000
## ENSMUSG00000102851       480 0.0000000   0.00000
## ENSMUSG00000103377      2819 0.0208333   1.04167
## ...                      ...       ...       ...
## ENSMUSG00000094431       100         0         0
## ENSMUSG00000094621       121         0         0
## ENSMUSG00000098647        99         0         0
## ENSMUSG00000096730      3077         0         0
## ENSMUSG00000095742       243         0         0
```

Furthermore, there is a special `rowRanges` slot to hold genomic coordinates in the form of a `GRanges` or `GRangesList`.
This stores describes the chromosome, start, and end coordinates of the features (genes, genomic regions) that can be easily queryed and manipulated via the *[GenomicRanges](https://bioconductor.org/packages/3.20/GenomicRanges)* framework.
In our case, `rowRanges(sce)` produces an empty list because we did not fill it with any coordinate information.


``` r
rowRanges(sce) # empty
```

```
## GRangesList object of length 46603:
## $ENSMUSG00000102693
## GRanges object with 0 ranges and 0 metadata columns:
##    seqnames    ranges strand
##       <Rle> <IRanges>  <Rle>
##   -------
##   seqinfo: no sequences
## 
## $ENSMUSG00000064842
## GRanges object with 0 ranges and 0 metadata columns:
##    seqnames    ranges strand
##       <Rle> <IRanges>  <Rle>
##   -------
##   seqinfo: no sequences
## 
## $ENSMUSG00000051951
## GRanges object with 0 ranges and 0 metadata columns:
##    seqnames    ranges strand
##       <Rle> <IRanges>  <Rle>
##   -------
##   seqinfo: no sequences
## 
## ...
## <46600 more elements>
```

The manner with which we populate the `rowRanges` depends on the organism and annotation used during alignment and quantification. 
Here, we have Ensembl identifiers, so we might use *[rtracklayer](https://bioconductor.org/packages/3.20/rtracklayer)* to load in a `GRanges` from an GTF file containing the Ensembl annotation used in this dataset:

<button class="rebook-collapse">Code to download file</button>
<div class="rebook-content">


``` r
# The paper uses Ensembl 82.
mm10.gtf <- bfcrpath(bfc, file.path("http://ftp.ensembl.org/pub/release-82",
    "gtf/mus_musculus/Mus_musculus.GRCm38.82.gtf.gz"))
```


</div>


``` r
gene.data <- rtracklayer::import(mm10.gtf)

# Cleaning up the object.
gene.data <- gene.data[gene.data$type=="gene"]
names(gene.data) <- gene.data$gene_id
is.gene.related <- grep("gene_", colnames(mcols(gene.data)))
mcols(gene.data) <- mcols(gene.data)[,is.gene.related]

rowRanges(sce) <- gene.data[rownames(sce)]
rowRanges(sce)[1:10,]
```

```
## GRanges object with 10 ranges and 6 metadata columns:
##                      seqnames          ranges strand |            gene_id
##                         <Rle>       <IRanges>  <Rle> |        <character>
##   ENSMUSG00000102693        1 3073253-3074322      + | ENSMUSG00000102693
##   ENSMUSG00000064842        1 3102016-3102125      + | ENSMUSG00000064842
##   ENSMUSG00000051951        1 3205901-3671498      - | ENSMUSG00000051951
##   ENSMUSG00000102851        1 3252757-3253236      + | ENSMUSG00000102851
##   ENSMUSG00000103377        1 3365731-3368549      - | ENSMUSG00000103377
##   ENSMUSG00000104017        1 3375556-3377788      - | ENSMUSG00000104017
##   ENSMUSG00000103025        1 3464977-3467285      - | ENSMUSG00000103025
##   ENSMUSG00000089699        1 3466587-3513553      + | ENSMUSG00000089699
##   ENSMUSG00000103201        1 3512451-3514507      - | ENSMUSG00000103201
##   ENSMUSG00000103147        1 3531795-3532720      + | ENSMUSG00000103147
##                      gene_version     gene_name    gene_source
##                       <character>   <character>    <character>
##   ENSMUSG00000102693            1 4933401J01Rik         havana
##   ENSMUSG00000064842            1       Gm26206        ensembl
##   ENSMUSG00000051951            5          Xkr4 ensembl_havana
##   ENSMUSG00000102851            1       Gm18956         havana
##   ENSMUSG00000103377            1       Gm37180         havana
##   ENSMUSG00000104017            1       Gm37363         havana
##   ENSMUSG00000103025            1       Gm37686         havana
##   ENSMUSG00000089699            1        Gm1992         havana
##   ENSMUSG00000103201            1       Gm37329         havana
##   ENSMUSG00000103147            1        Gm7341         havana
##                              gene_biotype havana_gene_version
##                               <character>         <character>
##   ENSMUSG00000102693                  TEC                   1
##   ENSMUSG00000064842                snRNA                <NA>
##   ENSMUSG00000051951       protein_coding                   2
##   ENSMUSG00000102851 processed_pseudogene                   1
##   ENSMUSG00000103377                  TEC                   1
##   ENSMUSG00000104017                  TEC                   1
##   ENSMUSG00000103025                  TEC                   1
##   ENSMUSG00000089699            antisense                   1
##   ENSMUSG00000103201                  TEC                   1
##   ENSMUSG00000103147 processed_pseudogene                   1
##   -------
##   seqinfo: 45 sequences from an unspecified genome; no seqlengths
```

### Other metadata 

Some analyses contain results or annotations that do not fit into the aforementioned slots, e.g., study metadata.
This can be stored in the `metadata` slot, a named list of arbitrary objects.
For example, say we have some favorite genes (e.g.,  highly variable genes) that we want to store inside of `sce` for use in our analysis at a later point. 
We can do this simply by appending to the metadata slot as follows:


``` r
my_genes <- c("gene_1", "gene_5")
metadata(sce) <- list(favorite_genes = my_genes)
metadata(sce)
```

```
## $favorite_genes
## [1] "gene_1" "gene_5"
```

Similarly, we can append more information via the `$` operator:


``` r
your_genes <- c("gene_4", "gene_8")
metadata(sce)$your_genes <- your_genes
metadata(sce)
```

```
## $favorite_genes
## [1] "gene_1" "gene_5"
## 
## $your_genes
## [1] "gene_4" "gene_8"
```

The main disadvantage of storing content in the `metadata()` is that it will not be synchronized with the rows or columns when subsetting or combining (see next chapter).
Thus, if an annotation field is related to the rows or columns, we suggest storing it in the `rowData()` or `colData()` instead.

## Subsetting and combining 

One of the major advantages of using the `SingleCellExperiment` is that operations on the rows or columns of the expression data are synchronized with the associated annotation.
This avoids embarrassing bookkeeping errors where we, e.g., subset the count matrix but forget to subset the corresponding feature/sample annotation. 
For example, if we subset our `sce` object to the first 10 cells, we can see that both the count matrix and the `colData()` are automatically subsetted:


``` r
first.10 <- sce[,1:10]
ncol(counts(first.10)) # only 10 columns.
```

```
## [1] 10
```

``` r
colData(first.10) # only 10 rows.
```

```
## DataFrame with 10 rows and 4 columns
##                                                   phenotype       sum  detected
##                                                 <character> <numeric> <numeric>
## SLX-9555.N701_S502.C89V9ANXX.s_1.r_1    wild type phenotype    854171      7617
## SLX-9555.N701_S503.C89V9ANXX.s_1.r_1    wild type phenotype   1044243      7520
## SLX-9555.N701_S504.C89V9ANXX.s_1.r_1    wild type phenotype   1152450      8305
## SLX-9555.N701_S505.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..   1193876      8142
## SLX-9555.N701_S506.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..   1521472      7153
## SLX-9555.N701_S507.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..    866705      6828
## SLX-9555.N701_S508.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..    608581      6966
## SLX-9555.N701_S517.C89V9ANXX.s_1.r_1    wild type phenotype   1113526      8634
## SLX-9555.N702_S502.C89V9ANXX.s_1.r_1    wild type phenotype   1308250      8364
## SLX-9555.N702_S503.C89V9ANXX.s_1.r_1    wild type phenotype    778605      8665
##                                          total
##                                      <numeric>
## SLX-9555.N701_S502.C89V9ANXX.s_1.r_1    854171
## SLX-9555.N701_S503.C89V9ANXX.s_1.r_1   1044243
## SLX-9555.N701_S504.C89V9ANXX.s_1.r_1   1152450
## SLX-9555.N701_S505.C89V9ANXX.s_1.r_1   1193876
## SLX-9555.N701_S506.C89V9ANXX.s_1.r_1   1521472
## SLX-9555.N701_S507.C89V9ANXX.s_1.r_1    866705
## SLX-9555.N701_S508.C89V9ANXX.s_1.r_1    608581
## SLX-9555.N701_S517.C89V9ANXX.s_1.r_1   1113526
## SLX-9555.N702_S502.C89V9ANXX.s_1.r_1   1308250
## SLX-9555.N702_S503.C89V9ANXX.s_1.r_1    778605
```

Similarly, if we only wanted wild-type cells, we could subset our `sce` object based on its `colData()` entries:


``` r
wt.only <- sce[, sce$phenotype == "wild type phenotype"]
ncol(counts(wt.only))
```

```
## [1] 48
```

``` r
colData(wt.only)
```

```
## DataFrame with 48 rows and 4 columns
##                                                phenotype       sum  detected
##                                              <character> <numeric> <numeric>
## SLX-9555.N701_S502.C89V9ANXX.s_1.r_1 wild type phenotype    854171      7617
## SLX-9555.N701_S503.C89V9ANXX.s_1.r_1 wild type phenotype   1044243      7520
## SLX-9555.N701_S504.C89V9ANXX.s_1.r_1 wild type phenotype   1152450      8305
## SLX-9555.N701_S517.C89V9ANXX.s_1.r_1 wild type phenotype   1113526      8634
## SLX-9555.N702_S502.C89V9ANXX.s_1.r_1 wild type phenotype   1308250      8364
## ...                                                  ...       ...       ...
## SLX-9555.N711_S517.C89V9ANXX.s_1.r_1 wild type phenotype   1317671      8581
## SLX-9555.N712_S502.C89V9ANXX.s_1.r_1 wild type phenotype   1736189      9687
## SLX-9555.N712_S503.C89V9ANXX.s_1.r_1 wild type phenotype   1521132      8983
## SLX-9555.N712_S504.C89V9ANXX.s_1.r_1 wild type phenotype   1759166      8480
## SLX-9555.N712_S517.C89V9ANXX.s_1.r_1 wild type phenotype   1436899      8469
##                                          total
##                                      <numeric>
## SLX-9555.N701_S502.C89V9ANXX.s_1.r_1    854171
## SLX-9555.N701_S503.C89V9ANXX.s_1.r_1   1044243
## SLX-9555.N701_S504.C89V9ANXX.s_1.r_1   1152450
## SLX-9555.N701_S517.C89V9ANXX.s_1.r_1   1113526
## SLX-9555.N702_S502.C89V9ANXX.s_1.r_1   1308250
## ...                                        ...
## SLX-9555.N711_S517.C89V9ANXX.s_1.r_1   1317671
## SLX-9555.N712_S502.C89V9ANXX.s_1.r_1   1736189
## SLX-9555.N712_S503.C89V9ANXX.s_1.r_1   1521132
## SLX-9555.N712_S504.C89V9ANXX.s_1.r_1   1759166
## SLX-9555.N712_S517.C89V9ANXX.s_1.r_1   1436899
```

The same logic applies to the `rowData()`.
Say we only want to keep protein-coding genes:


``` r
coding.only <- sce[rowData(sce)$gene_biotype == "protein_coding",]
nrow(counts(coding.only))
```

```
## [1] 22013
```

``` r
rowData(coding.only)
```

```
## DataFrame with 22013 rows and 6 columns
##                               gene_id gene_version      gene_name
##                           <character>  <character>    <character>
## ENSMUSG00000051951 ENSMUSG00000051951            5           Xkr4
## ENSMUSG00000025900 ENSMUSG00000025900            9            Rp1
## ENSMUSG00000025902 ENSMUSG00000025902           12          Sox17
## ENSMUSG00000033845 ENSMUSG00000033845           12         Mrpl15
## ENSMUSG00000025903 ENSMUSG00000025903           13         Lypla1
## ...                               ...          ...            ...
## ENSMUSG00000079808 ENSMUSG00000079808            3     AC168977.1
## ENSMUSG00000095041 ENSMUSG00000095041            6           PISD
## ENSMUSG00000063897 ENSMUSG00000063897            3          DHRSX
## ENSMUSG00000096730 ENSMUSG00000096730            6       Vmn2r122
## ENSMUSG00000095742 ENSMUSG00000095742            1 CAAA01147332.1
##                       gene_source   gene_biotype havana_gene_version
##                       <character>    <character>         <character>
## ENSMUSG00000051951 ensembl_havana protein_coding                   2
## ENSMUSG00000025900 ensembl_havana protein_coding                   2
## ENSMUSG00000025902 ensembl_havana protein_coding                   6
## ENSMUSG00000033845 ensembl_havana protein_coding                   3
## ENSMUSG00000025903 ensembl_havana protein_coding                   3
## ...                           ...            ...                 ...
## ENSMUSG00000079808        ensembl protein_coding                  NA
## ENSMUSG00000095041        ensembl protein_coding                  NA
## ENSMUSG00000063897        ensembl protein_coding                  NA
## ENSMUSG00000096730        ensembl protein_coding                  NA
## ENSMUSG00000095742        ensembl protein_coding                  NA
```

Conversely, if we were to combine multiple `SingleCellExperiment` objects, the class would take care of combining both the expression values and the associated annotation in a coherent manner.
We can use `cbind()` to combine objects by column, assuming that all objects involved have the same row annotation values and compatible column annotation fields.


``` r
sce2 <- cbind(sce, sce)
ncol(counts(sce2)) # twice as many columns
```

```
## [1] 192
```

``` r
colData(sce2) # twice as many rows
```

```
## DataFrame with 192 rows and 4 columns
##                                                   phenotype       sum  detected
##                                                 <character> <numeric> <numeric>
## SLX-9555.N701_S502.C89V9ANXX.s_1.r_1    wild type phenotype    854171      7617
## SLX-9555.N701_S503.C89V9ANXX.s_1.r_1    wild type phenotype   1044243      7520
## SLX-9555.N701_S504.C89V9ANXX.s_1.r_1    wild type phenotype   1152450      8305
## SLX-9555.N701_S505.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..   1193876      8142
## SLX-9555.N701_S506.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..   1521472      7153
## ...                                                     ...       ...       ...
## SLX-9555.N712_S505.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..    203221      5608
## SLX-9555.N712_S506.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..   1059853      6948
## SLX-9555.N712_S507.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..   1672343      6879
## SLX-9555.N712_S508.C89V9ANXX.s_1.r_1 induced CBFB-MYH11 o..   1939537      7213
## SLX-9555.N712_S517.C89V9ANXX.s_1.r_1    wild type phenotype   1436899      8469
##                                          total
##                                      <numeric>
## SLX-9555.N701_S502.C89V9ANXX.s_1.r_1    854171
## SLX-9555.N701_S503.C89V9ANXX.s_1.r_1   1044243
## SLX-9555.N701_S504.C89V9ANXX.s_1.r_1   1152450
## SLX-9555.N701_S505.C89V9ANXX.s_1.r_1   1193876
## SLX-9555.N701_S506.C89V9ANXX.s_1.r_1   1521472
## ...                                        ...
## SLX-9555.N712_S505.C89V9ANXX.s_1.r_1    203221
## SLX-9555.N712_S506.C89V9ANXX.s_1.r_1   1059853
## SLX-9555.N712_S507.C89V9ANXX.s_1.r_1   1672343
## SLX-9555.N712_S508.C89V9ANXX.s_1.r_1   1939537
## SLX-9555.N712_S517.C89V9ANXX.s_1.r_1   1436899
```

Similarly, we can use `rbind()` to combine objects by row, assuming all objects have the same column annotation values and compatible row annotation fields.


``` r
sce2 <- rbind(sce, sce)
nrow(counts(sce2)) # twice as many rows
```

```
## [1] 93206
```

``` r
rowData(sce2) # twice as many rows
```

```
## DataFrame with 93206 rows and 6 columns
##                               gene_id gene_version      gene_name
##                           <character>  <character>    <character>
## ENSMUSG00000102693 ENSMUSG00000102693            1  4933401J01Rik
## ENSMUSG00000064842 ENSMUSG00000064842            1        Gm26206
## ENSMUSG00000051951 ENSMUSG00000051951            5           Xkr4
## ENSMUSG00000102851 ENSMUSG00000102851            1        Gm18956
## ENSMUSG00000103377 ENSMUSG00000103377            1        Gm37180
## ...                               ...          ...            ...
## ENSMUSG00000094431 ENSMUSG00000094431            1 CAAA01205117.1
## ENSMUSG00000094621 ENSMUSG00000094621            1 CAAA01098150.1
## ENSMUSG00000098647 ENSMUSG00000098647            1 CAAA01064564.1
## ENSMUSG00000096730 ENSMUSG00000096730            6       Vmn2r122
## ENSMUSG00000095742 ENSMUSG00000095742            1 CAAA01147332.1
##                       gene_source         gene_biotype havana_gene_version
##                       <character>          <character>         <character>
## ENSMUSG00000102693         havana                  TEC                   1
## ENSMUSG00000064842        ensembl                snRNA                  NA
## ENSMUSG00000051951 ensembl_havana       protein_coding                   2
## ENSMUSG00000102851         havana processed_pseudogene                   1
## ENSMUSG00000103377         havana                  TEC                   1
## ...                           ...                  ...                 ...
## ENSMUSG00000094431        ensembl                miRNA                  NA
## ENSMUSG00000094621        ensembl                miRNA                  NA
## ENSMUSG00000098647        ensembl                miRNA                  NA
## ENSMUSG00000096730        ensembl       protein_coding                  NA
## ENSMUSG00000095742        ensembl       protein_coding                  NA
```

## Single-cell-specific fields

### Background

So far, we have covered the `assays` (primary data), `colData` (cell metadata), `rowData`/`rowRanges` (feature metadata), and `metadata` slots (other) of the `SingleCellExperiment` class.
These slots are actually inherited from the `SummarizedExperiment` parent class (see [here](https://bioconductor.org/packages/3.20/SummarizedExperiment/vignettes/SummarizedExperiment.html) for details), so any method that works on a `SummarizedExperiment` will also work on a `SingleCellExperiment` object.
But why do we need a separate `SingleCellExperiment` class?
This is motivated by the desire to streamline some single-cell-specific operations, which we will discuss in the rest of this section.

### Dimensionality reduction results

The `reducedDims` slot is specially designed to store reduced dimensionality representations of the primary data obtained by methods such as PCA and $t$-SNE (see [Basic Chapter 4](http://bioconductor.org/books/3.20/OSCA.basic/dimensionality-reduction.html#dimensionality-reduction) for more details).
This slot contains a list of numeric matrices of low-reduced representations of the primary data, where the rows represent the columns of the primary data (i.e., cells), and columns represent the dimensions.
As this slot holds a list, we can store multiple PCA/$t$-SNE/etc. results for the same dataset.

In our example, we can calculate a PCA representation of our data using the `runPCA()` function from *[scater](https://bioconductor.org/packages/3.20/scater)*. 
We see that the `sce` now shows a new `reducedDim` that can be retrieved with the accessor `reducedDim()`.


``` r
sce <- scater::logNormCounts(sce)
sce <- scater::runPCA(sce)
dim(reducedDim(sce, "PCA"))
```

```
## [1] 96 50
```

We can also calculate a tSNE representation using the `scater` package function `runTSNE()`:


``` r
sce <- scater::runTSNE(sce, perplexity = 0.1)
```

```
## Perplexity should be lower than K!
```

``` r
head(reducedDim(sce, "TSNE"))
```

```
##                                         TSNE1  TSNE2
## SLX-9555.N701_S502.C89V9ANXX.s_1.r_1   271.28  971.5
## SLX-9555.N701_S503.C89V9ANXX.s_1.r_1 -1234.19 -461.7
## SLX-9555.N701_S504.C89V9ANXX.s_1.r_1 -1040.93  421.0
## SLX-9555.N701_S505.C89V9ANXX.s_1.r_1    87.25 -371.7
## SLX-9555.N701_S506.C89V9ANXX.s_1.r_1  -720.77  775.0
## SLX-9555.N701_S507.C89V9ANXX.s_1.r_1   156.74 -607.3
```

We can view the names of all our entries in the `reducedDims` slot via the accessor, `reducedDims()`.
Note that this is plural and returns a list of all results, whereas `reducedDim()` only returns a single result.


``` r
reducedDims(sce)
```

```
## List of length 2
## names(2): PCA TSNE
```

We can also manually add content to the `reducedDims()` slot, much like how we added matrices to the `assays` slot previously.
To illustrate, we run the `umap()` function directly from the *[uwot](https://CRAN.R-project.org/package=uwot)* package to generate a matrix of UMAP coordinates that is added to the `reducedDims` of our `sce` object.
(In practice, *[scater](https://bioconductor.org/packages/3.20/scater)* has a `runUMAP()` wrapper function that adds the results for us, but we will manually call `umap()` here for demonstration purposes.)


``` r
u <- uwot::umap(t(logcounts(sce)), n_neighbors = 2)
reducedDim(sce, "UMAP_uwot") <- u
reducedDims(sce) # Now stored in the object.
```

```
## List of length 3
## names(3): PCA TSNE UMAP_uwot
```

``` r
head(reducedDim(sce, "UMAP_uwot"))
```

```
##                                        [,1]    [,2]
## SLX-9555.N701_S502.C89V9ANXX.s_1.r_1  4.133 -2.0302
## SLX-9555.N701_S503.C89V9ANXX.s_1.r_1  3.210 -3.2570
## SLX-9555.N701_S504.C89V9ANXX.s_1.r_1  5.003 -1.5169
## SLX-9555.N701_S505.C89V9ANXX.s_1.r_1  8.365 -3.7660
## SLX-9555.N701_S506.C89V9ANXX.s_1.r_1 -5.207  6.1162
## SLX-9555.N701_S507.C89V9ANXX.s_1.r_1 -1.456  0.9836
```

### Alternative Experiments

The `SingleCellExperiment` class provides the concept of "alternative Experiments" where we have data for a distinct set of features but the same set of samples/cells.
The classic application would be to store the per-cell counts for spike-in transcripts; this allows us to retain this data for downstream use but separate it from the `assays` holding the counts for endogenous genes.
The separation is particularly important as such alternative features often need to be processed separately, see Chapter [Advanced Chapter 12](http://bioconductor.org/books/3.20/OSCA.advanced/integrating-with-protein-abundance.html#integrating-with-protein-abundance) for examples with antibody-derived tags.

If we have data for alternative feature sets, we can store it in our `SingleCellExperiment` as an alternative Experiment.
For example, if we have some data for spike-in transcripts, we first create a separate `SummarizedExperiment` object:


``` r
# -1 to get rid of the first gene length column.
spike_se <- SummarizedExperiment(list(counts=spike.mat[,-1]))
spike_se
```

```
## class: SummarizedExperiment 
## dim: 92 96 
## metadata(0):
## assays(1): counts
## rownames(92): ERCC-00002 ERCC-00003 ... ERCC-00170 ERCC-00171
## rowData names(0):
## colnames(96): SLX-9555.N701_S502.C89V9ANXX.s_1.r_1
##   SLX-9555.N701_S503.C89V9ANXX.s_1.r_1 ...
##   SLX-9555.N712_S508.C89V9ANXX.s_1.r_1
##   SLX-9555.N712_S517.C89V9ANXX.s_1.r_1
## colData names(0):
```

Then we store this `SummarizedExperiment` in our `sce` object via the `altExp()` setter.
Like `assays()` and `reducedDims()`, we can also retrieve all of the available alternative Experiments with `altExps()`.


``` r
altExp(sce, "spike") <- spike_se
altExps(sce)
```

```
## List of length 1
## names(1): spike
```

The alternative Experiment concept ensures that all relevant aspects of a single-cell dataset can be held in a single object.
It is also convenient as it ensures that our spike-in data is synchronized with the data for the endogenous genes.
For example, if we subsetted `sce`, the spike-in data would be subsetted to match:


``` r
sub <- sce[,1:2] # retain only two samples.
altExp(sub, "spike")
```

```
## class: SummarizedExperiment 
## dim: 92 2 
## metadata(0):
## assays(1): counts
## rownames(92): ERCC-00002 ERCC-00003 ... ERCC-00170 ERCC-00171
## rowData names(0):
## colnames(2): SLX-9555.N701_S502.C89V9ANXX.s_1.r_1
##   SLX-9555.N701_S503.C89V9ANXX.s_1.r_1
## colData names(0):
```

Any `SummarizedExperiment` object can be stored as an alternative Experiment, including another `SingleCellExperiment`!
This allows power users to perform tricks like those described in [Basic Section 3.6](http://bioconductor.org/books/3.20/OSCA.basic/feature-selection.html#feature-selection-subsetting).

### Size factors 

The `sizeFactors()` function allows us to get or set a numeric vector of per-cell scaling factors used for normalization (see [Basic Chapter 2](http://bioconductor.org/books/3.20/OSCA.basic/normalization.html#normalization) for more details).
This is typically automatically added by normalization functions, as shown below for *[scran](https://bioconductor.org/packages/3.20/scran)*'s deconvolution-based size factors:


``` r
sce <- scran::computeSumFactors(sce)
summary(sizeFactors(sce))
```

```
##    Min. 1st Qu.  Median    Mean 3rd Qu.    Max. 
##   0.151   0.742   0.948   1.000   1.124   3.558
```

Alternatively, we can manually add the size factors, as shown below for library size-derived factors:


``` r
sizeFactors(sce) <- scater::librarySizeFactors(sce)
summary(sizeFactors(sce))
```

```
##    Min. 1st Qu.  Median    Mean 3rd Qu.    Max. 
##   0.170   0.766   0.951   1.000   1.106   3.605
```

Technically speaking, the `sizeFactors` concept is not unique to single-cell analyses.
Nonetheless, we mention it here as it is an extension beyond what is available in the `SummarizedExperiment` parent class.

### Column labels

The `colLabels()` function allows us to get or set a vector or factor of per-cell labels,
typically corresponding to groupings assigned by unsupervised clustering ([Basic Chapter 5](http://bioconductor.org/books/3.20/OSCA.basic/clustering.html#clustering)).
or predicted cell type identities from classification algorithms ([Basic Chapter 7](http://bioconductor.org/books/3.20/OSCA.basic/cell-type-annotation.html#cell-type-annotation)).


``` r
colLabels(sce) <- scran::clusterCells(sce, use.dimred="PCA")
table(colLabels(sce))
```

```
## 
##  1  2 
## 47 49
```

This is a convenient field to set as several functions (e.g., `scran::findMarkers`) will attempt to automatically retrieve the labels via `colLabels()`.
We can thus avoid the few extra keystrokes that would otherwise be necessary to specify, say, the cluster assignments in the function call.

## Conclusion 

The widespread use of the `SingleCellExperiment` class provides the foundation for interoperability between single-cell-related packages in the Bioconductor ecosystem.
`SingleCellExperiment` objects generated by one package can be used as input into another package, encouraging synergies that enable our analysis to be greater than the sum of its parts.
Each step of the analysis will also add new entries to the `assays`, `colData`, `reducedDims`, etc.,
meaning that the final `SingleCellExperiment` object effectively serves as a self-contained record of the analysis.
This is convenient as the object can be saved for future use or transferred to collaborators for further analysis.
Thus, for the rest of this book, we will be using the `SingleCellExperiment` as our basic data structure.

## Session Info {-}

<button class="rebook-collapse">View session info</button>
<div class="rebook-content">
```
R version 4.4.1 (2024-06-14)
Platform: x86_64-pc-linux-gnu
Running under: Ubuntu 24.04.1 LTS

Matrix products: default
BLAS:   /home/biocbuild/bbs-3.20-bioc/R/lib/libRblas.so 
LAPACK: /usr/lib/x86_64-linux-gnu/lapack/liblapack.so.3.12.0

locale:
 [1] LC_CTYPE=en_US.UTF-8       LC_NUMERIC=C              
 [3] LC_TIME=en_GB              LC_COLLATE=C              
 [5] LC_MONETARY=en_US.UTF-8    LC_MESSAGES=en_US.UTF-8   
 [7] LC_PAPER=en_US.UTF-8       LC_NAME=C                 
 [9] LC_ADDRESS=C               LC_TELEPHONE=C            
[11] LC_MEASUREMENT=en_US.UTF-8 LC_IDENTIFICATION=C       

time zone: America/New_York
tzcode source: system (glibc)

attached base packages:
[1] stats4    stats     graphics  grDevices utils     datasets  methods  
[8] base     

other attached packages:
 [1] BiocFileCache_2.14.0        dbplyr_2.5.0               
 [3] SingleCellExperiment_1.28.0 SummarizedExperiment_1.36.0
 [5] Biobase_2.66.0              GenomicRanges_1.58.0       
 [7] GenomeInfoDb_1.42.0         IRanges_2.40.0             
 [9] S4Vectors_0.44.0            BiocGenerics_0.52.0        
[11] MatrixGenerics_1.18.0       matrixStats_1.4.1          
[13] BiocStyle_2.34.0            rebook_1.16.0              

loaded via a namespace (and not attached):
  [1] DBI_1.2.3                bitops_1.0-9             gridExtra_2.3           
  [4] CodeDepends_0.6.6        rlang_1.1.4              magrittr_2.0.3          
  [7] scater_1.34.0            compiler_4.4.1           RSQLite_2.3.7           
 [10] dir.expiry_1.14.0        png_0.1-8                vctrs_0.6.5             
 [13] pkgconfig_2.0.3          crayon_1.5.3             fastmap_1.2.0           
 [16] XVector_0.46.0           scuttle_1.16.0           utf8_1.2.4              
 [19] Rsamtools_2.22.0         rmarkdown_2.28           graph_1.84.0            
 [22] UCSC.utils_1.2.0         ggbeeswarm_0.7.2         purrr_1.0.2             
 [25] bit_4.5.0                bluster_1.16.0           xfun_0.48               
 [28] zlibbioc_1.52.0          cachem_1.1.0             beachmat_2.22.0         
 [31] jsonlite_1.8.9           blob_1.2.4               highr_0.11              
 [34] DelayedArray_0.32.0      BiocParallel_1.40.0      cluster_2.1.6           
 [37] irlba_2.3.5.1            parallel_4.4.1           R6_2.5.1                
 [40] bslib_0.8.0              limma_3.62.0             rtracklayer_1.66.0      
 [43] jquerylib_0.1.4          Rcpp_1.0.13              bookdown_0.41           
 [46] knitr_1.48               FNN_1.1.4.1              igraph_2.1.1            
 [49] Matrix_1.7-1             tidyselect_1.2.1         abind_1.4-8             
 [52] yaml_2.3.10              viridis_0.6.5            codetools_0.2-20        
 [55] curl_5.2.3               lattice_0.22-6           tibble_3.2.1            
 [58] withr_3.0.2              Rtsne_0.17               evaluate_1.0.1          
 [61] Biostrings_2.74.0        pillar_1.9.0             BiocManager_1.30.25     
 [64] filelock_1.0.3           generics_0.1.3           RCurl_1.98-1.16         
 [67] ggplot2_3.5.1            munsell_0.5.1            scales_1.3.0            
 [70] glue_1.8.0               metapod_1.14.0           tools_4.4.1             
 [73] BiocIO_1.16.0            BiocNeighbors_2.0.0      ScaledMatrix_1.14.0     
 [76] locfit_1.5-9.10          GenomicAlignments_1.42.0 scran_1.34.0            
 [79] XML_3.99-0.17            grid_4.4.1               edgeR_4.4.0             
 [82] colorspace_2.1-1         GenomeInfoDbData_1.2.13  beeswarm_0.4.0          
 [85] BiocSingular_1.22.0      restfulr_0.0.15          vipor_0.4.7             
 [88] cli_3.6.3                rsvd_1.0.5               fansi_1.0.6             
 [91] viridisLite_0.4.2        S4Arrays_1.6.0           dplyr_1.1.4             
 [94] uwot_0.2.2               gtable_0.3.6             sass_0.4.9              
 [97] digest_0.6.37            dqrng_0.4.1              SparseArray_1.6.0       
[100] ggrepel_0.9.6            rjson_0.2.23             memoise_2.0.1           
[103] htmltools_0.5.8.1        lifecycle_1.0.4          httr_1.4.7              
[106] statmod_1.5.0            bit64_4.5.2             
```
</div>