---
title: 'PharmacoGx: An R Package for Analysis of Large Pharmacogenomic Datasets'

author:
- name: Petr Smirnov
  affilnum: 1

- name: Zhaleh Safikhani
  affilnum: '1,2'

- name: Benjamin Haibe-Kains
  affilation: '1, 2, 3'

affiliation:

- affilnum: 1
  affil: Princess Margaret Cancer Centre, University Health Network, Toronto Canada

- affilnum: 2
  affil: Department of Medical Biophysics, University of Toronto, Toronto Canada

- affilnum: 3
  affil: Department of Computer Science, University of Toronto, Toronto Canada

output:

  pdf_document:
    fig_caption: yes
    fig_width: 7
    fig_height: 7
    keep_tex: yes
    number_sections: no
    template: manuscript.latex
    includes:
      in_header: header.tex

  html_document: null

  word_document: null

documentclass: article
toc: true
classoption: a4paper
capsize: normalsize
geometry: margin=1in
fontsize: 11pt
spacing: singlespacing
footerdate: no
abstractt: no
bibliography:
  - pharmacogx.bib
csl: ecology.csl

vignette: >
  %\VignetteEngine{knitr::rmarkdown}
  %\VignetteEncoding{UTF-8}
  %\usepackage[UTF-8]{inputenc}
  %\VignetteIndexEntry{Creating a PharmacoSet Object}
---

\vspace{5pt}
\footnotesize
```{r setup, include=FALSE, cache=FALSE, message = FALSE}

library("knitr")

### Chunk options: see http://yihui.name/knitr/options/ ###

## Text results
opts_chunk$set(echo = TRUE, warning = TRUE, message = TRUE, include = TRUE)

## Code decoration
opts_chunk$set(tidy = FALSE, comment = NA, highlight = TRUE)

```


```{r knitcitation, include=FALSE}
library(knitcitations)
cleanbib()
cite_options(citation_format = "pandoc")
```


\normalsize

\clearpage

# Introduction

The PharmacoSet class is structured to contain several different types of
genomic data, as well as drug dose response data. It is built upon base R data
types and the `SummarizedExperiment` class. However, a `PharmacoSet` object
requires the presence of specific annotations for the data to be able to
function correctly with the function provided in PharmacoGx. The structure
allows users to then interrogate the data on the basis of cells and drugs,
removing the need for the user to deal with single experiments. We do not
recommend creating PharmacoSet objects by the end users, rather we recommend
contacting us to have the objects created for your dataset of interest.
However, for completeness and power users the process and structure is
documented below.

# PharmacoSet Structure

The base PharmacoSet structure is as follows:

## `sample`

Previously called `@cell`.

This slot contains a `data.frame` which contains information about all the cells
profiles across all the data types in the PharamcoSet, including both
perturbation and sensitivity experiments. It is crucial for the rownames of each
entry in the data frame to be the **unique cell identifier** used across all the
datatypes for each cell type. The content of this data frame will vary based on
what information each dataset provides. Mandatory columns in this data frame
must be `sampleid`, which should be equivalent to the rownames and `tissueid`,
which contains a curated annotation of the source tissue for each cell line.

## `treatment`

Previously called `@drug`.

This slot contains a `data.frame` which contains information about all the drugs
profiled across all the data types in the PharmacoSet, including both
perturbation and sensitivity experiments. Similar to the `sample` slot, it is
crucial for the rownames of each entry in the data frame to be the
**unique compound identifier** used across all the datatypes for each compound.
Once again, the content in this data frame will vary based on information
provided by each dataset. Mandatory columns must be `treatmentid`, which should
be equivalent to the object rownames.

## `curation`:

This slot contains three data.frames, one for drugs, tissues, and cells. Each
contains two columns, the first with the unique identifier that is used between
all PharmacoSet objects for this drug, and the second with the identifier used
within the dataset. At this time there is no set method to find the unique
identifiers between all PharmacoSets for arbitrary drugs, as much labour
intensive curation has gone into carefully matching identifiers between datasets.
However, these tables are used only by the intersecting function, and all other
functions will function without this data, therefore for PharmacoSet objects
created by users, we recommend just filling both columns with the identifiers
used in the datasets, to allow for at least some matching to be done.

* `sample`: data frame annotating all cell-lines investigated in the study.
* `treatment`: data frame annotating all the compounds investigated in the study.
* `tissue`: data.frame annotating all tissues investigated in the study.

## `molecularProfiles`:
* List of `SummarizedExperiment` objects containing the
molecular profiles of the cell lines, such as mutations, gene expressions, or
copy number variations.

The molecular profiles slot of a PharmacoSet object contains all the molecular
expression data profiled in the dataset. Each type of data is kept in a separate
SummarizedExperiment (SE) object, and they are all stored as a list. However, to
insure coordination between data types, there are specific annotations that must
be included in the SummarizedExperiment object. The annotations also differ
slightly in the cases of `perturbation` and `sensitivity` datasets.

First of all, each SummarizedExperiment object must be labelled with the type of
dataincluded within the object. Currently only `mutation`, `fusion`, and `rna`
molecular data types are recognized and handled differently by summarizing and
signature generating functions. This labelling is done by calling, for example:

```{r eval=FALSE }
SE@annotation <- "rna"
```

The phenoData in each SummarizedExperiment object also needs to contain specific
columns labelling each experiment. For sensitivity type datasets, this has to
include:

`sampleid`: This column contains a cell identifier that matches **exactly** the
rownames of the `sample` slot of the PSet.
`batchid`: This column contains and id of the batch of each experiment. If
such data is not available then it is customary to fill with NA, but this column
must be present.

Additionally, for the perturbation type datasets, there are several more columns
of metadata that must be included to enable the modelling of differential gene
expression. These are:

`treatmentid`: The identifier of the drug used in each experiment when a compound
was applied. For controls, it should be left as NA. These must match **exactly**
to the rownames of the `treatment` slot in the PharmacoSet.

`duration`: If available, the ength of the experiment. Should be 0 for
controls.

`concentration`: For experiments where compounds were applied, the
concentration. Should be 0 for controls.

`xptype`: A label of either `perturbation`, of `control` respectively.

Otherwise each SummarizedExperiment object should be constructed as specified
by the SummarizedExperiment package.

Once these SummarizedExperiment objects are created, they should be added to a
list, with the name of each object in the list being descriptive of the type of
data contained.

## `datasetType`

This slot is being deprecated, since `perturbation` data can effectively before
stored in the `colData` slot of the `SummarizedExperiment` in the
`molecularProfiles` slot

The `datasetType` slot is a character string which signifies whether the
PharmacoSet contains drug dose `sensitivity` data, genomic `perturbation` data,
or `both`. This slot is necessary for the subsetting and intersecting function
to be aware of what data types they should be looking for.

## `treatmentResponse`:

Previously called `@sensitivity` this slot contains viability measurements for
cell-lines treated with different therapeutic compounds.

* `n`: Number of experiments for each cell line treated with a given drug.
* `info`: Metadata for each pharmacological experiment.
* `raw`: All cell viability measurements at each drug concentration from the
drug dose-response curves.
* `profiles`: Drug sensitivity values summarizing each dose-response curve
(IC$_{50}$, AUC, etc.)

This slot is currently being redesigned to support drug combination experiments.
See the `LongTable` vignette for information about the new data strucutre.

This is a list containing all the data pertaining to drug dose response
experiments, usually only present in `sensitivity` or `both` type datasets. This
includes the names the following names slots in the list:

`info`: Metadata for each pharmacological experiment stored in a `data.frame`.
Each row of this data.frame should be labelled with a unique experiment
identifier. This data.frame must also contain specific columns:

`sampleid`: Contains a cell identifier that matches **exactly** the rownames of
the cell slot of the PSet.

`treatmentid`: The identifier of the drug used in each experiment when a compound was
applied. These must match **exactly** to the rownames of the drug slot in the
PharmacoSet.

`raw`: This is a 3-D `array` of raw drug dose response data. The first
dimension is the experiments, with the names of each row in this dimension
labelled exactly as the experiment ids used in the metadata data.frame `info`
above. The second dimension is the doses, with each "column" labelled as
`doses`, where the number is the column number. This is as long as there are
different number of doses for each experiment. The third dimension is always
fixed at 2, with names `Dose`, and `Viability`. `Dose} contains the actual dose
used (usually in micro-molar), while viability contains the cell viability
measurement at that dose. Therefore, for each experiment there are two vectors,
one of doses and one of viabilities at each dose.

`profiles` This is a data.frame containing down the rows, with **exactly**
matching rownames, the experiments as labelled in the `info` data.frame, and
each column being a summary of the drug dose sensitivity, such as
`auc\_published` or `ic50\_published`, as published with the data.

`n` This is a `matrix` containing cellids matching exactly the rownames of the
cell slot of the PSet down the rows, and drugids matching exactly the rownames
of the drug slot in the columns. This data.frame summaries how many experiments
are in the data for each pair, allowing quick identification of what pairs were
tested together. Note that this does not need to be generated before
constructing the object, it is generated by the constructor.

## `perturbation`:

This slot is being deprecated, as discussed above in `datasetType`.

* `n`: Number of experiments for each cell line perturbed by a given drug, for
  each molecular data type
* `profiles`: The metadata for the perturbation experiments is available for
each molecular type by calling the appropriate info function

`curation`: list of data frames containing the mapping between original drug,
cell line, and tissue names to standardized identifiers.

This slot is fully filled by the constructor, so nothing needs to be created for
it.

`n`: This is a 3-D `array` containing cellids matching exactly the rownames of
the cell slot of the PSet down the rows, and drugids matching exactly the
rownames of the drug slot in the columns, and the third dimension being the
names of the different molecular profile types. This array summarizes how many
perturbation experiments are in each molecular data type for each pair, allowing
quick identification of what pairs were tested together.

`info`: This is always exactly the string referring to each data type
separately: 'The metadata for the perturbation experiments is available for each
molecular type by calling the appropriate info function'

## `annotation`

The `annotation` slot contains information pertaining to the `PharmacoSet` as a
whole, including the full information on what packages were loaded into R when
the PharmacoSet was created, as well as the date and call to the constructor.
The only data that must be entered upon creation of the object is the name of
the PharmacoSet, which is passed to the constructor.

* `name`: Acronym of the pharmacogenomic dataset.
* `dateCreated`: When the object was created.
* `sessionInfo`: Software environment used to create the object.
* `call`: Set of parameters used to create the object.


# Creating the PharmacoSet

Once all the data is in the proper format, it can be passed to a the constructor
function as below:

```{r eval=FALSE}
PharmacoSet(name,
            molecularProfiles=list(),
            sample=data.frame(),
            treatment=data.frame(),
            sensitivityInfo=data.frame(),
            sensitivityRaw=array(dim=c(0,0,0)),
            sensitivityProfiles=matrix(),
            curationTreatment=data.frame(),
            curationSample=data.frame(),
            curationTissue=data.frame(),
            datasetType=c("sensitivity", "perturbation", "both"),
            verify = TRUE)
```

Here, `name` is the name of the PharmacoSet as described in annotations above,
`molecularProfiles` is the list of ExpressionSet objects described above, cell
and drug are the data.frames in the cell and drug slots. The `sensitivityInfo`,
`sensitivityRaw`, `sensitivityProfiles` are the elements of the `sensitivity`
slot, and curationTreatment, curationSample, and curationTissue the contents of the
curation slot. Finally, `datasetType` is a string to signify which type of data
isincluded in the datset, and verify is a flag for running the verification of
the pSet after its construction. Any data detailed above but missing from this
constructor call will be created by the constructor, and the default empty
values are as in the call above. Notice that none of the values should be set
as NA, they should be ommited if the data is not being provided.
