r-bioc-annotate 1.56.1+dfsg-1 / usr / lib / R / site-library / annotate / doc / useDataPkgs.Rnw

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\begin{document}
\title{Using Bioconductor's Annotation Libraries}

\author{Marc Carlson, Jianhua Zhang}
\date{}
\maketitle

\section*{Overview}

The Bioconductor project maintains a rich body of annotation data
assembled into R libraries. The purpose of this vignette
is to discuss the structure, contents, and usage of these
annotation data libraries. Executable code is provided as examples.

\section*{Contents}

Bioconductor's annotation data libraries are constructed by assembling data
collected from various public data repositories using Bioconductor's
\Rpackage{AnnotationDbi} package and distributed as regular R libraries that
can be installed and loaded in the same way an R library is
installed/loaded. Each annotation library is an independent unit that can be
used alone or in conjunction with other annotation libraries. Platform
specific libraries are a group annotation libraries assembled specifically for
given platforms (e. g. Affymetrix HG\_U95Av2). \texttt{org.XX.eg.db} are
libraries containing data assembled at genome level for specific organisms
such as human, mouse, fly, or rat. \Rpackage{KEGG.db} and \Rpackage{GO.db} are
source specific libraries containing generic data for various genomes.

% \begin{figure*}[htbp!]
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%    \caption{{\small \label{fig:DPChart}A diagram showing the overall
%        structure and inter-relationship of Bioconductor annotation
%        data packages. Boxes show a single or group of data
%        packages. Lines between two boxes indicate connections through
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Each annotation library, when installed, contains a sqlite database contained
within the \texttt{extdata} along with a \texttt{man} subdirectory filled with
documentation about the data. The data can be accessed using the standard
methods that would work for the classic environment objects (hash table with
key-value pairs) and act as if they were simple associations of annotation
values to a set of keys. For each of these emulated environment objects (which
we will refer to as mappings), there is a corresponding help file in the
\texttt{man} directory with detail descriptions of the data file and usage.
In addition to the traditional access to these data, these databases can also
be accessed directly by using DBI interfaces which allow for powerful new
combinations of these data.

Each platform specific library creates a series of these mapping objects
named by following the convention of package name plus mapping
name. The package name is in lower case letters and the mapping
names are in capital letters. When a given mapping maps platform
specific keys to annotation data, only the name of the annotation data
is used for the name of the mapping. Otherwise, the mapping
names have a pattern of key name and value name joined by a "2" in
between. For example, \Robject{hgu95av2ENTREZID} maps probe ids on 
an Affymetrix human genome U95Av2 chip to EntrezGene IDs while \Robject{hgu95av2GO2PROBE} 
maps Gene Ontology IDs to probe IDs. Names of the mappings available in a
platform specific data package are not listed here to save space but
are easily accessible as shown later in the section for usage.


Genome level annotation libraries are named in the form of org.Xx.yy.db where
Xx represents an abbreviation of the genus and species. Each of the organism
wide genome anotation packages is based upon some type of widely used gene
based identifier (such as an Entrez Gene id) that is mapped onto all the other
features in the package.  The yy part of the name corresponds to this
designation, where eg means a package is an entrez gene package and sgd is a
package based on the sgd database etc.  In many cases the org packages will
contain more different kinds of information that the platform based ones,
since not all types of information are as widely sought after.


The \Rpackage{KEGG.db} library contains mappings between ids such as Entrez
Gene IDs and \Rpackage{GO} to \Rpackage{KEGG} pathway ids and thus also to
pathway names.  The \Rpackage{GO.db} library maintain the directed acyclic
graph structure of the original data from Gene Ontology Consortium by
providing mappings of GO ids to their direct parents or children for each of
the three categories (molecular function, cellular component, and biological
process). Mappings between Entrez Gene and \Rpackage{GO} ids are also
available to complement the the GO.db package. These mappings are found within
the organism wide packages mentioned above. These mappings are provided with
evidence code that specifies the type of evidence that supports the annotation
of a gene to a particular \Rpackage{GO} term.

\section*{Usage}

All the annotation libraries can be obtained from the Bioconductor web
site (\url{http://www.bioconductor.org}). To illustrate their usages,
we use the library for Affymetrix HG\_U95Av2 chip (\Rpackage{hgu95av2.db}) as
an example for platform specific data packages and the \Rpackage{GO.db} library for
non-platform specific data packages. We assume that R
(\url{www.r-project.org}) and Bioconductor's Biobase and annotation
libraries have already been installed.

\subsection*{Package installation}

After downloading libraries \Rpackage{hgu95av2.db} and \Rpackage{GO.db} by
using biocLite, If the \Rpackage{reposTools} library has already been
installed/loaded, typing \Rfunction{install.packages2(library name)} installs
the library for both Unix and Windows.

Typing library(library name) in an R session will load the library
into R. For example,

<<loadLibs>>=
library("annotate")
library("hgu95av2.db")
library("GO.db")
@

\subsection*{Documentations}

Each library contains documentation for the library in general and each of the
individual mapping objects contained by the library. Two documents at the
library level can be accessed by typing a library basename proceeded by a
question mark (e. g. ?hgu95av2) and the library basename followed by a pair of
brackets (e. g. hgu95av2()), respectively. The former explains what the
package is and details how a user can get more information, while the latter
lists all the mappings contained by a library and provides information on
the total number of keys within each of the maps contained by the library and
how many of these keys are annotated.  In addition, the latter will indicate
the sources for the information provided by the package as well as the date
that these sources claim to have last been updated.

The documentation for a given mapping object can be accessed by
typing the name of an mapping object proceeded by a question mark
(e. g. \Robject{hgu95av2GO}). The resulting documentation provides detail
explanations to the mapping object, data source used to build the
object, and example code for accessing annotation data.

\subsection*{Accessing annotation data within a library}

Annotation data of a given library are stored as mapping objects
in the form of key (items to be annotated) and value (annotation for
an key item) pairs. Each mapping object provides annotation for keys
for a particular subject reflected by the name of the object. For
example, \Robject{hgu95av2GO} annotates probes on the HG\-U95Av2 chip
with ids of the Gene Ontology terms the probes correspond to.

The name of an mapping object consists of package basename (\Rpackage{hgu95av2.db}) and
mapping name (\Rpackage{GO}) to avoid confusion when multiple libraries are loaded
to the system at the same time. Data contained by an mapping can
be accessed easily using Bioconductor's existing functions. For example, the following code
stores all the keys contained by the \Robject{hgu95av2GO} mapping object to
variable \textit{temp} and displays the first five keys on the screen:

<<getGO>>=
as.list(hgu95av2GO[5])
@

To obtain annotation for a given set of keys, one may use the
\Rfunction{mget} function. Suppose we have run an experiment using the
HG\_U95Av2 chip and found three genes represented by Affymetrix probe ids
\textit{738\_at, 40840\_at}, and \textit{41668\_r\_at} interesting. To
get the names of genes the three probe ids corresponding to, we do:

<<showmget>>=
mget(c("738_at", "40840_at", "41668_r_at"), hgu95av2GENENAME)
@

Similarly, identifiers of Gene Ontology terms corrsponding to the
three probes can be obtained as shown below:

<<moremget>>=
temp <- mget(c("41561_s_at", "40840_at", "41668_r_at"), hgu95av2GO)
@

In this case, the function \Rfunction{mget} returns a list of
pre-defined S4 objects containing data for the ids, ontology, and
evidence code of Gene Ontology terms corresponding to the three
keys. The following code shows how to access the GO id, evidence code
and ontology of the Gene Ontology term corresponding to probe id
\textit{40840\_at}:

<<gettingGO>>=
temp <- get("738_at", hgu95av2GO)
names(temp)
temp[["GO:0008253"]][["Evidence"]]
temp[["GO:0008253"]][["Ontology"]]
@

As shown above, probe \textit{40840\_at} can be annotated by three Gene
Ontology terms identified by \textit{GO:0005829}, \textit{GO:0008253}, and
\textit{GO:0016787}. The evidence code for \textit{GO:0008253} is
\textit{TAS} (traceable author statement) and it belongs to ontology
\textit{MF} (molecular function).

\subsection*{Accessing annotation data across libraries}

Often, data available in a given data package alone may not
be sufficient and need to be sought across packages. Bioconductor's
annotation data packages are linked by common public data identifiers
to allow traverse between packages (Fig. 1). Using the example above,
we know that probe id \textit{738\_at} are annotated by three Gene Ontology
ids \textit{GO:0005829}, \textit{GO:0008253}, and \textit{GO:0016787}. The Gene Ontology
terms for various Gene Ontology ids, however, are stored in another
package named \Rpackage{GO.db}. AS package \Rpackage{hgu95av2.db} and
\Rpackage{GO.db} are linked by \Rpackage{GO} ids, one can annotate probe id
\textit{738\_at} with Gene Ontology terms by linking data in the
two packages using \Rpackage{GO} id as shown below:

<<>>=
mget(names(get("738_at", hgu95av2GO)), GOTERM)
@

It turns out that probe id \textit{738\_at} (corresponding to \textit{GO:0008253}, and \textit{GO:0016787}) has molecular function (MF)
\textit{5'-nucleotidase activity} and \textit{hydrolase activity}.

\section{Session Information}

The version number of R and packages loaded for generating the vignette were:

<<echo=FALSE>>=
sessionInfo()
@

\end{document}