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July 14, 2023 10:02
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Rnw vignette from the `annotate` package
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% \VignetteIndexEntry{Using Affymetrix Probe Level Data} | |
% \VignetteDepends{hgu95av2.db, rae230a.db, rae230aprobe, Biostrings} | |
% \VignetteKeywords{Annotation} | |
%\VignettePackage{annotate} | |
\documentclass{article} | |
\newcommand{\Rfunction}[1]{{\texttt{#1}}} | |
\newcommand{\Rmethod}[1]{{\texttt{#1}}} | |
\newcommand{\Robject}[1]{{\texttt{#1}}} | |
\newcommand{\Rpackage}[1]{{\textit{#1}}} | |
\newcommand{\Rclass}[1]{{\textit{#1}}} | |
\usepackage{hyperref} | |
\usepackage[authoryear,round]{natbib} | |
\usepackage{times} | |
\begin{document} | |
\title{Using Probe Information} | |
\author{Robert Gentleman} | |
\date{} | |
\maketitle | |
\section*{Overview} | |
The Bioconductor project maintains a rich body of annotation data | |
assembled into R libraries. For many different Affymetrix chips | |
information is provided on both the sequence of the mRNA that was | |
intended to be matched and the actual 25mers that were used for the | |
bindings. In this vignette we show how to make use of the probe | |
information. | |
\section*{A Simple Example} | |
To demonstrate the use of probe level data we will use the | |
\texttt{rae230a} chip (for rats). So we first need to load these | |
libraries. | |
<<loadlibs, results=hide>>= | |
library("annotate") | |
library("rae230a.db") | |
library("rae230aprobe") | |
@ | |
Now, we do not have any data so all we are going to do is to examine | |
the probe data and show how to use some of the different Bioconductor | |
tools to access that information, and potentially check on the mapping | |
information that has been given. | |
We will select a probe set, | |
<<selprobe>>= | |
ps = names(as.list(rae230aACCNUM)) | |
myp = ps[1001] | |
myA = get(myp, rae230aACCNUM) | |
wp = rae230aprobe$Probe.Set.Name == myp | |
myPr = rae230aprobe[wp,] | |
@ | |
The probe data is stored as a \Rclass{data.frame} with 6 columns. They | |
are | |
\begin{description} | |
\item[sequence] The sequence of the 25mer | |
\item[x] The x position of the probe on the array. | |
\item[y] The y position of the probe on the array. | |
\item[Probe.Set.Name] The Affymetrix ID for the probe set. | |
\item[Probe.Interrogation.Position] The location (in bases) of the | |
13th base in the 25mer, in the target sequence. | |
\item[Target.Strandedness] Whether the 25mer is a Sense or an | |
Antisense match to the target sequence. | |
\end{description} | |
We note that it is not always the case that the sequence reported is | |
found in the reference or if it is, it is not always at the location | |
reported. One can check that using other tools available in the | |
\Rpackage{annotate} package and in the \Rpackage{Biostrings} package. | |
%%FIXME: need to check for connectivity | |
<<getACC>>= | |
myseq = getSEQ(myA) | |
nchar(myseq) | |
library("Biostrings") | |
mybs = DNAString(myseq) | |
match1 = matchPattern(as.character(myPr[1,1]), mybs) | |
match1 | |
as.matrix(ranges(match1)) | |
myPr[1,5] | |
@ | |
And we can see that in this case the 13th nucleotide is indeed in | |
exactly the place that has been predicted. | |
One additional thing to note is that Affymetrix does not accurately report the strandedness of the | |
probes, so it is necessary to check the reverse complement of the sequence prior to | |
assuming that the probe does not interrogate the correct gene. | |
<<getRev>>= | |
myp = ps[100] | |
myA = get(myp, rae230aACCNUM) | |
wp = rae230aprobe$Probe.Set.Name == myp | |
myPr = rae230aprobe[wp,] | |
myseq = getSEQ(myA) | |
mybs = DNAString(myseq) | |
Prstr = as.character(myPr[1,1]) | |
match2 = matchPattern(Prstr, mybs) | |
## expecting 0 (no match) | |
length(match2) | |
match2 = matchPattern(reverseComplement(DNAString(Prstr)), mybs) | |
nchar(match2) | |
nchar(myseq) - as.matrix(ranges(match2)) | |
myPr[1,5] | |
@ | |
Again, we see that the 13th nucleotide is exactly where predicted. It is relatively | |
straightforward to check the other 25mers, and to develop different | |
visualization tools that can be used to investigate the available data. | |
\section*{Other Sources of Information} | |
There are other tools available that may also be of some interest. For instance, the | |
Mental Health Research Institute at the University of Michigan have various custom | |
cdf files for Affymetrix data analysis that have been updated using more current annotation | |
information from GenBank and Ensembl. | |
\url {http://brainarray.mhri.med.umich.edu/Brainarray/Database/CustomCDF/genomic_curated_CDF.asp} | |
The Weizmann Institute of Science have a database that can be queried to get the sensitivity and specificity | |
for the probes on the Affymetrix HG-U95av2 chip. Although the information here is limited to a particular chip, | |
this general idea is something that an enterprising end-user might want to replicate for other chips. | |
\url {http://genecards.weizmann.ac.il/geneannot/} | |
\section{Session Information} | |
The version number of R and packages loaded for generating the vignette were: | |
<<echo=FALSE>>= | |
sessionInfo() | |
@ | |
\end{document} |
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