r-bioc-geneplotter 1.56.0-1 / usr / lib / R / site-library / geneplotter / doc / byChroms.Rnw

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%
% NOTE -- ONLY EDIT THE .Rnw FILE!!!  The .tex file is
% likely to be overwritten.
%
% \VignetteIndexEntry{How to assemble a chromLocation object}
% \VignetteAuthor{R. Gentleman}
%\VignetteDepends{annotate, hu6800.db}
%\VignetteKeywords{chromosomes}
%\VignettePackage{geneplotter}
\documentclass[12pt]{article}

\usepackage{amsmath}
\usepackage{hyperref}

\newcommand{\Rfunction}[1]{{\texttt{#1}}}
\newcommand{\Robject}[1]{{\texttt{#1}}}
\newcommand{\Rpackage}[1]{{\textit{#1}}}


\textwidth=6.2in
\textheight=8.5in
%\parskip=.3cm
\oddsidemargin=.1in
\evensidemargin=.1in
\headheight=-.3in

\newcommand{\scscst}{\scriptscriptstyle}
\newcommand{\scst}{\scriptstyle}

\bibliographystyle{plainnat}

\begin{document}

\section*{How to Assemble a chromLocation Object}


In order to use the various \Rpackage{geneplotter} functions you will
need to assemble an object of class \Robject{chromLocation}.
This is relatively straightforward if you have access to a Bioconductor
data package. In this example we will consider using the
\Rpackage{hu6800.db} data package to construct our object. This vignette
was built with version \Sexpr{packageDescription("hu6800.db")$Version} of
the package.

<<loaddata>>=

 library("annotate")
 library("hu6800.db")
 lens <- unlist(eapply(hu6800CHR, length))

 table(lens)
 wh2 = mget(names(lens)[lens==2], env = hu6800CHR)

 wh2[1]
@

So somehow \Sexpr{length(wh2)} of the genes are mapped to two
 different chromosomes.  Based on OMIM the these genes are localized
 to the so called \textit{pseudoautosomal region} where the X and Y
 cromosomes are similar and there is actual recombination going on
 between them. So, we will take the expedient measure of assigning
 each of them to just one chromosome.

<<fixdata>>=
chrs2 <- unlist(eapply(hu6800CHR, function(x) x[1]))
chrs2 <- factor(chrs2)
length(chrs2)
 table(unlist(chrs2))
@

Now we are ready to obtain the chromosome location data and
orientation.  The chromosome location data tells us the (approximate)
location of the gene on the chromosome.  The positions for both the
sense and antisense strand are number of base pairs measured from the
p (5' end of the sense strand) to q (3' end of the sense strand) arms.
Chromosomes are double stranded and the gene is encoded on only one of
those two strands. The strands are labeled plus and minus (sense and
antisense).  We use both the location and the orientation when making
plots.

<<strandloc>>=

 strand <- as.list(hu6800CHRLOC)

 splits <- split(strand, chrs2)
 length(splits)
 names(splits)

@

Now we have processed the data and are ready to construct a new
\Robject{chromLocation} object.

<<chrloc>>=

 newChrClass <- buildChromLocation("hu6800")

@

And finally we can test it by calling \Rfunction{cPlot}.

<<cPlot, fig=TRUE>>=

  library(geneplotter)

  cPlot(newChrClass)

@

\end{document}

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