[Patchwork-commits] r55 - in pkg/patchwork: . R man
noreply at r-forge.r-project.org
noreply at r-forge.r-project.org
Wed Dec 14 16:23:20 CET 2011
Author: sebastian_d
Date: 2011-12-14 16:23:19 +0100 (Wed, 14 Dec 2011)
New Revision: 55
Modified:
pkg/patchwork/DESCRIPTION
pkg/patchwork/R/patchwork.readChroms.r
pkg/patchwork/man/karyotype.Rd
pkg/patchwork/man/karyotype_chroms.Rd
pkg/patchwork/man/patchwork.findCNs.Rd
Log:
some small fixes to get the new data system working
Modified: pkg/patchwork/DESCRIPTION
===================================================================
--- pkg/patchwork/DESCRIPTION 2011-12-14 14:23:48 UTC (rev 54)
+++ pkg/patchwork/DESCRIPTION 2011-12-14 15:23:19 UTC (rev 55)
@@ -7,5 +7,4 @@
Maintainer: Markus Rasmussen <Markus.Rasmussen at medsci.uu.se>
Description: Performs a copy number analysis of whole genome data.
License: GPL-2
-LazyLoad: no
Imports: DNAcopy,patchworkData
Modified: pkg/patchwork/R/patchwork.readChroms.r
===================================================================
--- pkg/patchwork/R/patchwork.readChroms.r 2011-12-14 14:23:48 UTC (rev 54)
+++ pkg/patchwork/R/patchwork.readChroms.r 2011-12-14 15:23:19 UTC (rev 55)
@@ -52,7 +52,6 @@
readlength=80 # this is currently hard coded and may be adjusted.
seglength=200 # (do not change)
data=NULL
- tmp = NULL
for (c in chroms)
{
@@ -62,8 +61,7 @@
system(paste("python .python/Pysamloader.py ",BamFile," ",c,sep =""))
# Load the newly created position file
unix = read.csv(".Tmp_chr_pos",sep='',header=F)$V1 + readlength/2
- tmp = paste(c,".mark",sep="")
- load(paste(datapath,"/data/",c,".mark.RData",sep=""))
+ gc = readRDS(paste(datapath,"/extdata/",c,".mark.rds",sep=""))
xpos=gc[,1]
xgc=gc[,2]
xgck=gc[,3]
Modified: pkg/patchwork/man/karyotype.Rd
===================================================================
--- pkg/patchwork/man/karyotype.Rd 2011-12-14 14:23:48 UTC (rev 54)
+++ pkg/patchwork/man/karyotype.Rd 2011-12-14 15:23:19 UTC (rev 55)
@@ -12,7 +12,7 @@
}
\usage{
-karyotype(chr,start,end,int,ai,chroms,name,xlim,ylim)
+karyotype(chr,start,end,int,ai,name,xlim,ylim)
}
\arguments{
@@ -31,9 +31,6 @@
\item{ai}{ %segs$ai
Allelic imbalance.
}
- \item{chroms}{
- Object created in patchwork.CNA which holds chromosome names.
- }
\item{name}{
Default is the name of the input BamFile from patchwork.CNA().
Plot generated as "name.karyotype.png" in your working directory.
Modified: pkg/patchwork/man/karyotype_chroms.Rd
===================================================================
--- pkg/patchwork/man/karyotype_chroms.Rd 2011-12-14 14:23:48 UTC (rev 54)
+++ pkg/patchwork/man/karyotype_chroms.Rd 2011-12-14 15:23:19 UTC (rev 55)
@@ -12,7 +12,7 @@
}
\usage{
-karyotype_chroms(chr,start,end,int,ai,chroms,mchr,mpos,mval,schr,spos,sval,name,xlim,ylim)
+karyotype_chroms(chr,start,end,int,ai,mchr,mpos,mval,schr,spos,sval,name,xlim,ylim)
}
\arguments{
@@ -31,9 +31,6 @@
\item{ai}{ %segs$ai
Allelic imbalance.
}
- \item{chroms}{
- Object created in patchwork.CNA which holds chromosome names.
- }
\item{mchr}{
Chromosomes name of kbsegs object. Final version of kbsegs created from patchwork.smoothing().
}
Modified: pkg/patchwork/man/patchwork.findCNs.Rd
===================================================================
--- pkg/patchwork/man/patchwork.findCNs.Rd 2011-12-14 14:23:48 UTC (rev 54)
+++ pkg/patchwork/man/patchwork.findCNs.Rd 2011-12-14 15:23:19 UTC (rev 55)
@@ -73,8 +73,8 @@
%% ~Make other sections like Warning with \section{Warning }{....} ~
\seealso{
-\code{\link{patchwork.CNA}} \cr
-\code{\link{subfunctions_findCNs}}
+\code{\link[patchwork]{patchwork.CNA}} \cr
+\code{\link[patchwork]{subfunctions_findCNs}}
}
%\examples{
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