[Patchwork-commits] r32 - in pkg/patchwork: R man

noreply at r-forge.r-project.org noreply at r-forge.r-project.org
Tue Nov 29 12:05:00 CET 2011


Author: sebastian_d
Date: 2011-11-29 12:04:59 +0100 (Tue, 29 Nov 2011)
New Revision: 32

Modified:
   pkg/patchwork/R/patchwork.findCNs.r
   pkg/patchwork/man/karyotype.Rd
   pkg/patchwork/man/karyotype_chroms.Rd
   pkg/patchwork/man/karyotype_chromsCN.Rd
   pkg/patchwork/man/patchwork.CNA.Rd
   pkg/patchwork/man/patchwork.findCNs.Rd
   pkg/patchwork/man/subfunctions_findCNs.Rd
Log:
More documentation and code updates.

Modified: pkg/patchwork/R/patchwork.findCNs.r
===================================================================
--- pkg/patchwork/R/patchwork.findCNs.r	2011-11-28 16:34:09 UTC (rev 31)
+++ pkg/patchwork/R/patchwork.findCNs.r	2011-11-29 11:04:59 UTC (rev 32)
@@ -1,4 +1,4 @@
-patchwork.findCNs = function(cn2=NULL,delta=NULL,het=NULL,hom=NULL,maxCn=8,ceiling=1)
+patchwork.findCNs = function(cn2,delta,het,hom,maxCn=8,ceiling=1)
 	{
 	
 	packagepath = system.file(package="patchwork")

Modified: pkg/patchwork/man/karyotype.Rd
===================================================================
--- pkg/patchwork/man/karyotype.Rd	2011-11-28 16:34:09 UTC (rev 31)
+++ pkg/patchwork/man/karyotype.Rd	2011-11-29 11:04:59 UTC (rev 32)
@@ -12,7 +12,7 @@
 }
 
 \usage{
-karyotype(chr,start,end,int,ai,name,xlim,ylim)
+karyotype(chr,start,end,int,ai,chroms,name,xlim,ylim)
 }
 
 \arguments{
@@ -47,8 +47,8 @@
 }
 
 \details{
-Vertical axis: Allelic imbalance. \\
-Horizontal axis: Total intensity. \\
+Vertical axis: Allelic imbalance. \cr
+Horizontal axis: Total intensity. \cr
 
 The plot is a overview, for a closer look see the plots generated by karyotype_chroms().
 }

Modified: pkg/patchwork/man/karyotype_chroms.Rd
===================================================================
--- pkg/patchwork/man/karyotype_chroms.Rd	2011-11-28 16:34:09 UTC (rev 31)
+++ pkg/patchwork/man/karyotype_chroms.Rd	2011-11-29 11:04:59 UTC (rev 32)
@@ -66,9 +66,9 @@
 \details{
 Walkthrough of the plot:
 
-\textbf{TOP} \\
-Vertical axis: Allelic Imbalance \\
-Horizontal axis: Total Intensity \\
+\bold{TOP} \cr
+Vertical axis: Allelic Imbalance \cr
+Horizontal axis: Total Intensity \cr
 
 The chromosome plotted against the complete genome background. The separation between
 clusters within the plot are due to the fluctuating intensity and allelic imbalance
@@ -76,15 +76,15 @@
 Longer/larger segments have bigger circles. Darker circles show more content as they are
 ontop of eachother.
 
-\textbf{MIDDLE} \\
-Vertical axis: Total Intensity \\
-Horizontal axis: Chromosomal coordinate \\
+\bold{MIDDLE} \cr
+Vertical axis: Total Intensity \cr
+Horizontal axis: Chromosomal coordinate \cr
 
 The chromosome in questions total intensity plotted against the position on the chromosome.
 
-\textbf{BOTTOM} \\
-Vertical axis: Allelic Imbalance \\
-Horizontal axis: Chromosomal coordinate \\
+\bold{BOTTOM} \cr
+Vertical axis: Allelic Imbalance \cr
+Horizontal axis: Chromosomal coordinate \cr
 
 The chromosome in questions allelic imbalance plotted against the position on the chromosome.
 }

Modified: pkg/patchwork/man/karyotype_chromsCN.Rd
===================================================================
--- pkg/patchwork/man/karyotype_chromsCN.Rd	2011-11-28 16:34:09 UTC (rev 31)
+++ pkg/patchwork/man/karyotype_chromsCN.Rd	2011-11-29 11:04:59 UTC (rev 32)
@@ -13,7 +13,7 @@
 }
 
 \usage{
-karyotype_chromsCN(chr,start,end,int,ai,chroms,mchr,mpos,mval,schr,spos,sval,name,xlim,ylim,maxCN=8)
+karyotype_chromsCN(chr,start,end,int,ai,Cn,mCn,mchr,mpos,mval,schr,spos,sval,name='',xlim=c(-1.02,1.82),ylim=0:1,maxCn=8)
 }
 
 \arguments{
@@ -32,9 +32,12 @@
 	\item{ai}{					%segs$ai
   	Allelic imbalance.
 	}
-	\item{chroms}{
-  	Object created in patchwork.CNA which holds chromosome names.
+	\item{Cn}{
+  	Copy number.
 	}
+	\item{mCn}{
+  	mCn.
+	}
 	\item{mchr}{
 	Chromosomes name of kbsegs object. Final version of kbsegs created from patchwork.smoothing().
 	}
@@ -57,12 +60,12 @@
   	Name of sample. patchwork.CNA sends it as name of the bamfile.
 	}
   	\item{xlim}{
-  	Default is c(0,2.4). Limit of x axis.
+  	Default is c(-1.02,1.82). Limit of x axis.
 	}
   	\item{ylim}{
-  	Default is c(0.3,1). Limit of y axis.
+  	Default is 0:1. Limit of y axis.
 	}
-	\item{maxCN}{
+	\item{maxCn}{
 	Default is 8. The highest copynumber of the sample to check for.
 	}
 }
@@ -70,9 +73,9 @@
 \details{
 Walkthrough of the plot:
 
-\textbf{TOP} \\
-Vertical axis: Allelic Imbalance \\
-Horizontal axis: Total Intensity \\
+\bold{TOP} \cr
+Vertical axis: Allelic Imbalance \cr
+Horizontal axis: Total Intensity \cr
 
 The chromosome plotted against the complete genome background. The separation between
 clusters within the plot are due to the fluctuating intensity and allelic imbalance
@@ -80,21 +83,21 @@
 Longer/larger segments have bigger circles. Darker circles show more content as they are
 ontop of eachother.
 
-\textbf{TOP MIDDLE} \\
-Vertical axis: Copynumber \\
-Horizontal axis: Chromosomal coordinate \\
+\bold{TOP MIDDLE} \cr
+Vertical axis: Copynumber \cr
+Horizontal axis: Chromosomal coordinate \cr
 
 Displays the total and minor copynumbers for different segments of the chromosome in question.
 
-\textbf{LOWER MIDDLE} \\
-Vertical axis: Total Intensity \\
-Horizontal axis: Chromosomal coordinate \\
+\bold{LOWER MIDDLE} \cr
+Vertical axis: Total Intensity \cr
+Horizontal axis: Chromosomal coordinate \cr
 
 The chromosome in questions total intensity plotted against the position on the chromosome.
 
-\textbf{BOTTOM} \\
-Vertical axis: Allelic Imbalance \\
-Horizontal axis: Chromosomal coordinate \\
+\bold{BOTTOM} \cr
+Vertical axis: Allelic Imbalance \cr
+Horizontal axis: Chromosomal coordinate \cr
 
 The chromosome in questions allelic imbalance plotted against the position on the chromosome.
 }
@@ -121,9 +124,9 @@
 
 %% ~Make other sections like Warning with \section{Warning }{....} ~
 
-%\seealso{
-%% ~~objects to See Also as \code{\link{help}}, ~~~
-%}
+\seealso{
+\code{\link{patchwork.findCNs}}
+}
 
 %\examples{
 %##---- Should be DIRECTLY executable !! ----

Modified: pkg/patchwork/man/patchwork.CNA.Rd
===================================================================
--- pkg/patchwork/man/patchwork.CNA.Rd	2011-11-28 16:34:09 UTC (rev 31)
+++ pkg/patchwork/man/patchwork.CNA.Rd	2011-11-29 11:04:59 UTC (rev 32)
@@ -45,7 +45,7 @@
 }
 
 \details{
-\textbf{Make sure to only run one sample at a time in a single working directory
+\bold{Make sure to only run one sample at a time in a single working directory
 as standard file names are created. If you do not heed this warning you
 will end up with a complete mess and probably runtime errors as patchwork.readChroms
 tries to run simultaniously for multiple samples in the same working directory.}

Modified: pkg/patchwork/man/patchwork.findCNs.Rd
===================================================================
--- pkg/patchwork/man/patchwork.findCNs.Rd	2011-11-28 16:34:09 UTC (rev 31)
+++ pkg/patchwork/man/patchwork.findCNs.Rd	2011-11-29 11:04:59 UTC (rev 32)
@@ -1,41 +1,44 @@
 \name{patchwork.findCNs}
+\alias{patchwork.findCNs}
 \alias{findCNs}
-\alias{patchwork.findCNs}
 
+
 \title{
-Function to find Copy Numbers
+Function plot allele-specific copy numbers of the genome
 }
 
 \description{
-Given input data from user regarding plots generated through patchwork.CNA
-this function will find copy numbers or something..
+Input data for this function should be assessed from any of the karyotype_chroms()
+plots. For example <yoursample>_karyotype.chr<1-22,X,Y>.png.
 
-Very important: For this function to work you must have the file findCNs.Rdata,
-generated using patchwork.CNA function, in your working directory!
+See argument details.
+
+\bold{Very important: For this function to work you must have the file findCNs.Rdata,
+generated using patchwork.CNA function, in your working directory!}
 }
 
 \usage{
-patchwork.findCNs(cn2=NULL,delta=NULL,het=NULL,hom=NULL,maxCn=8,ceiling=1))
+patchwork.findCNs(cn2,delta,het,hom,maxCn=8,ceiling=1)
 }
 
 \arguments{
   \item{cn2}{
-	description
+	The approximate position of copy number two on total intensity axis.
 	}
   \item{delta}{
-	description
+	The difference in total intensity between consecutive copy numbers. For example 1 and 2 or 2 and 3.
 	}
   \item{het}{
-	description
+	Allelic imbalance ratio of heterozygous copy number 2.
 	}
   \item{hom}{
-	description
+	Allelic imbalance ratio of Loss-of-heterozygosity copy number 2.
 	}
   \item{maxCn}{
-	description
+	Highest copy number to calculate for. Default is 8.
 	}
   \item{ceiling}{
-	description
+	Default is 1.
 	}
 }
 
@@ -70,7 +73,7 @@
 
 \seealso{
 \code{\link{patchwork.CNA}}
-\code{\link{subfunctions_findCNss}}
+\code{\link{subfunctions_findCNs}}
 }
 
 %\examples{

Modified: pkg/patchwork/man/subfunctions_findCNs.Rd
===================================================================
--- pkg/patchwork/man/subfunctions_findCNs.Rd	2011-11-28 16:34:09 UTC (rev 31)
+++ pkg/patchwork/man/subfunctions_findCNs.Rd	2011-11-29 11:04:59 UTC (rev 32)
@@ -25,19 +25,19 @@
 
 \arguments{
   \item{data}{
-  	description
+  	Object to be handled by the internal function.
 	}
   \item{weights}{
-	description
+	Weights to be applied.
 	}
   \item{vector}{
 	The segs objects chr column.
 	}
 }
 
-\details{
-Details
-}
+%\details{
+%Details
+%}
 
 %\value{
 %%  ~Describe the value returned



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