# HG changeset patch
# User fcaramia
# Date 1354495666 18000
# Node ID 576f9c85da252eb1ececdc2faa14bada8e246cf6
# Parent 3259b48e82c086cadaac6c2fbb96b27c1e8963b8
Deleted selected files
diff -r 3259b48e82c0 -r 576f9c85da25 Contra/baseline.xml
--- a/Contra/baseline.xml Sun Dec 02 19:46:37 2012 -0500
+++ /dev/null Thu Jan 01 00:00:00 1970 +0000
@@ -1,69 +0,0 @@
-
- : Control files for Contra
-
- bedtools
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- baseline_wrapper.pl
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- ##Required files
- "PLAYEROPTION::-t=$target_file"
-
- #for $group in $file_group
- "BAMLISTENTRY::${group.bam}"
- #end for
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- "PLAYEROPTION::--name=$sampleName"
- "PLAYEROPTION::--trim=$trim"
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- ##File to generate the bam list
- "BASELINEOUTPUT::$baseline_output"
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-**Reference**
- http://contra-cnv.sourceforge.net/
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------
-
-**What it does**
-
-Creating a baseline control from multiple samples is can be useful when a matched control is not available. In the CONTRA download page, we have provided several baseline files for some of the platforms that we have tried. Alternatively, the “baseline.py” script that comes with CONTRA can be used to generate a custom baseline file.
-
------
-
-**Parameters**
-
-::
-
- -t, --target Target region definition file [REQUIRED] [BED format]
-
- -f, --files Files to be converted to baselines [REQUIRED] [BAM]
-
- -o, --output Output folder [REQUIRED]
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- -c, --trim Portion of outliers to be removed before calculating
- average [Default: 0.2]
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- -n, --name Output baseline file name [Default: baseline]
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diff -r 3259b48e82c0 -r 576f9c85da25 Contra/contra.xml
--- a/Contra/contra.xml Sun Dec 02 19:46:37 2012 -0500
+++ /dev/null Thu Jan 01 00:00:00 1970 +0000
@@ -1,286 +0,0 @@
-
- : Copy Number Analysis for Targeted Resequencing
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- bedtools
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- contra_wrapper.pl
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- ##Ref Genome
- #if $genomeSource.refGenomeSource == "history":
- "PLAYEROPTION::-f=${genomeSource.ownFile}"
- #else:
- ##use precomputed indexes
- "PLAYEROPTION::-f=${genomeSource.indices.fields.path}"
- #end if
-
- ##Required files
- "PLAYEROPTION::-t=$target_file"
- "PLAYEROPTION::-s=$alignment_file"
- #if $controlSource.refControlSource == "history":
- "PLAYEROPTION::-c=${controlSource.control_file}"
- #else:
- ##use precomputed indexes
- "PLAYEROPTION::-c=${controlSource.indices.fields.path}"
- #end if
-
- ##Optional parameter
-
- #if $option.option == "modify_parameters":
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- "PLAYEROPTION::--numBin=$option.numBin"
- "PLAYEROPTION::--minReadDepth=$option.minReadDepth"
- "PLAYEROPTION::--minNBases=$option.minNbases"
-
- #if str($option.sam) == "true":
- "PLAYEROPTION::--sam"
- #end if
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- #if str($option.bed) == "true":
- "PLAYEROPTION::--bed"
- #end if
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- "PLAYEROPTION::--pval=$option.pval"
- "PLAYEROPTION::--sampleName=$option.sampleName"
-
- #if str($option.nomultimapped) == "true":
- "PLAYEROPTION::--nomultimapped"
- #end if
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- #if str($option.plot) == "true":
- "PLAYEROPTION::--plot"
- #end if
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- "PLAYEROPTION::--minExon=$option.minExon"
- "PLAYEROPTION::--minControlRdForCall=$option.minControlRdForCall"
- "PLAYEROPTION::--minTestRdForCall=$option.minTestRdForCall"
- "PLAYEROPTION::--minAvgForCall=$option.minAvgForCall"
- "PLAYEROPTION::--maxRegionSize=$option.maxRegionSize"
- "PLAYEROPTION::--targetRegionSize=$option.targetRegionSize"
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- #if str($option.largedeletion) == "true":
- "PLAYEROPTION::--largedeletion"
- #end if
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- "PLAYEROPTION::--smallSegment=$option.smallSegment"
- "PLAYEROPTION::--targetRegionSize=$option.targetRegionSize"
- "PLAYEROPTION::--largeSegment=$option.largeSegment"
- "PLAYEROPTION::--lrCallStart=$option.lrCallStart"
- "PLAYEROPTION::--lrCallEnd=$option.lrCallEnd"
- "PLAYEROPTION::--passSize=$option.passSize"
- #end if
-
- ##File to generate the bam list
- CONTRAOUTPUT::$html_file
- CONTRADIR::$html_file.files_path
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-**Reference**
- http://contra-cnv.sourceforge.net/
-
------
-
-**What it does**
-
-CONTRA is a tool for copy number variation (CNV) detection for targeted resequencing data such as those from whole-exome capture data. CONTRA calls copy number gains and losses for each target region with key strategies include the use of base-level log-ratios to remove GC-content bias, correction for an imbalanced library size effect on log-ratios, and the estimation of log-ratio variations via binning and interpolation. It takes standard alignment formats (BAM/SAM) and output in variant call format (VCF 4.0) for easy integration with other next generation sequencing analysis package.
-
-
------
-
-**Required Parameters**
-
-::
-
- -t, --target Target region definition file [BED format]
-
- -s, --test Alignment file for the test sample [BAM/SAM]
-
- -c, --control Alignment file for the control sample
- [BAM/SAM/BED – baseline file]
-
- --bed **option has to be supplied for control
- with baseline file.**
-
- -f, --fasta Reference genome [FASTA]
-
- -o, --outFolder the folder name (and its path) to store the output
- of the analysis (this new folder will be created –
- error message occur if the folder exists)
-
------
-
-**Optional Parameters**
-
-::
-
- --numBin Numbers of bins to group the regions. User can
- specify multiple experiments with different numbers
- of bins (comma separated). [Default: 20]
-
- --minReadDepth The threshold for minimum read depth for each bases
- (see Step 2 in CONTRA workflow) [Default: 10]
-
- --minNBases The threshold for minimum number of bases for each
- target regions (see Step 2 in CONTRA workflow)
- [Default: 10]
-
- --sam If the specified test and control samples are in
- SAM format. [Default: False] (It will always take
- BAM samples as default)
-
- --bed If specified, control will be a baseline file in
- BED format. [Default: False]
- Please refer to the Baseline Script section for
- instruction how to create baseline files from set
- of BAMfiles. A set of baseline files from different
- platform have also been provided in the CONTRA
- download page.
-
- --pval The p-value threshold for filtering. Based on Adjusted
- P-Values. Only regions that pass this threshold will
- be included in the VCF file. [Default: 0.05]
-
- --sampleName The name to be appended to the front of the default output
- name. By default, there will be nothing appended.
-
- --nomultimapped The option to remove multi-mapped reads
- (using SAMtools with mapping quality > 0).
- [default: FALSE]
-
- -p, --plot If specified, plots of log-ratio distribution for each
- bin will be included in the output folder [default: FALSE]
-
- --minExon Minimum number of exons in one bin (if less than this number
- , bin that contains small number of exons will be merged to
- the adjacent bins) [Default : 2000]
-
- --minControlRdForCall Minimum Control ReadDepth for call [Default: 5]
-
- --minTestRdForCall Minimum Test ReadDepth for call [Default: 0]
-
- --minAvgForCall Minimum average coverage for call [Default: 20]
-
- --maxRegionSize Maximum region size in target region (for breaking
- large regions into smaller regions. By default,
- maxRegionSize=0 means no breakdown). [Default : 0]
-
- --targetRegionSize Target region size for breakdown (if maxRegionSize
- is non-zero) [Default: 200]
-
- -l, --largeDeletion If specified, CONTRA will run large deletion analysis (CBS).
- User must have DNAcopy R-library installed to run the
- analysis. [False]
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- --smallSegment CBS segment size for calling large variations [Default : 1]
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- --largeSegment CBS segment size for calling large variations [Default : 25]
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- --lrCallStart Log ratios start range that will be used to call CNV
- [Default : -0.3]
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- --lrCallEnd Log ratios end range that will be used to call CNV
- [Default : 0.3]
-
- --passSize Size of exons that passed the p-value threshold compare
- to the original exons size [Default: 0.5]
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