Deleting old shell code
git-svn-id: file:///humgen/gsa-scr1/gsa-engineering/svn_contents/trunk@4962 348d0f76-0448-11de-a6fe-93d51630548a
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java -Xmx40000m -cp ../java/dist/AnalysisTK.jar org.broadinstitute.sting.atk.PrepareROD REF_FILE_ARG=/seq/references/Homo_sapiens_assembly18/v0/Homo_sapiens_assembly18.fasta ROD_FILE=/seq/references/dbsnp/downloads/snp129_hg18.txt OUT=`echo $1/snp129_hg18.txt.rod` ROD_TYPE=dbSNP ROD_NAME=dbSNP
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#!/bin/tcsh
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foreach model (ONE_STATE THREE_STATE EMPIRICAL)
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java -Xmx4096m -jar ~/dev/GenomeAnalysisTK/trunk/dist/GenomeAnalysisTK.jar -l INFO -L 1:10,000,000-11,000,000 -R /broad/1KG/reference/human_b36_both.fasta -T SingleSampleGenotyper -I /humgen/gsa-scr1/GATK_Data/Validation_Data/NA12878.1kg.p2.chr1_10mb_11_mb.SLX.bam -varout ./$model.geli.calls -lod 5 -m $model
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end
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wc -l *.geli.calls
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md5sum *.geli.calls
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cd dist/packages/GATKResources
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tar cvhzf gatk_resources_062309.tgz resources
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#!/usr/bin/csh
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# ##############################################################################
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# this file can be used to diff the flagstat values for a whole genome,
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# along with sub-diffs for each chromosome. This may be helpful if you're
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# debugging a specific reads problem, and you want to know the differences
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# between the output of the GATK and samtools
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# ##############################################################################
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if ($#argv != 3) then
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echo "usage readStatsDiff <bamfile.bam> <referenceSequence.fasta> <outputFile>"; exit 1
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endif
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if (! -f $1) then
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echo bam file $2 does not seem to exist; exit 1
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endif
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if (! -f $2) then
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echo reference file $2 does not seem to exist; exit 1
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endif
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if ( -e $3) then
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echo output file $3 already exists!; exit 1
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endif
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# set the bam and the reference index
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set bam = $1
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set seq = $2
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set out = $3
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# diff the whole chromosome
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java -ea -Xmx4096m \
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-Xdebug -Xrunjdwp:transport=dt_socket,server=y,suspend=n,address=8015 \
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-jar dist/GenomeAnalysisTK.jar \
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-S SILENT \
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-T FlagStatRead \
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-I $bam \
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-R $seq \
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-oe 1.out
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samtools flagstat $bam > 2.out
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echo "\n" >> $out
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echo results for whole bam file >> $out
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echo "\n" >> $out
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diff 1.out 2.out >> $out
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rm 1.out
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rm 2.out
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foreach chromosome (chr1 chr2 chr3 chr4 chr5 chr6 chr7 chr8 chr9 chr10 chr11 chr12 chr13 chr14 chr15 chr16 chr17 chr18 chr19 chr20 chr21 chr22 chrX)
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java -ea -Xmx4096m \
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-Xdebug -Xrunjdwp:transport=dt_socket,server=y,suspend=n,address=8015 \
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-jar dist/GenomeAnalysisTK.jar \
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-S SILENT \
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-T FlagStatRead \
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-I $bam \
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-R $seq \
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-oe 1.out \
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-L $chromosome
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samtools view -h -b $bam $chromosome > temp.bam
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samtools flagstat temp.bam > 2.out
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echo results for $chromosome >> $out
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echo "\n" >> $out
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diff 1.out 2.out >> $out
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rm temp.bam
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rm 1.out
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rm 2.out
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end
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#!/bin/tcsh
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setenv HERE java
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setenv HERE "java tribble"
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setenv THERE \~/dev/GenomeAnalysisTKFromLaptop/trunk
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rsync -e ssh -aCvz $HERE depristo@gsa2:$THERE
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rsync -e ssh -aCvz $HERE depristo@gsa1:$THERE
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