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comp-metadata/docs/quantification/dnase-seq/DHSv1.xml
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<?xml version="1.0"?> | |
<?xml-stylesheet type="text/css" href="http://deep.mpi-inf.mpg.de/DAC/files/style/deep_process_style.css"?> | |
<process> | |
<name>DHS</name> | |
<version>1</version> | |
<author> | |
<name>Karl Nordström, Peter Ebert</name> | |
<email>karl.nordstroem@uni-saarland.de, pebert@mpi-inf.mpg.de</email> | |
</author> | |
<description> | |
Process DHS is modelled using the CHP process as blueprint | |
</description> | |
<inputs> | |
<filetype> | |
<identifier>ALNvX_dnase.bam</identifier> | |
<format></format> | |
<quantity>single</quantity> | |
<comment></comment> | |
</filetype> | |
<filetype> | |
<identifier>ALNvX.bai</identifier> | |
<format></format> | |
<quantity>single</quantity> | |
<comment>Index files are renamed internally to .bam.bai since deepTools is expecting index naming like this</comment> | |
</filetype> | |
</inputs> | |
<references> | |
<filetype> | |
<identifier>reference_genome</identifier> | |
<format>2bit</format> | |
<quantity>single</quantity> | |
<comment>The reference genome file; see DCC/download/results/references/genomes</comment> | |
</filetype> | |
<filetype> | |
<identifier>plot_regions</identifier> | |
<format>BED</format> | |
<quantity>single</quantity> | |
<comment>Control regions?</comment> | |
</filetype> | |
</references> | |
<outputs> | |
<filetype> | |
<identifier>samplesID.PROCESS.DATE.corplot.cormethod</identifier> | |
<format>deepTools graphics PNG</format> | |
<quantity>single</quantity> | |
<comment></comment> | |
</filetype> | |
<filetype> | |
<identifier>samplesID.PROCESS.DATE.fgprplot</identifier> | |
<format>deepTools graphics PNG</format> | |
<quantity>single</quantity> | |
<comment></comment> | |
</filetype> | |
<filetype> | |
<identifier>sampleID.PROCESS.DATE.gcbplot</identifier> | |
<format>deepTools graphics PNG</format> | |
<quantity>collection</quantity> | |
<comment></comment> | |
</filetype> | |
<filetype> | |
<identifier>sampleID.PROCESS.DATE.gcbfreq</identifier> | |
<format>tab-separated text file</format> | |
<quantity>collection</quantity> | |
<comment></comment> | |
</filetype> | |
<filetype> | |
<identifier>sampleIDs.PROCESS.DATE.bamcomp.scalemethod</identifier> | |
<format>bigwig</format> | |
<quantity>collection</quantity> | |
<comment>Always compare a signal vs the input</comment> | |
</filetype> | |
<filetype> | |
<identifier>sampleID.PROCESS.DATE.bamcov.seqDepthNorm</identifier> | |
<format>bigwig</format> | |
<quantity>collection</quantity> | |
<comment></comment> | |
</filetype> | |
<filetype> | |
<identifier>sampleID.PROCESS.DATE.ctrlreg</identifier> | |
<format>graphics PNG</format> | |
<quantity>collection</quantity> | |
<comment></comment> | |
</filetype> | |
</outputs> | |
<software> | |
<tool> | |
<name>region_filter.py</name> | |
<version>0.1</version> | |
<command_line><![CDATA[ region_filter.py --bamfile {ALNvX_*.bam} --regions {filtered_regions} --output BAM_filtered.tmp ]]></command_line> | |
<loop></loop> | |
<comment>Script to generate a temporary BAM file with ENCODE blacklist regions excluded, only relevant for bamCorrelate tool. The filtered BAM file is discarded at the end of this process</comment> | |
</tool> | |
<tool> | |
<name>bamFingerprint (deepTools)</name> | |
<version>1.5.7-5-gcbab7b3</version> | |
<command_line><![CDATA[ bamFingerprint -p {numproc} --bamfiles {ALNvX_*.bam} --plotFile {samplesID.PROCESS.DATE.fgpplot} --labels {labels} --fragmentLength {all_median_fraglen} --numberOfSamples 500000 ]]></command_line> | |
<loop></loop> | |
<comment></comment> | |
</tool> | |
<tool> | |
<name>computeGCBias (deepTools)</name> | |
<version>1.5.7-5-gcbab7b3</version> | |
<command_line><![CDATA[ computeGCBias -p {numproc} --bamfile {ALNvX_*.bam} --effectiveGenomeSize {genomesize} --genome {reference_genome} --fragmentLength {_median_fraglen} --sampleSize 50000000 --GCbiasFrequenciesFile {sampleID.PROCESS.DATE.gcbfreq} --biasPlot {sampleID.PROCESS.DATE.gcbplot} ]]></command_line> | |
<loop></loop> | |
<comment></comment> | |
</tool> | |
<tool> | |
<name>MACS2</name> | |
<version>2.0.10.20131216 (tag:beta)</version> | |
<command_line><![CDATA[ macs2 callpeak -t {ALNvX_dnase.bam} -c {ALNvX_input.bam} -f BAM --gsize {genomesize} --keep-dup all --name {_name_prefix} --nomodel --extsize {_median_fraglen} --qvalue 0.05 {broad} ]]></command_line> | |
<loop></loop> | |
<comment>parameter "--broad" for samples H3K4me1/H3K27me3/H3K36me/H3K9me3; default q-value cutoff of 0.05 is recommended by the author at least for broad marks and approved by A. Richter for all marks</comment> | |
</tool> | |
<tool> | |
<name>bamCoverage (deepTools)</name> | |
<version>1.5.7-5-gcbab7b3</version> | |
<command_line><![CDATA[ bamCoverage -p {numproc} --bam {bamfile} --outFileName {sampleID.PROCESS.DATE.bamcov.seqDepthNorm} --outFileFormat bigwig --normalizeTo1x {genomesize} --fragmentLength {_median_fraglen} ]]></command_line> | |
<loop></loop> | |
<comment>report read coverage normalized to 1x sequencing depth</comment> | |
</tool> | |
<tool> | |
<name>signal_plotter.py</name> | |
<version>0.1</version> | |
<command_line><![CDATA[ signal_plotter.py --signal {sampleID_histone.PROCESS.DATE.bamcov.seqDepthNorm} --input {sampleID_input.PROCESS.DATE.bamcov.seqDepthNorm} --regions {plot_regions} --outfile {sampleID.PROCESS.DATE.ctrlreg} ]]></command_line> | |
<loop></loop> | |
<comment></comment> | |
</tool> | |
</software> | |
</process> |