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biowdl
tasks
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!30
add picard metrics tools
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add picard metrics tools
BIOWDL-51
into
develop
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Ruben Vorderman
requested to merge
BIOWDL-51
into
develop
6 years ago
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Created by: DavyCats
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d81eed41
Merge branch 'develop' into BIOWDL-51
· d81eed41
Cats
authored
6 years ago
picard.wdl
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15
Options
task
ScatterIntervalList
{
task
CollectMultipleMetrics
{
String? preCommand
File interval_list
Int scatter_count
File bamFile
File bamIndex
File refFasta
File refDict
File refFastaIndex
String basename
# These should proably be optional, but I'm not sure how to handle the ouput in that
# case (without a null literal).
Boolean collectAlignmentSummaryMetrics = true
Boolean collectInsertSizeMetrics = true
Boolean qualityScoreDistribution = true
Boolean meanQualityByCycle = true
Boolean collectBaseDistributionByCycle = true
Boolean collectGcBiasMetrics = true
#Boolean? rnaSeqMetrics = false # There is a bug in picard https://github.com/broadinstitute/picard/issues/999
Boolean collectSequencingArtifactMetrics = true
Boolean collectQualityYieldMetrics = true
String? picardJar
Float? memory
@@ -10,26 +27,139 @@ task ScatterIntervalList {
Int mem = ceil(select_first([memory, 4.0]))
String toolCommand = if defined(picardJar)
then "java -Xmx" + mem + "G -jar " + picardJar
else "picard -Xmx" + mem + "G"
then "java -Xmx" + mem + "G -jar " + picardJar
else "picard -Xmx" + mem + "G"
command {
set -e -o pipefail
mkdir -p $(dirname "${basename}")
${preCommand}
mkdir scatter_list
${toolCommand} \
IntervalListTools \
SCATTER_COUNT=${scatter_count} \
SUBDIVISION_MODE=BALANCING_WITHOUT_INTERVAL_SUBDIVISION_WITH_OVERFLOW \
UNIQUE=true \
SORT=true \
INPUT=${interval_list} \
OUTPUT=scatter_list
CollectMultipleMetrics \
I=${bamFile} \
R=${refFasta} \
O=${basename} \
PROGRAM=null \
${true="PROGRAM=CollectAlignmentSummaryMetrics" false="" collectAlignmentSummaryMetrics} \
${true="PROGRAM=CollectInsertSizeMetrics" false="" collectInsertSizeMetrics} \
${true="PROGRAM=QualityScoreDistribution" false="" qualityScoreDistribution} \
${true="PROGRAM=MeanQualityByCycle" false="" meanQualityByCycle} \
${true="PROGRAM=CollectBaseDistributionByCycle" false="" collectBaseDistributionByCycle} \
${true="PROGRAM=CollectGcBiasMetrics" false="" collectGcBiasMetrics} \
${true="PROGRAM=CollectSequencingArtifactMetrics" false=""
collectSequencingArtifactMetrics} \
${true="PROGRAM=CollectQualityYieldMetrics" false="" collectQualityYieldMetrics}
}
output {
Array[File] out = glob("scatter_list/*/*.interval_list")
Int interval_count = read_int(stdout())
File aligmentSummary = basename + ".alignment_summary_metrics"
File baitBiasDetail = basename + ".bait_bias_detail_metrics"
File baitBiasSummary = basename + ".bait_bias_summary_metrics"
File baseDistributionByCycle = basename + ".base_distribution_by_cycle_metrics"
File baseDistributionByCyclePdf = basename + ".base_distribution_by_cycle.pdf"
File errorSummary = basename + ".error_summary_metrics"
File gcBiasDetail = basename + ".gc_bias.detail_metrics"
File gcBiasPdf = basename + ".gc_bias.pdf"
File gcBiasSummary = basename + ".gc_bias.summary_metrics"
File insertSizeHistogramPdf = basename + ".insert_size_histogram.pdf"
File insertSize = basename + ".insert_size_metrics"
File preAdapterDetail = basename + ".pre_adapter_detail_metrics"
File preAdapterSummary = basename + ".pre_adapter_summary_metrics"
File qualityByCycle = basename + ".quality_by_cycle_metrics"
File qualityByCyclePdf = basename + ".quality_by_cycle.pdf"
File qualityDistribution = basename + ".quality_distribution_metrics"
File qualityDistributionPdf = basename + ".quality_distribution.pdf"
File qualityYield = basename + ".quality_yield_metrics"
}
runtime {
memory: ceil(mem * select_first([memoryMultiplier, 3.0]))
}
}
task CollectRnaSeqMetrics {
String? preCommand
File bamFile
File bamIndex
File refRefflat
String basename
String? strandSpecificity = "NONE"
String? picardJar
Float? memory
Float? memoryMultiplier
Int mem = ceil(select_first([memory, 4.0]))
String toolCommand = if defined(picardJar)
then "java -Xmx" + mem + "G -jar " + picardJar
else "picard -Xmx" + mem + "G"
command {
set -e -o pipefail
mkdir -p $(dirname "${basename}")
${preCommand}
${toolCommand} \
CollectRnaSeqMetrics \
I=${bamFile} \
O=${basename}.RNA_Metrics \
CHART_OUTPUT=${basename}.RNA_Metrics.pdf \
${"STRAND_SPECIFICITY=" + strandSpecificity} \
REF_FLAT=${refRefflat}
}
output {
File chart = basename + ".RNA_Metrics.pdf"
File metrics = basename + ".RNA_Metrics"
}
runtime {
memory: ceil(mem * select_first([memoryMultiplier, 3.0]))
}
}
task CollectTargetedPcrMetrics {
String? preCommand
File bamFile
File bamIndex
File refFasta
File refDict
File refFastaIndex
File ampliconIntervals
Array[File]+ targetIntervals
String basename
String? picardJar
Float? memory
Float? memoryMultiplier
Int mem = ceil(select_first([memory, 4.0]))
String toolCommand = if defined(picardJar)
then "java -Xmx" + mem + "G -jar " + picardJar
else "picard -Xmx" + mem + "G"
command {
set -e -o pipefail
mkdir -p $(dirname "${basename}")
${preCommand}
${toolCommand} \
CollectTargetedPcrMetrics \
I=${bamFile} \
R=${refFasta} \
AMPLICON_INTERVALS=${ampliconIntervals} \
TARGET_INTERVALS=${sep=" TARGET_INTERVALS=" targetIntervals} \
O=${basename}.targetPcrMetrics \
PER_BASE_COVERAGE=${basename}.targetPcrPerBaseCoverage \
PER_TARGET_COVERAGE=${basename}.targetPcrPerTargetCoverage
}
output {
File perTargetCoverage = basename + ".targetPcrPerTargetCoverage"
File perBaseCoverage = basename + ".targetPcrPerBaseCoverage"
File metrics = basename + ".targetPcrMetrics"
}
runtime {
@@ -201,6 +331,45 @@ task SamToFastq {
File? unpairedRead = outputUnpaired
}
runtime {
memory: ceil(mem * select_first([memoryMultiplier, 3.0]))
}
}
task ScatterIntervalList {
String? preCommand
File interval_list
Int scatter_count
String? picardJar
Float? memory
Float? memoryMultiplier
Int mem = ceil(select_first([memory, 4.0]))
String toolCommand = if defined(picardJar)
then "java -Xmx" + mem + "G -jar " + picardJar
else "picard -Xmx" + mem + "G"
command {
set -e -o pipefail
${preCommand}
mkdir scatter_list
${toolCommand} \
IntervalListTools \
SCATTER_COUNT=${scatter_count} \
SUBDIVISION_MODE=BALANCING_WITHOUT_INTERVAL_SUBDIVISION_WITH_OVERFLOW \
UNIQUE=true \
SORT=true \
INPUT=${interval_list} \
OUTPUT=scatter_list
}
output {
Array[File] out = glob("scatter_list/*/*.interval_list")
Int interval_count = read_int(stdout())
}
runtime {
memory: ceil(mem * select_first([memoryMultiplier, 3.0]))
}
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