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biopet.biopet
Commits
413f0bd1
Commit
413f0bd1
authored
10 years ago
by
Peter van 't Hof
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Remove unused code
parent
bbd005c3
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protected/biopet-gatk-pipelines/src/main/scala/nl/lumc/sasc/biopet/pipelines/gatk/GatkPipeline.scala
+0
-136
0 additions, 136 deletions
...ala/nl/lumc/sasc/biopet/pipelines/gatk/GatkPipeline.scala
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and
136 deletions
protected/biopet-gatk-pipelines/src/main/scala/nl/lumc/sasc/biopet/pipelines/gatk/GatkPipeline.scala
+
0
−
136
View file @
413f0bd1
...
...
@@ -40,17 +40,6 @@ class GatkPipeline(val root: Configurable) extends QScript with MultiSampleQScri
var
useAllelesOption
:
Boolean
=
config
(
"use_alleles_option"
,
default
=
false
)
val
externalGvcfs
=
config
(
"external_gvcfs_files"
,
default
=
Nil
).
asFileList
/**
* class LibraryOutput extends AbstractLibraryOutput {
* var mappedBamFile: File = _
* var variantcalling: GatkVariantcalling.ScriptOutput = _
* }
*
* class SampleOutput extends AbstractSampleOutput {
* var variantcalling: GatkVariantcalling.ScriptOutput = _
* }
*/
def
makeSample
(
id
:
String
)
=
new
Sample
(
id
)
class
Sample
(
sampleId
:
String
)
extends
AbstractSample
(
sampleId
)
{
def
makeLibrary
(
id
:
String
)
=
new
Library
(
id
)
...
...
@@ -217,131 +206,6 @@ class GatkPipeline(val root: Configurable) extends QScript with MultiSampleQScri
}
}
}
/*
// Called for each sample
def runSingleSampleJobs(sampleID: String): SampleOutput = {
val sampleOutput = new SampleOutput
var libraryBamfiles: List[File] = List()
sampleOutput.libraries = runLibraryJobs(sampleID)
val sampleDir = globalSampleDir + sampleID
for ((libraryID, libraryOutput) <- sampleOutput.libraries) {
libraryBamfiles ++= libraryOutput.variantcalling.bamFiles
}
if (libraryBamfiles.size > 0) {
finalBamFiles ++= libraryBamfiles
val gatkVariantcalling = new GatkVariantcalling(this)
gatkVariantcalling.inputBams = libraryBamfiles
gatkVariantcalling.outputDir = sampleDir + "/variantcalling/"
gatkVariantcalling.preProcesBams = false
if (!singleSampleCalling) {
gatkVariantcalling.useHaplotypecaller = false
gatkVariantcalling.useUnifiedGenotyper = false
}
gatkVariantcalling.sampleID = sampleID
gatkVariantcalling.init
gatkVariantcalling.biopetScript
addAll(gatkVariantcalling.functions)
sampleOutput.variantcalling = gatkVariantcalling.scriptOutput
gvcfFiles :+= gatkVariantcalling.scriptOutput.gvcfFile
} else logger.warn("No bamfiles for variant calling for sample: " + sampleID)
return sampleOutput
}
// Called for each run from a sample
def runSingleLibraryJobs(libraryId: String, sampleID: String): LibraryOutput = {
val libraryOutput = new LibraryOutput
val runDir: String = globalSampleDir + sampleID + "/run_" + libraryId + "/"
var inputType: String = config("inputtype", default = "dna")
def loadFromLibraryConfig(startJobs: Boolean = true): Mapping = {
val mapping = new Mapping(this)
mapping.input_R1 = config("R1")
mapping.input_R2 = config("R2")
mapping.RGLB = libraryId
mapping.RGSM = sampleID
mapping.RGPL = config("PL")
mapping.RGPU = config("PU")
mapping.RGCN = config("CN")
mapping.outputDir = runDir
if (startJobs) {
mapping.init
mapping.biopetScript
}
return mapping
}
if (config.contains("R1")) {
val mapping = loadFromLibraryConfig()
addAll(mapping.functions) // Add functions of mapping to curent function pool
libraryOutput.mappedBamFile = mapping.outputFiles("finalBamFile")
} else if (config.contains("bam")) {
var bamFile: File = config("bam")
if (!bamFile.exists) throw new IllegalStateException("Bam in config does not exist, file: " + bamFile)
if (config("bam_to_fastq", default = false).asBoolean) {
val samToFastq = SamToFastq(this, bamFile, runDir + sampleID + "-" + libraryId + ".R1.fastq",
runDir + sampleID + "-" + libraryId + ".R2.fastq")
add(samToFastq, isIntermediate = true)
val mapping = loadFromLibraryConfig(startJobs = false)
mapping.input_R1 = samToFastq.fastqR1
mapping.input_R2 = samToFastq.fastqR2
mapping.init
mapping.biopetScript
addAll(mapping.functions) // Add functions of mapping to curent function pool
libraryOutput.mappedBamFile = mapping.outputFiles("finalBamFile")
} else {
var readGroupOke = true
val inputSam = SamReaderFactory.makeDefault.open(bamFile)
val header = inputSam.getFileHeader.getReadGroups
for (readGroup <- inputSam.getFileHeader.getReadGroups) {
if (readGroup.getSample != sampleID) logger.warn("Sample ID readgroup in bam file is not the same")
if (readGroup.getLibrary != libraryId) logger.warn("Library ID readgroup in bam file is not the same")
if (readGroup.getSample != sampleID || readGroup.getLibrary != libraryId) readGroupOke = false
}
inputSam.close
if (!readGroupOke) {
if (config("correct_readgroups", default = false)) {
logger.info("Correcting readgroups, file:" + bamFile)
val aorrg = AddOrReplaceReadGroups(this, bamFile, new File(runDir + sampleID + "-" + libraryId + ".bam"))
aorrg.RGID = sampleID + "-" + libraryId
aorrg.RGLB = libraryId
aorrg.RGSM = sampleID
aorrg.RGPL = config("PL", default = "illumina")
aorrg.RGPU = config("PU", default = "na")
aorrg.RGCN = config("CN")
add(aorrg, isIntermediate = true)
bamFile = aorrg.output
} else throw new IllegalStateException("Sample readgroup and/or library of input bamfile is not correct, file: " + bamFile +
"\nPlease note that it is possible to set 'correct_readgroups' to true in the config to automatic fix this")
}
addAll(BamMetrics(this, bamFile, runDir + "metrics/").functions)
libraryOutput.mappedBamFile = bamFile
}
} else {
logger.error("Sample: " + sampleID + ": No R1 found for run: " + libraryId)
return libraryOutput
}
val gatkVariantcalling = new GatkVariantcalling(this)
gatkVariantcalling.inputBams = List(libraryOutput.mappedBamFile)
gatkVariantcalling.outputDir = runDir
gatkVariantcalling.variantcalling = config("library_variantcalling", default = false)
gatkVariantcalling.preProcesBams = true
gatkVariantcalling.sampleID = sampleID
gatkVariantcalling.init
gatkVariantcalling.biopetScript
addAll(gatkVariantcalling.functions)
libraryOutput.variantcalling = gatkVariantcalling.scriptOutput
return libraryOutput
}
*/
}
object
GatkPipeline
extends
PipelineCommand
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