Merge branch '63-on_error' into 'develop'

Test failure.

Closes #63

See merge request !47

.gitlab-ci.yml

@@ -130,7 +130,7 @@ dedupData:
   - singularity run 'docker://bicf/gudmaprbkdedup:2.0.0' samtools sort -@ 20 -O BAM -o Q-Y5F6_1M.se.sorted.deduped.bam ./test_data/bam/small/Q-Y5F6_1M.se.deduped.bam
   - singularity run 'docker://bicf/gudmaprbkdedup:2.0.0' samtools index -@ 20 -b ./test_data/bam/small/Q-Y5F6_1M.se.sorted.deduped.bam Q-Y5F6_1M.se.sorted.deduped.bam.bai
   - >
-    for i in {"chr8","chr4","chrY"}; do 
+    for i in {"chr8","chr4","chrY"}; do
       echo "samtools view -b Q-Y5F6_1M.se.sorted.deduped.bam ${i} > Q-Y5F6_1M.se.sorted.deduped.${i}.bam; samtools index -@ 20 -b Q-Y5F6_1M.se.sorted.deduped.${i}.bam Q-Y5F6_1M.se.sorted.deduped.${i}.bam.bai;";
       done | singularity run 'docker://bicf/gudmaprbkdedup:2.0.0' parallel -j 20 -k
   - pytest -m dedupData
@@ -145,7 +145,7 @@ countData:
   script:
   - ln -s /project/BICF/BICF_Core/shared/gudmap/references/GRCh38.p12.v31/geneID.tsv
   - ln -s /project/BICF/BICF_Core/shared/gudmap/references/GRCh38.p12.v31/Entrez.tsv
-  - singularity run 'docker://bicf/subread2:2.0.0' featureCounts -T 20 -a /project/BICF/BICF_Core/shared/gudmap/references/GRCh38.p12.v31/genome.gtf -G /project/BICF/BICF_Core/shared/gudmap/references/GRCh38.p12.v31/genome.fna -g 'gene_name' --extraAttributes 'gene_id' -o Q-Y5F6_1M.se.countData -s 1 -R SAM --primary --ignoreDup ./test_data/bam/small/Q-Y5F6_1M.se.sorted.deduped.bam 
+  - singularity run 'docker://bicf/subread2:2.0.0' featureCounts -T 20 -a /project/BICF/BICF_Core/shared/gudmap/references/GRCh38.p12.v31/genome.gtf -G /project/BICF/BICF_Core/shared/gudmap/references/GRCh38.p12.v31/genome.fna -g 'gene_name' --extraAttributes 'gene_id' -o Q-Y5F6_1M.se.countData -s 1 -R SAM --primary --ignoreDup ./test_data/bam/small/Q-Y5F6_1M.se.sorted.deduped.bam
   - singularity run 'docker://bicf/subread2:2.0.0' Rscript ./workflow/scripts/calculateTPM.R --count ./test_data/counts/small/Q-Y5F6_1M.se.countData
   - singularity run 'docker://bicf/subread2:2.0.0' Rscript ./workflow/scripts/convertGeneSymbols.R --repRID Q-Y5F6_1M.se
   - assignedReads=$(grep -m 1 'Assigned' *.summary | grep -oe '\([0-9.]*\)')
@@ -283,7 +283,7 @@ integration_se:
   script:
   - hostname
   - ulimit -a
-  - nextflow -q run ./workflow/rna-seq.nf --deriva ./test_data/auth/credential.json --bdbag ./test_data/auth/cookies.txt --repRID 16-1ZX4 -with-dag dag.png --ci true
+  - nextflow -q run ./workflow/rna-seq.nf --deriva ./test_data/auth/credential.json --bdbag ./test_data/auth/cookies.txt --repRID 16-1ZX4 -with-dag dag.png --ci true --email 'venkat.malladi@utsouthwestern.edu,Gervaise.Henry@UTSouthwestern.edu'
   - find . -type f -name "multiqc_data.json" -exec cp {} ./SE_multiqc_data.json \;
   artifacts:
     name: "$CI_JOB_NAME"
@@ -366,7 +366,7 @@ override_fastq:
     max: 1
     when:
       - always
-    
+
 override_species:
   stage: integration
   only: [merge_requests]
@@ -388,7 +388,7 @@ override_species:
     max: 1
     when:
       - always
-  
+
 
 consistency:
   stage: consistency
@@ -413,4 +413,4 @@ consistency:
       - assignedPE.txt
       - assignedExpectSE.txt
       - assignedExpectPE.txt
-    expire_in: 7 days
+    expire_in: 7 days
\ No newline at end of file

CHANGELOG.md

 # v0.0.4 (in development)
 **User Facing**
 * Add option to pull references from datahub
+* Add option to send email on workflow error, with pipeline error message
 
 **Background**
 * Remove (comment out) option to pull references from S3

README.md

@@ -43,6 +43,9 @@ To Run:
     * **biohpc_max** = process on high power BioHPC cluster nodes (=> 128GB nodes), for resource testing
     * **aws_ondemand** = AWS Batch on-demand instant requests
     * **aws_spot** = AWS Batch spot instance requests
+  * `--email` email address(es) to send failure notification (comma separated) ***(optional)***:
+    * e.g: `--email 'venkat.malladi@utsouthwestern.edu,Gervaise.Henry@UTSouthwestern.edu'`
+    
 * NOTES:
   * once deriva-auth is run and authenticated, the two files above are saved in ```~/.deriva/``` (see official documents from [deriva](https://github.com/informatics-isi-edu/deriva-client#installer-packages-for-windows-and-macosx) on the lifetime of the credentials)
   * reference version consists of Genome Reference Consortium version, patch release and GENCODE annotation release # (leaving the params blank will use the default version tied to the pipeline version)
@@ -126,4 +129,4 @@ Please cite in publications: Pipeline was developed by BICF from funding provide
 Pipeline Directed Acyclic Graph
 -------------------------------
 
-![dag](docs/dag.png "DAG")
+![dag](docs/dag.png "DAG")
\ No newline at end of file

workflow/nextflow.config

@@ -82,7 +82,7 @@ timeline {
   enabled = false
   file = 'timeline.html'
 }
-	
+
 report {
   enabled = false
   file = 'report.html'
@@ -94,6 +94,7 @@ tower {
 }
 
 manifest {
+  name = 'gudmap_rbk/rna-seq'
   homePage = 'https://git.biohpc.swmed.edu/gudmap_rbk/rna-seq'
   description = 'This pipeline was created to be a standard mRNA-sequencing analysis pipeline which integrates with the GUDMAP and RBK consortium data-hub.'
   mainScript = 'rna-seq.nf'

workflow/rna-seq.nf

 #!/usr/bin/env nextflow
 
-//  ########  ####  ######  ######## 
-//  ##     ##  ##  ##    ## ##       
-//  ##     ##  ##  ##       ##       
-//  ########   ##  ##       ######   
-//  ##     ##  ##  ##       ##       
-//  ##     ##  ##  ##    ## ##       
-//  ########  ####  ######  ##       
+//  ########  ####  ######  ########
+//  ##     ##  ##  ##    ## ##
+//  ##     ##  ##  ##       ##
+//  ########   ##  ##       ######
+//  ##     ##  ##  ##       ##
+//  ##     ##  ##  ##    ## ##
+//  ########  ####  ######  ##
 
 // Define input variables
 params.deriva = "${baseDir}/../test_data/auth/credential.json"
@@ -18,6 +18,8 @@ params.refMoVersion = "38.p6.vM22"
 params.refHuVersion = "38.p12.v31"
 params.refERCCVersion = "92"
 params.outDir = "${baseDir}/../output"
+params.email = ""
+
 
 // Define override input variable
 params.refSource = "biohpc"
@@ -25,6 +27,7 @@ params.inputBagForce = ""
 params.fastqsForce = ""
 params.speciesForce = ""
 
+
 // Parse input variables
 deriva = Channel
   .fromPath(params.deriva)
@@ -46,6 +49,7 @@ logsDir = "${outDir}/Logs"
 inputBagForce = params.inputBagForce
 fastqsForce = params.fastqsForce
 speciesForce = params.speciesForce
+email = params.email
 
 // Define fixed files
 derivaConfig = Channel.fromPath("${baseDir}/conf/replicate_export_config.json")
@@ -89,7 +93,7 @@ process trackStart {
   """
   hostname
   ulimit -a
-  
+
   curl -H 'Content-Type: application/json' -X PUT -d \
     '{ \
       "sessionId": "${workflow.sessionId}", \
@@ -199,16 +203,16 @@ process getData {
     mkdir -p ~/.bdbag
     ln -sf `readlink -e deriva-cookies.txt` ~/.bdbag/deriva-cookies.txt
     echo -e "LOG: linked" >> ${repRID}.getData.log
-    
+
     # get bag basename
     replicate=\$(basename "${inputBag}" | cut -d "." -f1)
     echo -e "LOG: bag replicate name \${replicate}" >> ${repRID}.getData.log
-    
+
     # unzip bag
     echo -e "LOG: unzipping replicate bag" >> ${repRID}.getData.log
     unzip ${inputBag}
     echo -e "LOG: unzipped" >> ${repRID}.getData.log
-    
+
     # bag fetch fastq's only and rename by repRID
     echo -e "LOG: fetching replicate bdbag" >> ${repRID}.getData.log
     sh ${script_bdbagFetch} \${replicate} ${repRID}
@@ -259,7 +263,7 @@ process parseMetadata {
     # get experiment RID metadata
     exp=\$(python3 ${script_parseMeta} -r ${repRID} -m "${file}" -p expRID)
     echo -e "LOG: experiment RID metadata parsed: \${exp}" >> ${repRID}.parseMetadata.log
-    
+
     # get study RID metadata
     study=\$(python3 ${script_parseMeta} -r ${repRID} -m "${file}" -p studyRID)
     echo -e "LOG: study RID metadata parsed: \${study}" >> ${repRID}.parseMetadata.log
@@ -267,7 +271,7 @@ process parseMetadata {
     # get endedness metadata
     endsMeta=\$(python3 ${script_parseMeta} -r ${repRID} -m "${experimentSettings}" -p endsMeta)
     echo -e "LOG: endedness metadata parsed: \${endsMeta}" >> ${repRID}.parseMetadata.log
-    
+
     # ganually get endness
     endsManual=\$(python3 ${script_parseMeta} -r ${repRID} -m "${file}" -p endsManual)
     echo -e "LOG: endedness manually detected: \${endsManual}" >> ${repRID}.parseMetadata.log
@@ -275,11 +279,11 @@ process parseMetadata {
     # get strandedness metadata
     stranded=\$(python3 ${script_parseMeta} -r ${repRID} -m "${experimentSettings}" -p stranded)
     echo -e "LOG: strandedness metadata parsed: \${stranded}" >> ${repRID}.parseMetadata.log
-    
+
     # get spike-in metadata
     spike=\$(python3 ${script_parseMeta} -r ${repRID} -m "${experimentSettings}" -p spike)
     echo -e "LOG: spike-in metadata parsed: \${spike}" >> ${repRID}.parseMetadata.log
-    
+
     # get species metadata
     species=\$(python3 ${script_parseMeta} -r ${repRID} -m "${experiment}" -p species)
     echo -e "LOG: species metadata parsed: \${species}" >> ${repRID}.parseMetadata.log
@@ -358,7 +362,7 @@ process trimData {
     fi
     echo -e "LOG: trimmed" >> ${repRID}.trimData.log
     echo -e "LOG: average trimmed read length: \${readLength}" >> ${repRID}.trimData.log
-    
+
     # save read length file
     echo -e "\${readLength}" > readLength.csv
     """
@@ -381,7 +385,7 @@ getRefInferInput = referenceInfer.combine(deriva_getRefInfer.combine(script_refD
 
 /*
   * getRefInfer: dowloads appropriate reference for metadata inference
-*/  
+*/
 process getRefInfer {
   tag "${refName}"
 
@@ -391,7 +395,7 @@ process getRefInfer {
   output:
     tuple val (refName), path ("hisat2", type: 'dir'), path ("*.fna"), path ("*.gtf")  into refInfer
     path ("${refName}", type: 'dir') into bedInfer
- 
+
   script:
     """
     hostname > ${repRID}.${refName}.getRefInfer.log
@@ -532,14 +536,14 @@ process alignSampleData {
     echo -e "LOG: aligning ${ends}" >> ${repRID}.${ref}.alignSampleData.log
     if [ "${ends}" == "se" ]
     then
-     
+
       hisat2 -p `nproc` --add-chrname -S ${ref}.sampled.sam -x hisat2/genome -U ${fastq1} --summary-file ${ref}.alignSampleSummary.txt --new-summary
     elif [ "${ends}" == "pe" ]
     then
       hisat2 -p `nproc` --add-chrname -S ${ref}.sampled.sam -x hisat2/genome --no-mixed --no-discordant -1 ${fastq1} -2 ${fastq2} --summary-file ${ref}.alignSampleSummary.txt --new-summary
     fi
     echo -e "LOG: aliged" >> ${repRID}.${ref}.alignSampleData.log
-    
+
     # convert the output sam file to a sorted bam file using Samtools
     echo -e "LOG: converting from sam to bam" >> ${repRID}.${ref}.alignSampleData.log
     samtools view -1 -@ `nproc` -F 4 -F 8 -F 256 -o ${ref}.sampled.bam ${ref}.sampled.sam
@@ -639,7 +643,7 @@ process inferMetadata {
 
     ended=`bash inferMeta.sh endness ${repRID}.infer_experiment.txt`
     fail=`bash inferMeta.sh fail ${repRID}.infer_experiment.txt`
-    if [ \${ended} == "PairEnd" ] 
+    if [ \${ended} == "PairEnd" ]
     then
       ends="pe"
       percentF=`bash inferMeta.sh pef ${repRID}.infer_experiment.txt`
@@ -728,7 +732,7 @@ process getRef {
 
   output:
     tuple path ("hisat2", type: 'dir'), path ("bed", type: 'dir'), path ("*.fna"), path ("*.gtf"), path ("geneID.tsv"), path ("Entrez.tsv")  into reference
- 
+
   script:
     """
     hostname > ${repRID}.getRef.log
@@ -847,7 +851,7 @@ process alignData {
         strandedParam="--rna-strandness R"
     elif [ "${stranded}" == "reverse" ] && [ "${ends}" == "pe" ]
     then
-      strandedParam="--rna-strandness RF"    
+      strandedParam="--rna-strandness RF"
     fi
 
     # align the reads with Hisat2
@@ -860,7 +864,7 @@ process alignData {
       hisat2 -p `nproc` --add-chrname --un-gz ${repRID}.unal.gz -S ${repRID}.sam -x hisat2/genome \${strandedParam} --no-mixed --no-discordant -1 ${fastq[0]} -2 ${fastq[1]} --summary-file ${repRID}.alignSummary.txt --new-summary
     fi
     echo -e "LOG: alignined" >> ${repRID}.align.log
-    
+
     # convert the output sam file to a sorted bam file using Samtools
     echo -e "LOG: converting from sam to bam" >> ${repRID}.align.log
     samtools view -1 -@ `nproc` -F 4 -F 8 -F 256 -o ${repRID}.bam ${repRID}.sam
@@ -892,7 +896,7 @@ process dedupData {
 
   output:
     tuple path ("${repRID}.sorted.deduped.bam"), path ("${repRID}.sorted.deduped.bam.bai") into dedupBam
-    tuple path ("${repRID}.sorted.deduped.*.bam"), path ("${repRID}.sorted.deduped.*.bam.bai") into dedupChrBam 
+    tuple path ("${repRID}.sorted.deduped.*.bam"), path ("${repRID}.sorted.deduped.*.bam.bai") into dedupChrBam
     path ("*.deduped.Metrics.txt") into dedupQC
 
   script:
@@ -908,7 +912,7 @@ process dedupData {
     # sort the bam file using Samtools
     echo -e "LOG: sorting the bam file" >> ${repRID}.dedup.log
     samtools sort -@ `nproc` -O BAM -o ${repRID}.sorted.deduped.bam ${repRID}.deduped.bam
-    
+
     # index the sorted bam using Samtools
     echo -e "LOG: indexing sorted bam file" >> ${repRID}.dedup.log
     samtools index -@ `nproc` -b ${repRID}.sorted.deduped.bam ${repRID}.sorted.deduped.bam.bai
@@ -1004,7 +1008,7 @@ process countData {
       featureCounts -T `nproc` -a ./genome.gtf -G ./genome.fna -g 'gene_name' --extraAttributes 'gene_id' -o ${repRID}.countData -s \${stranding} -p -B -R SAM --primary --ignoreDup ${repRID}.sorted.deduped.bam
     fi
     echo -e "LOG: counted" >> ${repRID}.countData.log
-    
+
     # extract assigned reads
     grep -m 1 'Assigned' *.countData.summary | grep -oe '\\([0-9.]*\\)' > assignedReads.csv
 
@@ -1069,12 +1073,12 @@ process dataQC {
     tuple path (bam), path (bai) from dedupBam_dataQC
     tuple path (chrBam), path (chrBai) from dedupChrBam
     val ends from endsInfer_dataQC
-    
+
   output:
     path "${repRID}.tin.hist.tsv" into tinHist
     path "${repRID}.tin.med.csv" into inferMetadata_tinMed
     path "${repRID}.insertSize.inner_distance_freq.txt" into innerDistance
-  
+
   script:
     """
     hostname > ${repRID}.dataQC.log
@@ -1179,8 +1183,8 @@ process aggrQC {
     echo -e "LOG: creating run table" >> ${repRID}.aggrQC.log
     echo -e "Session\tSession ID\tStart Time\tPipeline Version\tInput" > run.tsv
     echo -e "Session\t${workflow.sessionId}\t${workflow.start}\t${workflow.manifest.version}\t\${input}" >> run.tsv
-    
-    
+
+
     # make RID table
     echo -e "LOG: creating RID table" >> ${repRID}.aggrQC.log
     echo -e "Replicate\tReplicate RID\tExperiment RID\tStudy RID" > rid.tsv
@@ -1224,11 +1228,11 @@ process aggrQC {
 process outputBag {
   tag "${repRID}"
   publishDir "${outDir}/outputBag", mode: 'copy', pattern: "Replicate_${repRID}.outputBag.zip"
-  
+
   input:
     path multiqc
     path multiqcJSON
-  
+
   output:
     path ("Replicate_*.zip") into outputBag
 
@@ -1239,4 +1243,25 @@ process outputBag {
   cp ${multiqcJSON} Replicate_${repRID}.outputBag
   bdbag Replicate_${repRID}.outputBag --archiver zip
   """
-}
+}
\ No newline at end of file
+
+
+workflow.onError = {
+  subject = "$workflow.manifest.name FAILED: $params.repRID"
+
+  def msg = """\
+
+      Pipeline error summary
+      ---------------------------
+      RID         : ${params.repRID}
+      Version     : ${workflow.manifest.version}
+      Duration    : ${workflow.duration}
+      Nf Version  : ${workflow.nextflow.version}
+      Message     : ${workflow.errorMessage}
+      exit status : ${workflow.exitStatus}
+      """
+      .stripIndent()
+  if (email != '') {
+    sendMail(to: email, subject: subject , body: msg)
+  }
+}