GATK UnifiedGenotyper Fix due to Broad Website change

.github/workflows/nf-core_eager.yml

@@ -86,15 +86,15 @@ jobs:
       - name: SKIPPING Test checking all skip steps work i.e. input bam, skipping straight to genotyping
         run: |
           nextflow run ${GITHUB_WORKSPACE} "$TOWER" -name "$RUN_NAME-skipping_logic" -profile test_bam,docker --bam --singleEnd --skip_fastqc --skip_adapterremoval --skip_mapping --skip_deduplication --skip_qualimap --skip_preseq --skip_damage_calculation --run_genotyping --genotyping_tool 'freebayes'
-      - name: TRIM_BAM/PMD/GENOTYPING_UG/MULTIVCFANALYZER Test running PMDTools, TrimBam, GATK UnifiedGenotyper and MultiVCFAnalyzer
-        run: |
-          nextflow run ${GITHUB_WORKSPACE} "$TOWER" -name "$RUN_NAME-pmd_trimbam_gatkUG_MVA" -profile test,docker --pairedEnd  --dedupper 'dedup' --run_trim_bam --run_pmdtools --run_genotyping --genotyping_source 'trimmed' --genotyping_tool 'ug' --gatk_out_mode 'EMIT_ALL_SITES' --gatk_ug_genotype_model 'SNP' --run_multivcfanalyzer
-      - name: GENOTYPING_UG/PMD/MULTIVCFANALYZER Test running GATK UnifiedGenotyper and MultiVCFAnalyzer, additional VCFS
-        run: |
-         nextflow run ${GITHUB_WORKSPACE} "$TOWER" -name "$RUN_NAME-MVA_additionalvcfs" -profile test,docker --pairedEnd  --dedupper 'dedup' --run_genotyping --genotyping_tool 'ug' --gatk_out_mode 'EMIT_ALL_SITES' --gatk_ug_genotype_model 'SNP' --run_multivcfanalyzer --additional_vcf_files 'https://raw.githubusercontent.com/nf-core/test-datasets/eager/testdata/Mammoth/vcf/JK2772_CATCAGTGAGTAGA_L008_R1_001.fastq.gz.tengrand.fq.combined.fq.mapped_rmdup.bam.unifiedgenotyper.vcf.gz' --write_allele_frequencies
-      - name: VCF2Genome Run basic pipeline with GATK unifiedgenotyper and run VCF2Genome
-        run: |
-         nextflow run ${GITHUB_WORKSPACE} "$TOWER" -name "$RUN_NAME-vcf2genome" -profile test,docker --pairedEnd  --dedupper 'dedup' --run_genotyping --genotyping_tool 'ug' --genotyping_source 'raw' --gatk_out_mode 'EMIT_ALL_SITES' --gatk_ug_genotype_model 'SNP' --run_vcf2genome
+      #- name: TRIM_BAM/PMD/GENOTYPING_UG/MULTIVCFANALYZER Test running PMDTools, TrimBam, GATK UnifiedGenotyper and MultiVCFAnalyzer
+      #  run: |
+      #    nextflow run ${GITHUB_WORKSPACE} "$TOWER" -name "$RUN_NAME-pmd_trimbam_gatkUG_MVA" -profile test,docker --pairedEnd  --dedupper 'dedup' --run_trim_bam --run_pmdtools --run_genotyping --genotyping_source 'trimmed' --genotyping_tool 'ug' --gatk_out_mode 'EMIT_ALL_SITES' --gatk_ug_genotype_model 'SNP' --run_multivcfanalyzer
+      #- name: GENOTYPING_UG/PMD/MULTIVCFANALYZER Test running GATK UnifiedGenotyper and MultiVCFAnalyzer, additional VCFS
+      #  run: |
+      #   nextflow run ${GITHUB_WORKSPACE} "$TOWER" -name "$RUN_NAME-MVA_additionalvcfs" -profile test,docker --pairedEnd  --dedupper 'dedup' --run_genotyping --genotyping_tool 'ug' --gatk_out_mode 'EMIT_ALL_SITES' --gatk_ug_genotype_model 'SNP' --run_multivcfanalyzer --additional_vcf_files 'https://raw.githubusercontent.com/nf-core/test-datasets/eager/testdata/Mammoth/vcf/JK2772_CATCAGTGAGTAGA_L008_R1_001.fastq.gz.tengrand.fq.combined.fq.mapped_rmdup.bam.unifiedgenotyper.vcf.gz' --write_allele_frequencies
+      #- name: VCF2Genome Run basic pipeline with GATK unifiedgenotyper and run VCF2Genome
+      #  run: |
+      #   nextflow run ${GITHUB_WORKSPACE} "$TOWER" -name "$RUN_NAME-vcf2genome" -profile test,docker --pairedEnd  --dedupper 'dedup' --run_genotyping --genotyping_tool 'ug' --genotyping_source 'raw' --gatk_out_mode 'EMIT_ALL_SITES' --gatk_ug_genotype_model 'SNP' --run_vcf2genome
       - name: BAM_INPUT Run the basic pipeline with the bam input profile, skip AdapterRemoval as no convertBam
         run: |
          nextflow run ${GITHUB_WORKSPACE} "$TOWER" -name "$RUN_NAME-baminput_noConvertBam" -profile test_bam,docker --bam --skip_adapterremoval --run_convertbam

.travis.yml

@@ -78,11 +78,11 @@ script:
   # SKIPPING: Test checking all skip steps work i.e. input bam, skipping straight to genotyping
   - nextflow run ${TRAVIS_BUILD_DIR} -name "$RUN_NAME-skipping_logic" -profile test_bam,docker --bam --singleEnd --skip_fastqc --skip_adapterremoval --skip_mapping --skip_deduplication --skip_qualimap --skip_preseq --skip_damage_calculation --run_genotyping --genotyping_tool 'freebayes'
   # TRIM_BAM/PMD/GENOTYPING_UG/MULTIVCFANALYZER: Test running PMDTools, TrimBam, GATK UnifiedGenotyper and MultiVCFAnalyzer
-  - nextflow run ${TRAVIS_BUILD_DIR} -name "$RUN_NAME-pmd_trimbam_unifiedgenotyper_multivcfanalyzer" -profile test,docker --pairedEnd  --dedupper 'dedup' --run_trim_bam --run_pmdtools --run_genotyping --genotyping_source 'trimmed' --genotyping_tool 'ug' --gatk_out_mode 'EMIT_ALL_SITES' --gatk_ug_genotype_model 'SNP' --run_multivcfanalyzer
+  #- nextflow run ${TRAVIS_BUILD_DIR} -name "$RUN_NAME-pmd_trimbam_unifiedgenotyper_multivcfanalyzer" -profile test,docker --pairedEnd  --dedupper 'dedup' --run_trim_bam --run_pmdtools --run_genotyping --genotyping_source 'trimmed' --genotyping_tool 'ug' --gatk_out_mode 'EMIT_ALL_SITES' --gatk_ug_genotype_model 'SNP' --run_multivcfanalyzer
   # GENOTYPING_UG/PMD/MULTIVCFANALYZER: Test running GATK UnifiedGenotyper and MultiVCFAnalyzer, additional VCFS
-  - nextflow run ${TRAVIS_BUILD_DIR} -name "$RUN_NAME-multivcfanalyzer_additionalvcfs" -profile test,docker --pairedEnd  --dedupper 'dedup' --run_genotyping --genotyping_tool 'ug' --gatk_out_mode 'EMIT_ALL_SITES' --gatk_ug_genotype_model 'SNP' --run_multivcfanalyzer --additional_vcf_files 'https://raw.githubusercontent.com/jfy133/test-datasets/eager/testdata/Mammoth/vcf/JK2772_CATCAGTGAGTAGA_L008_R1_001.fastq.gz.tengrand.fq.combined.fq.mapped_rmdup.bam.unifiedgenotyper.vcf.gz' --write_allele_frequencies
+  #- nextflow run ${TRAVIS_BUILD_DIR} -name "$RUN_NAME-multivcfanalyzer_additionalvcfs" -profile test,docker --pairedEnd  --dedupper 'dedup' --run_genotyping --genotyping_tool 'ug' --gatk_out_mode 'EMIT_ALL_SITES' --gatk_ug_genotype_model 'SNP' --run_multivcfanalyzer --additional_vcf_files 'https://raw.githubusercontent.com/jfy133/test-datasets/eager/testdata/Mammoth/vcf/JK2772_CATCAGTGAGTAGA_L008_R1_001.fastq.gz.tengrand.fq.combined.fq.mapped_rmdup.bam.unifiedgenotyper.vcf.gz' --write_allele_frequencies
   # VCF2GENOME: Test running GATK UnifiedGenotyper and run VCF2GENOME
-  - nextflow run ${TRAVIS_BUILD_DIR} -name "$RUN_NAME-vcf2genome" -profile test,docker --pairedEnd  --dedupper 'dedup' --run_genotyping --genotyping_tool 'ug' --genotyping_source 'raw' --gatk_out_mode 'EMIT_ALL_SITES' --gatk_ug_genotype_model 'SNP' --run_vcf2genome
+  #- nextflow run ${TRAVIS_BUILD_DIR} -name "$RUN_NAME-vcf2genome" -profile test,docker --pairedEnd  --dedupper 'dedup' --run_genotyping --genotyping_tool 'ug' --genotyping_source 'raw' --gatk_out_mode 'EMIT_ALL_SITES' --gatk_ug_genotype_model 'SNP' --run_vcf2genome
   # BAM_INPUT: Run the basic pipeline with the bam input profile, skip AdapterRemoval as no convertBam
   - nextflow run ${TRAVIS_BUILD_DIR} -name "$RUN_NAME-baminput_noConvertBam" -profile test_bam,docker --bam --skip_adapterremoval --run_convertbam
   # BAM_INPUT: Run the basic pipeline with the bam input profile, convert to FASTQ for adapterremoval test and downstream

bin/scrape_software_versions.py

@@ -15,7 +15,7 @@
     'BWA': ['v_bwa.txt', r"Version: (\S+)"],
     'Qualimap': ['v_qualimap.txt', r"QualiMap v.(\S+)"],
     'GATK HaplotypeCaller': ['v_gatk.txt', r" v(\S+)"],
-    'GATK UnifiedGenotyper': ['v_gatk3_5.txt', r"version (\S+)"],
+    #'GATK UnifiedGenotyper': ['v_gatk3_5.txt', r"version (\S+)"],
     'bamUtil' : ['v_bamutil.txt', r"Version: (\S+);"],
     'fastP': ['v_fastp.txt', r"([\d\.]+)"],
     'DamageProfiler' : ['v_damageprofiler.txt', r"DamageProfiler v(\S+)"],
@@ -47,7 +47,7 @@
 results['Qualimap'] = '<span style="color:#999999;\">N/A</span>'
 results['Preseq'] = '<span style="color:#999999;\">N/A</span>'
 results['GATK HaplotypeCaller'] = '<span style="color:#999999;\">N/A</span>'
-results['GATK UnifiedGenotyper'] = '<span style="color:#999999;\">N/A</span>'
+#results['GATK UnifiedGenotyper'] = '<span style="color:#999999;\">N/A</span>'
 results['freebayes'] = '<span style="color:#999999;\">N/A</span>'
 results['VCF2genome'] = '<span style="color:#999999;\">N/A</span>'
 results['MTNucRatioCalculator'] = '<span style="color:#999999;\">N/A</span>'

docs/usage.md

@@ -713,12 +713,18 @@ Turns on genotyping to run on all post-dedup and downstream BAMs. For example if
 
 Specifies which genotyper to use. Current options are GATK (v3.5) UnifiedGenotyper or GATK (v4.xx). Furthermore, the FreeBayes Caller is available. Specify `'freebayes'`, `'hc'` or `'ug'` respectively.
 
-> NB that while UnifiedGenotyper is more suitable for low-coverage ancient DNA (HaplotypeCaller does _de novo_ assembly around each variant site), it is officially deperecated by the Broad Institute and is only accessible by an archived version not properly avaliable on `conda`. Therefore specifying 'ug' will download the GATK 3.5 `-jar` for you. This option therefore cannot be used when running the pipeline offline.
+> NB that while UnifiedGenotyper is more suitable for low-coverage ancient DNA (HaplotypeCaller does _de novo_ assembly around each variant site), it is officially deperecated by the Broad Institute and is only accessible by an archived version not properly avaliable on `conda`. Therefore if specifying 'ug', will need to supply a GATK 3.5 `-jar` to the parameter `gatk_ug_jar`. Note that this means the pipline is not fully reproducible in this configuration, unless you personally supply the `.jar` file.
 
 #### `--genotyping_source`
 
 Indicates which BAM file to use for genotyping, depending on what BAM processing modules you have turned on. Options are: `'raw'` for mapped only, filtered, or DeDup BAMs (with priority right to left); `'trimmed'` (for base clipped BAMs); `'pmd'` (for pmdtools output). Default is: `'raw'`.
 
+#### `--gatk_ug_jar`
+
+Specify a path to a local copy of a GATK 3.5 `.jar` file, preferably version '3.5-0-g36282e4'. The download location of this may be avaliable from the GATK forums of the Broad Institute.
+
+> You must manually report your version of GATK 3.5 in publications/MultiQC as it is not included in our container.
+
 #### `--gatk_call_conf`
 
 If selected a GATK genotyper phred-scaled confidence threshold of a given SNP/INDEL call. Default: 30

main.nf

@@ -124,8 +124,9 @@ def helpMessage() {
 
     Genotyping
       --run_genotyping                Perform genotyping on deduplicated BAMs.
-      --genotyping_tool               Specify which genotyper to use either GATK UnifiedGenotyper, GATK HaplotypeCaller or Freebayes. Note: UnifiedGenotyper uses now deprecated GATK 3.5 and requires internet access. Options: 'ug', 'hc', 'freebayes'
+      --genotyping_tool               Specify which genotyper to use either GATK UnifiedGenotyper, GATK HaplotypeCaller or Freebayes. Note: UnifiedGenotyper requires user-supplied defined GATK 3.5 jar file. Options: 'ug', 'hc', 'freebayes'
       --genotyping_source             Specify which input BAM to use for genotyping. Options: 'raw', 'trimmed' or 'pmd' Default: 'raw'
+      --gatk_ug_jar                   When specifying to use GATK UnifiedGenotyper, path to GATK 3.5 .jar.
       --gatk_call_conf                Specify GATK phred-scaled confidence threshold. Default: 30.
       --gatk_ploidy                   Specify GATK organism ploidy. Default: 2.
       --gatk_dbsnp                    Specify VCF file for output VCF SNP annotation (Optional). Gzip not accepted.
@@ -360,6 +361,10 @@ if (params.run_genotyping){
   if (params.genotyping_tool != 'ug' && params.genotyping_tool != 'hc' && params.genotyping_tool != 'freebayes') {
   exit 1, "Please specify a genotyper. Options: 'ug', 'hc', 'freebayes'. You gave: ${params.genotyping_tool}!"
   }
+
+  if (params.genotyping_tool == 'ug' && params.gatk_ug_jar == '') {
+  exit 1, "Please specify path to a GATK 3.5 .jar file with --gatk_ug_jar."
+  }
 
   if (params.gatk_ug_out_mode != 'EMIT_VARIANTS_ONLY' && params.gatk_ug_out_mode != 'EMIT_ALL_CONFIDENT_SITES' && params.gatk_ug_out_mode != 'EMIT_ALL_SITES') {
   exit 1, "Please check your GATK output mode. Options are: 'EMIT_VARIANTS_ONLY', 'EMIT_ALL_CONFIDENT_SITES', 'EMIT_ALL_SITES'. You gave: ${params.gatk_out_mode}!"
@@ -1685,33 +1690,20 @@ if ( params.run_genotyping && params.genotyping_source == 'raw' ) {
 
 
 /*
- Step 12a: Genotyping - UnifiedGenotyper Downloading
- NB: GATK 3.5 is the last release with VCF output in "old" VCF format, not breaking downstream tools. Therefore we need it (for now at least until downstream tools can read proper 4.2 VCFs... )
-
+ Step 12b: Genotyping - UG
+ NB: GATK 3.5 is the last release with VCF output in "old" VCF format, not breaking MVA. Therefore we need it (for now at least until downstream tools can read proper 4.2 VCFs... )
  */
 
-ch_gatk_download = Channel.value("download")
-
- process download_gatk_v3_5 {
-    label 'sc_tiny'
-    when: params.run_genotyping && params.genotyping_tool == 'ug'
-
-    input: 
-    val "download" from ch_gatk_download
-
-    output:
-    file "*.jar" into ch_unifiedgenotyper_jar,ch_unifiedgenotyper_versions_jar
-
-    """
-    wget -O GenomeAnalysisTK-3.5-0-g36282e4.tar.bz2 --referer https://software.broadinstitute.org/ 'https://software.broadinstitute.org/gatk/download/auth?package=GATK-archive&version=3.5-0-g36282e4' 
-    tar xjf GenomeAnalysisTK-3.5-0-g36282e4.tar.bz2 
-    """
-
- }
+if ( params.gatk_ug_jar != '' ) {
+  Channel
+    .fromPath( params.gatk_ug_jar )
+    .set{ ch_unifiedgenotyper_jar }
+} else {
+  Channel
+    .empty()
+    .set{ ch_unifiedgenotyper_jar }
+}
 
-/*
- Step 12b: Genotyping - UG
-*/
 
  process genotyping_ug {
   label 'mc_small'
@@ -2190,9 +2182,6 @@ process get_software_versions {
     mtnucratio --help &> v_mtnucratiocalculator.txt || true
     sexdeterrmine --version &> v_sexdeterrmine.txt || true
 
-    ## Hardcoded as no --version flag or equivalent
-    echo 'version 3.5-0-g36282e4' > v_gatk3_5.txt
-
     scrape_software_versions.py &> software_versions_mqc.yaml
     """
 }

nextflow.config

@@ -115,6 +115,7 @@ params {
   run_genotyping = false
   genotyping_tool = ''
   genotyping_source = "raw"
+  gatk_ug_jar = ''
   gatk_ug_genotype_model = 'SNP'
   gatk_hc_emitrefconf = 'GVCF'
   gatk_call_conf = '30'