Dealing with optional and mandatory GATK resource files

CHANGELOG.md

@@ -92,6 +92,7 @@ and this project adheres to [Semantic Versioning](https://semver.org/spec/v2.0.0
 - [#587](https://github.com/nf-core/sarek/pull/587) - Fix issue with VEP extra files
 - [#581](https://github.com/nf-core/sarek/pull/581) - `TIDDIT` is back
 - [#590](https://github.com/nf-core/sarek/pull/590) - Fix empty folders during scatter/gather
+- [#592](https://github.com/nf-core/sarek/pull/592) - Fix optional resources for Mutect2, GetPileupSummaries, and HaplotypeCaller: issue [#299](https://github.com/nf-core/sarek/issues/299), [#359](https://github.com/nf-core/sarek/issues/359), [#367](https://github.com/nf-core/sarek/issues/367)
 
 ### Deprecated
 

modules.json

@@ -130,7 +130,7 @@
                 "git_sha": "169b2b96c1167f89ab07127b7057c1d90a6996c7"
             },
             "gatk4/getpileupsummaries": {
-                "git_sha": "f40cfefc0899fd6bb6adc300142ca6c3a35573ff"
+                "git_sha": "1ac223ad436c1410e9c16a5966274b7ca1f8d855"
             },
             "gatk4/haplotypecaller": {
                 "git_sha": "169b2b96c1167f89ab07127b7057c1d90a6996c7"

subworkflows/local/prepare_genome.nf

@@ -52,7 +52,6 @@ workflow PREPARE_GENOME {
     TABIX_PON(pon.flatten().map{ it -> [[id:it.baseName], it] })
 
     chr_files = chr_dir
-    //TODO this works, but is not pretty. I will leave this in your hands during refactoring @Maxime
     if ( params.chr_dir.endsWith('tar.gz')){
         UNTAR_CHR_DIR(chr_dir.map{ it -> [[id:it[0].baseName], it] })
         chr_files = UNTAR_CHR_DIR.out.untar.map{ it[1] }
@@ -71,16 +70,16 @@ workflow PREPARE_GENOME {
     ch_versions = ch_versions.mix(TABIX_PON.out.versions)
 
     emit:
-        bwa                              = BWAMEM1_INDEX.out.index                                        // path: bwa/*
-        bwamem2                          = BWAMEM2_INDEX.out.index                                        // path: bwamem2/*
-        hashtable                        = DRAGMAP_HASHTABLE.out.hashmap                                  // path: dragmap/*
-        dbsnp_tbi                        = TABIX_DBSNP.out.tbi.map{ meta, tbi -> [tbi] }.collect()        // path: dbsnb.vcf.gz.tbi 
-        dict                             = GATK4_CREATESEQUENCEDICTIONARY.out.dict                        // path: genome.fasta.dict
-        fasta_fai                        = SAMTOOLS_FAIDX.out.fai.map{ meta, fai -> [fai] }               // path: genome.fasta.fai
-        germline_resource_tbi            = TABIX_GERMLINE_RESOURCE.out.tbi.map{ meta, tbi -> [tbi] }.collect()      // path: germline_resource.vcf.gz.tbi
-        known_indels_tbi                 = TABIX_KNOWN_INDELS.out.tbi.map{ meta, tbi -> [tbi] }.collect() // path: {known_indels*}.vcf.gz.tbi
-        msisensorpro_scan                = MSISENSORPRO_SCAN.out.list.map{ meta, list -> [list] }         // path: genome_msi.list
-        pon_tbi                          = TABIX_PON.out.tbi.map{ meta, tbi -> [tbi] }.collect()          // path: pon.vcf.gz.tbi
+        bwa                              = BWAMEM1_INDEX.out.index                                             // path: bwa/*
+        bwamem2                          = BWAMEM2_INDEX.out.index                                             // path: bwamem2/*
+        hashtable                        = DRAGMAP_HASHTABLE.out.hashmap                                       // path: dragmap/*
+        dbsnp_tbi                        = TABIX_DBSNP.out.tbi.map{ meta, tbi -> [tbi] }.collect()             // path: dbsnb.vcf.gz.tbi
+        dict                             = GATK4_CREATESEQUENCEDICTIONARY.out.dict                             // path: genome.fasta.dict
+        fasta_fai                        = SAMTOOLS_FAIDX.out.fai.map{ meta, fai -> [fai] }                    // path: genome.fasta.fai
+        germline_resource_tbi            = TABIX_GERMLINE_RESOURCE.out.tbi.map{ meta, tbi -> [tbi] }.collect() // path: germline_resource.vcf.gz.tbi
+        known_indels_tbi                 = TABIX_KNOWN_INDELS.out.tbi.map{ meta, tbi -> [tbi] }.collect()      // path: {known_indels*}.vcf.gz.tbi
+        msisensorpro_scan                = MSISENSORPRO_SCAN.out.list.map{ meta, list -> [list] }              // path: genome_msi.list
+        pon_tbi                          = TABIX_PON.out.tbi.map{ meta, tbi -> [tbi] }.collect()               // path: pon.vcf.gz.tbi
         chr_files                        = chr_files
-        versions                         = ch_versions                                                    // channel: [ versions.yml ]
+        versions                         = ch_versions                                                         // channel: [ versions.yml ]
 }

tests/test_tools.yml

@@ -430,10 +430,18 @@
     - no_intervals
     - tumor_only
     - variant_calling
-  exit_code: 1
-  stdout:
-    contains:
-      - "--tools mutect2 and --no_intervals cannot be used together."
+  files:
+    - path: results/variant_calling/sample2/mutect2/sample2.vcf.gz
+    - path: results/variant_calling/sample2/mutect2/sample2.vcf.gz.tbi
+    - path: results/variant_calling/sample2/mutect2/sample2.vcf.gz.stats
+    - path: results/variant_calling/sample2/mutect2/sample2.contamination.table
+    - path: results/variant_calling/sample2/mutect2/sample2.segmentation.table
+    - path: results/variant_calling/sample2/mutect2/sample2.artifactprior.tar.gz
+    - path: results/variant_calling/sample2/mutect2/sample2.pileupsummaries.table
+    - path: results/variant_calling/sample2/mutect2/sample2.filtered.vcf.gz
+    - path: results/variant_calling/sample2/mutect2/sample2.filtered.vcf.gz.tbi
+    - path: results/variant_calling/sample2/mutect2/sample2.filtered.vcf.gz.filteringStats.tsv
+    - path: results/csv/variantcalled.csv
 
 - name: Run variant calling on somatic sample with mutect2
   command: nextflow run main.nf -profile test,tools_somatic,docker --tools mutect2 -c ./tests/nextflow.config
@@ -462,10 +470,19 @@
     - no_intervals
     - somatic
     - variant_calling
-  exit_code: 1
-  stdout:
-    contains:
-      - "--tools mutect2 and --no_intervals cannot be used together."
+  files:
+    - path: results/variant_calling/sample4_vs_sample3/mutect2/sample4_vs_sample3.vcf.gz
+    - path: results/variant_calling/sample4_vs_sample3/mutect2/sample4_vs_sample3.vcf.gz.tbi
+    - path: results/variant_calling/sample4_vs_sample3/mutect2/sample4_vs_sample3.vcf.gz.stats
+    - path: results/variant_calling/sample4_vs_sample3/mutect2/sample4_vs_sample3.contamination.table
+    - path: results/variant_calling/sample4_vs_sample3/mutect2/sample4_vs_sample3.segmentation.table
+    - path: results/variant_calling/sample4_vs_sample3/mutect2/sample3.pileupsummaries.table
+    - path: results/variant_calling/sample4_vs_sample3/mutect2/sample4.pileupsummaries.table
+    - path: results/variant_calling/sample4_vs_sample3/mutect2/sample4_vs_sample3.artifactprior.tar.gz
+    - path: results/variant_calling/sample4_vs_sample3/mutect2/sample4_vs_sample3.filtered.vcf.gz
+    - path: results/variant_calling/sample4_vs_sample3/mutect2/sample4_vs_sample3.filtered.vcf.gz.tbi
+    - path: results/variant_calling/sample4_vs_sample3/mutect2/sample4_vs_sample3.filtered.vcf.gz.filteringStats.tsv
+    - path: results/csv/variantcalled.csv
 
 - name: Run variant calling on somatic sample with msisensor-pro
   command: nextflow run main.nf -profile test,tools_somatic,docker --tools msisensorpro

workflows/sarek.nf

@@ -59,10 +59,25 @@ if (params.wes) {
 }
 
 if(params.tools && params.tools.contains('mutect2')){
-    if(params.no_intervals){
-        log.error "--tools mutect2 and --no_intervals cannot be used together.\nOne of the tools within the Mutect2 subworkflow requires intervals. They can be provided to the pipeline with --intervals. If none are provided, they will be generated from the FASTA file.\nFor more information on the Mutect2 workflow, see here: https://gatk.broadinstitute.org/hc/en-us/articles/360035531132--How-to-Call-somatic-mutations-using-GATK4-Mutect2.\nFor more information on GetPileupsummaries, see here: https://gatk.broadinstitute.org/hc/en-us/articles/5358860217115-GetPileupSummaries"
+    if(!params.pon){
+        log.warn("No Panel-of-normal was specified for Mutect2.\nIt is highly recommended to use one: https://gatk.broadinstitute.org/hc/en-us/articles/5358911630107-Mutect2\nFor more information on how to create one: https://gatk.broadinstitute.org/hc/en-us/articles/5358921041947-CreateSomaticPanelOfNormals-BETA-")
+    }
+    if(!params.germline_resource){
+        log.warn("If Mutect2 is specified without a germline resource, no filtering will be done.\nIt is recommended to use one: https://gatk.broadinstitute.org/hc/en-us/articles/5358911630107-Mutect2")
+    }
+    if(params.pon && params.pon.contains("/Homo_sapiens/GATK/GRCh38/Annotation/GATKBundle/1000g_pon.hg38.vcf.gz")){
+        log.warn("The default Panel-of-Normals provided by GATK is used for Mutect2.\nIt is highly recommended to generate one from normal samples that are technical similar to the tumor ones.\nFor more information: https://gatk.broadinstitute.org/hc/en-us/articles/360035890631-Panel-of-Normals-PON-")
+    }
+}
+
+if(!params.dbsnp && !params.known_indels){
+    if(!params.skip_tools || params.skip_tools && !params.skip_tools.contains('baserecalibrator')){
+        log.error "Base quality score recalibration requires at least one resource file. Please provide at least one of `--dbsnp` or `--known_indels`\nYou can skip this step in the workflow by adding `--skip_tools baserecalibrator` to the command."
         exit 1
     }
+    if(params.tools && params.tools.contains('haplotypecaller')){
+        log.warn "If Haplotypecaller is specified, without `--dbsnp` or `--known_indels no filtering will be done. For filtering, please provide at least one of `--dbsnp` or `--known_indels`.\nFor more information see FilterVariantTranches (single-sample, default): https://gatk.broadinstitute.org/hc/en-us/articles/5358928898971-FilterVariantTranches\nFor more information see VariantRecalibration (--joint_germline): https://gatk.broadinstitute.org/hc/en-us/articles/5358906115227-VariantRecalibrator\nFor more information on GATK Best practice germline variant calling: https://gatk.broadinstitute.org/hc/en-us/articles/360035535932-Germline-short-variant-discovery-SNPs-Indels-"
+    }
 }
 
 // Save AWS IGenomes file containing annotation version
@@ -79,15 +94,16 @@ if (anno_readme && file(anno_readme).exists()) {
 */
 
 // Initialize file channels based on params, defined in the params.genomes[params.genome] scope
-chr_dir            = params.chr_dir            ? Channel.fromPath(params.chr_dir).collect()                  : []
-dbsnp              = params.dbsnp              ? Channel.fromPath(params.dbsnp).collect()                    : Channel.empty()
+chr_dir            = params.chr_dir            ? Channel.fromPath(params.chr_dir).collect()                  : Channel.value([])
+dbsnp              = params.dbsnp              ? Channel.fromPath(params.dbsnp).collect()                    : Channel.value([])
 fasta              = params.fasta              ? Channel.fromPath(params.fasta).collect()                    : Channel.empty()
 fasta_fai          = params.fasta_fai          ? Channel.fromPath(params.fasta_fai).collect()                : Channel.empty()
-germline_resource  = params.germline_resource  ? Channel.fromPath(params.germline_resource).collect()        : Channel.empty()
-known_indels       = params.known_indels       ? Channel.fromPath(params.known_indels).collect()             : Channel.empty()
-loci               = params.ac_loci            ? Channel.fromPath(params.ac_loci).collect()                  : []
-loci_gc            = params.ac_loci_gc         ? Channel.fromPath(params.ac_loci_gc).collect()               : []
-mappability        = params.mappability        ? Channel.fromPath(params.mappability).collect()              : []
+germline_resource  = params.germline_resource  ? Channel.fromPath(params.germline_resource).collect()        : Channel.value([]) //Mutec2 does not require a germline resource, so set to optional input
+known_indels       = params.known_indels       ? Channel.fromPath(params.known_indels).collect()             : Channel.value([])
+loci               = params.ac_loci            ? Channel.fromPath(params.ac_loci).collect()                  : Channel.value([])
+loci_gc            = params.ac_loci_gc         ? Channel.fromPath(params.ac_loci_gc).collect()               : Channel.value([])
+mappability        = params.mappability        ? Channel.fromPath(params.mappability).collect()              : Channel.value([])
+pon                = params.pon                ? Channel.fromPath(params.pon).collect()                      : Channel.value([]) //PON is optional for Mutect2 (but highly recommended)
 
 // Initialize value channels based on params, defined in the params.genomes[params.genome] scope
 snpeff_db          = params.snpeff_db          ?: Channel.empty()
@@ -96,7 +112,6 @@ vep_genome         = params.vep_genome         ?: Channel.empty()
 vep_species        = params.vep_species        ?: Channel.empty()
 
 // Initialize files channels based on params, not defined within the params.genomes[params.genome] scope
-pon                = params.pon                ? Channel.fromPath(params.pon).collect()                      : Channel.empty()
 snpeff_cache       = params.snpeff_cache       ? Channel.fromPath(params.snpeff_cache).collect()             : []
 vep_cache          = params.vep_cache          ? Channel.fromPath(params.vep_cache).collect()                : []
 
@@ -246,9 +261,9 @@ workflow SAREK {
     dragmap                = params.fasta                   ? params.dragmap               ? Channel.fromPath(params.dragmap).collect()               : PREPARE_GENOME.out.hashtable             : []
     dict                   = params.fasta                   ? params.dict                  ? Channel.fromPath(params.dict).collect()                  : PREPARE_GENOME.out.dict                  : []
     fasta_fai              = params.fasta                   ? params.fasta_fai             ? Channel.fromPath(params.fasta_fai).collect()             : PREPARE_GENOME.out.fasta_fai             : []
-    dbsnp_tbi              = params.dbsnp                   ? params.dbsnp_tbi             ? Channel.fromPath(params.dbsnp_tbi).collect()             : PREPARE_GENOME.out.dbsnp_tbi             : Channel.empty()
+    dbsnp_tbi              = params.dbsnp                   ? params.dbsnp_tbi             ? Channel.fromPath(params.dbsnp_tbi).collect()             : PREPARE_GENOME.out.dbsnp_tbi             : Channel.value([])
     germline_resource_tbi  = params.germline_resource       ? params.germline_resource_tbi ? Channel.fromPath(params.germline_resource_tbi).collect() : PREPARE_GENOME.out.germline_resource_tbi : []
-    known_indels_tbi       = params.known_indels            ? params.known_indels_tbi      ? Channel.fromPath(params.known_indels_tbi).collect()      : PREPARE_GENOME.out.known_indels_tbi      : Channel.empty()
+    known_indels_tbi       = params.known_indels            ? params.known_indels_tbi      ? Channel.fromPath(params.known_indels_tbi).collect()      : PREPARE_GENOME.out.known_indels_tbi      : Channel.value([])
     pon_tbi                = params.pon                     ? params.pon_tbi               ? Channel.fromPath(params.pon_tbi).collect()               : PREPARE_GENOME.out.pon_tbi               : []
     msisensorpro_scan      = PREPARE_GENOME.out.msisensorpro_scan
 
@@ -259,7 +274,6 @@ workflow SAREK {
 
     // known_sites is made by grouping both the dbsnp and the known indels ressources
     // Which can either or both be optional
-    // Actually BQSR has been throwing erros if no sides were provided so it must be at least one
     known_sites     = dbsnp.concat(known_indels).collect()
     known_sites_tbi = dbsnp_tbi.concat(known_indels_tbi).collect()