diff --git a/CHANGELOG.md b/CHANGELOG.md
index be1821cb50..1c4963826a 100644
--- a/CHANGELOG.md
+++ b/CHANGELOG.md
@@ -10,18 +10,22 @@ and this project adheres to [Semantic Versioning](http://semver.org/spec/v2.0.0.
 ### `Added`
 
 -   [#671](https://github.com/SciLifeLab/Sarek/pull/671) - New `publishDirMode` param and docs
--   [#673](https://github.com/SciLifeLab/Sarek/pull/673) - Profiles for BinAC and CFC clusters in Tübingen
+-   [#673](https://github.com/SciLifeLab/Sarek/pull/673), [#675](https://github.com/SciLifeLab/Sarek/pull/675),  [#676](https://github.com/SciLifeLab/Sarek/pull/676) - Profiles for BinAC and CFC clusters in Tübingen
+-   [#679](https://github.com/SciLifeLab/Sarek/pull/679) - Add container for `CreateIntervalBeds`
 
 ### `Changed`
 
 -   [#678](https://github.com/SciLifeLab/Sarek/pull/678) - Changing VEP to v92 and adjusting CPUs for VEP
 -   [#663](https://github.com/SciLifeLab/Sarek/pull/663) - Update `do_release.sh` script
 -   [#671](https://github.com/SciLifeLab/Sarek/pull/671) - publishDir modes are now params
+-   [#677](https://github.com/SciLifeLab/Sarek/pull/677) - Update docs
+-   [#679](https://github.com/SciLifeLab/Sarek/pull/679) - Update old awsbatch configuration
 
 ### `Fixed`
 
 -   [#665](https://github.com/SciLifeLab/Sarek/pull/665) - Input bam file now has always the same name (whether it is from a single fastq pair or multiple) in the MarkDuplicates process, so metrics too
 -   [#672](https://github.com/SciLifeLab/Sarek/pull/672) - process `PullSingularityContainers` from `buildContainers.nf` now expect a file with the correct `.simg` extension for singularity images, and no longer the `.img` one.
+-   [#679](https://github.com/SciLifeLab/Sarek/pull/679) - Add publishDirMode for `germlineVC.nf`
 
 ## [2.2.1] - 2018-10-04
 
diff --git a/Sarek-data b/Sarek-data
index c2da0d2a8a..d1f1848688 160000
--- a/Sarek-data
+++ b/Sarek-data
@@ -1 +1 @@
-Subproject commit c2da0d2a8a1c1a8e9b9b0930b84e34073ea43d03
+Subproject commit d1f1848688d2f0a4f8c792373c3002ab046063c0
diff --git a/annotate.nf b/annotate.nf
index 7ae5fb828a..1599239767 100644
--- a/annotate.nf
+++ b/annotate.nf
@@ -215,7 +215,7 @@ process RunVEP {
   script:
   finalannotator = annotator == "snpeff" ? 'merge' : 'vep'
   genome = params.genome == 'smallGRCh37' ? 'GRCh37' : params.genome
-  cache_version = params.genome == 'GRCh38' ? 92 : 91
+  cache_version = params.genome == 'GRCh38' || params.genome == 'iGRCh38' ? 92 : 91
   """
   /opt/vep/src/ensembl-vep/vep --dir /opt/vep/.vep/  \
   -i ${vcf} \
diff --git a/conf/aws-batch.config b/conf/aws-batch.config
index 4c4c837610..ec8a9e9139 100644
--- a/conf/aws-batch.config
+++ b/conf/aws-batch.config
@@ -8,7 +8,8 @@
  */
 
 params {
-  genome_base = params.genome == 'GRCh37' ? "s3://caw-references/grch37" : params.genome == 'GRCh38' ? "s3://caw-references/grch38" : "s3://caw-references/smallgrch37"
+  genome_base = params.genome == 'GRCh37' ? "s3://sarek-references/Homo_sapiens/GATK/GRCh37" : params.genome == 'iGRCh38' ? "s3://sarek-references/Homo_sapiens/GATK/GRCh38" : "s3://sarek-references/small"
+  publishDirMode = 'copy'
 }
 
 executor.name = 'awsbatch'
@@ -16,7 +17,7 @@ executor.awscli = '/home/ec2-user/miniconda/bin/aws'
 
 process {
   executor = 'awsbatch'
-  queue = 'caw-job-queue'
+  queue = 'Sarek-queue'
 
   errorStrategy = {task.exitStatus == 143 ? 'retry' : 'terminate'}
   maxErrors = '-1'
diff --git a/conf/containers.config b/conf/containers.config
index 6e0ab0a1ad..ad2becd9e5 100644
--- a/conf/containers.config
+++ b/conf/containers.config
@@ -26,6 +26,9 @@ process {
   withName:ConcatVCF {
     container = "${params.repository}/sarek:${params.tag}"
   }
+  withName:CreateIntervalBeds {
+    container = "${params.repository}/sarek:${params.tag}"
+  }
   withName:CreateRecalibrationTable {
     container = "${params.repository}/sarek:${params.tag}"
   }
diff --git a/conf/genomes.config b/conf/genomes.config
index 53ceecf9cf..b736bc9e4f 100644
--- a/conf/genomes.config
+++ b/conf/genomes.config
@@ -15,8 +15,6 @@ params {
   genomes {
     'GRCh37' {
       acLoci      = "${params.genome_base}/1000G_phase3_20130502_SNP_maf0.3.loci"
-      cosmic      = "${params.genome_base}/GRCh37_Cosmic_v83.vcf"
-      cosmicIndex = "${cosmic}.idx"
       dbsnp       = "${params.genome_base}/dbsnp_138.b37.vcf"
       dbsnpIndex  = "${dbsnp}.idx"
       genomeFile  = "${params.genome_base}/human_g1k_v37_decoy.fasta"
@@ -30,8 +28,6 @@ params {
     }
     'GRCh38' {
       acLoci        = "${params.genome_base}/1000G_phase3_GRCh38_maf0.3.loci"
-      cosmic        = "${params.genome_base}/COSMICv80.vcf"
-      cosmicIndex   = "${cosmic}.idx"
       dbsnp         = "${params.genome_base}/dbsnp_146.hg38.vcf.gz"
       dbsnpIndex    = "${dbsnp}.tbi"
       genomeFile    = "${params.genome_base}/Homo_sapiens_assembly38.fasta"
@@ -43,13 +39,24 @@ params {
       knownIndelsIndex = "${params.genome_base}/{Mills_and_1000G_gold_standard.indels.hg38,beta/Homo_sapiens_assembly38.known_indels}.vcf.gz.tbi"
       snpeffDb      = "GRCh38.86"
 			// This a nasty-looking list of allele-frequencies files. Add/remove files to match to your sets
-			//AF_files			= "${params.genome_base}/{00-All.dbsnp_151.hg38.CAF.TOPMED.alternate.allele.freq,hapmap_3.3_grch38_pop_stratified_af.HMAF,SweGen_hg38_stratified.SWAF}.vcf" 
-			//AF_indexes		= "${params.genome_base}/{00-All.dbsnp_151.hg38.CAF.TOPMED.alternate.allele.freq,hapmap_3.3_grch38_pop_stratified_af.HMAF,SweGen_hg38_stratified.SWAF}.vcf.idx" 
+			//AF_files			= "${params.genome_base}/{00-All.dbsnp_151.hg38.CAF.TOPMED.alternate.allele.freq,hapmap_3.3_grch38_pop_stratified_af.HMAF,SweGen_hg38_stratified.SWAF}.vcf"
+			//AF_indexes		= "${params.genome_base}/{00-All.dbsnp_151.hg38.CAF.TOPMED.alternate.allele.freq,hapmap_3.3_grch38_pop_stratified_af.HMAF,SweGen_hg38_stratified.SWAF}.vcf.idx"
+    }
+    'iGRCh38' {
+      acLoci           = "${params.genome_base}/Annotation/ASCAT/1000G_phase3_GRCh38_maf0.3.loci"
+      dbsnp            = "${params.genome_base}/Annotation/GATKBundle/dbsnp_146.hg38.vcf.gz"
+      dbsnpIndex       = "${params.genome_base}/Annotation/GATKBundle/dbsnp_146.hg38.vcf.gz.tbi"
+      genomeFile       = "${params.genome_base}/Sequence/WholeGenomeFasta/Homo_sapiens_assembly38.fasta"
+      genomeDict       = "${params.genome_base}/Sequence/WholeGenomeFasta/Homo_sapiens_assembly38.dict"
+      genomeIndex      = "${params.genome_base}/Sequence/WholeGenomeFasta/Homo_sapiens_assembly38.fasta.fai"
+      bwaIndex         = "${params.genome_base}/Sequence/BWAIndex/Homo_sapiens_assembly38.fasta.64.{alt,amb,ann,bwt,pac,sa}"
+      intervals        = "${params.genome_base}/Annotation/intervals/wgs_calling_regions.hg38.bed"
+      knownIndels      = "${params.genome_base}/Annotation/GATKBundle/{Mills_and_1000G_gold_standard.indels.hg38,Homo_sapiens_assembly38.known_indels}.vcf.gz"
+      knownIndelsIndex = "${params.genome_base}/Annotation/GATKBundle/{Mills_and_1000G_gold_standard.indels.hg38,Homo_sapiens_assembly38.known_indels}.vcf.gz.tbi"
+      snpeffDb         = "GRCh38.86"
     }
     'smallGRCh37' {
       acLoci      = "${params.genome_base}/1000G_phase3_20130502_SNP_maf0.3.small.loci"
-      cosmic      = "${params.genome_base}/b37_cosmic_v74.noCHR.sort.4.1.small.vcf"
-      cosmicIndex = "${cosmic}.idx"
       dbsnp       = "${params.genome_base}/dbsnp_138.b37.small.vcf"
       dbsnpIndex  = "${dbsnp}.idx"
       genomeFile  = "${params.genome_base}/human_g1k_v37_decoy.small.fasta"
diff --git a/conf/singularity-path.config b/conf/singularity-path.config
index 448e7d1432..d41cf45059 100644
--- a/conf/singularity-path.config
+++ b/conf/singularity-path.config
@@ -31,6 +31,9 @@ process {
   withName:ConcatVCF {
     container = "${params.containerPath}/sarek-${params.tag}.simg"
   }
+  withName:CreateIntervalBeds {
+    container = "${params.containerPath}/sarek-${params.tag}.simg"
+  }
   withName:CreateRecalibrationTable {
     container = "${params.containerPath}/sarek-${params.tag}.simg"
   }
diff --git a/germlineVC.nf b/germlineVC.nf
index 1cc9f39ddc..7b53d1006c 100644
--- a/germlineVC.nf
+++ b/germlineVC.nf
@@ -104,7 +104,7 @@ if (params.verbose) recalibratedBam = recalibratedBam.view {
 process RunSamtoolsStats {
   tag {idPatient + "-" + idSample}
 
-  publishDir directoryMap.samtoolsStats, mode: 'link'
+  publishDir directoryMap.samtoolsStats, mode: params.publishDirMode
 
   input:
     set idPatient, status, idSample, file(bam), file(bai) from bamForSamToolsStats
@@ -125,7 +125,7 @@ if (params.verbose) samtoolsStatsReport = samtoolsStatsReport.view {
 process RunBamQC {
   tag {idPatient + "-" + idSample}
 
-  publishDir directoryMap.bamQC, mode: 'link'
+  publishDir directoryMap.bamQC, mode: params.publishDirMode
 
   input:
     set idPatient, status, idSample, file(bam), file(bai) from bamForBamQC
@@ -356,7 +356,7 @@ if (params.verbose) vcfsToMerge = vcfsToMerge.view {
 process ConcatVCF {
   tag {variantCaller + "-" + idSampleNormal}
 
-  publishDir "${directoryMap."$variantCaller"}", mode: 'link'
+  publishDir "${directoryMap."$variantCaller"}", mode: params.publishDirMode
 
   input:
     set variantCaller, idPatient, idSampleNormal, idSampleTumor, file(vcFiles) from vcfsToMerge
@@ -394,7 +394,7 @@ if (params.verbose) vcfConcatenated = vcfConcatenated.view {
 process RunSingleStrelka {
   tag {idSample}
 
-  publishDir directoryMap.strelka, mode: 'link'
+  publishDir directoryMap.strelka, mode: params.publishDirMode
 
   input:
     set idPatient, status, idSample, file(bam), file(bai) from bamsForSingleStrelka
@@ -447,7 +447,7 @@ if (params.verbose) singleStrelkaOutput = singleStrelkaOutput.view {
 process RunSingleManta {
   tag {idSample + " - Single Diploid"}
 
-  publishDir directoryMap.manta, mode: 'link'
+  publishDir directoryMap.manta, mode: params.publishDirMode
 
   input:
     set idPatient, status, idSample, file(bam), file(bai) from bamsForSingleManta
@@ -511,7 +511,7 @@ vcfForQC = Channel.empty().mix(
 process RunBcftoolsStats {
   tag {vcf}
 
-  publishDir directoryMap.bcftoolsStats, mode: 'link'
+  publishDir directoryMap.bcftoolsStats, mode: params.publishDirMode
 
   input:
     set variantCaller, file(vcf) from vcfForBCFtools
@@ -534,7 +534,7 @@ bcfReport.close()
 process RunVcftools {
   tag {vcf}
 
-  publishDir directoryMap.vcftools, mode: 'link'
+  publishDir directoryMap.vcftools, mode: params.publishDirMode
 
   input:
     set variantCaller, file(vcf) from vcfForVCFtools
diff --git a/somaticVC.nf b/somaticVC.nf
index 89a814da2c..9a99aebebd 100644
--- a/somaticVC.nf
+++ b/somaticVC.nf
@@ -279,14 +279,12 @@ process RunMutect2 {
 
   input:
     set idPatient, idSampleNormal, file(bamNormal), file(baiNormal), idSampleTumor, file(bamTumor), file(baiTumor), file(intervalBed) from bamsFMT2
-    set file(genomeFile), file(genomeIndex), file(genomeDict), file(dbsnp), file(dbsnpIndex), file(cosmic), file(cosmicIndex) from Channel.value([
+    set file(genomeFile), file(genomeIndex), file(genomeDict), file(dbsnp), file(dbsnpIndex) from Channel.value([
       referenceMap.genomeFile,
       referenceMap.genomeIndex,
       referenceMap.genomeDict,
       referenceMap.dbsnp,
-      referenceMap.dbsnpIndex,
-      referenceMap.cosmic,
-      referenceMap.cosmicIndex
+      referenceMap.dbsnpIndex
     ])
 
   output:
@@ -832,9 +830,6 @@ def defineReferenceMap() {
     'acLoci'           : checkParamReturnFile("acLoci"),
     'dbsnp'            : checkParamReturnFile("dbsnp"),
     'dbsnpIndex'       : checkParamReturnFile("dbsnpIndex"),
-    // cosmic VCF with VCF4.1 header
-    'cosmic'           : checkParamReturnFile("cosmic"),
-    'cosmicIndex'      : checkParamReturnFile("cosmicIndex"),
     // genome reference dictionary
     'genomeDict'       : checkParamReturnFile("genomeDict"),
     // FASTA genome reference
@@ -923,8 +918,6 @@ def minimalInformationMessage() {
   log.info "  Tag          : " + params.tag
   log.info "Reference files used:"
   log.info "  acLoci      :\n\t" + referenceMap.acLoci
-  log.info "  cosmic      :\n\t" + referenceMap.cosmic
-  log.info "\t" + referenceMap.cosmicIndex
   log.info "  dbsnp       :\n\t" + referenceMap.dbsnp
   log.info "\t" + referenceMap.dbsnpIndex
   log.info "  genome      :\n\t" + referenceMap.genomeFile