A Cromwell workflow to call and filter variants from sequencing data.
- QC on samples raw sequencing data
java -Dconfig.file=sge.config -Xms32G -Xmx32G -jar cromwell.jar run fastQC.wdl --inputs fastQC.inputs.json > fastQC.log
- Align samples raw sequencing data (fastq -> bam)
java -Dconfig.file=sge.config -Xms32G -Xmx32G -jar cromwell.jar run alignment_WGS.wdl --inputs alignment_WGS.inputs.json > alignment_WGS.log
- Call variants (bam -> vcf)
java -Dconfig.file=sge.config -Xms32G -Xmx32G -jar cromwell.jar run VariantDiscovery.wdl --inputs VariantDiscovery.inputs.json > VariantDiscovery.log
- Filter variants
java -Dconfig.file=sge.config -Xms8G -Xmx8G -jar cromwell.jar run VariantFiltering.wdl --inputs VariantFiltering.inputs.json > VariantFiltering.log