task teprof_s1 { String sample_id File fastq1 File fastq2 File STAR_INDEX_DIR String disk_size String docker String cluster command <<< set -o pipefail set -e pigz -p 8 -dc ${fastq1} > ${sample_id}_R1.fastq pigz -p 8 -dc ${fastq2} > ${sample_id}_R2.fastq STAR \ --runThreadN 8 \ --genomeDir ${STAR_INDEX_DIR} \ --readFilesIn ${sample_id}_R1.fastq ${sample_id}_R2.fastq \ --outSAMstrandField intronMotif \ --outSAMtype BAM SortedByCoordinate \ --outFileNamePrefix ./${sample_id}. samtools view -@ 16 -q 255 -h ${sample_id}.Aligned.sortedByCoord.out.bam > ${sample_id}.filtered.Aligned.sortedByCoord.out.bam stringtie -p 8 ${sample_id}.filtered.Aligned.sortedByCoord.out.bam -o ${sample_id}.Aligned.sortedByCoord.out.gtf -m 100 -c 1 --rf python /database/rnapipelinerefhg38/rnapipeline/rmskhg38_annotate_gtf_update_test_tpm.py ${sample_id}.Aligned.sortedByCoord.out.gtf /database/rnapipelinerefhg38/rnapipeline/arguments.txt python /database/rnapipelinerefhg38/rnapipeline/annotationtpmprocess.py ${sample_id}.Aligned.sortedByCoord.out.gtf_annotated_filtered_test mkdir ${sample_id}_annotated cp ${sample_id}.Aligned.sortedByCoord.out.gtf_annotated_* ${sample_id}_annotated tar -zcvf ${sample_id}_annotated.tgz ${sample_id}_annotated rm ${sample_id}.filtered.Aligned.sortedByCoord.out.bam rm ${sample_id}_R1.fastq rm ${sample_id}_R2.fastq >>> runtime { docker: docker cluster: cluster systemDisk: "cloud_ssd 40" dataDisk: "cloud_ssd " + disk_size + " /cromwell_root/" } output { File annotated = "${sample_id}_annotated.tgz" File annotated_use = "${sample_id}.Aligned.sortedByCoord.out.gtf_annotated_filtered_test_c" File output_bam = "${sample_id}.Aligned.sortedByCoord.out.bam" File output_gtf = "${sample_id}.Aligned.sortedByCoord.out.gtf" } }