For RNA-seq data, from bam/fastq to AS sites files.
Nevar pievienot vairāk kā 25 tēmas
Tēmai ir jāsākas ar burtu vai ciparu, tā var saturēt domu zīmes ('-') un var būt līdz 35 simboliem gara.
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- task rmats {
- String sample_id
- File bam1
- File bam2
- File reference_gtf_file
-
-
- String docker
- String cluster
- String disk_size
-
-
-
- command <<<
- set -o pipefail
- set -e
-
- mkdir -p ${sample_id}/output
- mkdir -p ${sample_id}/tmp_output
-
- echo ${bam1} > b1_txt
- echo ${bam2} > b2_txt
-
- python /usr/local/bin/rmats.py --b1 b1_txt \
- --b2 b2_txt \
- --gtf ${reference_gtf_file} \
- -t paired \
- --readLength 150 \
- --nthread 4 \
- --od ${sample_id}/output \
- --tmp ${sample_id}/tmp_output
-
- find . -depth > fileList.txt
- >>>
-
- runtime {
- docker: docker
- cluster: cluster
- systemDisk: "cloud_ssd 40"
- dataDisk: "cloud_ssd " + disk_size + " /cromwell_root/"
- }
-
- output {
- File fileList = "fileList.txt"
- Array[File] AS_txt = glob("${sample_id}/output/*.txt")
- Array[File] tmp = glob("${sample_id}/output/tmp/*")
- }
- }
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