See this.
Output filename will be suffixed with .trimmed
and outputs will be stored on gs://input-data-mirrored/input_fastqs/trimmed
.
$ preprocess/trimmomatic_gs.sh [FASTQ_GS_URI] [BASENAME_OF_TRIMMED_FASTQ]
Find a template JSON process/sample.json
$ caper submit process/chip.ihec.docker.wdl -i INPUT_JSON
Check workflow's status. You can also get WORKFLOW_ID
, which will be used for post-processing.
$ caper list
Based on this code
Deidentify experiment BAMs and control BAMS. Then make a bamCoverage
signal track for experiment BAMs. This script will find all BAMs on WORKFLOW_ROOT_GS_URI
and store postprocessed outputs on OUTPUT_DIR_GS_URI
. NO TRAILING SLASH ALLOWED FOR GS URI!
$ cd postprocess # will make tmp directory inside it
$ ./postprocess_gs.sh [WORKFLOW_ROOT_GS_URI] [OUTPUT_DIR_GS_URI]