-
Download cromwell.
$ cd $ wget https://github.com/broadinstitute/cromwell/releases/download/34/cromwell-34.jar $ chmod +rx cromwell-34.jar
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Git clone this pipeline and move into it.
$ cd $ git clone https://github.com/ENCODE-DCC/atac-seq-pipeline $ cd atac-seq-pipeline
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Download a SUBSAMPLED (1/400) paired-end sample of ENCSR356KRQ.
$ wget https://storage.googleapis.com/encode-pipeline-test-samples/encode-atac-seq-pipeline/ENCSR356KRQ/ENCSR356KRQ_fastq_subsampled.tar $ tar xvf ENCSR356KRQ_fastq_subsampled.tar
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Download pre-built genome database for hg38.
$ wget https://storage.googleapis.com/encode-pipeline-genome-data/test_genome_database_hg38_atac.tar $ tar xvf test_genome_database_hg38_atac.tar
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CHECK YOUR SINGULARITY VERSION FIRST AND UPGRADE IT TO A VERSION
>=2.5.2
OR PIPELINE WILL NOT WORK CORRECTLY.$ singularity --version
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Pull a singularity container for the pipeline. This will pull pipeline's docker container first and build a singularity one on
~/.singularity
.$ mkdir -p ~/.singularity && cd ~/.singularity && SINGULARITY_CACHEDIR=~/.singularity SINGULARITY_PULLFOLDER=~/.singularity singularity pull --name atac-seq-pipeline-v1.3.0.simg -F docker://quay.io/encode-dcc/atac-seq-pipeline:v1.3.0
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Run a pipeline for the test sample.
$ INPUT=examples/local/ENCSR356KRQ_subsampled.json $ PIPELINE_METADATA=metadata.json $ java -jar -Xmx1G -Dconfig.file=backends/backend.conf -Dbackend.default=singularity cromwell-34.jar run atac.wdl -i ${INPUT} -o workflow_opts/singularity.json -m ${PIPELINE_METADATA}
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It will take about an hour. You will be able to find all outputs on
cromwell-executions/atac/[RANDOM_HASH_STRING]/
. See output directory structure for details. -
See full specification for input JSON file.
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You can resume a failed pipeline from where it left off by using
PIPELINE_METADATA
(metadata.json
) file. This file is created for each pipeline run. See here for details. Once you get a new input JSON file from the resumer, use itINPUT=resume.[FAILED_WORKFLOW_ID].json
instead ofINPUT=examples/local/ENCSR356KRQ_subsampled.json
. -
IF YOU WANT TO RUN PIPELINES WITH YOUR OWN INPUT DATA/GENOME DATABASE, PLEASE ADD THEIR DIRECTORIES TO
workflow_opts/singularity.json
. For example, you have input FASTQs on/your/input/fastqs/
and genome database installed on/your/genome/database/
then add/your/
tosingularity_bindpath
. You can also define multiple directories there. It's comma-separated.{ "default_runtime_attributes" : { "singularity_container" : "~/.singularity/chip-seq-pipeline-v1.3.0.simg", "singularity_bindpath" : "/your/,YOUR_OWN_DATA_DIR1,YOUR_OWN_DATA_DIR1,..." } }