Test data for ENCODE atac-seq-pipeline

Single ended dataset (ENCSR889WQX) and paired end dataset (ENCSR356KRQ) are subsampled down to 1/400 reads.

For genome data (/genome_data) sequences for chr19 and chrM are extracted from hg38 and mm10 and bowtie2 indices are built on them.

$ cd scripts
$ ./subsample_ref_fasta.sh

0. Make sure that you have an executable cromwell-30.1.jar in your PATH.

1. Specify correct file paths in subsample_fastq.sh and run to subsample test samples.

$ cd test_sample
$ ./subsample_fastq.sh

2. Generate base reference outputs by running the following shell scripts. These test samples are subsampled down to 1/200 reads.

$ cd scripts
$ ./ENCSR356KRQ.sh
$ ./ENCSR889WQX.sh

3. Wait until 2) is done. Link outputs of 2) to JSON files in test_sample/*.sh, run other shell scripts.

$ cd scripts
$ ./ENCSR356KRQ_disable_tn5_shift.sh
$ ./ENCSR356KRQ_no_dup_removal.sh
$ ./ENCSR356KRQ_no_multimapping.sh
$ ./ENCSR356KRQ_subsample.sh
$ ./ENCSR356KRQ_subsample_xcor.sh
$ ./ENCSR889WQX_disable_tn5_shift.sh
$ ./ENCSR889WQX_no_dup_removal.sh
$ ./ENCSR889WQX_no_multimapping.sh
$ ./ENCSR889WQX_subsample.sh
$ ./ENCSR889WQX_subsample_xcor.sh