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How to download genome database

  1. Choose GENOME from hg19, hg38, mm9 and mm10 and specify a destination directory. 
    $ bash scripts/download_genome_data.sh [GENOME] [DESTINATION_DIR]
  2. Find a TSV file on the destination directory and use it for "atac.genome_tsv" in your input JSON.

How to build genome database

  1. Install Conda.

  2. Install pipeline's Conda environment.

    $ bash scripts/uninstall_conda_env.sh  # to remove any existing pipeline env
$ bash scripts/install_conda_env.sh

  3. Choose GENOME from hg19, hg38, mm9 and mm10 and specify a destination directory. This will take several hours. We recommend not to run this installer on a login node of your cluster. It will take >8GB memory and >2h time.

    $ conda activate encd-atac
$ bash scripts/build_genome_data.sh [GENOME] [DESTINATION_DIR]

  4. Find a TSV file on the destination directory and use it for "atac.genome_tsv" in your input JSON.

How to build genome database for your own genome

  1. You can build your own genome database if your reference genome has one of the following file types.

    • .fasta.gz
    • .fa.gz
    • .fasta.bz2
    • .fa.gz2
    • .2bit

  2. Get a URL for your reference genome. You may need to upload it to somewhere on the internet.

  3. Get a URL for a gzipped blacklist BED file for your genome. If you don't have one then skip this step. An example blacklist for hg38 is here.

  4. Find the following lines in scripts/build_genome_data.sh and modify them as follows. Give a good name [YOUR_OWN_GENOME] for your genome. For MITO_CHR_NAME use a correct mitochondrial chromosome name of your genome (e.g. chrM or MT). For REGEX_BFILT_PEAK_CHR_NAME Perl style regular expression must be used to keep regular chromosome names only in a blacklist filtered (.bfilt.) peaks files. This .bfilt. peak files are considered final peaks output of the pipeline and peaks BED files for genome browser tracks (.bigBed and .hammock.gz) are converted from these .bfilt. peaks files. Chromosome name filtering with REGEX_BFILT_PEAK_CHR_NAME will be done even without the blacklist itself.

    ...

elif [[ $GENOME == "YOUR_OWN_GENOME" ]]; then
  # Perl style regular expression to keep regular chromosomes only.
  # this reg-ex will be applied to peaks after blacklist filtering (b-filt) with "grep -P".
  # so that b-filt peak file (.bfilt.*Peak.gz) will only have chromosomes matching with this pattern
  # this reg-ex will work even without a blacklist.
  # you will still be able to find a .bfilt. peak file
  REGEX_BFILT_PEAK_CHR_NAME="chr[\dXY]+"
  # mitochondrial chromosome name (e.g. chrM, MT)
  MITO_CHR_NAME="chrM"
  # URL for your reference FASTA (fasta, fasta.gz, fa, fa.gz, 2bit)
  REF_FA="https://some.where.com/your.genome.fa.gz"
  # 3-col blacklist BED file to filter out overlapping peaks from b-filt peak file (.bfilt.*Peak.gz file).
  # leave it empty if you don't have one
  BLACKLIST=
...

  5. Specify a destination directory for your genome database and run the installer. This will take several hours.

    $ bash scripts/build_genome_data.sh [YOUR_OWN_GENOME] [DESTINATION_DIR]

  6. Find a TSV file in the destination directory and use it for "atac.genome_tsv" in your input JSON.