Install java (jdk >= 1.7 or jre >= 1.7) and the latest git on your system.
Install Anaconda Python3 (or Miniconda3) on your system. Open a new terminal after installation.
Install BigDataScript v0.9999 on your system.
See details here
ATAC Seq pipeline is dependent on two external git repos and each has the following directory:
ataqc/ (public, https://bitbucket.org/csfoo/ataqc)
chipseq/ (public, https://github.com/kundajelab/TF_chipseq_pipeline)
To FULLY clone the repo:
$ git clone https://github.com/kundajelab/bds_atac --recursive
To FULLY pull the repo:
$ git pull --recurse-submodules
Install software dependencies automatically (DO NOT run this on kundaje clusters or SCG3). It will create two conda environments (aquas_chipseq and aquas_chipseq_py3) in Miniconda3.
$ ./install_dependencies.sh
Replace BDS's default bds.config with a correct one:
$ cp chipseq/bds.config $HOME/.bds
BDS and all dependencies have already been installed on lab servers (including SCG3). Do not run install_dependencies.sh on these servers. Get the latest version of chipseq pipelines. Don't forget to move bds.config to BigDataScript (BDS) directory
$ git clone https://github.com/kundajelab/bds_atac --recursive
$ cd bds_atac
$ mkdir -p $HOME/.bds
$ cp chipseq/bds.config $HOME/.bds/
For Kundaje lab servers (mitra, nandi, durga, kali, vayu, amold and wotan) and SCG3 (carmack*, crick*, scg3*), the pipeline automatically determines the type of servers and set shell environments and species database.
$ bds bds_atac.bds ... -species [SPECIES; hg19, mm9, ... ]
- Define parameters in command line argument (legacy method, NOT RECOMMENDED) This input method does not support multiple replicates and always generate V plot and perform preseq analysis.
$ bds atac.bds [BOWTIE2_INDEX] [READ1] [READ2] [NTHREADS_BWT2] [GENOMESIZE; hs for human, mm for mouse] [CHROMSIZES_FILE] [VPLOT_INDEX] [OUTPUT_DIR]
- Define parameters in command line argument. For general use, use the following command line:
$ bds atac.bds -fastq1 [READ1] -fastq2 [READ2] -bwt2_idx [BOWTIE2_INDEX] \
-gensz [GENOMESIZE; hs for human, mm for mouse] -chrsz [CHR_SIZES_FILE]
If your fastqs are already trimmed, add the following to the command line to skip trimming stage.
-trimmed_fastq
If your data are single ended, add the following to the command line.
-se
For ATAQC, you need to define the following parameters. parameters -preseq and -vplot will be ignored since they are already included in ATAQC. See help ($ bds atac.bds) for description of all parameters. Even though you don't use a species file -species_file, you need to specify a species name for ATAQC.
-species [hg19, mm9 or ...] -vplot_idx [] -ref_fa [] -blacklist [] -dnase [] -prom [] -enh [] -reg2map [] -roadmap_meta []
If you don't want ATAQC, add the following to command line.
-no_ataqc
If you have just one replicate (PE), define fastqs with -fastq[PAIR_NO].
-fastq1 [READ_PAIR1] -fastq2 [READ_PAIR2] \
For multiple replicates (PE), define fastqs with -fastq[REP_NO]_[PAIR_NO]. Add -fastq[]_[] for each replicate and pair to the command line:replicates.
-fastq1_1 [READ_REP1_PAIR1] -fastq1_2 [READ_REP1_PAIR2] -fastq2_1 [READ_REP2_PAIR1] -fastq2_2 [READ_REP2_PAIR2] ...
For multiple replicates (SE), define fastqs with -fastq[REP_NO]:
-se -fastq1 [READ_REP1] -fastq2 [READ_REP2] ...
You can also start from bam files. There are two kinds of bam files (raw or deduped) and you need to explicitly choose between raw bam (bam) and deduped one (nodup_bam) with -input [BAM_TYPE]. Don't forget to add -se if they are not paired end (PE).
For raw bams,
-bam1 [RAW_BAM_REP1] -bam2 [RWA_BAM_REP1] ...
For deduped (filtered) bams, preseq analysis and v plot will not be available since they need sorted raw bam.
-filt_bam1 [NODUP_BAM_REP1] -filt_bam2 [NODUP_BAM_REP1] ...
To subsample beds (tagaligns) add the following to the command line. This is different from subsampling for cross-corr. analysis. Peaks will be called with subsampled tagaligns.
-subsample [NO_READS_TO_SUBSAMPLE]
To disable pseudo replicate generation. By default, IDR will be done for true replicates and pseudo replicates, but if you have -true_rep in the command line, you will also get IDR on true replicates only. IDR on a single replicate and naive overlapped peak is not avaiable when this flag is on:
-true_rep
IDR analysis is included in the pipeline by default. For better IDR QC, add path to blacklist idr (for hg19, http://hgdownload.cse.ucsc.edu/goldenPath/hg19/encodeDCC/wgEncodeMapability/wgEncodeDacMapabilityConsensusExcludable.bed.gz).
-blacklist_idr [BLACKLIST_IDR]
If you don't want IDR analysis on peaks (two replicates are needed) add the following:
-no_idr
To change resource settings (# of processor, max memory and walltime) for bowtie2, add the following to command line, please note that memory is PER CPU:
-nth_bwt2 [NTHREADS_BWT2] -mem_bwt2 [MAX_MEMORY_PER_THREAD_BWT2; e.g. 20G] -wt_bwt2 [WALLTIME_BWT2; e.g. 20h]
For MACS2 peak calling:
-nth_macs2 [NTHREADS_MACS2] -mem_macs2 [MEMORY_MACS2; e.g. 20G] -wt_macs2 [WALLTIME_MACS2; e.g. 20h]
For Kundaje lab cluster and SCG3, skip all genome specific parameters (like bwt2_idx, chrsz, ... ) and just specify species.
$ bds atac.bds -fastq1 [READ1] -fastq2 [READ2] -species [hg19 or mm9]
For other clusters, add -mod, -addpath, -shcmd, -conda_env to set up enviroment variables for your jobs or make an environment file for your system. See details here.
To list all parameters and default values for them,
$ bds atac.bds
- Define parameters in configuration file. Key names in a configruation file are identical to parameter names on command line.
$ bds atac.bds [CONF_FILE]
or
$ bds atac.bds -c [CONF_FILE]
$ cat [CONF_FILE]
fastq1= [READ1]
fastq2= [READ2]
...
See details here
ATAC seq for each repliacte will go IN PARALLEL!. Consider your computation resources! # of processors taken will be :
max( [NTH_BWT2], [NTH_MACS2], [NTH_SPP] ) x [NUM_REP]
For completely serialized jobs:
-no_par
You can also set up the level of parallelization for the pipeline.
-par_lvl [PAR_LEVEL; 0-7]
0: no parallel jobs (equivalent to -no_par, all subtasks for each replicate will also be serialized)
1: no replicates/controls in parallel (subtasks for each replicate can be parallelized)
2: 2 replicates/controls in parallel
3: 2 replicates/controls and 2 peak-callings in parallel (default)
4: 4 replicates/controls and 2 peak-callings in parallel
5: 4 replicates/controls and 4 peak-callings in parallel
6: customized
7: unlimited
For customized parallelization:
-par_lvl 6 -reps_in_par [NO_REP_IN_PAR] -peaks_in_par [NO_PEAKCALLING_IN_PAR]
See details here
For python2 (python 2.x >= 2.7), here
For python3, here
For R-2.x, here
- [main_samview] random alignment retrieval only works for indexed BAM or CRAM files.
If your pipeline starts from BAM files, make sure that bam index (.bam.bai) exists together with BAM file. If not, build index with samtools index [YOUR_BAM_FILE]. BAM and BAI should be in the same directory.
- pysam backward compatibility issue
ATAQC currently does not work with pysam >= 0.9. Lower it to 0.8.3.
Traceback (most recent call last):
File "/users/leepc12/code/bds_atac/ataqc/run_ataqc.py", line 1303, in <module>
main()
File "/users/leepc12/code/bds_atac/ataqc/run_ataqc.py", line 1120, in main
chr_m_reads, fraction_chr_m = get_chr_m(COORDSORT_BAM)
File "/users/leepc12/code/bds_atac/ataqc/run_ataqc.py", line 160, in get_chr_m
tot_reads += int(chrom_stats[2])
IndexError: list index out of range
- Jin wook Lee - PhD Student, Mechanical Engineering Dept., Stanford University
- Chuan Sheng Foo - PhD Student, Computer Science Dept., Stanford University
- Daniel Kim - MD/PhD Student, Biomedical Informatics Program, Stanford University
- Anshul Kundaje - Assistant Professor, Dept. of Genetics, Stanford University