Find documentation and examples at http://nservant.github.io/HiC-Pro/
For any question about HiC-Pro, please contact nicolas.servant@curie.fr or use the HiC-Pro forum
HiC-Pro was designed to process Hi-C data, from raw fastq files (paired-end Illumina data) to normalized contact maps. It supports the main Hi-C protocols, including digestion protocols as well as protocols that do not require restriction enzymes such as DNase Hi-C. In practice, HiC-Pro was successfully applied to many data-sets including dilution Hi-C, in situ Hi-C, DNase Hi-C, Micro-C, capture-C, capture Hi-C or HiChip data.
The pipeline is flexible, scalable and optimized. It can operate either on a single laptop or on a computational cluster. HiC-Pro is sequential and each step of the workflow can be run independantly.
HiC-Pro includes a fast implementatation of the iterative correction method (see the iced python package for more information).
Finally, HiC-Pro can use phasing data to build allele-specific contact maps.
If you use HiC-Pro, please cite :
Servant N., Varoquaux N., Lajoie BR., Viara E., Chen CJ., Vert JP., Dekker J., Heard E., Barillot E. HiC-Pro: An optimized and flexible pipeline for Hi-C processing. Genome Biology 2015, 16:259 doi:10.1186/s13059-015-0831-x
HiC-Pro provides a Singularity container to ease its installation process. A ready-to-use container is available here.
In order to build you own Singularity image;
1- Install singularity
- Linux : http://singularity.lbl.gov/install-linux
- MAC : http://singularity.lbl.gov/install-mac
- Windows : http://singularity.lbl.gov/install-windows
2- Build the singularity HiC-Pro image using the 'Singularity' file available in the HiC-Pro root directory.
sudo singularity build hicpro_latest_ubuntu.img MY_INSTALL_PATH/HiC-Pro/Singularity
3- Run HiC-pro
You can then either use HiC-Pro using the 'exec' command ;
singularity exec hicpro_latest_ubuntu.img HiC-Pro -h
Or directly use HiC-Pro within the Singularity shell
singularity shell hicpro_latest_ubuntu.img
HiC-Pro -h
The HiC-Pro pipeline requires the following dependencies :
- The bowtie2 mapper
- Python (>2.7) with pysam (>=0.8.3), bx-python(>=0.5.0), numpy(>=1.8.2), and scipy(>=0.15.1) libraries.
Note that the current version does not support python 3 - R with the RColorBrewer and ggplot2 (>2.2.1) packages
- g++ compiler
- samtools (>1.1)
- Unix sort (which support -V option) is required ! For Mac OS user, please install the GNU core utilities !
Note that Bowtie >2.2.2 is strongly recommanded for allele specific analysis.
To install HiC-Pro (>=2.7.8), be sure to have the appropriate rights and run :
tar -zxvf HiC-Pro-master.tar.gz
cd HiC-Pro-master
## Edit config-install.txt file if necessary
make configure
make install
For older version (<2.7.8), the following process can be used
tar -zxvf HiC-Pro-master.tar.gz
cd HiC-Pro-master
## Edit config-install.txt file if necessary
make CONFIG_SYS=config-install.txt install
Note that if some of these dependencies are not installed (i.e. not detected in the $PATH), HiC-Pro will try to install them.
You can also edit the config-install.txt file and manually defined the paths to dependencies.
| SYSTEM CONFIGURATION | |
|---|---|
| PREFIX | Path to installation folder |
| BOWTIE2_PATH | Full path the bowtie2 installation directory |
| SAMTOOLS_PATH | Full path to the samtools installation directory (>1.1 ) |
| R_PATH | Full path to the R installation directory |
| PYTHON_PATH | Full path to the python installation directory (>2.7 - python3 not supported) |
| CLUSTER_SYS | Scheduler to use for cluster submission. Must be TORQUE, SGE, SLURM or LSF |
In order to process the raw data, HiC-Pro requires three annotation files. Note that the pipeline is provided with some Human and Mouse annotation files.
Please be sure that the chromosome names are the same than the ones used in your bowtie indexes !
- A BED file of the restriction fragments after digestion. This file depends both of the restriction enzyme and the reference genome. See the FAQ and the HiC-Pro utilities for details about how to generate this file. A few annotation files are provided with the HiC-Pro sources as examples.
chr1 0 16007 HIC_chr1_1 0 +
chr1 16007 24571 HIC_chr1_2 0 +
chr1 24571 27981 HIC_chr1_3 0 +
chr1 27981 30429 HIC_chr1_4 0 +
chr1 30429 32153 HIC_chr1_5 0 +
chr1 32153 32774 HIC_chr1_6 0 +
chr1 32774 37752 HIC_chr1_7 0 +
chr1 37752 38369 HIC_chr1_8 0 +
chr1 38369 38791 HIC_chr1_9 0 +
chr1 38791 39255 HIC_chr1_10 0 +
(...)
- A table file of chromosomes' size. This file can be easily find on the UCSC genome browser. Of note, pay attention to the contigs or scaffolds, and be aware that HiC-pro will generate a map per chromosomes pair. For model organisms such as Human or Mouse, which are well annotated, we usually recommand to remove all scaffolds.
chr1 249250621
chr2 243199373
chr3 198022430
chr4 191154276
chr5 180915260
chr6 171115067
chr7 159138663
chr8 146364022
chr9 141213431
chr10 135534747
(...)
- The bowtie2 indexes. See the bowtie2 manual page for details about how to create such indexes.
First have a look at the help message !
HiC-Pro --help
usage : HiC-Pro -i INPUT -o OUTPUT -c CONFIG [-s ANALYSIS_STEP] [-p] [-h] [-v]
Use option -h|--help for more information
HiC-Pro 2.10.0
---------------
OPTIONS
-i|--input INPUT : input data folder; Must contains a folder per sample with input files
-o|--output OUTPUT : output folder
-c|--conf CONFIG : configuration file for Hi-C processing
[-p|--parallel] : if specified run HiC-Pro on a cluster
[-s|--step ANALYSIS_STEP] : run only a subset of the HiC-Pro workflow; if not specified the complete workflow is run
mapping: perform reads alignment
proc_hic: perform Hi-C filtering
quality_checks: run Hi-C quality control plots
build_contact_maps: build raw inter/intrachromosomal contact maps
ice_norm: run ICE normalization on contact maps
[-h|--help]: help
[-v|--version]: version
-
Copy and edit the configuration file 'config-hicpro.txt' in your local folder. See the manual for details about the configuration file
-
Put all input files in a rawdata folder. The input files have to be organized with one folder per sample, such as;
+ PATH_TO_MY_DATA
+ sample1
++ file1_R1.fastq.gz
++ file1_R2.fastq.gz
++ ...
+ sample2
++ file1_R1.fastq.gz
++ file1_R2.fastq.gz
*...
- Run HiC-Pro on your laptop in standalone model
MY_INSTALL_PATH/bin/HiC-Pro -i FULL_PATH_TO_DATA_FOLDER -o FULL_PATH_TO_OUTPUTS -c MY_LOCAL_CONFIG_FILE
- Run HiC-Pro on a cluster (TORQUE/SGE/SLURM/LSF)
MY_INSTALL_PATH/bin/HiC-Pro -i FULL_PATH_TO_DATA_FOLDER -o FULL_PATH_TO_OUTPUTS -c MY_LOCAL_CONFIG_FILE -p
In the latter case, you will have the following message :
Please run HiC-Pro in two steps :
1- The following command will launch the parallel workflow through 12 torque jobs:
qsub HiCPro_step1.sh
2- The second command will merge all outputs to generate the contact maps:
qsub HiCPro_step2.sh
Execute the displayed command from the output folder:
qsub HiCPro_step1.sh
Once executed succesfully (may take several hours), run the step using:
qsub HiCPro_step2.sh
The test dataset and associated results are available here. Small fastq files (2M reads) extracted from the Dixon et al. 2012 paper are available for test.
## Get the data. Will download a test_data folder and a configuration file
wget https://zerkalo.curie.fr/partage/HiC-Pro/HiCPro_testdata.tar.gz && tar -zxvf HiCPro_testdata.tar.gz
## Edit the configuration file and set the path to Human bowtie2 indexes
## Run HiC-Pro
time HICPRO_INSTALL_DIR/bin/HiC-Pro -c config_test_latest.txt -i test_data -o hicpro_latest_test
Run HiC-Pro 2.11.0-beta
--------------------------------------------
vendredi 13 juillet 2018, 14:55:21 (UTC+0200)
Bowtie2 alignment step1 ...
Logs: logs/dixon_2M_2/mapping_step1.log
Logs: logs/dixon_2M/mapping_step1.log
--------------------------------------------
vendredi 13 juillet 2018, 14:56:06 (UTC+0200)
Bowtie2 alignment step2 ...
Logs: logs/dixon_2M_2/mapping_step2.log
Logs: logs/dixon_2M/mapping_step2.log
--------------------------------------------
vendredi 13 juillet 2018, 14:56:15 (UTC+0200)
Combine R1/R2 alignment files ...
Logs: logs/dixon_2M_2/mapping_combine.log
Logs: logs/dixon_2M/mapping_combine.log
--------------------------------------------
vendredi 13 juillet 2018, 14:56:20 (UTC+0200)
Mapping statistics for R1 and R2 tags ...
Logs: logs/dixon_2M_2/mapping_stats.log
Logs: logs/dixon_2M/mapping_stats.log
--------------------------------------------
vendredi 13 juillet 2018, 14:56:21 (UTC+0200)
Pairing of R1 and R2 tags ...
Logs: logs/dixon_2M_2/mergeSAM.log
Logs: logs/dixon_2M/mergeSAM.log
--------------------------------------------
vendredi 13 juillet 2018, 14:56:29 (UTC+0200)
Assign alignments to restriction fragments ...
Logs: logs/dixon_2M_2/mapped_2hic_fragments.log
Logs: logs/dixon_2M/mapped_2hic_fragments.log
--------------------------------------------
vendredi 13 juillet 2018, 14:57:09 (UTC+0200)
Merge chunks from the same sample ...
Logs: logs/dixon_2M/merge_valid_interactions.log
Logs: logs/dixon_2M_2/merge_valid_interactions.log
--------------------------------------------
vendredi 13 juillet 2018, 14:57:09 (UTC+0200)
Merge stat files per sample ...
Logs: logs/dixon_2M/merge_stats.log
Logs: logs/dixon_2M_2/merge_stats.log
--------------------------------------------
vendredi 13 juillet 2018, 14:57:10 (UTC+0200)
Run quality checks for all samples ...
Logs: logs/dixon_2M/make_Rplots.log
Logs: logs/dixon_2M_2/make_Rplots.log
--------------------------------------------
vendredi 13 juillet 2018, 14:57:22 (UTC+0200)
Generate binned matrix files ...
Logs: logs/dixon_2M/build_raw_maps.log
Logs: logs/dixon_2M_2/build_raw_maps.log
--------------------------------------------
vendredi 13 juillet 2018, 14:57:23 (UTC+0200)
Run ICE Normalization ...
Logs: logs/dixon_2M/ice_500000.log
Logs: logs/dixon_2M/ice_1000000.log
Logs: logs/dixon_2M_2/ice_500000.log
Logs: logs/dixon_2M_2/ice_1000000.log
real 2m5.660s
user 3m44.816s
sys 0m25.612s