This is the Hi-C pipeline from the Sequana project.
- Overview:
Hi-C pipeline to capture 3D chromatin interactions in a genome
- Input:
Paired FastQ files and a reference genome in FASTA format
- Output:
Cooler contact matrices, Hi-C QC reports, and a MultiQC summary
- Status:
Production
- Citation:
Cokelaer et al, (2017), ‘Sequana’: a Set of Snakemake NGS pipelines, Journal of Open Source Software, 2(16), 352, JOSS DOI https://doi:10.21105/joss.00352
Installation
If you already have all requirements, install the package with pip:
pip install sequana_hic --upgrade
You will need third-party tools (see Requirements below). Use apptainer images to avoid installing them locally.
Usage
Set up the pipeline directory with your input data and reference:
sequana_hic --input-directory DATAPATH --reference-file genome.fa sequana_hic --input-directory DATAPATH --reference-file genome.fa --aligner-choice bwa_split
This creates a hic/ directory containing the pipeline and configuration file. Execute the pipeline locally:
cd hic sh hic.sh
See .sequana/profile/config.yaml to tune Snakemake behaviour (cores, cluster settings, etc.).
Usage with apptainer
With Apptainer, initiate the working directory as follows:
sequana_hic --input-directory DATAPATH --reference-file genome.fa --use-apptainer
Images can be stored in a shared location:
sequana_hic --input-directory DATAPATH --reference-file genome.fa --use-apptainer --apptainer-prefix ~/.sequana/apptainers
then:
cd hic sh hic.sh
If running Snakemake manually, add apptainer options:
snakemake -s hic.rules --cores 4 --use-apptainer --apptainer-prefix ~/.sequana/apptainers --apptainer-args "-B /home:/home"
By default the home directory is already bound. Additional paths can be set via:
export APPTAINER_BINDPATH="-B /pasteur"
Requirements
This pipeline requires the following executables (install via bioconda/conda):
bwa — short-read aligner (default mapper)
samtools — BAM/SAM manipulation
pairtools — processing of Hi-C read pairs
cooler — storage and analysis of Hi-C contact matrices
qc3c — Hi-C quality control
fastqc — raw read quality control
multiqc — aggregate QC reports
Optional:
chromap — fast Hi-C aligner (experimental, use --aligner-choice chromap)
seqkit — split FastQ files (required for --aligner-choice bwa_split)
Pipeline description
FastQC — quality control on raw reads
Reference indexing — BWA index build from the provided FASTA reference
Alignment — BWA-MEM alignment with Hi-C-specific options (-5SP), producing sorted BAM files
Pairtools — parse alignments into Hi-C contact pairs, sort, deduplicate, and split
Cooler — load pairs into a contact matrix and generate multi-resolution .mcool file
qc3C — Hi-C library quality assessment (ligation efficiency, distance distribution)
Visualisation — contact matrix PNG at 5 kb resolution
MultiQC — aggregated QC report
Changelog
Version |
Description |
|---|---|
0.2.0 |
Production release. |
0.1.0 |
Migration to modern sequana_pipetools framework (get_shell/get_run, schema validation, apptainer support, Python 3.10+). |
0.0.1 |
First release. |
Contribute & Code of Conduct
To contribute to this project, please take a look at the Contributing Guidelines first. Please note that this project is released with a Code of Conduct. By contributing to this project, you agree to abide by its terms.
Metadata
Release files for sequana-hic 0.2.0
For a detailed explanation of source distributions (sdists) and built distributions (wheels), please see the package formats documentation.
Source distribution (sdist)
| File | Size | Uploaded | |
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| sequana_hic-0.2.0.tar.gz | 136.0 kB | Details |
Built distribution (wheel)
| File | Interpreter | ABI | Platform | Reset |
|---|---|---|---|---|
| sequana_hic-0.2.0-py3-none-any.whl | Python 3 | none | any | Details |
Total release size: 272.6 kB
Release files / sequana_hic-0.2.0.tar.gz
| Download URL | sequana_hic-0.2.0.tar.gz |
|---|---|
| Size | 136.0 kB |
| Tags | Source |
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Release files / sequana_hic-0.2.0-py3-none-any.whl
| Download URL | sequana_hic-0.2.0-py3-none-any.whl |
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