oligopipe 1.1.2

Python package for Oligogenic Variant Analysis pipelines

oligopipe - Python package for Oligogenic Variant Analysis pipelines

This package offers a command-line interface to the Oligogenic Variant Analysis pipelines developed at the Interuniversity Institute of Bioinformatics in Brussels.

It contains two modules:

• prediction with VarCoPP2.0, as discussed in the paper “Faster and more accurate pathogenic combination predictions with VarCoPP2.0":

  takes a patient's variants from VCF/TSV along with additional parameters and predicts the pathogenicity of all digenic variant combinations.

• prioritization with HOP, as discussed in the paper "Prioritization of oligogenic variant combinations in whole exomes":

  takes a patient's variants from VCF/TSV along with information about the patient's disease (HPO terms or a gene panel) and ranks variant combinations based on how likely they are to cause the patient's disease.

Requirements

The package requires Python 3.8-3.10 (currently higher versions are not supported yet).

Additional requirements are specified in the requirements.txt file and automatically satisfied when installing with pip.

Installation

PIP-based installation

The easiest way to install is via the PyPI archive with the command

pip install oligopipe

It is recommended to use a virtual environment for the management of dependencies.

Source-based installation

The source code can be installed by cloning the repository or unpacking from a source code archive and running

pip install .

in the source directory.

For the purposes of testing or development, you may prefer to install as an editable module via PIP by running

pip install -e .

in the source directory.

Usage

Running oligopipe without any arguments or with --help returns the overview of the CLI:

$ oligopipe
usage: oligopipe [-h] {predict,prioritize,config} ...

CLI for oligopipe - oligogenic variant analysis pipelines

optional arguments:
  -h, --help            show this help message and exit

Commands:
  Run oligopipe {command} -h to get detailed help

  {predict,prioritize,config}
    predict             Run a VarCoPP prediction
    prioritize          Run a prioritization analysis with HOP -- under construction
    config              Show the template config file

The individual pipelines are available as submodules of the CLI, and also have dedicated help pages.

Both modules allow using a YAML config file for submitting input parameters and file paths, as well as passing them as command-line arguments (which will be favored if both are given). Running the oligopipe config module will print out a template for that config file.

Running a prediction

Please refer to the docs for extensive documentation on the pipeline logic, the expected inputs and outputs.

Check the available arguments:

$ oligopipe predict --help

The input arguments are grouped in categories:

• Variant input: VCF or TSV file and genome build (both required), patient's sex
• Filtering options
• Output options
• Database credentials (required; see below)

An example prediction run could then look like this (with database credentials in the config file):

$ oligopipe predict --config path/to/input_config.yaml \
                    --variants-vcf path/to/example_vcf_2_hg19.vcf --genome-build hg19 --patient-sex F \
                    --panel path/to/example_vcf_2_gene_panel.txt \
                    --outdir results 

Which will create the following result files:

• metadata.json: summary of the pipeline run (inputs, statistics)
• predictions_with_annotations.json: "raw" output of the predictions, containing also feature annotations
• predicted_variant_combinations.tsv: table of variant combinations with their predictions
• predicted_gene_pairs.tsv: table of gene pairs with prediction statistics
• one file per type of variants that were discarded by the pipeline (if applicable):
  • filtered_variants.txt
  • missing_variants.txt (missing from the annotation database)
  • invalid_zygosity_variants.txt

Note: if no variant combinations remain after the filtering, then the gene pair/variant combination files are not created

Running a prioritization

Not available yet

Annotation database

The pipelines rely on an annotation database for quick retrieval of the variant, gene and gene pair input features for VarCoPP.

We currently offer limited access to such a database for use in this package. If you wish to get access, please email us so that we can provide you with the credentials.

Additional documentation

Extensive documentation (and a FAQ page) about the pipelines can be found in the docs.

Citations

Prediction with VarCoPP(2.0):

• Versbraegen N., Gravel B., Nachtegael C., Renaux A., Verkinderen E., Nowé A., Lenaerts T., Papadimitriou S. (2023) Faster and more accurate pathogenic combination predictions with VarCoPP2.0. BMC Bioinformatics. 24:179. DOI: https://doi.org/10.1186/s12859-023-05291-3
• Papadimitriou S., Gazzo A., Versbraegen N., Nachtegael C., Aerts J., Moreau Y., Van Dooren S., Nowé A., Smits G., Lenaerts T. (2019) Predicting disease-causing variant combinations. Proceedings of the National Academy of Sciences. 116(24):11878-11887. DOI: https://doi.org/10.1073/pnas.1815601116

Prioritization with HOP:

• Gravel B., Renaux A., Papadimitriou S., Smits G., Nowé A., Lenaerts T. (2024) Prioritization of oligogenic variant combinations in whole exomes. Bioinformatics. Volume 40, Issue 4, April 2024, btae184. DOI: https://doi.org/10.1093/bioinformatics/btae184

Support

If you are having issues, please let us know via [e-mail].

Known issues

If you run oligopipe on a Macbook with M1 chip, you might get errors related to dependencies psycopg2 and python-magic. Try to resolve them by running:

• pip uninstall psycopg2 and then pip install psycopg2-binary
• pip install python-magic-bin

License

The package is licensed under the MIT license.