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2 changes: 1 addition & 1 deletion .bumpversion.toml
Original file line number Diff line number Diff line change
@@ -1,5 +1,5 @@
[tool.bumpversion]
current_version = "2.3.1"
current_version = "2.3.1.9001"
search = "{current_version}"
replace = "{new_version}"
message = "Bump version: {current_version} → {new_version}"
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2 changes: 1 addition & 1 deletion .github/workflows/build_conda_recipes.yaml
Original file line number Diff line number Diff line change
Expand Up @@ -12,7 +12,7 @@ env:
conda_env_yaml: conda/env/yaml
conda_env_lock: conda/env/lock
conda_org: pcgr
VERSION: '2.3.1' # bump
VERSION: '2.3.1.9001' # bump
jobs:
conda_build:
# When merging to one of the branches above and the commit message matches
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2 changes: 1 addition & 1 deletion CODE_OF_CONDUCT.md
Original file line number Diff line number Diff line change
Expand Up @@ -60,7 +60,7 @@ representative at an online or offline event.

Instances of abusive, harassing, or otherwise unacceptable behavior may be
reported to the community leaders responsible for enforcement at
sigven@ifi.uio.no.
sigven@ifi.uio.no or peterdiakumis@gmail.com.
All complaints will be reviewed and investigated promptly and fairly.

All community leaders are obligated to respect the privacy and security of the
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133 changes: 133 additions & 0 deletions CONTRIBUTING.md
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@@ -0,0 +1,133 @@
# Contributing to PCGR

Thanks for your interest in contributing to the Personal Cancer Genome Reporter
(PCGR). Contributions of all kinds are welcome — bug reports, documentation
improvements, feature suggestions, and code.

This document explains how to report problems and how to propose changes.

## Code of conduct

This project follows a [Code of Conduct](CODE_OF_CONDUCT.md). By participating,
you are expected to uphold it. Please report unacceptable behaviour to the
maintainers.

## Ways to contribute

- **Report a bug** — open an issue (see below for what to include)
- **Request a feature** — open an issue describing the use case
- **Ask a question** — use GitHub Discussions or open an issue
- **Improve documentation** — corrections and clarifications are very welcome
- **Contribute code** — see *Development workflow* below

## Reporting bugs

Most issues we receive can only be diagnosed with the full run context, so
please include **all** of the following. Issues without this information will
usually need a follow-up before we can help.

1. **PCGR version** (`pcgr --version`)
2. **Reference data bundle version** and the genome assembly used
(`grch37` or `grch38`)
3. **Installation method** — Conda, Docker, Singularity/Apptainer —
including the image tag or environment specification
4. **Operating system** and, if relevant, the compute environment
(laptop, HPC/cluster, cloud)
5. **The exact command you ran**, in full, with all arguments
6. **The complete error message and log output** (please paste as text in a
fenced code block rather than as a screenshot)
7. **Input characteristics** — variant caller used, approximate number of
variants, tumour type, whether CNA/expression/fusion input was supplied
8. **A minimal example input** that reproduces the problem, if you are able to
share one

Please do not attach patient-identifiable data to a public issue. If a problem
can only be reproduced with sensitive data, say so in the issue and we will
find another way to investigate.

## Requesting features

When proposing a feature, describe the scientific or clinical use case rather
than only the implementation. PCGR aims to produce clinically interpretable
output aligned with established guidelines (AMP/ASCO/CAP, ClinGen/CGC/VICC), so
proposals that affect variant classification or tier assignment should reference
the relevant guideline or evidence source.

## Development workflow

We use a simple two-branch model:

- **`main`** — reflects the current released version. Do not open pull requests
against `main`.
- **`dev`** — the active development branch. **All pull requests should target
`dev`.**

To contribute code:

1. Fork the repository and create a branch from `dev`
(e.g. `feature/short-description` or `fix/short-description`)
2. Make your changes, keeping the pull request focused on a single concern
3. Update documentation and the changelog where relevant
4. Open a pull request against `dev`, describing **what** the change does and
**why** it is needed

For anything substantial — new annotation sources, changes to classification or
tiering logic, or architectural changes — please open an issue to discuss the
approach before writing code. This saves time on both sides.

## Code organisation

PCGR spans two languages, and it helps to know where a change belongs:

- **Python** — the pipeline, variant annotation, and much of the interpretation
logic (including oncogenicity classification and biomarker matching)
- **R** (the [`pcgrr`](https://github.com/sigven/pcgrr) package) — report
generation and visualisation via Quarto, together with parts of the clinical
interpretation logic, notably AMP/ASCO/CAP tier assignment

Note that this split is not absolute: some classification logic currently lives
in `pcgrr` alongside the reporting code. If you are unsure where a change
belongs, open an issue and ask before starting work.

## Coding conventions

- Follow the style of the surrounding code
- Python: follow PEP 8 where practical; add docstrings to new functions
- R: follow the existing style in `pcgrr`
- Keep commits reasonably self-contained with descriptive messages
- Do **not** commit reference data bundles, large binary files, or test data
containing patient information

## Testing and validation

Automated test coverage is currently limited and is actively being expanded. In
the meantime, we ask contributors to describe how a change was validated:

- State the command(s) you ran to exercise the change
- For changes affecting annotation, classification or tiering, show the effect
on output — for example, the relevant rows or fields before and after
- Confirm that an end-to-end run completes on example data
- Where tests exist, please run them and add new ones covering your change

Continuous integration runs automatically on pull requests. Please make sure it
passes before requesting review.

## Releases and versioning

PCGR follows semantic versioning. Releases are cut from `dev` into `main` by the
maintainers, accompanied by an updated changelog. Reference data bundles are
versioned separately and tied to specific releases — see the documentation for
the compatible bundle for each version.

## Licence

PCGR is released under the MIT licence. By contributing, you agree that your
contributions will be licensed under the same terms.

## Getting in touch

- **Bugs and feature requests** — GitHub Issues
- **Questions and general discussion** — GitHub Discussions (to come)
- **Documentation** — https://sigven.github.io/pcgr/

Thanks for your effort to improve PCGR!
9 changes: 9 additions & 0 deletions README.md
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Expand Up @@ -153,6 +153,15 @@ Sigve Nakken, Ghislain Fournous, Daniel Vodák, Lars Birger Aaasheim, Ola Mykleb

Sigve Nakken, Vladislav Saveliev, Oliver Hofmann, Pål Møller, Ola Myklebost, and Eivind Hovig. **Cancer Predisposition Sequencing Reporter (CPSR): a flexible variant report engine for high-throughput germline screening in cancer** (2021). *Int J Cancer*. [doi:[10.1002/ijc.33749](doi:%5B10.1002/ijc.33749)](https://doi.org/10.1002/ijc.33749)

## Contributing

Contributions are welcome — bug reports, documentation improvements, feature
suggestions, and code. See [CONTRIBUTING.md](CONTRIBUTING.md) for how to report
issues and submit pull requests (note that all PRs should target the `dev`
branch).

This project follows a [Code of Conduct](CODE_OF_CONDUCT.md).

## Contact

sigven AT ifi.uio.no
8 changes: 4 additions & 4 deletions conda/env/lock/pcgr-linux-64.lock
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@@ -1,6 +1,6 @@
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Expand Down Expand Up @@ -300,7 +300,7 @@ https://conda.anaconda.org/bioconda/noarch/perl-www-robotrules-6.03-pl5321hdfd78
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8 changes: 4 additions & 4 deletions conda/env/lock/pcgr-osx-64.lock
Original file line number Diff line number Diff line change
@@ -1,6 +1,6 @@
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Expand Down Expand Up @@ -102,7 +102,7 @@ https://conda.anaconda.org/bioconda/osx-64/muscle-3.8.1551-h5fa12a8_9.tar.bz2#5c
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Expand Down Expand Up @@ -167,7 +167,7 @@ https://conda.anaconda.org/bioconda/osx-64/probcons-1.12-hd174df1_1.tar.bz2#bdf9
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Expand Down Expand Up @@ -284,7 +284,7 @@ https://conda.anaconda.org/bioconda/osx-64/pybedtools-0.10.0-py312ha99f805_2.tar
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8 changes: 4 additions & 4 deletions conda/env/lock/pcgrr-linux-64.lock
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https://conda.anaconda.org/conda-forge/osx-64/libiconv-1.18-h57a12c2_2.conda#210a85a1119f97ea7887188d176db135
https://conda.anaconda.org/conda-forge/osx-64/libjpeg-turbo-3.1.4.1-ha1e9b39_0.conda#57cc1464d457d01ac78f5860b9ca1714
https://conda.anaconda.org/conda-forge/osx-64/libjpeg-turbo-3.2.0-ha1e9b39_0.conda#d86c1b9259377fb4dcd76fe7472bd2d2
https://conda.anaconda.org/conda-forge/osx-64/liblzma-5.8.3-hbb4bfdb_0.conda#becdfbfe7049fa248e52aa37a9df09e2
https://conda.anaconda.org/conda-forge/osx-64/libmpdec-4.0.0-hf3981d6_1.conda#ec88ba8a245855935b871a7324373105
https://conda.anaconda.org/conda-forge/osx-64/libuv-1.52.1-ha3d0635_0.conda#703303067839cd1da659528a84b3c0cc
Expand Down Expand Up @@ -338,5 +338,5 @@ https://conda.anaconda.org/bioconda/noarch/bioconductor-bsgenome.hsapiens.ucsc.h
https://conda.anaconda.org/bioconda/noarch/bioconductor-bsgenome.hsapiens.ucsc.hg38-1.4.5-r45hdfd78af_4.conda#4baa0dd494a2955755bb00fcd0242f00
https://conda.anaconda.org/bioconda/osx-64/bioconductor-variantannotation-1.56.0-r45h010771c_0.conda#2bc0fa9167469b8ee04400d3b7d3e7f3
https://conda.anaconda.org/bioconda/noarch/bioconductor-mutationalpatterns-3.19.1-r45hdfd78af_0.conda#8a1832a474ae43bb4b015b5a106dbe04
https://conda.anaconda.org/pcgr/noarch/r-pcgrr-2.3.1-h4616a5c_0.conda#15cb05daf8edd1b6b488651bd553dd1a
https://conda.anaconda.org/pcgr/noarch/r-cpsr-2.3.0-h4616a5c_0.conda#00834de27a1f7e2a41953f72b48dfcdb
https://conda.anaconda.org/pcgr/label/dev/noarch/r-pcgrr-2.3.1.9001-h4616a5c_0.conda#b44c3c14e2af1087ad753de83a2a2601
https://conda.anaconda.org/pcgr/label/dev/noarch/r-cpsr-2.2.5.9012-h4616a5c_0.conda#28080c1c508222229783123de6b5e4e7
2 changes: 1 addition & 1 deletion conda/env/yaml/pcgr.yaml
Original file line number Diff line number Diff line change
Expand Up @@ -6,7 +6,7 @@ channels:
- bioconda

dependencies:
- pcgr ==2.3.1 # bump
- pcgr ==2.3.1.9001 # bump
- bioconda::bedtools
- bioconda::bcftools
- bioconda::ensembl-vep ==115.1
Expand Down
2 changes: 1 addition & 1 deletion conda/env/yaml/pcgrr.yaml
Original file line number Diff line number Diff line change
Expand Up @@ -7,7 +7,7 @@ channels:

dependencies:
- python
- r-pcgrr ==2.3.1 # bump
- r-pcgrr ==2.3.1.9001 # bump
- r-cpsr
- r-argparse
- bioconductor-bsgenome.hsapiens.ucsc.hg38
Expand Down
2 changes: 1 addition & 1 deletion conda/env/yaml/pkgdown.yaml
Original file line number Diff line number Diff line change
Expand Up @@ -4,7 +4,7 @@ channels:
- bioconda
- conda-forge
dependencies:
- r-pcgrr ==2.3.1 # bump
- r-pcgrr ==2.3.1.9001 # bump
- r-pkgdown
- r-readr
- r-glue
Expand Down
2 changes: 1 addition & 1 deletion conda/recipe/pcgr/recipe.yaml
Original file line number Diff line number Diff line change
@@ -1,6 +1,6 @@
context:
name: pcgr
version: 2.3.1 # bump
version: 2.3.1.9001 # bump

package:
name: ${{ name|lower }}
Expand Down
2 changes: 1 addition & 1 deletion conda/recipe/pcgrr/recipe.yaml
Original file line number Diff line number Diff line change
@@ -1,6 +1,6 @@
context:
name: r-pcgrr
version: 2.3.1 # bump
version: 2.3.1.9001 # bump

package:
name: ${{ name|lower }}
Expand Down
2 changes: 1 addition & 1 deletion pcgr/_version.py
Original file line number Diff line number Diff line change
@@ -1 +1 @@
__version__ = '2.3.1' # bump
__version__ = '2.3.1.9001' # bump
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