Skip to content

Commit

Permalink
Merge pull request #69 from Clinical-Genomics/update_coveralls_image
Browse files Browse the repository at this point in the history
swap coveralls image for codecov
  • Loading branch information
dnil authored Jul 1, 2024
2 parents b8f4820 + 219f371 commit 4155acf
Show file tree
Hide file tree
Showing 2 changed files with 8 additions and 4 deletions.
5 changes: 5 additions & 0 deletions CHANGELOG.md
Original file line number Diff line number Diff line change
Expand Up @@ -2,6 +2,11 @@
All notable changes to this project will be documented in this file.
This project adheres to [Semantic Versioning](http://semver.org/).

## [unreleased]
### Fixed
- Use codecov badge on README page


## [0.9.1]
### Added
- Added github action test and release workflows
Expand Down
7 changes: 3 additions & 4 deletions README.md
Original file line number Diff line number Diff line change
@@ -1,6 +1,5 @@
# Stranger
![Build Status - GitHub][actions-build-status]
[![Coverage Status][coveralls-image]][coveralls-url]
[![PyPI Version][pypi-img]][pypi-url]
[![DOI][doi-image]][doi-url]
![GitHub Release Date][github-release-date]
Expand Down Expand Up @@ -45,7 +44,7 @@ Options:
The repeats are called with Expansion Hunter as mentioned earlier. ExpansionHunter will annotate the number of times that a repeat has been seen in the bam files of each individual and what repeat id the variant has.
Stranger will annotate the level of pathogenicity for the repeat number. The intervals that comes with the package are manually collected from the literature since there is no single source where this information can be collected.

You can find a demo repeat definitions json file that comes with Stranger [here](https://github.com/Clinical-Genomics/stranger/blob/master/stranger/resources/variant_catalog_grch37.json). It is based on the ExpansionHunter variant catalog, but extended with a few disease locus relevant keys:
You can find a demo repeat definitions json file that comes with Stranger [here](https://github.com/Clinical-Genomics/stranger/blob/main/stranger/resources/variant_catalog_grch37.json). It is based on the ExpansionHunter variant catalog, but extended with a few disease locus relevant keys:
It is advisable to use an up to date file, perhaps based on a curated public repostitory such as [STRchive][strchive] or [STRipy][stripy]. The ones we use in our routine pipelines can be found at our [Reference-files repository][reference-files] and include our literature curation.

| Column/Key | Content/Value |
Expand Down Expand Up @@ -219,8 +218,8 @@ and

[pypi-img]: https://img.shields.io/pypi/v/stranger.svg?style=flat-square
[pypi-url]: https://pypi.python.org/pypi/stranger/
[coveralls-url]: https://coveralls.io/github/moonso/stranger
[coveralls-image]: https://coveralls.io/repos/github/moonso/stranger/badge.svg?branch=master
[codecov-img]: https://codecov.io/gh/Clinical-Genomics/stranger/branch/main/graph/badge.svg
[codecov-url]: https://codecov.io/gh/Clinical-Genomics/stranger
[doi-image]: https://zenodo.org/badge/158848858.svg
[doi-url]: https://zenodo.org/badge/latestdoi/158848858
[github-release-date]: https://img.shields.io/github/release-date/Clinical-Genomics/scout
Expand Down

0 comments on commit 4155acf

Please sign in to comment.