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bump version to 0.2.0
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nvnieuwk committed Jul 19, 2024
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4 changes: 2 additions & 2 deletions CHANGELOG.md
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The format is based on [Keep a Changelog](https://keepachangelog.com/en/1.0.0/)
and this project adheres to [Semantic Versioning](https://semver.org/spec/v2.0.0.html).

## v0.2.0dev
## v0.2.0 - [19 July 2024] - Mighty Manneken Pis

### `Added`

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### `Changes`

1. Updated all WisecondorX modules to version 1.2.6 and added the `--seed` argument to `WisecondorX predict`
2. Removed support for the `phenotypes` VEP plugin. Commen VEP plugin support will be added later
2. Removed support for the `phenotypes` VEP plugin. Common VEP plugin support will be added later
3. Made the main workflow pluggable, making it possible to use this pipeline in a meta pipeline
4. Updated all modules to their latest version

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4 changes: 2 additions & 2 deletions assets/multiqc_config.yml
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report_comment: >
This report has been generated by the <a href="https://github.com/nf-core/structural/tree/dev" target="_blank">nf-core/structural</a> analysis pipeline. For information about how to interpret these results, please see the <a
href="https://nf-co.re/structural/dev/docs/output" target="_blank">documentation</a>.
This report has been generated by the <a href="https://github.com/nf-core/structural/releases/tag/0.2.0" target="_blank">nf-core/structural</a> analysis pipeline. For information about how to interpret these results, please see the <a
href="https://nf-co.re/structural/0.2.0/docs/output" target="_blank">documentation</a>.
report_section_order:
"nf-cmgg-structural-methods-description":
order: -1000
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2 changes: 1 addition & 1 deletion nextflow.config
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description = 'A bioinformatics best-practice analysis pipeline for calling structural variants (SVs), copy number variants (CNVs) and repeat region expansions (RREs) from short DNA reads'
mainScript = 'main.nf'
nextflowVersion = '!>=23.10.0'
version = '0.2.0dev'
version = '0.2.0'
doi = ''
}

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