From 17082326fa7e168fbb3fa5943fcfe7e9d4109e7a Mon Sep 17 00:00:00 2001 From: Nicolas Vannieuwkerke Date: Fri, 19 Jul 2024 14:49:46 +0200 Subject: [PATCH] bump version to 0.2.0 --- CHANGELOG.md | 4 ++-- assets/multiqc_config.yml | 4 ++-- nextflow.config | 2 +- 3 files changed, 5 insertions(+), 5 deletions(-) diff --git a/CHANGELOG.md b/CHANGELOG.md index 44760594..340a58bf 100644 --- a/CHANGELOG.md +++ b/CHANGELOG.md @@ -3,7 +3,7 @@ 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` @@ -17,7 +17,7 @@ and this project adheres to [Semantic Versioning](https://semver.org/spec/v2.0.0 ### `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 diff --git a/assets/multiqc_config.yml b/assets/multiqc_config.yml index 66263b52..dc167595 100644 --- a/assets/multiqc_config.yml +++ b/assets/multiqc_config.yml @@ -1,6 +1,6 @@ report_comment: > - This report has been generated by the nf-core/structural analysis pipeline. For information about how to interpret these results, please see the documentation. + This report has been generated by the nf-core/structural analysis pipeline. For information about how to interpret these results, please see the documentation. report_section_order: "nf-cmgg-structural-methods-description": order: -1000 diff --git a/nextflow.config b/nextflow.config index c4ae6e42..d2a30631 100644 --- a/nextflow.config +++ b/nextflow.config @@ -279,7 +279,7 @@ manifest { 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 = '' }