Merge pull request #325 from nf-core/bump-version

Bump version for v2.7 release

CHANGELOG.md

@@ -3,9 +3,15 @@
 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).
 
-## v2.7.0dev
+## v2.7.0 - 2024-06-03
 
+- Apply `check_max` to AlevinQC time limit ([#335](https://github.com/nf-core/scrnaseq/pull/335))
+- Update template to v2.14.1 ([#328](https://github.com/nf-core/scrnaseq/pull/328))
+- Avoid filename collisions in cellranger-arc ([#321](https://github.com/nf-core/scrnaseq/pull/321))
 - Add cellranger multi subworkflow ([#247](https://github.com/nf-core/scrnaseq/issues/247))
+  - Add support for 10x multiplexed, multi-omics and FFPE samples
+  - Allow the use of gzipped fasta and GTF files
+- Fix that pipeline couldn't run without GTF file, even when an aligner index was specified ([#322](https://github.com/nf-core/scrnaseq/pull/322))
 
 ## v2.6.0 - 2024-04-16
 

assets/multiqc_config.yml

@@ -1,7 +1,7 @@
 report_comment: >
-  This report has been generated by the <a href="https://github.com/nf-core/scrnaseq/releases/tag/2.6.0" target="_blank">nf-core/scrnaseq</a>
+  This report has been generated by the <a href="https://github.com/nf-core/scrnaseq/releases/tag/2.7.0" target="_blank">nf-core/scrnaseq</a>
   analysis pipeline. For information about how to interpret these results, please see the
-  <a href="https://nf-co.re/scrnaseq/2.6.0/docs/output" target="_blank">documentation</a>.
+  <a href="https://nf-co.re/scrnaseq/2.7.0/docs/output" target="_blank">documentation</a>.
 report_section_order:
   "nf-core-scrnaseq-methods-description":
     order: -1000

nextflow.config

@@ -303,7 +303,7 @@ manifest {
     description     = """Pipeline for processing 10x Genomics single cell rnaseq data"""
     mainScript      = 'main.nf'
     nextflowVersion = '!>=23.04.0'
-    version         = '2.6.0'
+    version         = '2.7.0'
     doi             = '10.5281/zenodo.3568187'
 }