Release prep v.0.1.0 (#89)

* bump versions * clear changelog
genomic-medicine-sweden · Apr 22, 2024 · 9a523d2 · 9a523d2
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diff --git a/CHANGELOG.md b/CHANGELOG.md
@@ -15,7 +15,7 @@ Initial release of genomic-medicine-sweden/nallo, created with the [nf-core](htt
 - Call SNVs with DeepVariant and merge with GLNexus
 - Annotate SNVs with echtvar and VEP
 - Call SVs with Sniffles, tandem repeats with TRGT and CNVs with HiFiCNV
-- Phase and haplotag reads with whatshap or HiPhase
+- Phase variants and haplotag reads with whatshap or HiPhase
 - Create methylation pileups with modkit
 - Assemble genomes with hifiasm
 - Align assemly to reference and call variants with dipcall
diff --git a/assets/multiqc_config.yml b/assets/multiqc_config.yml
@@ -1,4 +1,5 @@
 report_comment: >
+<<<<<<< HEAD
   This report has been generated by the <a href="https://github.com/genomic-medicine-sweden/nallo/releases/tag/0.1.0" target="_blank">genomic-medicine-sweden/nallo</a>
   analysis pipeline.
 report_section_order: