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Added
Added the samplesheet to the pipeline output as OUTDIR/samplesheet.csv
Added the --bedpe parameter. This makes the pipeline output BEDPE files alongside the VCF files.
Added parallelization on SV type to the delly flow
Added a --gtf parameter for annotation of gene and transcript overlap using gatk SVAnnotate.
Added StrVCTVRE as a new annotation tool
Changes
Updated the pipeline to be compatible with future nextflow updates
Removed the max_cpus, max_memory and max_time parameter in favor of the new built-in resourceLimits
Replaced nf-validation with nf-schema
Updated to nf-core template v3.2.0
Fixed language server errors
Removed the old output publishing code and used the new workflow output definitions instead
Bumped the minimal nextflow version to 25.10.0
Changed the --annotations_filter parameter to a --filter parameter. This parameter takes an argument of bcftools filter to filter the resulting VCFs.
Removed the --delly_sv_types parameter.
Moved all wisecondorx and qdnaseq outputs to a separate directory in each sample output.
Bumped all annotation modules to the latest versions
Reworked the annotation structure to a per tool structure. Specify the annotations tools you want to run with --annotate_tools. This parameter takes a comma-separated list of tool names (options: vep, vcfanno, svannotate, strvctvre or all (=> all tools))
Updated to nf-core template v3.5.1
Removed AnnotSV from the pipeline
Removed the small_variants field from the samplesheet. Small variant VCFs are no longer used in the pipeline
Fixed
Fail the pipeline when the sex determination failed. This will now prompt the user to add the sex to the samplesheet so the pipeline doesn't do any wrong assumptions
Fixed the Jasmine module output VCFs being empty when no variants have been merged. This file now contains the header of one of the input VCFs
Fixed a map issue when the sex field is empty in the samplesheet