Pipelines & Workflow Elements
Nfcore Variantcatalogue
Pileup-based variant calling for research data artifact. Groups reads by genomic position, counts base frequencies, calls the reference as the most common base, and emits research data artifact records for minority alleles exceeding 20%...
Runnablealigned sequencing readsnf-core/variantcatalogue | 13 stars
Catalog entry
About this entry
Pileup-based variant calling for research data artifact. Groups reads by genomic position, counts base frequencies, calls the reference as the most common base, and emits research data artifact records for minority alleles exceeding 20% frequency.
Use in DarwinOmics
How to use it
Use this workflow element when the submitted analysis needs a multi-step execution path, imported workflow, Darwinomics wrapper, or workflow-scale comparison rather than a single module.