Initial release of nf-core/variantprioritization, created with the nf-core template.

This is a bioinformatics analysis pipeline for the functional annotation and translation of somatic SNVs/InDels and copy number abberations for precision cancer medicine using the Personal Cancer Genome Reporter (PCGR). The pipeline offers germline SNVs/INDELS intepretation and annotation using the Cancer Predisposition Sequencing Reporter (CPSR).

Originally written by @barrydigby, @yussab and @matbonfanti. Adapted to nf-core standards by @famosab.

The team from the October 2025 nf-core Hackathon who worked on issues related to this pipeline: @georgiakes, @petanska, @maxibor, @eolaniru, @colorstorm, @mkatsanto, @dhtt and @famosab.