nf-core/variantprioritization
Bioinformatics analysis pipeline for the functional annotation and translation of somatic SNVs/InDels and copy number abberations for precision cancer medicine using Personal Cancer Genome Reporter (PCGR). The pipeline offers germline SNVs/INDELS intepretation and annotation using Cancer Predisposition Sequencing Reporter (CPSR).
This is the development version of the pipeline. View the latest v1.0.0 release.
Launch development versionhttps://github.com/nf-core/variantprioritization