This repo contains RNAseq SNV calling pipelines using:
- Broad GATK4 best practices
- The overall workflow picks up from post-STAR alignment, starting at Picard mark duplicates.
- For the most part, tool parameters follow defaults from the GATK Best Practices WDL, written in cwl with added optimatization for use on the Cavatica platform.
- Strelka2
- This workflow is pretty straight forward, with a
PASS
filter step added to get PASS
calls.
- VarDict Java
- This workflow is based on the Vardict run style of BC Bio.