Clindet documentation#
Contents:
- Quick Start
- DNAseq analysis
- RNAseq analysis
- Use Case
- 1. Use case I: SNV and CNV calling from Whole exome sequencing data
- 2. Use case II: Fusion genes detection from multiple myeloma patient RNA-seq
- 3. Use case III: Whole genome sequencing of COLO829 cell line
- 4. Use case IV: Quantifying the contributions of DNA repair defective gene mutations to mutational signatures(C.elegans)
- 5. Use case V: Switching to different genome version (e.g. hg38)
- snakemake/clindet: Citations