All Published Workflows
2 workflows that have been reviewed and published
RNA-seq analysis pipeline for detection gene-fusions
nf-core/rnafusion is a bioinformatics best-practice analysis pipeline for RNA sequencing analysis pipeline with curated li...
Call and score variants from WGS/WES of rare disease patients.
Introduction
Pipeline summary
Usage
Pipeline output
Credits
Contributions and Su...
Sequence variations
Variant calling
gatk
hmtnote
manta
peddy
rhocall
smncopynumbercaller
tabix
BCFtools
BWA
Bwa-mem2
ExpansionHunter Denovo
FastQC
haplocheck
HaploGrep
mosdepth
MultiQC
Picard
QualiMap
SAMtools
Sentieon DNASeq
TIDDIT
Variant Effect Predictor (VEP)
vcfanno
GENMOD
GLnexus
Stranger
SVDB
wigToBigWig
Rare diseases
Whole genome sequencing