RNA sequencing analysis pipeline using STAR, RSEM, HISAT2 or Salmon with gene/isoform counts and extensive quality control.

Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing

Repository to host tool-specific module files for the Nextflow DSL2 community!

Python package with helper tools for the nf-core community.

Assembly and binning of metagenomes

A single-cell RNAseq pipeline for 10X genomics data

ChIP-seq peak-calling, QC and differential analysis pipeline.

ATAC-seq peak-calling and QC analysis pipeline

Amplicon sequencing analysis workflow using DADA2 and QIIME2

Nanopore demultiplexing, QC and alignment pipeline

Pipeline to fetch metadata and raw FastQ files from public databases

A fully reproducible and state-of-the-art ancient DNA analysis pipeline

RNA-seq analysis pipeline for detection of gene-fusions

Methylation (Bisulfite-Sequencing) analysis pipeline using Bismark or bwa-meth + MethylDackel

Highly parallelised multi-taxonomic profiling of shotgun short- and long-read metagenomic data

Assembly and intrahost/low-frequency variant calling for viral samples

Test data to be used for automated testing with the nf-core pipelines

Analysis of Chromosome Conformation Capture data (Hi-C)

Config files used to define parameters specific to compute environments at different Institutions

Call and score variants from WGS/WES of rare disease patients.