Pinned Repositories
ampliseq
Amplicon sequencing analysis workflow using DADA2 and QIIME2
chipseq
ChIP-seq peak-calling, QC and differential analysis pipeline.
configs
Config files used to define parameters specific to compute environments at different Institutions
mag
Assembly and binning of metagenomes
modules
Repository to host tool-specific module files for the Nextflow DSL2 community!
proposals
Where new ideas for nf-core pipelines, special interest groups and more are proposed
rnaseq
RNA sequencing analysis pipeline using STAR, RSEM, HISAT2 or Salmon with gene/isoform counts and extensive quality control.
sarek
Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing
scrnaseq
Single-cell RNA-Seq pipeline for barcode-based protocols such as 10x, DropSeq or SmartSeq, offering a variety of aligners and empty-droplet detection
tools
Python package with helper tools for the nf-core community.
nf-core's Repositories
nf-core/sarek
Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing
nf-core/modules
Repository to host tool-specific module files for the Nextflow DSL2 community!
nf-core/tools
Python package with helper tools for the nf-core community.
nf-core/mag
Assembly and binning of metagenomes
nf-core/ampliseq
Amplicon sequencing analysis workflow using DADA2 and QIIME2
nf-core/atacseq
ATAC-seq peak-calling and QC analysis pipeline
nf-core/eager
A fully reproducible and state-of-the-art ancient DNA analysis pipeline
nf-core/taxprofiler
Highly parallelised multi-taxonomic profiling of shotgun short- and long-read metagenomic data
nf-core/viralrecon
Assembly and intrahost/low-frequency variant calling for viral samples
nf-core/test-datasets
Test data to be used for automated testing with the nf-core pipelines
nf-core/configs
Config files used to define parameters specific to compute environments at different Institutions
nf-core/website
Code and files for the main nf-core website.
nf-core/epitopeprediction
A bioinformatics best-practice analysis pipeline for epitope prediction and annotation
nf-core/variantbenchmarking
Pipeline to evaluate and validate the accuracy of variant calling methods in genomic research
nf-core/hgtseq
A pipeline to investigate horizontal gene transfer from NGS data
nf-core/phaseimpute
A bioinformatics pipeline to phase and impute genetic data
nf-core/detaxizer
A pipeline to identify (and remove) certain sequences from raw genomic data. Default taxon to identify (and remove) is Homo sapiens. Removal is optional.
nf-core/genomeqc
Compare the quality of multiple genomes, along with their annotations.
nf-core/createtaxdb
Parallelised and automated construction of metagenomic classifier databases of different tools
nf-core/seqinspector
QC pipeline to inspect your sequences
nf-core/molkart
A pipeline for processing Molecular Cartography data from Resolve Bioscience (combinatorial FISH)
nf-core/metapep
From metagenomes to epitopes and beyond
nf-core/rnadnavar
Pipeline for RNA and DNA integrated analysis for somatic mutation detection
nf-core/meerpipe
nf-core/meerpipe is a astronomy pipeline that processes MeerKAT pulsar data to produce images and data products for pulsar timing analysis
nf-core/logos
Host nf-core logos and templates for making new logos
nf-core/lsmquant
A pipeline for processing and analysis of light-sheet microscopy images.
nf-core/sammyseq
Pipeline for Sequential Analysis of MacroMolecules accessibilitY sequencing (SAMMY-seq) data, to analyze chromatin state.
nf-core/ops
Different *Ops related scripts for the nf-core org.
nf-core/panoramaseq
a pipeline to process sequencing based spatial transccriptomics data from in-situ arrays
nf-core/rarevariantburden
Pipeline for performing consistent summary count based rare variant burden test, which is useful when we only have sequenced cases data. For example, we can compare the cases against public summary count data, such as gnomAD.