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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 sequencingmodules
Repository to host tool-specific module files for the Nextflow DSL2 community!tools
Python package with helper tools for the nf-core community.mag
Assembly and binning of metagenomesscrnaseq
A single-cell RNAseq pipeline for 10X genomics datachipseq
ChIP-seq peak-calling, QC and differential analysis pipeline.atacseq
ATAC-seq peak-calling and QC analysis pipelineampliseq
Amplicon sequencing analysis workflow using DADA2 and QIIME2nanoseq
Nanopore demultiplexing, QC and alignment pipelinefetchngs
Pipeline to fetch metadata and raw FastQ files from public databaseseager
A fully reproducible and state-of-the-art ancient DNA analysis pipelinernafusion
RNA-seq analysis pipeline for detection of gene-fusionsmethylseq
Methylation (Bisulfite-Sequencing) analysis pipeline using Bismark or bwa-meth + MethylDackeltaxprofiler
Highly parallelised multi-taxonomic profiling of shotgun short- and long-read metagenomic dataviralrecon
Assembly and intrahost/low-frequency variant calling for viral samplestest-datasets
Test data to be used for automated testing with the nf-core pipelinesconfigs
Config files used to define parameters specific to compute environments at different Institutionsraredisease
Call and score variants from WGS/WES of rare disease patients.hic
Analysis of Chromosome Conformation Capture data (Hi-C)cutandrun
Analysis pipeline for CUT&RUN and CUT&TAG experiments that includes QC, support for spike-ins, IgG controls, peak calling and downstream analysis.smrnaseq
A small-RNA sequencing analysis pipelinefuncscan
(Meta-)genome screening for functional and natural product gene sequenceswebsite
Code and files for the main nf-core website.pangenome
Renders a collection of sequences into a pangenome graph.hlatyping
Precision HLA typing from next-generation sequencing databacass
Simple bacterial assembly and annotation pipelinedifferentialabundance
Differential abundance analysis for feature/ observation matrices from platforms such as RNA-seqairrflow
B-cell and T-cell Adaptive Immune Receptor Repertoire (AIRR) sequencing analysis pipeline using the Immcantation frameworkbactmap
A mapping-based pipeline for creating a phylogeny from bacterial whole genome sequencesproteinfold
Protein 3D structure prediction pipelinespatialvi
Pipeline for processing spatially-resolved gene counts with spatial coordinates and image data. Designed for 10x Genomics Visium transcriptomics.circrna
circRNA quantification, differential expression analysis and miRNA target prediction of RNA-Seq datarnasplice
rnasplice is a bioinformatics pipeline for RNA-seq alternative splicing analysisdemultiplex
Demultiplexing pipeline for sequencing dataepitopeprediction
A bioinformatics best-practice analysis pipeline for epitope prediction and annotationoncoanalyser
A comprehensive cancer DNA/RNA analysis and reporting pipelinernavar
gatk4 RNA variant calling pipelineproteomicslfq
Proteomics label-free quantification (LFQ) analysis pipelinemhcquant
Identify and quantify MHC eluted peptides from mass spectrometry raw datacircdna
Pipeline for the identification of extrachromosomal circular DNA (ecDNA) from Circle-seq, WGS, and ATAC-seq data that were generated from cancer and other eukaryotic cells.isoseq
Genome annotation with PacBio Iso-Seq. Takes raw subreads as input, generate Full Length Non Chemiric (FLNC) sequences and produce a bed annotation.readsimulator
A pipeline to simulate sequencing reads, such as Amplicon, Target Capture, Metagenome, and Whole genome data.scdownstream
A single cell transcriptomics pipeline for QC, integration and making the data presentablecrisprseq
A pipeline for the analysis of CRISPR edited data. It allows the evaluation of the quality of gene editing experiments using targeted next generation sequencing (NGS) data (`targeted`) as well as the discovery of important genes from knock-out or activation CRISPR-Cas9 screens using CRISPR pooled DNA (`screening`).imcyto
Image Mass Cytometry analysis pipelinemetatdenovo
Assembly and annotation of metatranscriptomic or metagenomic data for prokaryotic, eukaryotic and viruses.bamtofastq
Converts bam or cram files to fastq format and does quality control.gwas
UNDER CONSTRUCTION: A pipeline for Genome Wide Association Studieshgtseq
A pipeline to investigate horizontal gene transfer from NGS datafastquorum
Pipeline to produce consensus reads using unique molecular indexes/barcodes (UMIs)clipseq
CLIP sequencing analysis pipeline for QC, pre-mapping, genome mapping, UMI deduplication, and multiple peak-calling options.cookiecutter
DEPRECIATED! Please use nf-core/tools insteadkmermaid
k-mer similarity analysis pipelinedualrnaseq
Analysis of Dual RNA-seq data - an experimental method for interrogating host-pathogen interactions through simultaneous RNA-seq.nascent
Nascent Transcription Processing Pipelinegenomeannotator
Pipeline for the identification of (coding) gene structures in draft genomes.viralintegration
Analysis pipeline for the identification of viral integration events in genomes using a chimeric read approach.exoseq
Please consider using/contributing to https://github.com/nf-core/sarekphaseimpute
metaboigniter
Pre-processing of mass spectrometry-based metabolomics data with quantification and identification based on MS1 and MS2 data.genomeassembler
vipr
Assembly and intrahost / low-frequency variant calling for viral samplesvscode-extensionpack
A VSCode extension pack for nf-core developers.multiplesequencealign
A pipeline to run and systematically evaluate Multiple Sequence Alignment (MSA) methods.nanostring
An analysis pipeline for Nanostring nCounter expression data.scnanoseq
Single-cell/nuclei pipeline for data derived from Oxford Nanopore and 10X Genomicsdetaxizer
A pipeline to identify (and remove) certain sequences from raw genomic data. Default taxa to identify (and remove) are Homo and Homo sapiens. Removal is optional.diaproteomics
Automated quantitative analysis of DIA proteomics mass spectrometry measurements.setup-nextflow
A GitHub action to install Nextflowcageseq
CAGE-sequencing analysis pipeline with trimming, alignment and counting of CAGE tags.pathogensurveillance
Surveillance of pathogens using population genomics and sequencingphageannotator
Pipeline for identifying, annotation, and quantifying phage sequences in (meta)-genomic sequences.mnaseseq
MNase-seq analysis pipeline using BWA and DANPOS2.coproid
Coprolite host Identification pipelinemolkart
A pipeline for processing Molecular Cartography data from Resolve Bioscience (combinatorial FISH)variantbenchmarking
A nextflow variant benchmarking pipeline - prematuretfactivity
Bioinformatics pipeline that makes use of expression and open chromatin data to identify differentially active transcription factors across conditions.variantcatalogue
Pipeline to generate variant catalogues, a list of variants and their frequencies in a population, from whole genome sequences.metapep
From metagenomes to epitopes and beyondpixelator
Pipeline to generate Molecular Pixelation data with Pixelator (Pixelgen Technologies AB)datasync
nf-core/datasync is a system operation pipeline that provides several workflows for handling system operation / automation tasksphyloplace
nf-core/phyloplace is a bioinformatics best-practice analysis pipeline that performs phylogenetic placement with EPA-NG.createtaxdb
Parallelised and automated construction of metagenomic classifier databases of different toolsmcmicro
An end-to-end processing pipeline that transforms multi-channel whole-slide images into single-cell data.createpanelrefs
Generate Panel of Normals, models or other similar references from lots of samplesprettier-plugin-nextflow
hicar
Pipeline for HiCAR data, a robust and sensitive multi-omic co-assay for simultaneous measurement of transcriptome, chromatin accessibility and cis-regulatory chromatin contacts.radseq
Variant-calling pipeline for Restriction site-associated DNA sequencing (RADseq).reportho
nf-core pipeline for comparative analysis of ortholog predictionsriboseq
Pipeline for the analysis of ribosome profiling, or Ribo-seq (also named ribosome footprinting) data.omicsgenetraitassociation
A nextflow pipeline which integrates multiple omic data streams and performs coordinated analysisgh-actions-lint
GitHub Action to run nf-core code linting on a Nextflow pipelinecrisprvar
[WIP] Evaluate outcomes from genome editing experimentsawsmegatests
CloudFormation templates to setup the aws megatests necessary cloud infrastructuremarsseq
MARS-seq v2 pre-processing pipeline with velocitytbanalyzer
An nf-core (meta) pipeline for analysis of different members of Mycobacterium tuberculosis complex.rnadnavar
Pipeline for RNA and DNA integrated analysis for somatic mutation detectionmeerpipe
nf-core/meerpipe is a astronomy pipeline that processes MeerKAT pulsar data to produce images and data products for pulsar timing analysiscallingcards
A pipeline for processing calling cards dataLove Open Source and this site? Check out how you can help us