516 Followers
34 Following
742 Posts
A community effort to collect a curated set of analysis pipelines built using Nextflow
Websitehttps://nf-co.re
Githubhttps://github.com/nf-core
Release v4.0.0 - Chinese Baozi - 2026-06-27 · nf-core/funcscan

v4.0.0 - Chinese Baozi - [2026-06-27] Breaking change #530 Updated AMPcombi, changed parameter amp_ampcombi_cluster_removesingletons into amp_ampcombi_cluster_keepsingletons. (by @jasmezz, @jfy13...

GitHub

Pipeline release! nf-core/scnanoseq v1.3.0 - nf-core/scnanoseq v1.3.0 - Steel Elephant!
Single-cell/nuclei pipeline for data derived from Oxford Nanopore and 10X Genomics
Please see the changelog: https://github.com/nf-core/scnanoseq/releases/tag/1.3.0

#10xgenomics #longreadsequencing #nanopore #rnaseq #rnaseq #scrnaseq #singlecell #nfcore #openscience #nextflow #bioinformatics

Release nf-core/scnanoseq v1.3.0 - Steel Elephant · nf-core/scnanoseq

v1.3.0 [2026-06-26] Credits Special thanks to a new contributor to scnanoseq: Nick Youngblut Enhancements #94 Strict syntax conversion: converted entire workflow to strict syntax and reorganized...

GitHub

Pipeline release! nf-core/longraredisease v1.0.0 - 1.0.0!
Long read sequencing pipeline to identify variants in patients with neurodevelopmental disorders
Please see the changelog: https://github.com/nf-core/longraredisease/releases/tag/1.0.0

#nfcore #openscience #nextflow #bioinformatics

Release 1.0.0 · nf-core/longraredisease

Initial release of nf-core/longraredisease, created with the nf-core template. This release provides an end-to-end pipeline for comprehensive variant detection: structural variants (SV), single-nuc...

GitHub

Pipeline release! nf-core/pairgenomealign v3.0.0 - nf-core/pairgenomealign v3.0.0 – Tokoroten!
Pairwise genome comparison pipeline using the LAST software to align a list of query genomes to a target genome, and plot the results
Please see the changelog: https://github.com/nf-core/pairgenomealign/releases/tag/3.0.0

#comparativegenomics #dotplot #genomics #last #pairwisealignment #synteny #wholegenomealignment #nfcore #openscience #nextflow #bioinformatics

Release nf-core/pairgenomealign v3.0.0 – Tokoroten · nf-core/pairgenomealign

v3.0.0 "Tokoroten" - [June 26th 2026] Breaking changes Simplify output file names by removing _aln and _plt. Update all modules to latest versions. Use the default CRAM format from samtools (CRAM ...

GitHub

Pipeline release! nf-core/metatdenovo v1.4.0 - Download improvements and more!
Assembly and annotation of metatranscriptomic or metagenomic data for prokaryotic, eukaryotic and viruses.
Please see the changelog: https://github.com/nf-core/metatdenovo/releases/tag/1.4.0

#eukaryotes #metagenomics #metatranscriptomics #prokaryotes #viruses #nfcore #openscience #nextflow #bioinformatics

Release Download improvements and more · nf-core/metatdenovo

This release addresses key issues with database files: The inbuilt domain for the eggNOG database has disappeared. The download tool now bypasses that to retrieve files from an alternative source....

GitHub

Pipeline release! nf-core/pacvar v1.1.0 - Neon tetra!
Longread PacBio sequencing processing for WGS and PureTarget
Please see the changelog: https://github.com/nf-core/pacvar/releases/tag/1.1.0

#alignment #longread #pacbio #puretarget #variantcalling #wgs #nfcore #openscience #nextflow #bioinformatics

Release Neon tetra · nf-core/pacvar

nf-core/pacvar 1.1.0 - Neon tetra nf-core/pacvar 1.1.0 expands the WGS workflow with major new PacBio long-read analysis capabilities, including copy number variant calling (hificnv), optional sawf...

GitHub

Pipeline release! nf-core/raredisease v3.1.1 - 3.1.1 - Princess Peach (patch)!
Call and score variants from WGS/WES of rare disease patients.
Please see the changelog: https://github.com/nf-core/raredisease/releases/tag/3.1.1

#diagnostics #raredisease #snv #structuralvariants #variantannotation #variantcalling #wes #wgs #nfcore #openscience #nextflow #bioinformatics

Release 3.1.1 - Princess Peach (patch) · nf-core/raredisease

What's Changed Release 3.1.1 (Patch deepvariant/rundeepvariant to detect silent failures) by @ramprasadn in #889 Full Changelog: 3.1.0...3.1.1

GitHub

Pipeline release! nf-core/demo v1.2.0 - nf-core/demo 1.2.0 - Sleeping Kiwi!
nf-core/demo is a simple nf-core style bioinformatics pipeline for workshops and demos.
Please see the changelog: https://github.com/nf-core/demo/releases/tag/1.2.0

#demo #minimalexample #training #tutorial #nfcore #openscience #nextflow #bioinformatics

Release nf-core/demo 1.2.0 - Sleeping Kiwi · nf-core/demo

Changed #54 Changed the test_full.config input samplesheet #56 Updated to nf-core template 4.0.2 #57 Added a new local module COWPY without resource label Dependencies Dependency Old version N...

GitHub

Pipeline release! nf-core/fastquorum v2.0.0 - 2.0.0!
Pipeline to produce consensus reads using unique molecular indexes/barcodes (UMIs)
Please see the changelog: https://github.com/nf-core/fastquorum/releases/tag/2.0.0

#consensus #umi #umis #uniquemolecularidentifier #nfcore #openscience #nextflow #bioinformatics

Release 2.0.0 · nf-core/fastquorum

What's Changed New Features Add non-random UMI correction via fgbio CorrectUmis, enabled by an optional umi_file column in the samplesheet #145 Add optional library_id, lane, and flowcell samplesh...

GitHub

Pipeline release! nf-core/differentialabundance v2.0.0 - v2.0.0 - 2026-06-23!
Differential abundance analysis for feature/ observation matrices from platforms such as RNA-seq
Please see the changelog: https://github.com/nf-core/differentialabundance/releases/tag/2.0.0

#atacseq #chipseq #deseq2 #differentialabundance #differentialexpression #gsea #limma #microarray #rnaseq #shiny #nfcore #openscience #nextflow #bioinformatics

Release v2.0.0 - 2026-06-23 · nf-core/differentialabundance

What's Changed Template update for nf-core/tools v2.14.1 by @WackerO in #273 Show >10 contrasts in report by @pinin4fjords in #272 Fix pagination on samples table by @pinin4fjords in #274 Fix gpro...

GitHub