3 blog posts, 10 pipeline releases, 6 upcoming events.

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nf-core newsletter

1st April 2025

Blog posts

nf-core survey 2025: the results
Results summary from the nf-core community survey 2025
26 Mar 2025 · by jfy133, FranBonath
Spring cleaning 2025
🧹
20 Mar 2025 · by maxulysse, jfy133
nf-core weekly help desk is coming to Asia-Pacific!
Join the APAC community for a weekly help desk.
10 Mar 2025 · by awgymer, christopher-hakkaart

New pipeline first releases! 🎉

These pipelines just had their very first release.

nf-core/genomeassembler v1.0.0 v1.0.1
Assembly and scaffolding of haploid / unphased genomes from long ONT or PacBio HiFi reads

Pipeline releases

nf-core/eager
v2.5.3 18 Mar 2025
nf-core/funcscan
v2.1.0 5 Mar 2025
nf-core/metatdenovo
v1.1.1 13 Mar 2025
nf-core/molkart
v1.1.0 6 Mar 2025
nf-core/pacvar
v1.0.1 6 Mar 2025
nf-core/scnanoseq
v1.1.0 18 Mar 2025
nf-core/scrnaseq
v4.0.0 11 Mar 2025
nf-core/taxprofiler
v1.2.3 13 Mar 2025
nf-core/variantbenchmarking
v1.1.0 v1.2.0 31 Mar 2025

Upcoming events

Talk Bytesize: nf-core/variantbenchmarking 1 Apr 2025
Kübra Narci, German Human Genome-Penome Archieve, DKFZ Heidelberg
Talk Bytesize: nf-core/proteinfamilies 8 Apr 2025
Evangelos Karatzas, EMBL-EBI, Cambridge
Talk #animal-genomics: April Meeting 16 Apr 2025
Damir Baranasic (MRC, London Institute of Medical Sciences, UK)
Talk Bytesize: nf-core/fastqrepair 13 May 2025
Tommaso Mazza, IRCCS Casa Sollievo della Sofferenza - Mendel
Hackathon Hackathon - May 2025 (Boston) 13 May 2025 – 14 May 2025
An in-person hackathon held in Boston
Talk #animal-genomics: May Meeting 21 May 2025
James Reecy (Iowa State University, USA)

In case you missed it

Nextflow Training Week - March 2025
10 Mar 2025 – 14 Mar 2025 Training
Hackathon - March 2025 (Online / Distributed)
24 Mar 2025 – 26 Mar 2025 Hackathon

New pipelines & proposals

New pipeline repositories

nf-core/proteinannotator
Generation of sequence-level annotations for amino acid sequences
nf-core/rarevariantburden In Development
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.
nf-core/variantprioritization In Development
Analysis pipeline for the functional annotation and translation of somatic SNVs/InDels and copy number aberations for precision cancer medicine.

Pipeline proposals

From nf-core/proposals

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