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10 repository supportati

Mostra repository con issue indicizzate
nf-core/crisprvarNextflow

[WIP] Evaluate outcomes from genome editing experiments

Ultimo commit 10 lug 2019

 (5 star) (5 fork) (0 issue indicizzate) (0 good first issue aperte)
nf-core/deepmodeloptimNextflow

Stochastic Testing and Input Manipulation for Unbiased Learning Systems

Ultimo commit 30 apr 2026

 (31 star) (15 fork) (6 issue indicizzate) (6 good first issue aperte)
nf-core/deepvariantNextflow

Please consider using/contributing to https://github.com/nf-core/sarek

Ultimo commit 13 lug 2021

 (41 star) (26 fork) (4 issue indicizzate) (4 good first issue aperte)
nf-core/genomeqcNextflow

Compare the quality of multiple genomes, along with their annotations.

Ultimo commit 24 lug 2026

 (24 star) (24 fork) (3 issue indicizzate) (1 good first issue aperta)
nf-core/hlatypingNextflow

Precision HLA typing from next-generation sequencing data

Ultimo commit 10 lug 2026

 (81 star) (37 fork) (0 issue indicizzate) (0 good first issue aperte)
nf-core/kmermaidNextflow

k-mer similarity analysis pipeline

Ultimo commit 27 lug 2026

 (24 star) (16 fork) (0 issue indicizzate) (0 good first issue aperte)
nf-core/pathogensurveillanceNextflow

Surveillance of pathogens using population genomics and sequencing

Ultimo commit 24 lug 2026

 (61 star) (9 fork) (3 issue indicizzate) (1 good first issue aperta)
nf-core/proteinannotatorNextflow

Generation of sequence-level annotations for amino acid sequences

Ultimo commit 27 lug 2026

 (14 star) (13 fork) (0 issue indicizzate) (0 good first issue aperte)
nf-core/sarekNextflow

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

Ultimo commit 30 lug 2026

 (589 star) (539 fork) (6 issue indicizzate) (6 good first issue aperte)
nf-core/variantprioritizationNextflow

Bioinformatics analysis pipeline for the functional annotation and translation of somatic SNVs/InDels and copy number abberations for precision cancer medicine using Personal Cancer Genome Reporter (PCGR). The pipeline offers germline SNVs/INDELS intepretation and annotation using Cancer Predisposition Sequencing Reporter (CPSR).

Ultimo commit 3 giu 2026

 (15 star) (12 fork) (0 issue indicizzate) (0 good first issue aperte)