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scnanoseq

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software/scnanoseq

Single-cell/nuclei pipeline for data derived from Oxford Nanopore and 10X Genomics

Machine-generated from the listed sources and not yet reviewed by a human.

record
Category
Software & Systems
Subcategory
unknown
License
MIT(osi)
Status
active
Maturity
deployed
Organization
nf-core
Country
unknown
Documentation
unknown
Tags
10xgenomics · long-read-sequencing · nanopore · nextflow · nf-core · pipeline · rna-seq · rnaseq
Regulatory
unknown
built by · 6

Top contributors by commit count, from the project’s public repository. Avatars are served by their origin, not stored here. To be removed from this list, open an issue.

similar by tags

Computed from shared tags, weighted so a rare tag counts for more than a common one. These are suggestions, not curated relationships.

  • spatialvi10xgenomics · nextflow · nf-core · pipeline

    Pipeline for processing spatially-resolved gene counts with spatial coordinates and image data. Designed for 10x Genomics Visium transcriptomics.

  • rnavarnextflow · nf-core · pipeline · rnaseq

    gatk4 RNA variant calling pipeline

  • Clair3-RNAlong-read-sequencing · nanopore · rna-seq

    Clair3-RNA - a long-read small variant caller for RNA sequencing data

  • zUMIspipeline · rna-seq · rnaseq

    zUMIs: A fast and flexible pipeline to process RNA sequencing data with UMIs

  • scrnaseq10xgenomics · nextflow · nf-core

    Single-cell RNA-Seq pipeline for barcode-based protocols such as 10x, DropSeq or SmartSeq, offering a variety of aligners and empty-droplet detection

  • diaproteomicsnextflow · nf-core · pipeline

    Automated quantitative analysis of DIA proteomics mass spectrometry measurements.

sources
  1. api.github.com/repos/nf-core/scnanoseq
    retrieved 2026-08-05 · via github-api

    Machine-imported from GitHub search. Last push 2026-07-28, 56 stars, license reported as MIT. Category and schematic were assigned by keyword heuristics and are unreviewed.

Not yet verified by a human. Correct this record →

machine-readable

/v1/entries/40.json→ .entries["scnanoseq"]

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