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variantbenchmarking

imported

software/variantbenchmarking

Pipeline to evaluate and validate the accuracy of variant calling methods in genomic research

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
benchmark · nextflow · nf-core · pipeline · small-variants · structural-variants · variant-calling · workflow
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.

  • rarediseasenextflow · nf-core · pipeline · structural-variants

    Call and score variants from WGS/WES of rare disease patients.

  • diaproteomicsnextflow · nf-core · pipeline · workflow

    Automated quantitative analysis of DIA proteomics mass spectrometry measurements.

  • proteinannotatornextflow · nf-core · pipeline · workflow

    Generation of sequence-level annotations for amino acid sequences

  • toolsnextflow · nf-core · pipeline · workflow

    Python package with helper tools for the nf-core community.

  • pacvarnextflow · nf-core · pipeline · variant-calling

    Longread PacBio sequencing processing for WGS and PureTarget

  • rnavarnextflow · nf-core · pipeline · variant-calling

    gatk4 RNA variant calling pipeline

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

    Machine-imported from GitHub search. Last push 2026-07-28, 51 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/51.json→ .entries["variantbenchmarking"]

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