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cievad

imported

software/cievad

A tool suite for a simple, streamlined and rapid evaluation of variant callsets

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

record
Category
Software & Systems
Subcategory
unknown
License
GPL-3.0(osi)
Status
dormant
Maturity
deployed
Organization
rki-mf1
Country
unknown
Documentation
unknown
Tags
benchmarking · bioinformatics · genomics · indels · nextflow · ngs · oxford-nanopore · snps
Regulatory
unknown
built by · 2

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.

  • snpkitgenomics · ngs · snps

    Modular workflow for Microbial Variant Calling and SNP diagnostics.

  • readfishbioinformatics · genomics · oxford-nanopore

    CLI tool for flexible and fast adaptive sampling on ONT sequencers

  • CalliNGS-NFbioinformatics · genomics · nextflow · ngs

    GATK RNA-Seq Variant Calling in Nextflow

  • ClairSbioinformatics · genomics · indels

    ClairS: a deep-learning method for long-read tumor–normal pair somatic small variant calling

  • snippybioinformatics · genomics · snps

    :scissors: :zap: Rapid haploid variant calling and core genome alignment

  • VariantCallerindels · snps

    VariantCaller is a wrapper for the 2022 gatk & bcftools best practices + phasing with WhatsHap.

sources
  1. api.github.com/repos/rki-mf1/cievad
    retrieved 2026-08-05 · via github-api

    Machine-imported from GitHub search. Last push 2024-09-16, 6 stars, license reported as GPL-3.0. Category and schematic were assigned by keyword heuristics and are unreviewed.

Not yet verified by a human. Correct this record →

machine-readable

/v1/entries/27.json→ .entries["cievad"]

Entries are sharded 64 ways by a stable hash of the id, so a consumer can find any record without an index.