NAVIP

Category

Software & Systems

Subcategory

unknown

License

GPL-3.0(osi)

Status

maintained

Maturity

deployed

Organization

unknown

Country

unknown

Homepage

unknown

Repository

github.com/bpucker/NAVIP

Documentation

unknown

Tags

genomics · re-sequencing · variant-annotation · variant-calling · variants

Regulatory

unknown

• janbaasner
• bpucker
• andreas-rempel

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.

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

• dv-triovariant-calling · variants

  dv-trio provides a pipeline to call variants for a trio (father-mother-child) using DeepVariants [1]. Genomic Variant Calling Files (gVCFs) created by DeepVariants are then co_called together using…

• peppervariant-calling · variants

  PEPPER-Margin-DeepVariant

• rarediseasevariant-annotation

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

• variantstore-servicegenomics · variants

  The Variantstore is a Java/Groovy-based service application implemented using the Micronaut framework and enables storage and access to information on genomic variants and metadata from a connected…

• Exomisergenomics · variants

  A Tool to Annotate and Prioritize Exome Variants

• arcsvgenomics · variant-calling

  Complex structural variant detection from WGS data

1. api.github.com/repos/bpucker/NAVIP
   retrieved 2026-08-05 · via github-api

   Machine-imported from GitHub search. Last push 2025-03-05, 9 stars, license reported as GPL-3.0. Category and schematic were assigned by keyword heuristics and are unreviewed.

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/v1/entries/35.json→ .entries["navip"]

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