variantkey

Category

Software & Systems

Subcategory

unknown

License

MIT(osi)

Status

dormant

Maturity

deployed

Organization

genomics-dev

Country

unknown

Homepage

unknown

Repository

github.com/genomics-dev/variantkey

Documentation

unknown

Tags

alternate-allele · base · chromosome · dna · genetic · genomics · human-genetic-variants · nucleotides · position · reference-allele · reference-genome · reference-position · rsid · variant-normalization · variantkey · variants

Regulatory

unknown

• nicolaasuni
• jrandall
• jebob
• Adriandorr
• thomasd-gen

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.

• pgltoolschromosome · genomics

  Paired Genomic Loci Tool Suite

• ref-solvergenomics · reference-genome

  Identify which human reference genome was used to align a BAM/SAM/CRAM file

• CuteVCFgenomics · variants

  simple viewer for variant call format using htslib

• NAVIPgenomics · variants

  Neighborhood-Aware Variant Impact Predictor

• rare-disease-wfgenomics · variants

  (WIP) best-practices workflow for rare disease

• 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…

1. api.github.com/repos/genomics-dev/variantkey
   retrieved 2026-08-25 · via github-api

   Machine-imported from GitHub search. Last push 2023-06-08, 43 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 →

/v1/entries/29.json→ .entries["variantkey"]

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