truvari
importedsoftware/truvari
Structural variant toolkit for VCFs
Machine-generated from the listed sources and not yet reviewed by a human.
- Category
- Software & Systems
- Subcategory
- unknown
- License
- MIT(osi)
- Status
- active
- Maturity
- deployed
- Organization
- unknown
- Country
- unknown
- Homepage
- unknown
- Repository
- github.com/ACEnglish/truvari
- Documentation
- unknown
- Tags
- annotation-tool · benchmarking · bioinformatics · data-science · genomics · sequencing · structural-variation · sv-merging
- Regulatory
- unknown
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.
- open-cravatannotation-tool · bioinformatics · genomics
A modular annotation tool for genomic variants
- nRexsequencing · structural-variation
nRex: Germline and somatic single-nucleotide, short indel and structural variant calling
- dysgubioinformatics · genomics · structural-variation
Toolkit for calling structural variants using short or long reads
- gatk-svbioinformatics · genomics · structural-variation
A structural variation pipeline for short-read sequencing
- cievadbenchmarking · bioinformatics · genomics
A tool suite for a simple, streamlined and rapid evaluation of variant callsets
- GenomicSQLitebioinformatics · genomics · sequencing
Genomics Extension for SQLite
- api.github.com/repos/ACEnglish/truvariretrieved 2026-08-05 · via github-api
Machine-imported from GitHub search. Last push 2026-05-22, 420 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/50.json→ .entries["truvari"]
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