dysgu
importedsoftware/dysgu
Toolkit for calling structural variants using short or long reads
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/kcleal/dysgu
- Documentation
- unknown
- Tags
- bioinformatics · genomics · long-read · paired-end · structural · structural-variation · variant · variant-calling
- 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.
- pacvarlong-read · variant-calling
Longread PacBio sequencing processing for WGS and PureTarget
- arcsvgenomics · structural-variation · variant-calling
Complex structural variant detection from WGS data
- Varathongenomics · structural-variation · variant-calling
A scalable variant calling and benchmarking framework supporting both short and long reads.
- PopDelbioinformatics · structural-variation · variant-calling
Population-wide Deletion Calling
- gatk-svbioinformatics · genomics · structural-variation
A structural variation pipeline for short-read sequencing
- truvaribioinformatics · genomics · structural-variation
Structural variant toolkit for VCFs
- api.github.com/repos/kcleal/dysguretrieved 2026-08-05 · via github-api
Machine-imported from GitHub search. Last push 2026-07-14, 115 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/31.json→ .entries["dysgu"]
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