Sniphles
importedsoftware/sniphles
Sniphles is a read-based phasing approach for phased variant calling of structural variants.
Machine-generated from the listed sources and not yet reviewed by a human.
- Category
- Software & Systems
- Subcategory
- unknown
- License
- MIT(osi)
- Status
- dormant
- Maturity
- deployed
- Organization
- collaborativebioinformatics
- Country
- unknown
- Homepage
- unknown
- Documentation
- unknown
- Tags
- structural-variation · 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.
- arcsvstructural-variation · variant-calling
Complex structural variant detection from WGS data
- dysgustructural-variation · variant-calling
Toolkit for calling structural variants using short or long reads
- nRexstructural-variation · variant-calling
nRex: Germline and somatic single-nucleotide, short indel and structural variant calling
- PopDelstructural-variation · variant-calling
Population-wide Deletion Calling
- Varathonstructural-variation · variant-calling
A scalable variant calling and benchmarking framework supporting both short and long reads.
- dupholdstructural-variation
don't get DUP'ed or DEL'ed by your putative SVs.
- api.github.com/repos/collaborativebioinformatics/Sniphlesretrieved 2026-08-05 · via github-api
Machine-imported from GitHub search. Last push 2020-10-14, 12 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/13.json→ .entries["sniphles"]
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