vc
importedsoftware/vc
A tutorial on structural variant calling for short read sequencing data
Machine-generated from the listed sources and not yet reviewed by a human.
- Category
- Software & Systems
- Subcategory
- unknown
- License
- BSD-3-Clause(osi)
- Status
- dormant
- Maturity
- deployed
- Organization
- unknown
- Country
- unknown
- Repository
- github.com/tobiasrausch/vc
- Documentation
- unknown
- Tags
- delly · genomics · genomics-analysis · genomics-visualization · structural-variation
- 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.
- FinaleToolkitgenomics · genomics-analysis
FinaleToolkit is a package and standalone program to extract fragmentation features of cell-free DNA from paired-end sequencing data.
- vcfdistgenomics · genomics-analysis
vcfdist: Accurately benchmarking phased variant calls
- cellargenomics · genomics-visualization
Interactive software tool for the assignment of cell types in single-cell studies.
- cogegenomics · genomics-visualization
CoGe (Comparative Genomics) Platform
- deepStatsgenomics · genomics-visualization
deepStats: a stastitical toolbox for deeptools and genomic signals
- ezancestrygenomics · genomics-visualization
Easy genetic ancestry predictions in Python
- api.github.com/repos/tobiasrausch/vcretrieved 2026-08-25 · via github-api
Machine-imported from GitHub search. Last push 2024-10-24, 46 stars, license reported as BSD-3-Clause. Category and schematic were assigned by keyword heuristics and are unreviewed.
Not yet verified by a human. Correct this record →
/v1/entries/30.json→ .entries["vc"]
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