svtyper
importedsoftware/svtyper
Bayesian genotyper for structural variants
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
- hall-lab
- Country
- unknown
- Homepage
- unknown
- Repository
- github.com/hall-lab/svtyper
- Documentation
- unknown
- Tags
- bioinformatics · genomics · genotype · vcf
- 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.
- peddybioinformatics · genomics · genotype · vcf
genotype :: ped correspondence check, ancestry check, sex check. directly, quickly on VCF
- adVNTRbioinformatics · genomics · genotype
A tool for genotyping Variable Number Tandem Repeats (VNTR) from sequence data
- phaseimputebioinformatics · genomics · genotype
A bioinformatics pipeline to phase and impute genetic data
- cljambioinformatics · genomics · vcf
A DNA Sequence Alignment/Map (SAM) library for Clojure
- CuteVCFbioinformatics · genomics · vcf
simple viewer for variant call format using htslib
- cyvcf2bioinformatics · genomics · vcf
cython + htslib == fast VCF and BCF processing
- api.github.com/repos/hall-lab/svtyperretrieved 2026-08-05 · via github-api
Machine-imported from GitHub search. Last push 2026-04-13, 136 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["svtyper"]
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