adVNTR
importedsoftware/advntr
A tool for genotyping Variable Number Tandem Repeats (VNTR) from sequence 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
- Homepage
- advntr.readthedocs.io/
- Repository
- github.com/mehrdadbakhtiari/adVNTR
- Documentation
- unknown
- Tags
- bioinformatics · genomics · genotype · next-generation-sequencing · 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.
- peddybioinformatics · genomics · genotype
genotype :: ped correspondence check, ancestry check, sex check. directly, quickly on VCF
- phaseimputebioinformatics · genomics · genotype
A bioinformatics pipeline to phase and impute genetic data
- svtyperbioinformatics · genomics · genotype
Bayesian genotyper for structural variants
- 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
- kGWASflowbioinformatics · genomics · structural-variation
kGWASflow is a Snakemake workflow for performing k-mers-based GWAS.
- api.github.com/repos/mehrdadbakhtiari/adVNTRretrieved 2026-08-25 · via github-api
Machine-imported from GitHub search. Last push 2024-12-06, 49 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/46.json→ .entries["advntr"]
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