CuteVCF
importedsoftware/cutevcf
simple viewer for variant call format using htslib
Machine-generated from the listed sources and not yet reviewed by a human.
- Category
- Software & Systems
- Subcategory
- unknown
- License
- GPL-3.0(osi)
- Status
- dormant
- Maturity
- deployed
- Organization
- labsquare
- Country
- unknown
- Homepage
- unknown
- Repository
- github.com/labsquare/CuteVCF
- Documentation
- unknown
- Tags
- bioinformatics · genomics · gui · qt5 · variants · vcf
- Regulatory
- unknown
Computed from shared tags, weighted so a rare tag counts for more than a common one. These are suggestions, not curated relationships.
- FastQtbioinformatics · gui · qt5
FastQC port to Qt5: A quality control tool for high throughput sequence data.
- ugenebioinformatics · qt5
UGENE is free open-source cross-platform bioinformatics software
- cljambioinformatics · genomics · vcf
A DNA Sequence Alignment/Map (SAM) library for Clojure
- cyvcf2bioinformatics · genomics · vcf
cython + htslib == fast VCF and BCF processing
- gnomAD_DBbioinformatics · genomics · vcf
Scalable SQLite database for fast querying of gnomAD variant annotations (allele frequency, depth, population metrics). Supports gnomAD v2-v4, WGS and WES.
- gorbioinformatics · genomics · vcf
GORpipe is a tool based on a genomic ordered relational architecture and allows analysis of large sets of genomic and phenotypic tabular data using declarative query language, in a parallel…
- api.github.com/repos/labsquare/CuteVCFretrieved 2026-08-25 · via github-api
Machine-imported from GitHub search. Last push 2017-01-17, 33 stars, license reported as GPL-3.0. Category and schematic were assigned by keyword heuristics and are unreviewed.
Not yet verified by a human. Correct this record →
/v1/entries/33.json→ .entries["cutevcf"]
Entries are sharded 64 ways by a stable hash of the id, so a consumer can find any record without an index.