MindTheGap
importedsoftware/mindthegap
MindTheGap is a SV caller for short read sequencing data dedicated to insertion variants (all sizes and types). It can also be used as a local assembly tool.
Machine-generated from the listed sources and not yet reviewed by a human.
- Category
- Software & Systems
- Subcategory
- unknown
- License
- AGPL-3.0(osi)
- Status
- dormant
- Maturity
- deployed
- Organization
- GATB
- Country
- unknown
- Homepage
- unknown
- Repository
- github.com/GATB/MindTheGap
- Documentation
- unknown
- Tags
- bioinformatics · debruijn-graph · gatb · genomics · structural-variants
- Regulatory
- unknown
Computed from shared tags, weighted so a rare tag counts for more than a common one. These are suggestions, not curated relationships.
- gatk-svbioinformatics · genomics · structural-variants
A structural variation pipeline for short-read sequencing
- veritigbioinformatics · genomics · structural-variants
Sequence-level verification of structural variant assemblies against haplotype-resolved references
- OctopuSVgenomics · structural-variants
Merge and compare structural variants across callers, samples, and platforms. Standardizes BND-heavy output from GRIDSS, SvABA, Sniffles, and more.
- rarediseasestructural-variants
Call and score variants from WGS/WES of rare disease patients.
- variantbenchmarkingstructural-variants
Pipeline to evaluate and validate the accuracy of variant calling methods in genomic research
- adambioinformatics · genomics
ADAM is a genomics analysis platform with specialized file formats built using Apache Avro, Apache Spark, and Apache Parquet. Apache 2 licensed.
- api.github.com/repos/GATB/MindTheGapretrieved 2026-08-25 · via github-api
Machine-imported from GitHub search. Last push 2022-04-20, 37 stars, license reported as AGPL-3.0. Category and schematic were assigned by keyword heuristics and are unreviewed.
Not yet verified by a human. Correct this record →
/v1/entries/44.json→ .entries["mindthegap"]
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