echtvar
importedsoftware/echtvar
using all the bits for echt rapid variant annotation and filtering
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
- unknown
- Country
- unknown
- Repository
- github.com/brentp/echtvar
- Documentation
- unknown
- Tags
- genetic-variants · genomics · variant-analysis · variant-annotations
- 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.
- NCHHSTP-DTBE-Varpipe-WGSgenomics · variant-annotations
This repository contains an analysis pipeline developed to characterize WGS output
- hgvsgenomics · variant-analysis
Python library to parse, format, validate, normalize, and map sequence variants according to HGVS Nomenclature (https://hgvs-nomenclature.org/).
- slivargenomics · variant-analysis
genetic variant expressions, annotation, and filtering for great good.
- vcf_filteringgenomics · variant-analysis
Filter a VCF to discard false positive variants
- cellSNPgenetic-variants
Pileup biallelic SNPs from single-cell and bulk RNA-seq data
- cellsnp-litegenetic-variants
Efficient genotyping bi-allelic SNPs on single cells
- api.github.com/repos/brentp/echtvarretrieved 2026-08-05 · via github-api
Machine-imported from GitHub search. Last push 2026-07-22, 163 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 →
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