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echtvar

imported

software/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.

record
Category
Software & Systems
Subcategory
unknown
License
MIT(osi)
Status
active
Maturity
deployed
Organization
unknown
Country
unknown
Documentation
unknown
Tags
genetic-variants · genomics · variant-analysis · variant-annotations
Regulatory
unknown
built by · 6

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.

similar by tags

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

sources
  1. api.github.com/repos/brentp/echtvar
    retrieved 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 →

machine-readable

/v1/entries/46.json→ .entries["echtvar"]

Entries are sharded 64 ways by a stable hash of the id, so a consumer can find any record without an index.