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arcsv

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software/arcsv

Complex structural variant detection from WGS data

Machine-generated from the listed sources and not yet reviewed by a human.

record
Category
Software & Systems
Subcategory
unknown
License
MIT(osi)
Status
dormant
Maturity
deployed
Organization
SUwonglab
Country
unknown
Homepage
unknown
Documentation
unknown
Tags
genomics · structural-variation · variant-calling
Regulatory
unknown
built by · 2

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.

  • dysgugenomics · structural-variation · variant-calling

    Toolkit for calling structural variants using short or long reads

  • Varathongenomics · structural-variation · variant-calling

    A scalable variant calling and benchmarking framework supporting both short and long reads.

  • nRexstructural-variation · variant-calling

    nRex: Germline and somatic single-nucleotide, short indel and structural variant calling

  • PopDelstructural-variation · variant-calling

    Population-wide Deletion Calling

  • Sniphlesstructural-variation · variant-calling

    Sniphles is a read-based phasing approach for phased variant calling of structural variants.

  • dupholdgenomics · structural-variation

    don't get DUP'ed or DEL'ed by your putative SVs.

sources
  1. api.github.com/repos/SUwonglab/arcsv
    retrieved 2026-08-05 · via github-api

    Machine-imported from GitHub search. Last push 2025-01-10, 31 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/10.json→ .entries["arcsv"]

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