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Sniphles

imported

software/sniphles

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

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
collaborativebioinformatics
Country
unknown
Homepage
unknown
Documentation
unknown
Tags
structural-variation · variant-calling
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.

  • arcsvstructural-variation · variant-calling

    Complex structural variant detection from WGS data

  • dysgustructural-variation · variant-calling

    Toolkit for calling structural variants using short or 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

  • Varathonstructural-variation · variant-calling

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

  • dupholdstructural-variation

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

sources
  1. api.github.com/repos/collaborativebioinformatics/Sniphles
    retrieved 2026-08-05 · via github-api

    Machine-imported from GitHub search. Last push 2020-10-14, 12 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/13.json→ .entries["sniphles"]

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