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RUN-DVC

imported

software/run-dvc

Generalizing deep learning-based variant callers via domain adaptation and semi-supervised learning

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

record
Category
Software & Systems
Subcategory
unknown
License
BSD-3-Clause(osi)
Status
dormant
Maturity
deployed
Organization
kaist-ina
Country
unknown
Homepage
unknown
Documentation
unknown
Tags
bioinformatics · deep-learning · dna-sequencing · domain-adaptation · generalization · genomics · long-read-sequencing · ngs
Regulatory
unknown
built by · 1

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.

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  • ClairSbioinformatics · genomics · long-read-sequencing

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  • ClairS-TObioinformatics · genomics · long-read-sequencing

    ClairS-TO - a deep-learning method for tumor-only somatic variant calling

  • veritigbioinformatics · genomics · long-read-sequencing

    Sequence-level verification of structural variant assemblies against haplotype-resolved references

  • basevarbioinformatics · genomics · ngs

    This is the official development repository for BaseVar, which call variants for large-scale ultra low-pass (<1.0x) WGS data, especially for NIPT data

  • CalliNGS-NFbioinformatics · genomics · ngs

    GATK RNA-Seq Variant Calling in Nextflow

sources
  1. api.github.com/repos/kaist-ina/RUN-DVC
    retrieved 2026-08-05 · via github-api

    Machine-imported from GitHub search. Last push 2024-02-04, 9 stars, license reported as BSD-3-Clause. Category and schematic were assigned by keyword heuristics and are unreviewed.

Not yet verified by a human. Correct this record →

machine-readable

/v1/entries/20.json→ .entries["run-dvc"]

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