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brentp avatar

brentp/smoove

0
View on GitHub↗
266 stars·21 forks·Go·Apache-2.0·4 views

Smoove

structural variant calling and genotyping with existing tools, but, smoothly.

Features

  • Variant Calling - Tool for streamlined structural variant calling.

Star history

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Open-source alternatives to Smoove

Similar open-source projects, ranked by how many features they share with Smoove.
  • broadgsa/gatkbroadgsa avatar

    broadgsa/gatk

    300View on GitHub↗

    Official code repository for GATK versions 1.0 through 3.7 (core engine). For GATK 4 code, see the https://github.com/broadinstitute/gatk repository

    Java
    View on GitHub↗300
  • dellytools/dellydellytools avatar

    dellytools/delly

    525View on GitHub↗

    DELLY2: Structural variant discovery by integrated paired-end and split-read analysis

    C++
    View on GitHub↗525
  • ekg/freebayesekg avatar

    ekg/freebayes

    871View on GitHub↗

    Bayesian haplotype-based genetic polymorphism discovery and genotyping.

    C++
    View on GitHub↗871
  • arq5x/lumpy-svarq5x avatar

    arq5x/lumpy-sv

    343View on GitHub↗

    lumpy: a general probabilistic framework for structural variant discovery

    C
    View on GitHub↗343
See all 9 alternatives to Smoove→

Frequently asked questions

What does brentp/smoove do?

structural variant calling and genotyping with existing tools, but, smoothly.

What are the main features of brentp/smoove?

The main features of brentp/smoove are: Variant Calling.

What are some open-source alternatives to brentp/smoove?

Open-source alternatives to brentp/smoove include: arq5x/lumpy-sv — lumpy: a general probabilistic framework for structural variant discovery. broadgsa/gatk — Official code repository for GATK versions 1.0 through 3.7 (core engine). For GATK 4 code, see the… dellytools/delly — DELLY2: Structural variant discovery by integrated paired-end and split-read analysis. ekg/freebayes — Bayesian haplotype-based genetic polymorphism discovery and genotyping. google/deepvariant — DeepVariant is a deep learning genotyping tool and DNA sequence analysis pipeline used to identify single nucleotide… illumina/manta — Structural variant and indel caller for mapped sequencing data.