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  1. Clinical-Genomics/scout Clinical-Genomics/scout Public

    VCF visualization interface

    HTML 150 46

  2. Clinical-Genomics/stranger Clinical-Genomics/stranger Public

    Tool to annotate outfiles from ExpansionHunter and TRGT with the pathologic implications of the repeat

    Python 28 6

  3. NBISweden/vcf2cytosure NBISweden/vcf2cytosure Public

    Convert VCF with structural variations to CytoSure format

    Python 2 2

  4. SciLifeLab/TIDDIT SciLifeLab/TIDDIT Public

    TIDDIT - structural variant calling

    Cython 66 13

  5. hbvdtools hbvdtools Public

    Human Background Variantion Database Tools

    Perl 2

  6. rhocall rhocall Public

    Call regions of homozygosity and make tentative UPD calls

    Python 9 3