Skip to content
View dnil's full-sized avatar

Organizations

@Clinical-Genomics

Block or report dnil

Block user

Prevent this user from interacting with your repositories and sending you notifications. Learn more about blocking users.

You must be logged in to block users.

Maximum 250 characters. Please don't include any personal information such as legal names or email addresses. Markdown supported. This note will be visible to only you.
Report abuse

Contact GitHub support about this user’s behavior. Learn more about reporting abuse.

Report abuse

Pinned Loading

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

    VCF visualization interface

    HTML 175 51

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

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

    Python 37 6

  3. NBISweden/vcf2cytosure NBISweden/vcf2cytosure Public

    Convert VCF with structural variations to CytoSure format

    Python 2 4

  4. SciLifeLab/TIDDIT SciLifeLab/TIDDIT Public

    TIDDIT - structural variant calling

    Cython 77 16

  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 12 3