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  1. HAT HAT Public

    HAT is a set of tools for calling de novo variants from whole-genome sequencing data.

    Python 24

  2. acorn acorn Public

    acorn is an R package that examines various features of de novo variants including subsetting DNVs by individual, variant type, or genomic region; calculating features including variant change coun…

    R 7

  3. ACES ACES Public

    ACES is a workflow to query small sequences in a large set of genomes. It provides several outputs including BLAST results, a multiple sequence alignment file, a graphical fragment assembly file, a…

    Python 6

  4. 3D-CLUMP 3D-CLUMP Public

    Software to test for clustering of missense variants in 3D protein structures.

    Python 2

  5. CNPI CNPI Public

    Software for Rapid Analyses of Human Copy Number Data

    C++ 6

  6. DiamondsDenovo DiamondsDenovo Public

    DiamondsDenovo is a tool to calculate enrichment of de novo variants in the genome

    Python 2

Repositories

Showing 10 of 19 repositories
  • Hare Public

    A de novo variant caller leveraging Parabricks GPU accelerated variant calling

    TNTurnerLab/Hare’s past year of commit activity
    Python 8 MIT 0 0 0 Updated Dec 12, 2025
  • HAT-FLEX Public

    Flexible Trio DNV detection on existing VCFs.

    TNTurnerLab/HAT-FLEX’s past year of commit activity
    Python 5 MIT 0 0 0 Updated Dec 8, 2025
  • acorn Public

    acorn is an R package that examines various features of de novo variants including subsetting DNVs by individual, variant type, or genomic region; calculating features including variant change counts, lengths, and presence/absence at CpG sites; and characteristics of parental age and number of DNVs.

    TNTurnerLab/acorn’s past year of commit activity
    R 7 MIT 0 0 0 Updated Nov 26, 2025
  • DiamondsDenovo Public

    DiamondsDenovo is a tool to calculate enrichment of de novo variants in the genome

    TNTurnerLab/DiamondsDenovo’s past year of commit activity
    Python 2 MIT 0 0 0 Updated Nov 21, 2025
  • HAT Public

    HAT is a set of tools for calling de novo variants from whole-genome sequencing data.

    TNTurnerLab/HAT’s past year of commit activity
    Python 24 MIT 0 0 0 Updated Nov 18, 2025
  • CNPI Public

    Software for Rapid Analyses of Human Copy Number Data

    TNTurnerLab/CNPI’s past year of commit activity
    C++ 6 MIT 0 0 0 Updated Aug 14, 2025
  • 3D-CLUMP Public

    Software to test for clustering of missense variants in 3D protein structures.

    TNTurnerLab/3D-CLUMP’s past year of commit activity
    Python 2 MIT 0 0 0 Updated Aug 5, 2025
  • TNTurnerLab/denovo-db_helper_scripts’s past year of commit activity
    Python 0 MIT 1 0 0 Updated Aug 4, 2025
  • ElGenomaPequeno Public Forked from tycheleturner/ElGenomaPequeno

    El genoma pequeño - analysis workflow for "the little genome"

    TNTurnerLab/ElGenomaPequeno’s past year of commit activity
    R 0 MIT 1 0 0 Updated Sep 25, 2024
  • fitDNM Public

    Code for running fitDNM genome-wide by using Snakemake

    TNTurnerLab/fitDNM’s past year of commit activity
    Python 5 MIT 0 0 0 Updated Mar 21, 2024

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