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  1. HAT Public

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

    Python 23

  2. 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 6

  3. 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 5

  4. 3D-CLUMP Public

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

    Python 1

  5. CNPI Public

    Software for Rapid Analyses of Human Copy Number Data

    C++ 3

  6. fitDNM Public

    Code for running fitDNM genome-wide by using Snakemake

    Python 4

Repositories

Showing 10 of 19 repositories
  • DiamondsDenovo Public

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

    0 MIT 0 0 0 Updated Mar 9, 2025
  • CNPI Public

    Software for Rapid Analyses of Human Copy Number Data

    C++ 3 MIT 0 0 0 Updated Feb 5, 2025
  • Hare Public

    A de novo variant caller leveraging Parabricks GPU accelerated variant calling

    Python 6 MIT 0 0 0 Updated Nov 4, 2024
  • ElGenomaPequeno Public Forked from tycheleturner/ElGenomaPequeno

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

    R 0 MIT 1 0 0 Updated Sep 25, 2024
  • diamonds Public
    0 MIT 0 0 0 Updated May 21, 2024
  • EBVDetector Public
    0 MIT 0 0 0 Updated May 5, 2024
  • HAT Public

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

    Python 23 MIT 0 1 0 Updated Mar 21, 2024
  • fitDNM Public

    Code for running fitDNM genome-wide by using Snakemake

    Python 4 MIT 0 0 0 Updated Mar 21, 2024
  • 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, and a phylogenetic tree file.

    Python 5 MIT 0 0 0 Updated Mar 21, 2024
  • WTC-11 Public

    WTC-11 Genome Cell Line Analysis

    1 MIT 0 0 0 Updated Feb 19, 2024

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