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    • Ultima Genomics bioinfo-utils
      Python
      11011Updated Aug 21, 2025Aug 21, 2025
    • jalign

      Public
      Alignment for SV/CNV calls
      Jupyter Notebook
      0001Updated Aug 20, 2025Aug 20, 2025
    • parascopy

      Public
      Copy number estimation and variant calling for duplicated genes using WGS.
      Python
      4001Updated Aug 20, 2025Aug 20, 2025
    • gatk

      Public
      Official code repository for GATK versions 4 and up
      Java
      610004Updated Aug 12, 2025Aug 12, 2025
    • UltimaGenomics repository for workflows compatible with AWS HealthOmics
      WDL
      51721Updated Aug 10, 2025Aug 10, 2025
    • hmftools

      Public
      Various algorithms for analysing genomics data
      Java
      62000Updated Aug 7, 2025Aug 7, 2025
    • gridss

      Public
      GRIDSS: the Genomic Rearrangement IDentification Software Suite
      Java
      73000Updated Aug 6, 2025Aug 6, 2025
    • Ultima scripts related to downstream processing of WGS, MRD, methylation analysis
      Jupyter Notebook
      0954Updated Jul 28, 2025Jul 28, 2025
    • HLA-LA

      Public
      Fast HLA type inference from whole-genome data
      C++
      42000Updated Jul 17, 2025Jul 17, 2025
    • cn.mops

      Public
      Fork of Bioconductor git repository for cn.mops. Contains UG-specific changes
      R
      4001Updated May 27, 2025May 27, 2025
    • picard

      Public
      A set of command line tools (in Java) for manipulating high-throughput sequencing (HTS) data and formats such as SAM/BAM/CRAM and VCF.
      Java
      380000Updated May 25, 2025May 25, 2025
    • igv

      Public
      Integrative Genomics Viewer. Fast, efficient, scalable visualization tool for genomics data and annotations
      Java
      397000Updated May 17, 2025May 17, 2025
    • tools for working with Bisulfite Sequencing data while preserving reads intrinsic dependencies
      Python
      46000Updated Dec 24, 2024Dec 24, 2024
    • FREEC

      Public
      Control-FREEC: Copy number and genotype annotation in whole genome and whole exome sequencing data
      C++
      51100Updated Aug 26, 2024Aug 26, 2024
    • On-demand self-hosted AWS EC2 runner for GitHub Actions
      JavaScript
      369000Updated Aug 11, 2024Aug 11, 2024
    • Assignment of known mutational signatures to individual samples and individual somatic mutations
      Python
      15000Updated Jun 24, 2024Jun 24, 2024
    • STAR

      Public
      RNA-seq aligner
      C
      530000Updated Feb 15, 2024Feb 15, 2024
    • Python
      16000Updated Jan 4, 2023Jan 4, 2023
    • leviosam2

      Public
      Fast and accurate coordinate conversion between assemblies
      C++
      17000Updated Nov 26, 2022Nov 26, 2022
    • delly

      Public
      DELLY2: Structural variant discovery by integrated paired-end and split-read analysis
      C++
      139000Updated Sep 13, 2022Sep 13, 2022
    • test-lfs

      Public
      test git lfs issues
      0000Updated May 17, 2022May 17, 2022
    • levioSAM

      Public
      Lift-over alignments from variant-aware references
      C++
      4000Updated Apr 1, 2022Apr 1, 2022